Genetics of Type III Bartter Syndrome in Spain, Proposed Diagnostic Algorithm-Reference-Cited by-同舟云学术

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

Published:2013-09-18 Issue:9 Volume:8 Page:e74673
ISSN:1932-6203
Container-title:PLoS ONE
language:en
Short-container-title:PLoS ONE

Author:

García Castaño Alejandro,Pérez de Nanclares Gustavo,Madariaga Leire,Aguirre Mireia,Madrid Alvaro,Nadal Inmaculada,Navarro Mercedes,Lucas Elena,Fijo Julia,Espino Mar,Espitaletta Zilac,Castaño Luis,Ariceta Gema,

Publisher

Public Library of Science (PLoS)

Subject

Multidisciplinary

Reference30 articles.

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3. Congenital hypokalemia with hypercalciuria in preterm infants: a hyperprostaglandinuric tubular syndrome different from Bartter syndrome;HW Seyberth;J Pediatr,1985

4. Bartter syndrome and its neonatal variant;W Proesmans;Eur J Pediatr,1997

5. Bartter’s syndrome comes of age;J Rodríguez Soriano;Pediatrics,1999

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3. Genetic diagnosis of Bartter syndrome in Iranian patients and detection of a novel homozygous CLCNKB mutation;Clinical Case Reports;2022-12

4. Phenotypic and genotypic characteristics of children with bartter syndrome;The Turkish Journal of Pediatrics;2022

5. Identification of a Novel CLCNKB Mutation in an Iranian Family with Bartter Syndrome Type 3.;Journal of Advances in Medical and Biomedical Research;2022-01-01