Á. Madrid

发表

Mesangial C4d Deposits in Early IgA Nephropathy.

G. Ariceta, E. Jatem, A. Segarra, 2017, Clinical journal of the American Society of Nephrology : CJASN.

A kidney-disease gene panel allows a comprehensive genetic diagnosis of cystic and glomerular inherited kidney diseases.

D. Torrents, E. Ars, I. Llano‐Rivas, 2018, Kidney international.

Novel mutations associated with nephrogenic diabetes insipidus. A clinical-genetic study

G. Ariceta, F. Santos, J. A. Camacho, 2015, European Journal of Pediatrics.

The Density of Renal Lymphatics Correlates With Clinical Outcomes in IgA Nephropathy

L. Quintana, E. Poch, M. Blasco, 2022, Kidney international reports.

Single-cycle rituximab-induced immunologic changes in children

M. Juan, A. Vlagea, L. Alsina, 2020, Neurology: Neuroimmunology & Neuroinflammation.

SARS-CoV-2 infection in Spanish children with chronic kidney pathologies

Á. Madrid, M. Melgosa, F. Nieto, 2020, Pediatric Nephrology.

Charcoal Hemoperfusion for Methotrexate Toxicity: A Safe and Effective Life-Rescue Alternative When Glucarpidase Is Not Available

G. Ariceta, Á. Madrid, J. Dapena, 2021, Frontiers in Pediatrics.

Multidimensional inflammatory and immunological endotypes of idiopathic focal segmental glomerulosclerosis and their association with treatment outcomes

E. Jatem, Jorge González, A. Segarra, 2020, Clinical kidney journal.

CD44-negative parietal–epithelial cell staining in minimal change disease: association with clinical features, response to corticosteroids and kidney outcome

M. Santacana, E. Jatem, Jorge González, 2021, Clinical kidney journal.

Long-term eculizumab improves clinical outcomes in atypical hemolytic uremic syndrome

Á. Madrid, R. Vilalta, M. Muňoz, 2012, Pediatric Nephrology.

Intracranial Hypertension in Cystinosis Is a Challenge: Experience in a Children's Hospital.

Sílvia Alarcón, G. Ariceta, N. Martín-Begué, 2016, JIMD reports.

Mutations in sphingosine-1-phosphate lyase cause nephrosis with ichthyosis and adrenal insufficiency

K. Schwarz, T. Giese, R. Lifton, 2017, The Journal of clinical investigation.

Activation of the acute inflammatory phase response in idiopathic nephrotic syndrome: association with clinicopathological phenotypes and with response to corticosteroids

E. Jatem, A. Segarra, Cristina Martínez, 2021, Clinical kidney journal.

Targeted next-generation sequencing in steroid-resistant nephrotic syndrome: mutations in multiple glomerular genes may influence disease severity

X. Estivill, S. Ossowski, D. Trujillano, 2014, European Journal of Human Genetics.

Claudin-19 Mutations and Clinical Phenotype in Spanish Patients with Familial Hypomagnesemia with Hypercalciuria and Nephrocalcinosis

G. Ariceta, F. Claverie-Martin, F. Santos, 2013, PloS one.

Nephrin mutations cause childhood- and adult-onset focal segmental glomerulosclerosis.

P. Fernández-Llama, E. Ars, J. Ballarín, 2009, Kidney international.

TRPC6 mutational analysis in a large cohort of patients with focal segmental glomerulosclerosis.

P. Fernández-Llama, E. Ars, J. Rosell, 2009, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Dent’s disease: Identification of seven new pathogenic mutations in the CLCN5 gene

G. Ariceta, F. Claverie-Martin, M. García-Ramírez, 2013, Journal of Pediatric Genetics.

Genetics of Type III Bartter Syndrome in Spain, Proposed Diagnostic Algorithm

G. Ariceta, E. Lucas, L. Castaño, 2013, PloS one.

Complement Genetic Variants and FH Desialylation in S. pneumoniae-Haemolytic Uraemic Syndrome

P. Sánchez-Corral, Á. Szilágyi, Z. Prohászka, 2021, Frontiers in Immunology.

Very low-molecular-mass fragments of albumin in the plasma of patients with focal segmental glomerulosclerosis.

R. Torra, A. Meseguer, F. Canals, 2009, American journal of kidney diseases : the official journal of the National Kidney Foundation.

Primary distal renal tubular acidosis: novel findings in patients studied by next-generation sequencing

E. Coto, F. Santos, H. Gil-Peña, 2016, Pediatric Research.

Vascular thrombosis in pediatric kidney transplantation: Graft survival is possible with adequate management.

G. Ariceta, J. Molino, Á. Madrid, 2018, Journal of pediatric urology.

Overcoming limits: First ABO incompatible living donor paired kidney transplant in an hypersensitized pediatric recipient in Spain

F. Diekmann, I. Revuelta, F. Oppenheimer, 2022, Pediatric transplantation.

Poor phenotype-genotype association in a large series of patients with Type III Bartter syndrome

G. Ariceta, E. Lucas, L. Castaño, 2017, PloS one.

Improvement of refractory pruritus after lipoprotein‐apheresis in arthrogryposis‐renal failure‐cholestasis syndrome

G. Ariceta, Á. Madrid, A. Rosales, 2018, Journal of clinical apheresis.

Delayed graft function is reduced with antithymocyte globulin induction in pediatric kidney transplantation.

Á. Madrid, R. Vilalta, J. Nieto, 2009, Transplantation proceedings.

Reversal of hyperoxaluric cardiomyopathy with severe cardiac dysfunction after combined liver and kidney transplantation.

J. Girona, Á. Madrid, D. Albert, 2013, Revista espanola de cardiologia.

Primary distal renal tubular acidosis: novel findings in patients studied by next-generation sequencing

E. Coto, F. Santos, H. Gil-Peña, 2018, Pediatric Research.