Hereditary renal amyloidosis caused by a heterozygous G654A gelsolin mutation: a report of two cases-Reference-Cited by-同舟云学术

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Hereditary renal amyloidosis caused by a heterozygous G654A gelsolin mutation: a report of two cases

Published:2013-03-27 Issue:2 Volume:6 Page:189-193
ISSN:2048-8505
Container-title:Clinical Kidney Journal
language:en
Short-container-title:Clinical Kidney Journal

Author:

Yamanaka S.,Miyazaki Y.,Kasai K.,Ikeda S.-i.,Kiuru-Enari S.,Hosoya T.

Publisher

Oxford University Press (OUP)

Subject

Transplantation,Nephrology

Link

http://academic.oup.com/ckj/article-pdf/6/2/189/1086423/sft007.pdf

Reference24 articles.

1. A New Human Hereditary Amyloidosis: The Result of a Stop-Codon Mutation in the Apolipoprotein AII Gene

2. Diagnosis, Pathogenesis, Treatment, and Prognosis of Hereditary Fibrinogen Aα-Chain Amyloidosis

3. HEREDITARY GENERALIZED AMYLOIDOSIS WITH POLYNEUROPATHY

4. Familial amyloidosis of the Finnish type (FAF)

5. Finnish hereditary amyloidosis

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1. Urological and Kidney Involvements in Amyloidosis;Amyloidosis and Fabry Disease;2023

2. Renal amyloidosis: a new time for a complete diagnosis;Brazilian Journal of Medical and Biological Research;2022

3. Hearing problems in patients with hereditary gelsolin amyloidosis;Orphanet Journal of Rare Diseases;2021-10-24

4. The first Chinese renal gelsolin amyloidosis with the p.Asp174Asn mutation in the GSN gene: Nephrology picture;Journal of Nephrology;2021-01-04

5. Renal amyloidosis: an update on diagnosis and pathogenesis;Protoplasma;2020-05-24

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