G. Ghiggeri

L. Gesualdo, G. Ghiggeri, G. Caridi, 2009, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Uromodulin: from monogenic to multifactorial diseases.

F. Scolari, C. Izzi, G. Ghiggeri, 2015, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Allelism of MCKD, FJHN and GCKD caused by impairment of uromodulin export dynamics.

F. Scolari, A. Amoroso, G. Ghiggeri, 2003, Human molecular genetics.

Immature renal structures associated with a novel UMOD sequence variant.

G. Ghiggeri, G. Caridi, E. Benetti, 2009, American journal of kidney diseases : the official journal of the National Kidney Foundation.

Defective Intracellular Trafficking of Uromodulin Mutant Isoforms

F. Scolari, A. Amoroso, G. Ghiggeri, 2006, Traffic.

IgA nephropathy: the presence of familial disease does not confer an increased risk for progression.

F. Scolari, C. Izzi, B. F. Viola, 2006, American journal of kidney diseases : the official journal of the National Kidney Foundation.

Clinical Characteristics and Treatment Patterns of Children and Adults With IgA Nephropathy or IgA Vasculitis: Findings From the CureGN Study

Craig S. Wong, V. D’Agati, C. Alpers, 2018, Kidney international reports.

Active focal segmental glomerulosclerosis is associated with massive oxidation of plasma albumin.

F. Scolari, G. Ghiggeri, G. Caridi, 2007, Journal of the American Society of Nephrology : JASN.

Characterization of cationic albumin in minimal change nephropathy.

G. Ghiggeri, R. Oleggini, F. Ginevri, 1987, Kidney international.

Type IV Collagen Mutations in Familial IgA Nephropathy

V. D’Agati, A. Gharavi, K. Kiryluk, 2020, Kidney international reports.

Diffusion-Weighted MRI in the Evaluation of Renal Parenchymal Involvement during Febrile Urinary Tract Infections in Children: Preliminary Data

G. Ghiggeri, M. Bodria, A. Pistorio, 2021, Journal of clinical medicine.

Autoantibody-mediated impairment of DNASE1L3 activity in sporadic systemic lupus erythematosus

Mimi Y. Kim, A. Tsirigos, Ali Rashidfarrokhi, 2021, The Journal of experimental medicine.

Drug-induced lupus: Traditional and new concepts.

G. Ghiggeri, A. Vaglio, P. Grayson, 2018, Autoimmunity reviews.

Lupus nephritis in children and adolescents: results of the Italian Collaborative Study.

A. Edefonti, L. Peruzzi, R. Coppo, 2013, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Randomised controlled trial comparing rituximab to mycophenolate mofetil in children and young adults with steroid-dependent idiopathic nephrotic syndrome: study protocol

P. Ravani, G. Ghiggeri, G. Caridi, 2021, BMJ Open.

Rituximab for very low dose steroid-dependent nephrotic syndrome in children: a randomized controlled study

M. Prunotto, P. Ravani, G. Ghiggeri, 2020, Pediatric Nephrology.

Rituximab in Children with Steroid-Dependent Nephrotic Syndrome: A Multicenter, Open-Label, Noninferiority, Randomized Controlled Trial.

A. Edefonti, F. Scolari, P. Ravani, 2015, Journal of the American Society of Nephrology : JASN.

Persistent Disease Activity in Patients With Long-Standing Glomerular Disease

Craig S. Wong, B. Rovin, J. Klein, 2020, Kidney international reports.

Searching for IgA nephropathy candidate genes: genetic studies combined with high throughput innovative investigations.

F. Scolari, A. Amoroso, G. Ghiggeri, 2007, Contributions to nephrology.

A prospective observational study of associated anomalies in Hirschsprung’s disease

G. Ghiggeri, G. Mattioli, C. Granata, 2013, Orphanet Journal of Rare Diseases.

Full Reviews Uromodulin: from monogenic to multifactorial diseases

F. Scolari, C. Izzi, G. Ghiggeri, 2015 .

Effects of hemodialysis on guanidinopropionic acid metabolism.

G. Ghiggeri, G. Deferrari, G. Salvidio, 1986, Nephron.

Micro‐injection of recombinant lysyl oxidase blocks oncogenic p21‐Ha‐Ras and progesterone effects on Xenopus laevis oocyte maturation

G. Ghiggeri, J. Lacal, A. Di Donato, 1997, FEBS letters.

Mutational Spectrum of CYP24A1 Gene in a Cohort of Italian Patients with Idiopathic Infantile Hypercalcemia

G. Ardissino, L. Gesualdo, G. Ghiggeri, 2016, Nephron.

Genetic approaches to human renal agenesis/hypoplasia and dysplasia

A. Gharavi, F. Scolari, S. Sanna-Cherchi, 2007, Pediatric Nephrology.

Hirschsprung Disease and Congenital Anomalies of the Kidney and Urinary Tract (CAKUT): A Novel Syndromic Association

G. Ghiggeri, M. Musso, G. Mattioli, 2009, Medicine.

Biological surface properties in extracellular vesicles and their effect on cargo proteins

G. Ghiggeri, I. Panfoli, Genny Del Zotto, 2019, Scientific Reports.

Combinatorial Peptide Ligand Library and two dimensional electrophoresis: new frontiers in the study of peritoneal dialysis effluent in pediatric patients.

A. Scaloni, G. Ghiggeri, E. Verrina, 2015, Journal of proteomics.

Proteome profile of peritoneal effluents in children on glucose- or icodextrin-based peritoneal dialysis.

G. Ghiggeri, E. Verrina, G. Candiano, 2011, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Glomerular Macrophages in Human Auto- and Allo-Immune Nephritis

A. Cavalli, M. Prunotto, L. Scapozza, 2021, Cells.

De Novo Donor-Specific HLA Antibodies Developing Early or Late after Transplant Are Associated with the Same Risk of Graft Damage and Loss in Nonsensitized Kidney Recipients

G. Ghiggeri, C. Klersy, M. Cioni, 2017, Journal of immunology research.

Acquisition of C3d‐Binding Activity by De Novo Donor‐Specific HLA Antibodies Correlates With Graft Loss in Nonsensitized Pediatric Kidney Recipients

G. Ghiggeri, C. Klersy, M. Cioni, 2016, American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons.

Posttransplant Soluble B-Cell Activating Factor Kinetics in Pediatric Recipients of First Kidney Allograft

G. Ghiggeri, C. Klersy, M. Cioni, 2015, Transplantation.

Posttransplant De Novo Donor‐Specific HLA Antibodies Identify Pediatric Kidney Recipients at Risk for Late Antibody‐Mediated Rejection

G. Ghiggeri, M. Cioni, A. Nocera, 2012, American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons.

Inhibition of renal permeability towards albumin: A new function of apolipoproteins with possible pathogenetic relevance in focal glomerulosclerosis

G. Ghiggeri, F. Ginevri, L. Musante, 2001, Electrophoresis.

Genetic variant of C1GalT1 contributes to the susceptibility to IgA nephropathy.

S. Ulivi, F. Scolari, A. Amoroso, 2009, Journal of nephrology.

Novel ELISA for thrombospondin type 1 domain-containing 7A autoantibodies in membranous nephropathy.

J. Wetzels, G. Ghiggeri, G. Lambeau, 2019, Kidney international.

Membranous glomerulonephritis: histological and serological features to differentiate cancer-related and non-related forms

G. Ghiggeri, C. Murtas, 2016, Journal of Nephrology.

Coexistence of different circulating anti-podocyte antibodies in membranous nephropathy.

A. Magnano, L. Gesualdo, F. Scolari, 2012, Clinical journal of the American Society of Nephrology : CJASN.

In vivo characterization of renal auto‐antigens involved in human auto‐immune diseases: The case of membranous glomerulonephritis

M. Prunotto, G. Ghiggeri, L. Allegri, 2011, Proteomics. Clinical applications.

Glycosylation of human abumin in diabetes mellitus: Extensive microheterogeneity of serum and urinary species as revealed by isoelectric focusing

G. Ghiggeri, P. Righetti, E. Gianazza, 1984 .

Genetic screening in adolescents with steroid-resistant nephrotic syndrome.

A. Anarat, G. Ardissino, G. Ghiggeri, 2013, Kidney international.

Glomerular autoimmune multicomponents of human lupus nephritis in vivo: α-enolase and annexin AI.

A. Scaloni, L. Bianchi, F. Scolari, 2014, Journal of the American Society of Nephrology : JASN.

Urinary excretion of brush-border antigen and plasma proteins in early stages of diabetic nephropathy.

G. Ghiggeri, R. Alinovi, A. Mutti, 1990, Clinica chimica acta; international journal of clinical chemistry.

Rat model of perchloroethylene-induced renal dysfunctions.

G. Ghiggeri, G. Olivetti, R. Alinovi, 1992, Environmental research.

Cell-speciﬁc regulation of a 1 (III ) and a 2 ( V ) collagen by TGF- b 1 in tubulointerstitial cell models

R. Ravazzolo, G. Ghiggeri, G. Caridi, 1998 .

Neutrophil Extracellular Traps-DNase Balance and Autoimmunity

M. Prunotto, G. Ghiggeri, F. Lugani, 2021, Cells.

IgA nephropathy, the most common cause of glomerulonephritis, is linked to 6q22–23

R. Lifton, B. Julian, C. Nelson-Williams, 2000, Nature Genetics.

Urinary proteome in a snapshot: normal urine and glomerulonephritis.

