Clinical Features and Long-Term Outcome of Nephrotic Syndrome Associated with HeterozygousNPHS1andNPHS2Mutations-Reference-Cited by-同舟云学术

Clinical Features and Long-Term Outcome of Nephrotic Syndrome Associated with HeterozygousNPHS1andNPHS2Mutations

Published:2009-04-30 Issue:6 Volume:4 Page:1065-1072
ISSN:1555-9041
Container-title:Clinical Journal of the American Society of Nephrology
language:en
Short-container-title:CJASN

Author:

Caridi Gianluca,Gigante Maddalena,Ravani Pietro,Trivelli Antonella,Barbano Giancarlo,Scolari Francesco,Dagnino Monica,Murer Luisa,Murtas Corrado,Edefonti Alberto,Allegri Landino,Amore Alessandro,Coppo Rosanna,Emma Francesco,De Palo Tommaso,Penza Rosa,Gesualdo Loreto,Ghiggeri Gian Marco

Publisher

American Society of Nephrology (ASN)

Subject

Transplantation,Nephrology,Critical Care and Intensive Care Medicine,Epidemiology

Reference30 articles.

1. Mutations in ACTN4, encoding α-actinin-4, cause familial focal segmental glomerulosclerosis

2. NPHS2, encoding the glomerular protein podocin, is mutated in autosomal recessive steroid-resistant nephrotic syndrome

3. Broadening the Spectrum of Diseases Related to Podocin Mutations

4. Patients with Mutations in NPHS2 (Podocin) Do Not Respond to Standard Steroid Treatment of Nephrotic Syndrome

Cited by 40 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. Estimation of the Age of the Kashubian-Specific Pathogenic NPHS2 Variant Responsible for Hereditary Steroid-Resistant Nephrotic Syndrome Points to Its Recent Local Origin;Human Mutation;2024-03-21

2. NPHS1 Gene Mutations in Children with Focal Segmental Glomerulosclerosis and Literature Review;Advances in Clinical Medicine;2024

3. Mono- and biallelic variant effects on disease at biobank scale;Nature;2023-01-18

4. Genetic diversity in Kashubs: the regional increase in the frequency of several disease-causing variants;Journal of Applied Genetics;2022-08-15

5. The Clinical and Genetic Features in Chinese Children With Steroid-Resistant or Early-Onset Nephrotic Syndrome: A Multicenter Cohort Study;Frontiers in Medicine;2022-06-09