Challenge in pathologic diagnosis of Alport syndrome: evidence from correction of previous misdiagnosis-Reference-Cited by-同舟云学术

Challenge in pathologic diagnosis of Alport syndrome: evidence from correction of previous misdiagnosis

Published:2012 Issue:1 Volume:7 Page:100
ISSN:1750-1172
Container-title:Orphanet Journal of Rare Diseases
language:en
Short-container-title:Orphanet Journal of Rare Diseases

Author:

Yao Xiao-dan,Chen Xin,Huang Gao-yuan,Yu Yan-ting,Xu Shu-tian,Hu Yang-lin,Wang Qing-wen,Chen Hui-ping,Zeng Cai-hong,Ji Da-xi,Hu Wei-xin,Tang Zheng,Liu Zhi-hong

Publisher

Springer Science and Business Media LLC

Subject

Pharmacology (medical),Genetics(clinical),General Medicine

Reference30 articles.

1. The clinical spectrum of hereditary nephritis

2. HEREDITARY FAMILIAL CONGENITAL HAEMORRHAGIC NEPHRITIS

3. Genetic heterogeneity of Alport syndrome

4. Identification of mutations in the α3(IV) and α4(IV) collagen genes in autosomal recessive Alport syndrome

5. Identification of Mutations in the COL4A5 Collagen Gene in Alport Syndrome

Cited by 19 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. Frail inner limiting membrane maculopathy suggested to describe a new retinal Alport-like condition with two variants in three generations of females;Ophthalmic Genetics;2024-01-10

2. Clinicopathological Features of Hereditary Nephritis in the Iranian Population: Analysis of a 14-Year Survey in Kidney Biopsies From a Large Referral Center;Archives of Iranian Medicine;2024-01-01

3. Alport syndrome: new advances in the last decade;Childhood Kidney Diseases;2022-05-27

4. Role of Ultrastructural Study in the Diagnosis of Medical Renal Diseases: A Tertiary Medical Center Experience and Review of the Literature;Saudi Journal of Kidney Diseases and Transplantation;2022

5. Genetic testing in the diagnosis of chronic kidney disease: recommendations for clinical practice;Nephrology Dialysis Transplantation;2021-07-15