List of works - Alvaro Madrid

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

article

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

article published in 2013

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

scientific article published in July 2009

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

scientific article

Genetics of type III Bartter syndrome in Spain, proposed diagnostic algorithm

scientific article

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

scientific article published on 24 October 2017

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

scientific article

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

scientific article

Mesangial C4d Deposits in Early IgA Nephropathy.

scientific article published on 16 November 2017

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

scientific article published on 06 February 2017

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

article

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

scientific article published on 23 April 2015

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

scientific article

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

scientific article published in November 2017

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

scientific article published on 16 November 2015

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

scientific article published on 25 September 2012

Single-cycle rituximab-induced immunologic changes in children: Enhanced in neuroimmunologic disease?

scientific article published on 06 May 2020

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

scientific article published on 20 May 2009

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

scientific article

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

scientific article published on 20 March 2018

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

scientific article published on 25 September 2009

List of works by Alvaro Madrid

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

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

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

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

Genetics of type III Bartter syndrome in Spain, proposed diagnostic algorithm

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

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

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

Mesangial C4d Deposits in Early IgA Nephropathy.

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

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

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

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

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

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

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

Single-cycle rituximab-induced immunologic changes in children: Enhanced in neuroimmunologic disease?

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

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

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

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