G. Ghiggeri, M. Bodria, G. Candiano, 2013, Journal of nephrology.

Renal selectivity properties towards endogenous albumin in minimal change nephropathy.

G. Ghiggeri, F. Ginevri, G. Candiano, 1987, Kidney international.

Prognostic Factors and Long-Term Outcome with ANCA-Associated Kidney Vasculitis in Childhood

G. Ghiggeri, M. Bodria, A. Vaglio, 2021, Clinical journal of the American Society of Nephrology : CJASN.

Annexin A1 and Autoimmunity: From Basic Science to Clinical Applications

G. Ghiggeri, A. Vaglio, G. Candiano, 2018, International journal of molecular sciences.

Atypical IgM on T cells predict relapse and steroid dependence in idiopathic nephrotic syndrome.

M. Rastaldi, G. Ghiggeri, F. Emma, 2019, Kidney international.

Glomerular Autoimmune Multicomponents of Human Lupus Nephritis In Vivo (2): Planted Antigens.

F. Scolari, P. Ravani, G. Ghiggeri, 2015, Journal of the American Society of Nephrology : JASN.

Apolipoproteins prevent glomerular albumin permeability induced in vitro by serum from patients with focal segmental glomerulosclerosis.

G. Ghiggeri, F. Ginevri, L. Musante, 2001, Journal of the American Society of Nephrology : JASN.

Urine proteome analysis in Dent's disease shows high selective changes potentially involved in chronic renal damage.

E. Tosetto, F. Anglani, A. Scaloni, 2016, Journal of proteomics.

Resolution of fibronectin and other uncharacterized proteins by two-dimensional polyacrylamide electrophoresis with thiourea.

G. Ghiggeri, L. Musante, G. Candiano, 1998, Journal of chromatography. B, Biomedical sciences and applications.

Oxidized albumin. The long way of a protein of uncertain function.

G. Ghiggeri, G. Candiano, M. Bruschi, 2013, Biochimica et biophysica acta.

Analysis of the oxido-redox status of plasma proteins. Technology advances for clinical applications.

M. Prunotto, R. Camilla, R. Coppo, 2011, Journal of chromatography. B, Analytical technologies in the biomedical and life sciences.

Determination of the oxido-redox status of plasma albumin in hemodialysis patients.

F. Scolari, G. Ghiggeri, A. Urbani, 2008, Journal of chromatography. B, Analytical technologies in the biomedical and life sciences.

Protein-protein interaction heterogeneity of plasma apolipoprotein A1 in nephrotic syndrome.

G. Ghiggeri, A. Urbani, G. Federici, 2011, Molecular bioSystems.

Renal ammoniagenesis in an early stage of metabolic acidosis in man.

G. Ghiggeri, G. Deferrari, G. Garibotto, 1982, The Journal of clinical investigation.

Brain metabolism of amino acids and ammonia in patients with chronic renal insufficiency.

G. Ghiggeri, G. Deferrari, G. Garibotto, 1981, Kidney international.

Cyclosporin and organ specific toxicity: clinical aspects, pharmacogenetics and perspectives.

G. Ghiggeri, P. Catarsi, A. Magnasco, 2008, Current clinical pharmacology.

Characterisation of the phenylhydrazone derivatives of "glycated albumin" purified from diabetic sera.

G. Ghiggeri, F. Ginevri, G. Candiano, 1986, Carbohydrate research.

COQ2 nephropathy: a newly described inherited mitochondriopathy with primary renal involvement.

E. Bertini, F. Santorelli, G. Ghiggeri, 2007, Journal of the American Society of Nephrology : JASN.

SIX2 and BMP4 mutations associate with anomalous kidney development.

A. Bakkaloğlu, C. Antignac, M. Litwin, 2008, Journal of the American Society of Nephrology : JASN.

Familial vesicoureteral reflux: testing replication of linkage in seven new multigenerational kindreds.

R. Ravazzolo, T. Hensle, A. Gharavi, 2005, Journal of the American Society of Nephrology : JASN.

Renal denervation for severe hypertension in a small child with Turner syndrome: miniaturisation of the procedure and results

G. Ghiggeri, C. Gandolfo, A. Bonanni, 2015, BMJ Case Reports.

Proteomics of plasma and urine in primary nephrotic syndrome in children.

F. Scolari, G. Ghiggeri, A. Urbani, 2008, Contributions to nephrology.

The Journal of Rheumatology Neutrophil Extracellular Traps (NETs) profiles in patients with incident SLE and

Pesce, F. Scolari, G. Ghiggeri, 2019 .

Refractory Minimal Change Disease and Focal Segmental Glomerular Sclerosis Treated With Anakinra

G. Ghiggeri, G. Caridi, F. Lugani, 2021 .

Refractory minimal change disease and FSGS treated with Anakinra

G. Ghiggeri, G. Caridi, F. Lugani, 2021, Kidney International Reports.

Prevalence of mutations in renal developmental genes in children with renal hypodysplasia: results of the ESCAPE study.

R. Salomon, C. Antignac, G. Ghiggeri, 2006, Journal of the American Society of Nephrology : JASN.

The spatially resolved transcriptional profile of acute T-cell mediated rejection in a kidney allograft.

G. Ghiggeri, S. Sedrakyan, L. Perin, 2021, Kidney international.

Nephronophthisis-medullary cystic disease: clinical and genetic aspects.

G. Ghiggeri, G. Caridi, R. Gusmano, 1998, Journal of nephrology.

Copy Number Variant Analysis and Genome-wide Association Study Identify Loci with Large Effect for Vesicoureteral Reflux.

Craig S. Wong, H. Hakonarson, C. Willer, 2021, Journal of the American Society of Nephrology : JASN.

Regulatory T cells and minimal change nephropathy: in the midst of a complex network

P. Ravani, G. Ghiggeri, A. Di Donato, 2016, Clinical and experimental immunology.

Regulatory T Cells and Oxidative Stress in Minimal Change Nephropathy

P. Ravani, G. Ghiggeri, A. Bonanni, 2016 .

A Pilot Study of IL2 in Drug-Resistant Idiopathic Nephrotic Syndrome

P. Ravani, G. Ghiggeri, A. Di Donato, 2015, PloS one.

A Pilot Study of IL 2 in Drug-Resistant Idiopathic Nephrotic Syndrome

Donato, P. Ravani, G. Ghiggeri, 2015 .

LPS Nephropathy in Mice Is Ameliorated by IL-2 Independently of Regulatory T Cells Activity

M. Rastaldi, G. Ghiggeri, A. Di Donato, 2014, PloS one.

Genetic and Clinical Predictors of Age of ESKD in Individuals With Autosomal Dominant Tubulointerstitial Kidney Disease Due to UMOD Mutations

G. Cavalleri, J. Divers, F. Scolari, 2020, Kidney international reports.

Mapping of the human COL5A1 gene to chromosome 9q34.3

G. Gimelli, G. Ghiggeri, G. Caridi, 1992, Human Genetics.

Locus heterogeneity of Dent’s disease: OCRL1 and TMEM27 genes in patients with no CLCN5 mutations

E. Tosetto, F. Anglani, A. D'Angelo, 2009, Pediatric Nephrology.

Protracted high-dose interferon gamma therapy for chronic experimental nephropathy.

G. Ghiggeri, G. Salvidio, A. Trivelli, 1994, Life sciences.

Discovery of anti-Formin-like 1 protein (FMNL1) antibodies in membranous nephropathy and other glomerular diseases

John C. Tan, M. Prunotto, L. Scapozza, 2022, Scientific Reports.

α1‐Antitrypsin (AAT) deficiency and ANCA‐positive systemic vasculitis: genetic and clinical implications

F. Callea, G. Ghiggeri, G. Salvidio, 1997 .

alpha 1-Antitrypsin (AAT) deficiency and ANCA-positive systemic vasculitis: genetic and clinical implications.

F. Callea, G. Ghiggeri, G. Salvidio, 1997, European journal of clinical investigation.

Purification of alpha-1-antitrypsin monomer by preparative electrophoresis.

F. Callea, G. Ghiggeri, C. Sergi, 1994, Journal of clinical pathology.

TRPC6 mutations in children with steroid-resistant nephrotic syndrome and atypical phenotype.

L. Gesualdo, G. Ghiggeri, G. Caridi, 2011, Clinical journal of the American Society of Nephrology : CJASN.

Recurrent autosomal-dominant focal segmental glomerulosclerosis.

S. Sanna-Cherchi, G. Ghiggeri, L. Allegri, 2006, Kidney international.

Anti-CD20 Antibodies for Idiopathic Nephrotic Syndrome in Children.

P. Ravani, G. Ghiggeri, G. Caridi, 2016, Clinical journal of the American Society of Nephrology : CJASN.

Anti-CD 20 Antibodies for Idiopathic Nephrotic Syndrome in Children

P. Ravani, G. Ghiggeri, G. Caridi, 2016 .

Childhood Idiopathic Nephrotic Syndrome: Does the Initial Steroid Treatment Modify the Outcome? A Multicentre, Prospective Cohort Study

A. Edefonti, G. Ghiggeri, E. Monti, 2021, Frontiers in Pediatrics.

Short-term effects of rituximab in children with steroid- and calcineurin-dependent nephrotic syndrome: a randomized controlled trial.

A. Edefonti, F. Scolari, N. Dallera, 2011, Clinical journal of the American Society of Nephrology : CJASN.

Weighted Gene Co-Expression Network Analysis and Support Vector Machine Learning in the Proteomic Profiling of Cerebrospinal Fluid from Extraventricular Drainage in Child Medulloblastoma

G. Ghiggeri, I. Panfoli, G. Candiano, 2022, Metabolites.

Collapsing glomerulopathy associated with inherited mitochondrial injury.

