Clinical and pathological phenotype of genetic causes of focal segmental glomerulosclerosis in adults-Reference-Cited by-同舟云学术

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Clinical and pathological phenotype of genetic causes of focal segmental glomerulosclerosis in adults

Published:2018-01-09 Issue:2 Volume:11 Page:179-190
ISSN:2048-8505
Container-title:Clinical Kidney Journal
language:en
Short-container-title:

Author:

Lepori Nicola¹²,Zand Ladan¹,Sethi Sanjeev³,Fernandez-Juarez Gema¹⁴,Fervenza Fernando C¹

Affiliation:

1. Division of Nephrology and Hypertension, Mayo Clinic, Rochester, MN, USA

2. Division of Nephrology and Dialysis, Azienda Ospedaliera G. Brotzu, Cagliari, Italy

3. Division of Anatomic Pathology, Mayo Clinic, Rochester, MN, USA

4. Nephrology Division, Hospital Universitario Fundacion Alcorcon, Madrid, Spain

Publisher

Oxford University Press (OUP)

Subject

Transplantation,Nephrology

Link

http://academic.oup.com/ckj/article-pdf/11/2/179/25084934/sfx143.pdf

Reference73 articles.

1. Focal segmental glomerulosclerosis: towards a better understanding for the practicing nephrologist;Sethi;Nephrol Dial Transplant,2015

2. Focal segmental glomerulosclerosis;D’Agati;N Engl J Med,2011

3. Podocyte foot process effacement as a diagnostic tool in focal segmental glomerulosclerosis;Deegens;Kidney Int,2008

4. The incidence of primary versus secondary focal segmental glomerulosclerosis: a clinicopathological study;Hommos;Mayo Clin Proc,2017

5. Genetic testing in steroid-resistant nephrotic syndrome: when and how?;Lovric;Nephrol Dial Transplant,2016

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1. Kidney involvement in rare hereditary diseases;Terapevticheskii arkhiv;2024-07-07

2. Genetic Causes of Nephrotic Syndrome and Focal and Segmental Glomerulosclerosis;Advances in Kidney Disease and Health;2024-07

3. A Review of Focal Segmental Glomerulosclerosis Classification With a Focus on Genetic Associations;Kidney Medicine;2024-06

4. Novel Pathogenic Mutation of P209L in TRPC6 Gene Causes Adult Focal Segmental Glomerulosclerosis;Biochemical Genetics;2024-02-05

5. The most common founder pathogenic variant c.868G > A (p.Val290Met) in the NPHS2 gene in a representative adult Czech cohort with focal segmental glomerulosclerosis is associated with a milder disease and its underdiagnosis in childhood;Frontiers in Medicine;2023-12-19

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