Typical Features of Amelogenesis Imperfecta in Two Patients with Bartter’s Syndrome-Reference-Cited by-同舟云学术

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Typical Features of Amelogenesis Imperfecta in Two Patients with Bartter’s Syndrome

Published:2012-12-18 Issue:1 Volume:2 Page:319-325
ISSN:1664-5529
Container-title:Nephron Extra
language:en
Short-container-title:Nephron Extra

Author:

Martelli-Júnior Hercílio,Ferreira Shirlene Pimentel,Pereira Paula Cristina B.,Coletta Ricardo D.,de Aquino Sibele Nascimento,Miranda Débora Marques,Simões e Silva Ana Cristina

Publisher

S. Karger AG

Subject

Nephrology

Cited by 7 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Dentofacial manifestations in a child with Jalili syndrome;Special Care in Dentistry;2023-12-27

2. Abnormal teeth and renal calcifications: Answers;Pediatric Nephrology;2023-03-14

3. Genetic evaluation of paediatric nephrocalcinosis: phenotype-driven genetic panels reveal a rare diagnosis;Clinical Kidney Journal;2021-12-17

4. Late-onset Bartter syndrome type II;Clinical Kidney Journal;2017-05-08

5. Amelogenesis imperfecta in familial hypomagnesaemia and hypercalciuria with nephrocalcinosis caused byCLDN19gene mutations;Journal of Medical Genetics;2016-08-16

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