F. Santorelli, G. Ghiggeri, G. Caridi, 2008, Kidney international.

Characterization of oxidation end product of plasma albumin 'in vivo'.

G. Ghiggeri, A. Urbani, L. Musante, 2006, Biochemical and biophysical research communications.

Interaction between cationic dyes and erythrocyte membranes in minimal change nephropathy: an electrophoretic approach

G. Ghiggeri, R. Oleggini, F. Ginevri, 1991, Pediatric Nephrology.

Peroxidative damage of the erythrocyte membrane in children with nephrotic syndrome

G. Ghiggeri, R. Oleggini, F. Ginevri, 2004, Pediatric Nephrology.

Studies by conventional and “low denaturing” isoelectric focusing on albumin microheterogeneity under normal conditions and in experimental nephrosis

G. Remuzzi, G. Ghiggeri, F. Ginevri, 1987 .

Protracted remission of proteinuria after combined therapy with plasmapheresis and anti-CD20 antibodies/cyclophosphamide in a child with oligoclonal IgM and glomerulosclerosis

G. Ghiggeri, A. Trivelli, L. Musante, 2007, Pediatric Nephrology.

Uromodulin storage diseases: clinical aspects and mechanisms.

F. Scolari, C. Izzi, A. Amoroso, 2004, American journal of kidney diseases : the official journal of the National Kidney Foundation.

Molecular analysis of uromodulin and SAH genes, positional candidates for autosomal dominant medullary cystic kidney disease linked to 16p12.

F. Scolari, B. F. Viola, A. Amoroso, 2001, JN. Journal of Nephrology (Milano. 1992).

Phenotypic expansion of DGKE-associated diseases.

V. D’Agati, R. Lifton, A. Gharavi, 2014, Journal of the American Society of Nephrology : JASN.

Familial forms of nephrotic syndrome

S. Sanna-Cherchi, G. Ghiggeri, G. Caridi, 2010, Pediatric Nephrology.

Wolfram Syndrome: New Mutations, Different Phenotype

G. d’Annunzio, R. Lorini, G. Ghiggeri, 2012, PloS one.

Mesenchymal Stem Cells Protective Effect in Adriamycin Model of Nephropathy

G. Ghiggeri, A. Ibatici, A. Magnasco, 2008, Cell transplantation.

Immunity to Polyomavirus BK Infection: Immune Monitoring to Regulate the Balance between Risk of BKV Nephropathy and Induction of Alloimmunity

G. Ghiggeri, M. Luppi, M. Cioni, 2013, Clinical & developmental immunology.

Depletion of clusterin in renal diseases causing nephrotic syndrome.

M. Rastaldi, F. Scolari, G. Ghiggeri, 2002, Kidney international.

Recurrent lymphomatoid papulosis associated with nephrotic syndrome. An occurrence of uncertain origin

G. Ghiggeri, G. Caridi, C. Gambini, 2009, Pediatric Nephrology.

Circulating suPAR in two cohorts of primary FSGS.

A. Anarat, D. Gipson, G. Ghiggeri, 2012, Journal of the American Society of Nephrology : JASN.

Characterization of a DNA binding site that mediates the stimulatory effect of cyclosporin-A on type III collagen expression in renal cells.

R. Ravazzolo, G. Botti, G. Ghiggeri, 2000, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Expression of collagen by renal fibroblasts treated with FK 506 in vitro.

R. Ravazzolo, G. Ghiggeri, G. Caridi, 1998, Transplantation proceedings.

Activation of COL3A1 promoter activity by cyclosporine.

R. Ravazzolo, G. Botti, G. Ghiggeri, 1998, Transplantation proceedings.

Silver stain of proteins in ultra-thin gels containing carrier ampholytes--detection of glycosyl albumin with anionic and cationic charge in serums of diabetic patients.

G. Ghiggeri, G. Candiano, C. Queirolo, 1984, Clinica chimica acta; international journal of clinical chemistry.

Podocin mutations in sporadic focal-segmental glomerulosclerosis occurring in adulthood.

F. Scolari, S. Sanna-Cherchi, G. Ghiggeri, 2003, Kidney international.

Broadening the spectrum of diseases related to podocin mutations.

G. Mazzucco, G. Rizzoni, F. Scolari, 2003, Journal of the American Society of Nephrology : JASN.

'Congenital solitary functioning kidneys: which ones warrant follow-up into adult life?'.

S. Sanna-Cherchi, G. Ghiggeri, Valentina Corbani, 2011, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Soluble CD40 ligand directly alters glomerular permeability and may act as a circulating permeability factor in FSGS

G. Camussi, G. Ghiggeri, S. Doublier, 2017, PloS one.

Analysis of albumin charge by direct immunofixation in ultrathin gels.

G. Ghiggeri, F. Ginevri, G. Candiano, 1990, Kidney international.

Stromal-like Wilms tumor cells induce human Natural Killer cell degranulation and display immunomodulatory properties towards NK cells

G. Ghiggeri, L. Moretta, G. Candiano, 2021, Oncoimmunology.

Rituximab is a safe and effective long-term treatment for children with steroid and calcineurin inhibitor-dependent idiopathic nephrotic syndrome.

A. Edefonti, F. Scolari, P. Ravani, 2013, Kidney international.

The Case | Cystic renal disease, nephrogenic diabetes insipidus, and polycytemia.

F. Scolari, C. Izzi, N. Dallera, 2014, Kidney international.

Unexpectedly high prevalence of rare genetic disorders in kidney transplant recipients with an unknown causal nephropathy

G. Ghiggeri, F. Settanni, P. Stratta, 2014, Clinical transplantation.

Neutrophil Extracellular Traps in the Autoimmunity Context

M. Prunotto, F. Scolari, G. Ghiggeri, 2021, Frontiers in Medicine.

Post-translational modified proteins are biomarkers of autoimmune-processes: NETosis and the inflammatory-autoimmunity connection.

G. Ghiggeri, A. Vaglio, P. Migliorini, 2017, Clinica chimica acta; international journal of clinical chemistry.

Circulating antipodocyte antibodies in membranous nephropathy: new findings.

G. Ghiggeri, L. Allegri, C. Murtas, 2013, American journal of kidney diseases : the official journal of the National Kidney Foundation.

Patients with primary membranous nephropathy lack auto-antibodies against LDL receptor, the homologue of megalin in human glomeruli

M. Prunotto, F. Scolari, G. Ghiggeri, 2012, Clinical kidney journal.

2 Immunological Basis of Membranous Glomerulonephritis

M. Prunotto, R. Magistroni, G. Ghiggeri, 2012 .

Immunological Basis of Membranous Glomerulonephritis

M. Prunotto, R. Magistroni, G. Ghiggeri, 2011 .

Direct characterization of target podocyte antigens and auto-antibodies in human membranous glomerulonephritis: Alfa-enolase and borderline antigens.

M. Prunotto, L. Gesualdo, F. Scolari, 2011, Journal of proteomics.

Medullary cystic kidney disease: past and present.

F. Scolari, B. F. Viola, A. Amoroso, 2001, Contributions to nephrology.

Extracellular matrix formation by epithelial cells from human polycystic kidney cysts in culture

G. Ghiggeri, G. Caridi, A. Sessa, 1993, Virchows Archiv. B, Cell pathology including molecular pathology.

Adverse events linked with the use of chimeric and humanized anti‐CD20 antibodies in children with idiopathic nephrotic syndrome

P. Ravani, G. Ghiggeri, G. Caridi, 2018, British journal of clinical pharmacology.

Proteomics and Extracellular Vesicles as Novel Biomarker Sources in Peritoneal Dialysis in Children

G. Ghiggeri, F. Lugani, E. Verrina, 2022, International journal of molecular sciences.

Regulation of innate immunity by the nucleotide pathway in children with idiopathic nephrotic syndrome

G. Ghiggeri, M. Bodria, S. Alloisio, 2011, Clinical and experimental immunology.

Endocellular polyamine availability modulates epithelial-to-mesenchymal transition and unfolded protein response in MDCK cells

M. Prunotto, G. Ghiggeri, G. Gabbiani, 2010, Laboratory Investigation.

New iodo‐acetamido cyanines for labeling cysteine thiol residues. A strategy for evaluating plasma proteins and their oxido‐redox status

F. Scolari, G. Ghiggeri, A. Urbani, 2009, Proteomics.

Morphological and Biochemical Characteristics of Human Tubular Epithelial Cells “In Culture” Deriving from Nephronophthisis

G. Ghiggeri, F. Ginevri, P. Altieri, 1991 .

Fractionation of human serum albumin isoforms with chromatofocusing.

G. Ghiggeri, G. Candiano, C. Queirolo, 1986, Journal of chromatography.

Highly selective one-step chromatography of serum and urinary albumin on immobilized Cibacron Blue F3GA. Studies on normal and glycosyl albumin.

G. Ghiggeri, G. Candiano, C. Queirolo, 1985, Clinica chimica acta; international journal of clinical chemistry.

Glycosylation of human albumin in diabetes mellitus II. Extensive in vitro modification by trioses and hexoses as revealed by isoelectric focusing

G. Ghiggeri, P. Righetti, E. Gianazza, 1985 .

Proteomic analysis of urinary extracellular vesicles of kidney transplant recipients with BKV viruria and viremia: A pilot study

G. Ghiggeri, G. Stallone, G. Zaza, 2022, Frontiers in Medicine.

Genetics, clinical and pathological features of glomerulonephritis associated with mutations of nonmuscle myosin IIA (Fechtner syndrome).

