ALPORT'S SYNDROME OF HEREDITARY NEPHRITIS WITH DEAFNESS-Reference-Cited by-同舟云学术

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ALPORT'S SYNDROME OF HEREDITARY NEPHRITIS WITH DEAFNESS

Published:1961-12 Issue:7216 Volume:278 Page:1321-1323
ISSN:0140-6736
Container-title:The Lancet
language:en
Short-container-title:The Lancet

Author:

Williamson D.A.J.

Publisher

Elsevier BV

Subject

General Medicine

Reference27 articles.

1. CONGENITAL, HEREDITARY, AND FAMILY HqMATURIA.

2. HEREDITARY FAMILIAL CONGENITAL HAEMORRHAGIC NEPHRITIS

Cited by 58 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. Metabolic Analysis and Renal Protective Effects of Linagliptin and Empagliflozin in Alport Syndrome;Kidney360;2024-05-23

2. Multidisciplinary management improves the genetic diagnosis of hereditary kidney diseases in the next generation sequencing (NGS) era;Nefrología (English Edition);2024-01

3. A Current Landscape on Alport Syndrome Cases: Characterization, Therapy and Management Perspectives;Biomedicines;2023-10-12

4. Empagliflozin reduces podocyte lipotoxicity in experimental Alport syndrome;eLife;2023-05-02

5. El manejo multidisciplinar mejora el diagnóstico genético de las enfermedades renales hereditarias en la era de next generation sequencing (NGS);Nefrología;2022-11

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