Urinary titin as a biomarker in Fukuyama congenital muscular dystrophy-Reference-Cited by-同舟云学术

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Urinary titin as a biomarker in Fukuyama congenital muscular dystrophy

Published:2021-03 Issue:3 Volume:31 Page:194-197
ISSN:0960-8966
Container-title:Neuromuscular Disorders
language:en
Short-container-title:Neuromuscular Disorders

Author:

Sato Takatoshi,Awano Hiroyuki,Ishiguro Kumiko,Shichiji Minobu,Murakami Terumi,Shirakawa Taku,Matsuo Masafumi,Nagata Satoru,Ishigaki Keiko

Funder

National Center of Neurology and Psychiatry

Japan Agency for Medical Research and Development

Publisher

Elsevier BV

Subject

Genetics(clinical),Clinical Neurology,Neurology,Pediatrics, Perinatology, and Child Health

Reference15 articles.

1. Congenital progressive muscular dystrophy of the Fukuyama type – clinical, genetic and pathological considerations;Fukuyama;Brain Dev,1981

2. An ancient retrotransposal insertion causes Fukuyama-type congenital muscular dystrophy;Kobayashi;Nature,1998

3. Establishment of a highly sensitive sandwich ELISA for the N-terminal fragment of titin in urine;Maruyama;Sci Rep,2016

4. Titin gene and protein functions in passive and active muscle;Linke;Annu Rev Physiol,2018

5. Diagnostic and clinical significance of the titin fragment in urine of Duchenne muscular dystrophy patients;Awano;Clin Chim Acta,2018

Cited by 3 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. An insight to Fukuyama congenital muscular dystrophy (FCMD): Report of a rare case;Medical Reports;2024-02

2. Urinary titin in myotonic dystrophy type 1;Muscle & Nerve;2023-06-08

3. A sandwich ELISA kit reveals marked elevation of titin N‐terminal fragment levels in the urine of mdx mice;Animal Models and Experimental Medicine;2022-02

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