R. Ravazzolo, P. Noris, G. Ghiggeri, 2003, American journal of kidney diseases : the official journal of the National Kidney Foundation.

Purification and partial characterization of a new 85 KDa amyloidosis-related protein in chronic hemodialysis.

G. Ghiggeri, D. Brancaccio, F. Ginevri, 1991, Biochemical and Biophysical Research Communications - BBRC.

Parathyroid hormone and phosphate homeostasis in patients with Bartter and Gitelman syndrome: an international cross-sectional study

F. Trepiccione, P. Houillier, L. Weber, 2022, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Immunocytochemistry for the heavy chain of the non‐muscle myosin IIA as a diagnostic tool for MYH9‐related disorders

P. Noris, G. Ghiggeri, A. Savoia, 2002, British journal of haematology.

Unbiased next generation sequencing analysis confirms the existence of autosomal dominant Alport syndrome in a relevant fraction of cases

F. Brancati, G. Ghiggeri, S. Feriozzi, 2014, Clinical Genetics.

The effect of proteinase inhibitors on glomerular albumin permeability induced in vitro by serum from patients with idiopathic focal segmental glomerulosclerosis.

G. Ghiggeri, L. Musante, G. Candiano, 2004, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

WT1 mutations in nephrotic syndrome revisited. High prevalence in young girls, associations and renal phenotypes

L. Gesualdo, G. Ghiggeri, G. Caridi, 2006, Pediatric Nephrology.

Both the rituximab dose and maintenance immunosuppression in steroid-dependent/frequently-relapsing nephrotic syndrome have important effects on outcomes.

A. Sinha, A. Bagga, G. Ghiggeri, 2019, Kidney international.

Randomised controlled trial comparing ofatumumab to rituximab in children with steroid-dependent and calcineurin inhibitor-dependent idiopathic nephrotic syndrome: study protocol

P. Ravani, G. Ghiggeri, A. Bonanni, 2017, BMJ Open.

Low-dose ofatumumab for rituximab-resistant nephrotic syndrome

G. Ghiggeri, A. Bonanni, C. Murtas, 2015, BMJ Case Reports.

Prediction and treatment of recurrent focal segmental glomerulosclerosis after renal transplantation in children.

G. Ghiggeri, M. Cardillo, F. Ginevri, 1999, American journal of kidney diseases : the official journal of the National Kidney Foundation.

Cytotoxic effect of adriamycin and agarose-coupled adriamycin on glomerular epithelial cells: Role of free radicals

G. Ghiggeri, F. Ginevri, R. Bertelli, 1991, In Vitro Cellular & Developmental Biology - Animal.

Glomerular clusterin is associated with PKC-α/β regulation and good outcome of membranous glomerulonephritis in humans

S. Parodi, M. Rastaldi, G. Camussi, 2006 .

Multiple mechanisms for doxorubicin cytotoxicity on glomerular epithelial cells 'in vitro'.

G. Ghiggeri, R. Oleggini, A. Trivelli, 1992, European journal of pharmacology.

Puromycin aminonucleoside metabolism by glomeruli and glomerular epithelial cells in vitro.

G. Ghiggeri, A. Trivelli, F. Ginevri, 1991, Kidney international.

Apolipoprotein E in idiopathic nephrotic syndrome and focal segmental glomerulosclerosis.

M. Rastaldi, F. Scolari, S. Sanna-Cherchi, 2003, Kidney international.

Exome-wide Association Study Identifies GREB1L Mutations in Congenital Kidney Malformations.

D. Goldstein, S. Mane, G. Ardissino, 2017, American journal of human genetics.

Novel INF2 mutations in an Italian cohort of patients with focal segmental glomerulosclerosis, renal failure and Charcot-Marie-Tooth neuropathy.

L. Gesualdo, G. Ghiggeri, G. Caridi, 2014, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

New Insights into the Pathogenesis and the Therapy of Recurrent Focal Glomerulosclerosis

G. Ghiggeri, F. Vincenti, 2005, American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons.

NPHS2 (Podocin) Mutations in Nephrotic Syndrome. Clinical Spectrum and Fine Mechanisms

G. Ghiggeri, G. Caridi, F. Perfumo, 2005, Pediatric Research.

Prevalence, genetics, and clinical features of patients carrying podocin mutations in steroid-resistant nonfamilial focal segmental glomerulosclerosis.

G. Ghiggeri, G. Caridi, P. Catarsi, 2001, Journal of the American Society of Nephrology : JASN.

Multicentric Carpotarsal Osteolysis Syndrome Associated Nephropathy: Novel Variants of MAFB Gene and Literature Review

G. Ghiggeri, G. Caridi, F. Lugani, 2022, Journal of clinical medicine.

Stable incorporation of α‐smooth muscle actin into stress fibers is dependent on specific tropomyosin isoforms

G. Schevzov, P. Gunning, A. Scaloni, 2015, Cytoskeleton.

Ofatumumab in two pediatric nephrotic syndrome patients allergic to rituximab

G. Ghiggeri, F. Emma, Jessica Serafinelli, 2016, Pediatric Nephrology.

Renal purine efflux and xanthine oxidase activity during experimental nephrosis in rats: difference between puromycin aminonucleoside and adriamycin nephrosis.

G. Ghiggeri, R. Oleggini, F. Ginevri, 1990, Clinical science.

Separation of the 9-anthryldiazomethane derivates of fatty acids by high-performance liquid chromatography on a Fatty Acid Analysis Column. Application to albumin-bound fatty acid analysis.

G. Ghiggeri, F. Ginevri, G. Candiano, 1986, Journal of chromatography.

Clinical trials in minimal change disease.

P. Ravani, G. Ghiggeri, Simardeep Gill, 2017, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Vaccines and Disease Relapses in Children with Nephrotic Syndrome.

G. Ghiggeri, F. Lugani, P. Cravedi, 2021, Clinical journal of the American Society of Nephrology : CJASN.

Ofatumumab or Rituximab for Children with Steroid- and Calcineurin Inhibitor -Dependent Nephrotic Syndrome - A Superiority Randomized Controlled Trial (OFA2)

M. Prunotto, P. Ravani, G. Ghiggeri, 2021 .

Rituximab vs Low-Dose Mycophenolate Mofetil In Recurrence of Steroid-Dependent Nephrotic Syndrome in Children and Young Adults: A Randomized Clinical Trial.

P. Ravani, G. Ghiggeri, G. Caridi, 2021, JAMA pediatrics.

Low-dose ofatumumab for multidrug-resistant nephrotic syndrome in children: a randomized placebo-controlled trial

P. Ravani, G. Ghiggeri, G. Caridi, 2020, Pediatric Nephrology.

A mild form of rituximab-associated lung injury in two adolescents treated for nephrotic syndrome

G. Ghiggeri, M. Spatafora, T. Bellini, 2015, BMJ Case Reports.

Rituximab in children with resistant idiopathic nephrotic syndrome.

A. Edefonti, F. Scolari, P. Ravani, 2012, Journal of the American Society of Nephrology : JASN.

Recurrent focal glomerulosclerosis in the era of genetics of podocyte proteins: theory and therapy.

G. Ghiggeri, F. Vincenti, M. Carraro, 2004, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Human or Chimeric Monoclonal Anti-CD20 Antibodies for Children with Nephrotic Syndrome: A Superiority Randomized Trial

M. Prunotto, P. Ravani, G. Ghiggeri, 2021, Journal of the American Society of Nephrology : JASN.

Regarding Maas's editorial letter on serum suPAR levels.

D. Gipson, G. Ghiggeri, F. Schaefer, 2012, Kidney International.

FCGR2A single nucleotide polymorphism confers susceptibility to childhood-onset idiopathic nephrotic syndrome.

G. Ghiggeri, M. Bodria, A. Vaglio, 2018, Immunology letters.

Cyclosporine enhances the synthesis of selected extracellular matrix proteins by renal cells "in culture". Different cell responses and phenotype characterization.

G. Ghiggeri, R. Oleggini, F. Ginevri, 1994, Transplantation.

[TRPC6 mutations in children with steroid-resistant nephrotic syndrome].

L. Gesualdo, G. Ghiggeri, G. Caridi, 2011, Giornale italiano di nefrologia : organo ufficiale della Societa italiana di nefrologia.

Late onset of pANCA renal and pulmonary vasculitis in a girl affected by undifferentiated connective tissue disease

R. Lorini, G. Ghiggeri, G. Barbano, 2010, Lupus.

Editorial: The kidney in auto-immune and auto-inflammatory processes: Definitions, mechanisms, and biomarkers

G. Ghiggeri, A. Vaglio, L. Obici, 2023, Frontiers in Medicine.

Evidence for charge-based mimicry in anti dsDNA antibody generation.

M. Prunotto, F. Scolari, G. Ghiggeri, 2022, Journal of autoimmunity.

Blue silver: A very sensitive colloidal Coomassie G‐250 staining for proteome analysis

Pier Giorgio Righetti, Maurizio Bruschi, G. Ghiggeri, 2004, Electrophoresis.

Autosomal dominant medullary cystic disease: a disorder with variable clinical pictures and exclusion of linkage with the NPH1 locus.

F. Scolari, B. F. Viola, A. Amoroso, 1998, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Magnetic resonance urography and laparoscopy in paediatric urology: a case series

G. Ghiggeri, G. Mattioli, V. Jasonni, 2013, Pediatric Radiology.

Mutation of the Mg2+ transporter SLC41A1 results in a nephronophthisis-like phenotype.

