» Articles » PMID: 16998221

Amyloidosis-related Nephrotic Syndrome Due to a G654A Gelsolin Mutation: the First Report from the Middle East

Overview
Date 2006 Sep 26
PMID 16998221
Citations 18
Authors
Affiliations
Soon will be listed here.
Citing Articles

Photoreceptor Disc Morphogenesis: Who Are the Conductors of This Highly Metronomic Process?.

Megaw R Adv Exp Med Biol. 2025; 1468:305-308.

PMID: 39930213 DOI: 10.1007/978-3-031-76550-6_50.


Gelsolin amyloidosis associated with the p.D214N gelsolin gene mutation in a Chinese family.

Wang S, Li D, Xu J, Song W, Wang S Kidney Res Clin Pract. 2024; 43(5):693-696.

PMID: 39390625 PMC: 11467366. DOI: 10.23876/j.krcp.24.130.


Clinical Features and Brain MRI Findings in Korean Patients with AGel Amyloidosis.

Cheong E, Paik W, Choi Y, Lim Y, Kim H, Shim W Yonsei Med J. 2021; 62(5):431-438.

PMID: 33908214 PMC: 8084699. DOI: 10.3349/ymj.2021.62.5.431.


Analyses Mutations in , and Genes in Chinese Patients With Alzheimer's Disease.

Jiang Y, Jiao B, Liao X, Xiao X, Liu X, Shen L Front Aging Neurosci. 2020; 12:581524.

PMID: 33192475 PMC: 7533594. DOI: 10.3389/fnagi.2020.581524.


Clinical, histopathological, and in silico pathogenicity analyses in a pedigree with familial amyloidosis of the Finnish type (Meretoja syndrome) caused by a novel gelsolin mutation.

Cabral-Macias J, Garcia-Montano L, Perezpena-Diazconti M, Aguilar M, Garcia G, Vencedor-Meraz C Mol Vis. 2020; 26:345-354.

PMID: 32368002 PMC: 7195602.