Re-evaluation of the symptoms of Hirayama disease through anatomical perspective-Reference-Cited by-同舟云学术

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Re-evaluation of the symptoms of Hirayama disease through anatomical perspective

Published:2023-02-28 Issue:1 Volume:12 Page:62-66
ISSN:2186-361X
Container-title:Intractable & Rare Diseases Research
language:en
Short-container-title:IRDR

Author:

Tekin Bahar¹,Ansen Gamze²,Ormeci Tugrul³,Helvaci Yilmaz Nesrin⁴,Sakul Bayram Ufuk¹

Affiliation:

1. Department of Anatomy, Faculty of Medicine, Istanbul Medipol University, Istanbul, Turkey.

2. Department of Anatomy, School of Medicine, Institute of Health Sciences, Istanbul Medipol University, Istanbul, Turkey.

3. Department of Radiology, Faculty of Medicine, Istanbul Medipol University, Istanbul, Turkey.

4. Department of Neurology, Faculty of Medicine, Istanbul Medipol University, Istanbul, Turkey.

Publisher

International Research and Cooperation Association for Bio & Socio-Sciences Advancement (IRCA-BSSA)

Subject

General Medicine

Link

https://www.jstage.jst.go.jp/article/irdr/12/1/12_2022.01117/_pdf

Reference21 articles.

1. 1. Hirayama K. Juvenile muscular atrophy of distal upper extremity (Hirayama disease). Internal medicine. 2000; 39:283-290.

2. 2. Sitt CM, Fung LW, Yuen HY, Ahuja AT. Hirayama disease in a 17-year-old Chinese man. Singapore Med J. 2014; 55:e87-89.

3. 3. Zahid M, Wasim M, Ghaffar YA, Shahbaz NN, Abdullah M, Khatri IA. A case of Hirayama disease in Pakistan. J Pak Med Assoc. 2007; 57:41-44.

4. 4. de Carvalho M, Swash M. Monomelic neurogenic syndromes: a prospective study. J Neurol Sci. 2007; 263:26-34.

5. 5. O’Brien M. Aids to the examination of the peripheral nervous system (Fifth Edition). WB Saunders, London, UK, 2010; pp. 64-66.

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