T. Abe, T. Hurd, G. Ghiggeri, 2013, Journal of the American Society of Nephrology : JASN.

Proteomic Analysis of Urinary Extracellular Vesicles Reveals a Role for the Complement System in Medullary Sponge Kidney Disease

G. Gambaro, A. Fabris, G. Ghiggeri, 2019, International journal of molecular sciences.

Proteomic Analysis of Urinary Microvesicles and Exosomes in Medullary Sponge Kidney Disease and Autosomal Dominant Polycystic Kidney Disease.

G. Gambaro, A. Fabris, A. Lupo, 2019, Clinical journal of the American Society of Nephrology : CJASN.

The rediscovery of uromodulin (Tamm-Horsfall protein): from tubulointerstitial nephropathy to chronic kidney disease.

F. Scolari, A. Amoroso, G. Ghiggeri, 2011, Kidney international.

GWAS defines pathogenic signaling pathways and prioritizes drug targets for IgA nephropathy

F. Kronenberg, P. Gregersen, C. Wijmenga, 2021, medRxiv.

2DE maps in the discovery of human autoimmune kidney diseases: the case of membranous glomerulonephritis.

G. Ghiggeri, G. Candiano, M. Bruschi, 2015, Methods in molecular biology.

Autoimmunity in membranous nephropathy targets aldose reductase and SOD2.

M. Prunotto, F. Scolari, G. Ghiggeri, 2010, Journal of the American Society of Nephrology : JASN.

Soft immobilized pH gradient gels in proteome analysis: A follow‐up

G. Ghiggeri, P. Righetti, B. Herbert, 2003, Expert review of neurotherapeutics.

Two‐dimensional maps in soft immobilized pH gradient gels: A new approach to the proteome of the Third Millennium

G. Ghiggeri, P. Righetti, B. Herbert, 2002, Electrophoresis.

Glomerulocystic kidney disease in hypomelanosis of Ito

G. Ghiggeri, G. Caridi, F. Emma, 2008, Pediatric Nephrology.

Genetic basis of human congenital anomalies of the kidney and urinary tract

A. Gharavi, S. Sanna-Cherchi, G. Ghiggeri, 2018, The Journal of clinical investigation.

Potential biomarkers of childhood brain tumor identified by proteomics of cerebrospinal fluid from extraventricular drainage (EVD)

L. Ramenghi, G. Ghiggeri, I. Panfoli, 2021, Scientific Reports.

High-Content Screening Identifies Vanilloids as a Novel Class of Inhibitors of NET Formation

N. Pedemonte, G. Ghiggeri, Elvira Sondo, 2019, Front. Immunol..

R. Ravazzolo, P. Noris, P. Koivisto, 2003, Medicine.

The copy number variation landscape of congenital anomalies of the kidney and urinary tract

Craig S. Wong, H. Hakonarson, A. Latos-Bieleńska, 2018, Nature Genetics.

Copy-number disorders are a common cause of congenital kidney malformations.

Stephan J Sanders, V. Jobanputra, W. Chung, 2012, American journal of human genetics.

De novo TRIM8 variants impair its protein localization to nuclear bodies and cause developmental delay, epilepsy, and focal segmental glomerulosclerosis.

V. Jobanputra, D. Goldstein, S. Mane, 2021, American journal of human genetics.

Stop codon at arginine 586 is the prevalent nephronopthisis type 1 mutation in Italy.

G. Ghiggeri, G. Caridi, F. Emma, 2006, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Protective Role of the M-Sec–Tunneling Nanotube System in Podocytes

M. Papotti, G. Camussi, G. Ghiggeri, 2021, Journal of the American Society of Nephrology : JASN.

AHI1 is required for outer segment development and is a modifier for retinal degeneration in nephronophthisis

Madeline A. Lancaster, A. D. den Hollander, F. Cremers, 2010, Nature Genetics.

Proteomic profile of mesothelial exosomes isolated from peritoneal dialysis effluent of children with focal segmental glomerulosclerosis

G. Ghiggeri, I. Panfoli, G. Zaza, 2021, Scientific Reports.

Genetic Drivers of Kidney Defects in the DiGeorge Syndrome

Craig S. Wong, E. Zackai, H. Hakonarson, 2017, The New England journal of medicine.

Longitudinal Changes in Health-Related Quality of Life in Primary Glomerular Disease: Results From the CureGN Study

Craig S. Wong, V. D’Agati, M. Kretzler, 2020, Kidney international reports.

Genome-wide association study identifies susceptibility loci for IgA nephropathy

Loreto Gesualdo, Krzysztof Kiryluk, Murim Choi, 2011, Nature Genetics.

Exome sequencing identified MYO1E and NEIL1 as candidate genes for human autosomal recessive steroid-resistant nephrotic syndrome.

T. Palomero, V. D’Agati, H. Kim, 2011, Kidney international.

Clinical features and long-term outcome of nephrotic syndrome associated with heterozygous NPHS1 and NPHS2 mutations.

A. Edefonti, R. Coppo, L. Gesualdo, 2009, Clinical journal of the American Society of Nephrology : CJASN.

Repetitive Fragmentation Products of Albumin and α1-Antitrypsin in Glomerular Diseases Associated with Nephrotic Syndrome

F. Scolari, G. Ghiggeri, A. Urbani, 2006 .

Permeability plasma factors in nephrotic syndrome: more than one factor, more than one inhibitor.

G. Ghiggeri, F. Perfumo, M. Artero, 2001, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Molecular and Cellular Mechanisms for Proteinuria in Minimal Change Disease

G. Ghiggeri, G. Caridi, A. Bonanni, 2018, Front. Med..

A recessive gene for primary vesicoureteral reflux maps to chromosome 12p11-q13.

R. Ravazzolo, R. Burk, R. Cheng, 2009, Journal of the American Society of Nephrology : JASN.

Urinary excretion of brush border antigens and other proteins in children with vesico-ureteric reflux

G. Ghiggeri, E. Verrina, F. Ginevri, 1992, Pediatric Nephrology.

Mutations in SOX17 are Associated with Congenital Anomalies of the Kidney and the Urinary Tract

S. Gimelli, G. Gimelli, G. Ghiggeri, 2010, Human mutation.

Microvesicles as promising biological tools for diagnosis and therapy

L. Ramenghi, G. Ghiggeri, I. Panfoli, 2018, Expert review of proteomics.

The genetic architecture of membranous nephropathy and its potential to improve non-invasive diagnosis

L. Kiemeney, A. Köttgen, I. Ionita-Laza, 2020, Nature Communications.

Identification of a new locus for medullary cystic disease, on chromosome 16p12.

A. Ballabio, P. Aridon, F. Scolari, 1999, American journal of human genetics.

The genetic architecture of membranous nephropathy and its potential to improve non-invasive diagnosis

L. Kiemeney, A. Köttgen, I. Ionita-Laza, 2020, Nature Communications.

Selective enhancement by cyclosporin A of collagen expression by mesangial cells 'in culture'.

G. Ghiggeri, R. Oleggini, F. Ginevri, 1994, European journal of pharmacology.

Different renal manifestations associated with very early onset pediatric inflammatory bowel disease: case report and review of literature

G. Ghiggeri, S. Arrigo, M. Molteni, 2021, BMC Nephrology.

Expression of Nuclear Transcription Factor PAX2 in Renal Biopsies of Juvenile Nephronophthisis

G. Ghiggeri, G. Caridi, G. Montini, 2002, Nephron.

The impact of eNOS, MTR and MTHFR polymorphisms on renal graft survival in children and young adults.

A. Edefonti, G. Ghiggeri, S. Centi, 2009, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Determination of a glycosyl subunit of human serum albumin by concanavalin A-sepharose.

G. Ghiggeri, G. Candiano, C. Queirolo, 1983, Clinica chimica acta; international journal of clinical chemistry.

Phenotypic and genetic heterogeneity in Dent's disease—the results of an Italian collaborative study

G. Gambaro, L. Citron, E. Tosetto, 2006 .

Impaired urinary concentration ability is a sensitive predictor of renal disease progression in Joubert syndrome

E. Bertini, R. Borgatti, E. Valente, 2018, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Case Report: Atypical Manifestations Associated With FOXP3 Mutations. The “Fil Rouge” of Treg Between IPEX Features and Other Clinical Entities?

E. Fiaccadori, G. Ghiggeri, G. Caridi, 2022, Frontiers in Immunology.

Localization of a gene for nonsyndromic renal hypodysplasia to chromosome 1p32-33.

R. Ravazzolo, A. Gharavi, F. Scolari, 2007, American journal of human genetics.

Post-transplant recurrence of steroid resistant nephrotic syndrome in children: the Italian experience

S. Testa, L. Peruzzi, G. Ghiggeri, 2019, Journal of Nephrology.

Local TNF causes NFATc1-dependent cholesterol-mediated podocyte injury.

C. Forsblom, P. Groop, O. Kretz, 2016, The Journal of clinical investigation.

Glomerulocystic kidney disease in a family.

G. Ghiggeri, G. Caridi, I. Ceccherini, 2002, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Recurrence of focal segmental glomerulosclerosis after renal transplantation in patients with mutations of podocin.

G. Rizzoni, F. Scolari, S. Sanna-Cherchi, 2003, American journal of kidney diseases : the official journal of the National Kidney Foundation.

