A. Carrea

发表

Mutations in DSTYK and dominant urinary tract malformations.

R. Ravazzolo, A. Latos-Bieleńska, V. D’Agati, 2013, The New England journal of medicine.

Failure of regulation results in an amplified oxidation burst by neutrophils in children with primary nephrotic syndrome

G. Ghiggeri, M. Bodria, M. Cioni, 2010, Clinical and experimental immunology.

Cyclosporine in patients with steroid-resistant nephrotic syndrome: an open-label, nonrandomized, retrospective study.

G. Rizzoni, F. Scolari, S. Sanna-Cherchi, 2004, Clinical therapeutics.

Continuous Ambulatory Peritoneal Dialysis (CAPD) of Children with Amino Acid Solutions: Technical and Metabolic Aspects

A. Carrea, R. Gusmano, F. Perfumo, 1990, Peritoneal dialysis international : journal of the International Society for Peritoneal Dialysis.

Hyperinsulinemia and Insulin Resistance, Early Cardiovascular Risk Factors in Children with Chronic Kidney Disease

B. Lindholm, J. Axelsson, A. Qureshi, 2008, Blood Purification.

Acute effects of simultaneous intraperitoneal infusion of glucose and amino acids.

A. Trivelli, E. Verrina, A. Carrea, 2001, Kidney international.

Long-term effect of amino-acid dialysis solution in children on continuous ambulatory peritoneal dialysis

E. Verrina, A. Carrea, R. Gusmano, 1991, Pediatric Nephrology.

Nutritional status and muscle amino acids in children with end-stage renal failure

J. C. Divino Filho, A. Carrea, F. Perfumo, 1993, Pediatric Nephrology.

Nutritional status and muscle amino acids in children with end-stage renal failure.

A. Carrea, R. Gusmano, F. Perfumo, 1992 .

Measurement of free amino acids in polymorphonuclear leukocytes by high-performance liquid chromatography.

A. Carrea, R. Gusmano, F. Perfumo, 1989, Journal of chromatography.

Value of Intraperitoneal Amino Acids in Children Treated with Chronic Peritoneal Dialysis

E. Verrina, A. Carrea, R. Gusmano, 1999, Peritoneal dialysis international : journal of the International Society for Peritoneal Dialysis.

Nutritional Status in Children Receiving Chronic Peritoneal Dialysis

A. Trivelli, A. Carrea, R. Gusmano, 1996, Peritoneal dialysis international : journal of the International Society for Peritoneal Dialysis.

Biochemical and Hormonal Abnormalities of Mineral Metabolism in Children on Continuous Ambulatory Peritoneal Dialysis

R. Oleggini, F. Ginevri, A. Carrea, 1985 .

Phenotypic expansion of DGKE-associated diseases.

V. D’Agati, R. Lifton, A. Gharavi, 2014, 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.

Broadening the spectrum of diseases related to podocin mutations.

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

Proteolytic Activity and Free Amino Acid Concentrations in Polymorphonuclear Leucocytes

E. Verrina, A. Carrea, R. Gusmano, 1993, Annals of clinical biochemistry.

Apolipoprotein E in idiopathic nephrotic syndrome and focal segmental glomerulosclerosis.

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

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.

Homocysteine, folate, vitamin B12 levels, and C677T MTHFR mutation in children with renal failure

G. Caridi, G. Minniti, M. Calevo, 2003, Pediatric Nephrology.

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.

Genetic Drivers of Kidney Defects in the DiGeorge Syndrome

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

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.

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

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

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

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

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

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

Free amino acids in plasma, red blood cells, polymorphonuclear leukocytes, and muscle in normal and uraemic children.

E. Verrina, A. Carrea, F. Perfumo, 2002, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

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.

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.

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

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

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.

Phenotypic expansion of DGKE-associated diseases.

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

Nutritional status and muscle amino acids in children with end-stage renal failure

J. C. Divino Filho, A. Carrea, F. Perfumo, 1992, Pediatric Nephrology.

Muscle and plasma amino acids and nutritional status in kidney-transplanted children.

E. Verrina, J. Bergström, A. Carrea, 1994, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.