Constitutional Nephrin Deficiency in Conditionally Immortalized Human Podocytes Induced Epithelial-Mesenchymal Transition, Supported by β-Catenin/NF-kappa B Activation: A Consequence of Cell Junction Impairment?

G. Ghiggeri, M. Gigante, A. Di Donato, 2013, International journal of nephrology.

Minimal-change nephropathy and chronic hepatitis C infection : coincidental or associated ?

R. Coppo, A. Amore, G. Ghiggeri, 2007 .

Diagnostic specificity of autoantibodies to M-type phospholipase A2 receptor (PLA2R) in differentiating idiopathic membranous nephropathy (IMN) from secondary forms and other glomerular diseases

F. Pieruzzi, G. Ghiggeri, R. Sinico, 2018, Journal of Nephrology.

Anti-glutathione S-transferase theta 1 antibodies correlate with graft loss in non-sensitized pediatric kidney recipients

G. Ghiggeri, G. Caridi, C. Klersy, 2022, Frontiers in Medicine.

Long-Term Efficacy and Safety of Repeated Rituximab to Maintain Remission in Idiopathic Childhood Nephrotic Syndrome: An International Study

D. Gipson, G. Ghiggeri, J. Hogan, 2022, Journal of the American Society of Nephrology : JASN.

The oxido-redox potential of albumin methodological approach and relevance to human diseases.

M. Prunotto, G. Ghiggeri, A. Urbani, 2009, Journal of proteomics.

New and Old Anti-CD20 Monoclonal Antibodies for Nephrotic Syndrome. Where We Are?

G. Ghiggeri, A. Angeletti, B. Basu, 2022, Frontiers in Immunology.

Lysyl Oxidase Activates the Transcription Activity of Human Collagene III Promoter

R. Ravazzolo, G. Ghiggeri, A. Di Donato, 2000, The Journal of Biological Chemistry.

The latest advancements in proteomic two-dimensional gel electrophoresis analysis applied to biological samples.

G. Ghiggeri, G. Candiano, M. Bruschi, 2015, Methods in molecular biology.

Spectrophotometric determination of advanced products of non-enzymatic glycosylation of lysine by means of their reaction with diazonium salts

G. Ghiggeri, F. Ginevri, G. Candiano, 1986 .

Proteomic-based research strategy identified laminin subunit alpha 2 as a potential urinary-specific biomarker for the medullary sponge kidney disease.

G. Gambaro, A. Fabris, A. Lupo, 2017, Kidney international.

The European Rare Kidney Disease Registry (ERKReg): objectives, design and initial results

G. Capasso, G. Remuzzi, J. Wetzels, 2021, Orphanet Journal of Rare Diseases.

Nephrectomy for multicystic dysplastic kidney and renal hypodysplasia in children: where do we stand?

G. Ghiggeri, A. Magnasco, G. Mattioli, 2010, Pediatric Surgery International.

Results of the PROPINE randomized controlled study suggest tapering of prednisone treatment for relapses of steroid sensitive nephrotic syndrome is not necessary in children.

L. Ravà, M. L. Ciofi Degli Atti, G. Ghiggeri, 2020, Kidney international.

Two cases of swine H1N1 influenza presenting with hematuria as prodrome

G. Ghiggeri, F. Ansaldi, A. Magnasco, 2010, Pediatric Nephrology.

COVID-19 in Children with Nephrotic Syndrome on Anti-CD20 Chronic Immunosuppression.

G. Ghiggeri, G. Caridi, P. Cravedi, 2020, Clinical journal of the American Society of Nephrology : CJASN.

Molecular basis for idiopathic nephrotic syndrome in children

G. Ghiggeri, F. Ginevri, G. Candiano, 1986 .

Ofatumumab‐associated acute respiratory manifestations: clinical characteristics and treatment

P. Ravani, G. Ghiggeri, M. Bodria, 2016, British journal of clinical pharmacology.

Serum glomerular permeability activity in patients with podocin mutations (NPHS2) and steroid-resistant nephrotic syndrome.

G. Ghiggeri, G. Caridi, L. Musante, 2002, Journal of the American Society of Nephrology : JASN.

Glomerular albumin permeability as an in vitro model for characterizing the mechanism of focal glomerulosclerosis and predicting post‐transplant recurrence

G. Ghiggeri, G. Caridi, F. Ginevri, 2004, Pediatric transplantation.

S. Sanna-Cherchi, G. Ghiggeri, G. Caridi, 2006 .

Effect of dietary protein restriction on renal purines and purine-metabolizing enzymes in adriamycin nephrosis in rats: a mechanism for protection against acute proteinuria involving xanthine oxidase inhibition.

G. Ghiggeri, R. Oleggini, F. Ginevri, 1990, Clinical science.

Direct effect of plasma permeability factors from patients with idiopatic FSGS on nephrin and podocin expression in human podocytes.

G. Camussi, G. Ghiggeri, G. Caridi, 2005, International journal of molecular medicine.

Vaccines and nephrotic syndrome: efficacy and safety

G. Ghiggeri, G. Caridi, F. Lugani, 2022, Pediatric Nephrology.

Rituximab or Cyclophosphamide in the Treatment of Membranous Nephropathy: The RI-CYCLO Randomized Trial.

L. Gesualdo, F. Scolari, N. Dallera, 2021, Journal of the American Society of Nephrology : JASN.

Functional Magnetic Resonance Urography in Ureteropelvic Junction Obstruction: Proposal for a Pediatric Quantitative Score

G. Ghiggeri, M. Bodria, A. Pistorio, 2022, Frontiers in Pediatrics.

Multi-Autoantibody Signature and Clinical Outcome in Membranous Nephropathy.

M. Prunotto, F. Scolari, G. Ghiggeri, 2020, Clinical journal of the American Society of Nephrology : CJASN.

Editorial: Immune dysfunction in nephrotic syndrome - recent advances and new roads ahead

G. Ghiggeri, V. Audard, B. Seitz-Polski, 2022, Frontiers in Immunology.

Disseminated autoimmune disease during levamisole treatment of nephrotic syndrome

G. Ghiggeri, F. Ginevri, G. Barbano, 1999, Pediatric Nephrology.

Protracted levamisole in children with frequent-relapse nephrotic syndrome.

G. Ghiggeri, A. Trivelli, F. Ginevri, 1996, Pediatric nephrology.

An update on COVID-19 in paediatric and young adults with nephrotic syndrome, receiving chronic immunosuppression during the Omicron pandemic

G. Ghiggeri, F. Lugani, E. Verrina, 2022, JN. Journal of Nephrology (Milano. 1992).

Handling immune-suppressive therapies during SARS-CoV-2 pandemic: insights from pediatric datasets

G. Ghiggeri, P. Cravedi, A. Angeletti, 2020, Journal of Nephrology.

Ofatumumab‐associated acute pneumonitis: Not new but still the first case

P. Ravani, G. Ghiggeri, A. Bonanni, 2016, Pharmacology research & perspectives.

Nephrotic urine prevents increased rat glomerular albumin permeability induced by serum from the same patient with idiopathic nephrotic syndrome.

G. Ghiggeri, L. Musante, G. Candiano, 2003, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Discordant evolution of nephrotic syndrome in mono- and dizygotic twins

S. Parodi, A. Amoroso, G. Ghiggeri, 2006, Pediatric Nephrology.

Heterozygous NPHS1 or NPHS2 mutations in responsive nephrotic syndrome and the multifactorial origin of proteinuria.

G. Ghiggeri, G. Caridi, F. Perfumo, 2004, Kidney international.

Endogenous albumin as a marker of renal selectivity in steroid-unresponsive nephrotic syndrome.

G. Ghiggeri, R. Oleggini, F. Ginevri, 1989, Nephron.

Cis and trans regulatory elements in NPHS2 promoter: implications in proteinuria and progression of renal diseases.

S. Parodi, F. Scolari, S. Sanna-Cherchi, 2006, Kidney international.

Rare functional variants of podocin (NPHS2) promoter in patients with nephrotic syndrome.

R. Coppo, G. Camussi, F. Scolari, 2006, Gene Expression.

Intraureteral injection of NASHA/Dx gel under direct ureteroscopic visualization for the treatment of primary high-grade vesicoureteral reflux.

G. Ghiggeri, G. Mattioli, V. Jasonni, 2012, Journal of laparoendoscopic & advanced surgical techniques. Part A.

Surgical validation of functional magnetic resonance urography in the study of ureteropelvic junction obstruction in a pediatric cohort.

G. Ghiggeri, M. Bodria, A. Pistorio, 2019, Journal of pediatric urology.

A challenging case of renovascular hypertension

G. Ghiggeri, D. Palombo, C. Gandolfo, 2013, Vascular medicine.

Copy number variation analysis identifies novel CAKUT candidate genes in children with a solitary functioning kidney

V. D’Agati, A. Gharavi, S. Sanna-Cherchi, 2015, Kidney international.

An Update on Antibodies to Necleosome Components as Biomarkers of Sistemic Lupus Erythematosus and of Lupus Flares

M. Prunotto, G. Ghiggeri, F. Lugani, 2019, International journal of molecular sciences.

Cell-specific regulation of alpha1(III) and alpha2(V) collagen by TGF-beta1 in tubulointerstitial cell models.

R. Ravazzolo, G. Botti, G. Ghiggeri, 1998, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

New insights into membranous glomerulonephritis: from bench to bedside.

P. Ravani, G. Ghiggeri, C. Murtas, 2011, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Risk of COVID‐19 in young kidney transplant recipients. Results from a single‐center observational study

G. Ghiggeri, P. Cravedi, A. Magnasco, 2020, Clinical transplantation.

Genetic approaches to human renal agenesis/hypoplasia and dysplasia

A. Gharavi, F. Scolari, S. Sanna-Cherchi, 2007, Pediatric nephrology (Berlin, West).

What is measured by the alcian blue binding to red blood cells?

G. Ghiggeri, R. Alinovi, A. Mutti, 1989, British journal of industrial medicine.

Exome-wide Association Study Identifies GREB1L Mutations in Congenital Kidney Malformations.

D. Goldstein, S. Mane, G. Ardissino, 2017, American journal of human genetics.

Circulating Anti-Rituximab Antibodies Do Not Affect Response to Rituximab in Steroid-Dependent Nephrotic Syndrome

P. Ravani, G. Ghiggeri, G. Caridi, 2022, Kidney international reports.

Lack of cardiac anomalies in children with NPHS2 mutations.

R. Coppo, A. Amore, G. Ghiggeri, 2007, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Electrical charge of serum and urinary albumin in normal and diabetic humans.

G. Ghiggeri, G. Candiano, G M Ghiggeri, 1985, Kidney international.

Glycosyl albumin and diabetic microalbuminuria: demonstration of an altered renal handling.

G. Ghiggeri, G. Candiano, F. Bianchini, 1984, Kidney international.

A modification of the 5,5'-dithiobis(2-nitrobenzoic acid) (DTNB) method for the determination of the sulphhydryl content of human serum albumin.

G. Ghiggeri, G. Candiano, C. Queirolo, 1983, Clinica chimica acta; international journal of clinical chemistry.

Anti-alpha enolase multi-antibody specificity in human diseases. Clinical significance and molecular mechanisms.

M. Prunotto, G. Ghiggeri, P. Migliorini, 2021, Autoimmunity reviews.

Infantile steroid-resistant nephrotic syndrome associated with double homozygous mutations of podocin.

R. Ravazzolo, G. Ghiggeri, G. Caridi, 2004, American journal of kidney diseases : the official journal of the National Kidney Foundation.

Post‐transplant proteinuria associated with everolimus: Definition of main features with proteomics

M. Salvadori, M. Rastaldi, G. Ghiggeri, 2008, Proteomics. Clinical applications.

High‐resolution 2‐DE for resolving proteins, protein adducts and complexes in plasma

G. Ghiggeri, A. Urbani, G. Federici, 2008, Electrophoresis.

Angiotensin-converting enzyme (ACE) haplotypes and cyclosporine A (CsA) response: a model of the complex relationship between ACE quantitative trait locus and pathological phenotypes.

R. Ravazzolo, L. Finos, G. Ghiggeri, 2005, Human molecular genetics.

Genetic risk factors in typical haemolytic uraemic syndrome.

S. Ferracuti, A. Edefonti, L. Mannucci, 2009, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

2D-electrophoresis and the urine proteome map: where do we stand?

G. Ghiggeri, A. Urbani, G. Candiano, 2010, Journal of proteomics.

From hundreds to thousands: Widening the normal human Urinome (1).

G. Ghiggeri, P. Righetti, G. Candiano, 2015, Journal of proteomics.

"Cheek-to-cheek" urinary proteome profiling via combinatorial peptide ligand libraries: A novel, unexpected elution system.

A. Scaloni, G. Ghiggeri, P. Righetti, 2012, Journal of proteomics.

Neutrophil Extracellular Traps protein composition is specific for patients with Lupus nephritis and includes methyl-oxidized αenolase (methionine sulfoxide 93)

M. Prunotto, G. Ghiggeri, A. Vaglio, 2019, Scientific Reports.

Anti-Atp synthase β-chain autoantibodies

G. Ghiggeri, L. Musante, G. Candiano, 2007 .

CyTOF-Enabled Analysis Identifies Class-Switched B Cells as the Main Lymphocyte Subset Associated With Disease Relapse in Children With Idiopathic Nephrotic Syndrome

G. Ghiggeri, L. Perin, P. Cravedi, 2021, Frontiers in Immunology.

Teaching molecular genetics: chapter 4—positional cloning of genetic disorders

R. Ravazzolo, G. Ghiggeri, G. Caridi, 2007, Pediatric Nephrology.

Human urinary exosome proteome unveils its aerobic respiratory ability.

L. Ramenghi, G. Ghiggeri, I. Panfoli, 2016, Journal of proteomics.

Are the nail-patella syndrome and the autosomal Goltz-like syndrome the phenotypic expressions of different alleles at the COL5A1 locus?

G. Gimelli, G. Ghiggeri, G. Caridi, 1993, Human Genetics.

The kidney as a target organ in pharmaceutical research.

M. Prunotto, G. Ghiggeri, G. Gabbiani, 2011, Drug discovery today.

Urinary secretion and extracellular aggregation of mutant uromodulin isoforms.

F. Scolari, C. Izzi, A. Amoroso, 2012, Kidney international.

Juvenile nephronophthisis and related variants: clinical features and molecular approach.

G. Ghiggeri, G. Caridi, A. Carrea, 2001, Contributions to nephrology.

Posttransplant proteinuria associated with everolimus.

M. Salvadori, G. Ghiggeri, C. Boccardi, 2009, Transplantation Proceedings.

Combinatorial peptide ligand libraries for the analysis of low‐expression proteins: Validation for normal urine and definition of a first protein MAP

A. Scaloni, G. Ghiggeri, A. Urbani, 2012, Proteomics.

Neutrophil Extracellular Traps protein composition is specific for patients with Lupus nephritis and includes methyl-oxidized αenolase (methionine sulfoxide 93)

M. Prunotto, G. Ghiggeri, A. Vaglio, 2019, Scientific Reports.

Literature Abstracts

A. Farhi, F. Scolari, A. Amoroso, 2001, Pediatric Nephrology.

Metabolic Signature of Microvesicles from Umbilical Cord Mesenchymal Stem Cells of Preterm and Term Infants

L. Ramenghi, G. Ghiggeri, I. Panfoli, 2018, Proteomics. Clinical applications.

Proteome of Bovine Mitochondria and Rod Outer Segment Disks: Commonalities and Differences.

L. Manni, L. Ramenghi, G. Ghiggeri, 2018, Journal of proteome research.

Serum IgG2 antibody multicomposition in systemic lupus erythematosus and lupus nephritis (Part 1): cross-sectional analysis.

M. Prunotto, F. Locatelli, F. Scolari, 2020, Rheumatology.

IEF of Albumin in Low Denaturing Media. I: Analytical Aspects Related to Uremia

G. Ghiggeri, G. Candiano, C. Queirolo, 1985 .

A Comprehensive Proteomics Analysis of Urinary Extracellular Vesicles Identifies a Specific Kinase Protein Profile as a Novel Hallmark of Medullary Sponge Kidney Disease

G. Ghiggeri, G. Stallone, G. Zaza, 2022, Kidney international reports.

Proteomics Insights into Medullary Sponge Kidney Disease: Review of the Recent Results of an Italian Research Collaborative Network

G. Ghiggeri, G. Stallone, G. Zaza, 2022, Kidney and Blood Pressure Research.

Oxidative stress and galactose-deficient IgA1 as markers of progression in IgA nephropathy.

B. Julian, J. Novak, R. Camilla, 2011, Clinical journal of the American Society of Nephrology : CJASN.

Neutrophil Extracellular Traps in Systemic Lupus Erythematosus Stimulate IgG2 Production From B Lymphocytes

N. Pedemonte, G. Ghiggeri, S. Negrini, 2021, Frontiers in Medicine.

Reaction of 2-amino-2-deoxy-D-glucose and lysine: isolation and characterization of 2,5-bis(tetrahydroxybutyl)pyrazine.

E. Benfenati, G. Ghiggeri, G. Candiano, 1988, Carbohydrate research.

Serum IgG2 antibody multi-composition in systemic lupus erythematosus and in lupus nephritis (Part 2): prospective study

M. Prunotto, F. Locatelli, F. Scolari, 2020, Rheumatology.

Reaction of Aldoses with Amino Acids and Proteins. Part 3. Reaction of 2‐Amino‐2‐deoxy‐D‐glucose and Lysine: Isolation and Characterization of 2,5‐Bis(tetrahydroxybutyl)pyrazine.

E. Benfenati, G. Ghiggeri, G. Candiano, 1989 .

Characterization of the Major Browning Derivatives of Lysine with 2-Amino-2-Deoxy-D-Glucose

E. Benfenati, G. Ghiggeri, G. Candiano, 1990 .

Preparative high performance chromatography of a major browning compound derived from lysine and glucose.

G. Ghiggeri, R. Oleggini, F. Ginevri, 1989, Preparative biochemistry.

Reaction of human serum albumin with aldoses.

G. Vecchio, G. Ghiggeri, P. Righetti, 1985, Carbohydrate research.

Reaction of lysine with aldoses

G. Ghiggeri, P. Righetti, E. Gianazza, 1985 .

Post-transplant de novo non donor-specific HLA antibodies are not associated with poor graft outcome in non-sensitized pediatric recipients of kidney transplantation.

G. Ghiggeri, C. Klersy, M. Cioni, 2021, Transplant immunology.

DQ molecules are the principal stimulators of de novo donor‐specific antibodies in nonsensitized pediatric recipients receiving a first kidney transplant

G. Ghiggeri, C. Klersy, D. Palombo, 2014, Transplant international : official journal of the European Society for Organ Transplantation.

Kidney Intragraft Homing of De Novo Donor‐Specific HLA Antibodies Is an Essential Step of Antibody‐Mediated Damage but Not Per Se Predictive of Graft Loss

G. Ghiggeri, C. Klersy, M. Cioni, 2017, American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons.

Mechanisms Limiting Renal Tissue Protection and Repair in Glomerulonephritis

M. Prunotto, G. Ghiggeri, F. Lugani, 2023, International journal of molecular sciences.

Atypical presentation of Dent disease in a patient with interstitial Xp11.22 deletion

G. Ghiggeri, G. Caridi, A. Puliti, 2021, Journal of Nephrology.

Kidney Involvement in PSTPIP1 Associated Inflammatory Diseases (PAID): A Case Report and Review of the Literature

G. Ghiggeri, I. Ceccherini, G. Piaggio, 2021, Frontiers in Medicine.

Biological surface properties in extracellular vesicles and their effect on cargo proteins

G. Ghiggeri, I. Panfoli, Genny Del Zotto, 2019, Scientific Reports.

Second Wave Antibodies in Autoimmune Renal Diseases: The Case of Lupus Nephritis.

M. Prunotto, F. Locatelli, F. Scolari, 2021, Journal of the American Society of Nephrology : JASN.

State of the art in childhood nephrotic syndrome: concrete discoveries and unmet needs

G. Ghiggeri, F. Vincenti, A. Angeletti, 2023, Frontiers in immunology.

Transforming growth factor β blocks cystogenesis by MDCK epithelium in vitro by enhancing the paracellular flux: Implication of collagen V

G. Ghiggeri, A. Sessa, P. Altieri, 1998, Journal of cellular physiology.

Genome-wide association analyses define pathogenic signaling pathways and prioritize drug targets for IgA nephropathy

F. Kronenberg, P. Gregersen, C. Wijmenga, 2023, Nature Genetics.

Hyponatremic-hypertensive syndrome with extensive and reversible renal defects

G. Ghiggeri, A. Trivelli, F. Perfumo, 2004, Pediatric nephrology (Berlin, West).

Five cases of severe vesico-ureteric reflux in a family with an X-linked compatible trait

G. Ghiggeri, G. Caridi, M. Abbaszadegan, 2010, Pediatric Nephrology.

Neutrophil Extracellular Traps Profiles in Patients with Incident Systemic Lupus Erythematosus and Lupus Nephritis

F. Scolari, G. Ghiggeri, L. Allegri, 2019, The Journal of Rheumatology.

Age and memory B cells at baseline are associated with risk of relapse and memory B-cell reappearance following anti-CD20 treatment in pediatric frequently-relapsing/steroid-dependent nephrotic syndrome.

L. Ravà, P. Ravani, G. Ghiggeri, 2023, Kidney international.

Negative staining of proteins in polyacrylamide gels with methyl trichloroacetate.

G. Ghiggeri, M. Porotto, G. Candiano, 1996, Analytical biochemistry.

A novel WT1 gene mutation in a three-generation family with progressive isolated focal segmental glomerulosclerosis.

G. Ghiggeri, G. Caridi, S. Tosatto, 2010, Clinical journal of the American Society of Nephrology : CJASN.

Multi-population genome-wide association study implicates immune and non-immune factors in pediatric steroid-sensitive nephrotic syndrome

S. Raychaudhuri, V. Tasic, R. Loos, 2023, Nature communications.

Progression of chronic adriamycin nephropathy in leukopenic rats.

F. Callea, G. Ghiggeri, G. Salvidio, 1993, Nephron.

Amoxicillin-associated interference in an HPLC-EC assay for urinary fractionated metanephrines: potential pitfall in pheochromocytoma biochemical diagnosis.

G. Ghiggeri, G. Tripodi, M. Talio, 2014, Clinical biochemistry.

Anti-alpha-enolase antibodies in membranous nephropathy: isotype matters

G. Ghiggeri, G. Candiano, A. Bonanni, 2017, Clinical and Experimental Nephrology.

Erratum : Exome-wide Association Study Identifies GREB1L Mutations in Congenital Kidney Malformations (The American Journal of Human Genetics (2017) 101(5) (789–802) (S0002929717303877) (10.1016/j.ajhg.2017.09.018))

D. Goldstein, S. Mane, G. Ardissino, 2017 .

Combinatorial peptide ligand libraries for urine proteome analysis: Investigation of different elution systems

G. Ghiggeri, P. Righetti, E. Boschetti, 2009, Electrophoresis.

Mutations in MYH9 result in the May-Hegglin anomaly, and Fechtner and Sebastian syndromes. The May-Heggllin/Fechtner Syndrome Consortium.

U Magrini, R. Ravazzolo, P. Noris, 2000, Nature genetics.

Association between maternal omega‐3 polyunsaturated fatty acids supplementation and preterm delivery: A proteomic study

L. Ramenghi, G. Ghiggeri, I. Panfoli, 2020, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

Rare Single Nucleotide and Copy Number Variants and the Etiology of Congenital Obstructive Uropathy: Implications for Genetic Diagnosis

A. Latos-Bieleńska, J. McKiernan, Shrikant Mane, 2023, Journal of the American Society of Nephrology : JASN.

RPGRIP1L mutations are mainly associated with the cerebello‐renal phenotype of Joubert syndrome‐related disorders

T. Sanger, E. Bertini, M. Koenig, 2008, Clinical genetics.

Widening and diversifying the proteome capture by combinatorial peptide ligand libraries via Alcian Blue dye binding.

G. Ghiggeri, P. Righetti, E. Boschetti, 2015, Analytical chemistry.

Letter and Reply

G. Ghiggeri, C. Murtas, Sujoy Khan, 2011 .

A Novel WT 1 Gene Mutation in a Three-Generation Family with Progressive Isolated Focal Segmental Glomerulosclerosis

G. Ghiggeri, G. Caridi, S. Tosatto, 2010 .

Clinical and molecular heterogeneity of juvenile nephronophthisis in Italy: insights from molecular screening.

G. Ghiggeri, G. Caridi, F. Ginevri, 2000, American journal of kidney diseases : the official journal of the National Kidney Foundation.

Biologics in steroid resistant nephrotic syndrome in childhood: review and new hypothesis-driven treatment

G. Ghiggeri, G. Caridi, F. Lugani, 2023, Frontiers in immunology.

Nephronophthisis-medullary cystic kidney disease: from bedside to bench and back again.

F. Scolari, G. Ghiggeri, 2003, Saudi Journal of Kidney Diseases and Transplantation.

Evidence of further genetic heterogeneity in autosomal dominant medullary cystic kidney disease.

F. Scolari, G. Ghiggeri, G. Caridi, 2000, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Spectrophotometric determination of browning products of glycation of protein amino groups based on their reactivity with nitro blue tetrazolium salts.

G. Ghiggeri, R. Oleggini, F. Ginevri, 1988, The Analyst.

CureGN Study Rationale, Design, and Methods: Establishing a Large Prospective Observational Study of Glomerular Disease.

Krzysztof Kiryluk, Matthias Kretzler, Brenda W Gillespie, 2019, American journal of kidney diseases : the official journal of the National Kidney Foundation.

Circulating antipodocyte antibodies in membranous nephropathy: new findings.

G. Ghiggeri, L. Allegri, C. Murtas, 2013, American journal of kidney diseases : the official journal of the National Kidney Foundation.

Phenotypic expansion of DGKE-associated diseases.

V. D’Agati, R. Lifton, A. Gharavi, 2014, Journal of the American Society of Nephrology : JASN.

COQ2 nephropathy: a newly described inherited mitochondriopathy with primary renal involvement.

E. Bertini, F. Santorelli, G. Ghiggeri, 2007, Journal of the American Society of Nephrology : JASN.

The IgA nephropathy Biobank. An important starting point for the genetic dissection of a complex trait

K. Zerres, F. Scolari, A. Amoroso, 2005, BMC nephrology.

Urinary proteomics and drug discovery in chronic kidney disease: a new perspective.

P. Lescuyer, D. Hochstrasser, M. Prunotto, 2011, Journal of proteome research.

The impact of eNOS, MTR and MTHFR polymorphisms on renal graft survival in children and young adults.

A. Edefonti, G. Ghiggeri, S. Centi, 2009, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Immunity to Polyomavirus BK Infection: Immune Monitoring to Regulate the Balance between Risk of BKV Nephropathy and Induction of Alloimmunity

G. Ghiggeri, M. Luppi, M. Cioni, 2013, Clinical & developmental immunology.

Circulating anti‐actin and anti‐ATP synthase antibodies identify a sub‐set of patients with idiopathic nephrotic syndrome

G. Camussi, S. Sanna-Cherchi, G. Ghiggeri, 2005, Clinical and experimental immunology.

Microplastics and Kidneys: An Update on the Evidence for Deposition of Plastic Microparticles in Human Organs, Tissues and Fluids and Renal Toxicity Concern

G. Ghiggeri, G. Caridi, F. Lugani, 2023, International journal of molecular sciences.

Isoelectric focusing in low-denaturing media: visualization in renal disease of variation of the isoelectric point of albumin not related to a remarkable conformational variation.

G. Vecchio, G. Ghiggeri, G. Candiano, 1986, Journal of chromatography.

Purification of intact concanavalin A in tetramers by isoelectric focusing.

G. Vecchio, G. Ghiggeri, G. Candiano, 1987, Journal of Chromatography A.

Urinary secretion and extracellular aggregation of mutant uromodulin isoforms.

F. Scolari, C. Izzi, A. Amoroso, 2012, Kidney international.