Expanded clinical spectrum of oculopharyngodistal myopathy type 1-Reference-Cited by-同舟云学术

Expanded clinical spectrum of oculopharyngodistal myopathy type 1

Published:2022-09-27 Issue:6 Volume:66 Page:679-685
ISSN:0148-639X
Container-title:Muscle & Nerve
language:en
Short-container-title:Muscle and Nerve

Author:

Shimizu Takahiro¹^ORCID,Ishiura Hiroyuki¹,Hara Manato¹,Shibata Shota¹,Unuma Atsushi¹,Kubota Akatsuki¹,Sakuishi Kaori¹²,Inoue Kiyoharu³,Goto Jun¹⁴,Takahashi Yuji¹⁵,Shirota Yuichiro¹⁶,Hamada Masashi¹,Shimizu Jun¹⁷,Tsuji Shoji¹⁸⁹,Toda Tatsushi¹

Affiliation:

1. Department of Neurology, Graduate School of Medicine University of Tokyo Tokyo Japan

2. Department of Neurology Teikyo University Chiba Medical Center Chiba Japan

3. Department of Neurology Fujieda Heisei Memorial Hospital Shizuoka Japan

4. Department of Neurology International University of Health and Welfare Mita Hospital Tokyo Japan

5. Department of Neurology National Center Hospital, National Center of Neurology and Psychiatry Tokyo Japan

6. Department of Clinical Laboratory University of Tokyo Hospital Tokyo Japan

7. Department of Physical Therapy, School of Health Sciences Tokyo University of Technology Tokyo Japan

8. Department of Molecular Neurology, Graduate School of Medicine University of Tokyo Tokyo Japan

9. Institute of Medical Genomics International University of Health and Welfare Chiba Japan

Funder

Japan Agency for Medical Research and Development

Japan Society for the Promotion of Science

Publisher

Wiley

Subject

Physiology (medical),Cellular and Molecular Neuroscience,Neurology (clinical),Physiology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/mus.27717

Reference22 articles.

1. Oculopharyngodistal Myopathy

2. Autosomal recessive oculopharyngodistal myopathy in light of distal myopathy with rimmed vacuoles and oculopharyngeal muscular dystrophy

3. Oculopharyngodistal myopathy is genetically heterogeneous and most cases are distinct from oculopharyngeal muscular dystrophy

4. Autosomal recessive oculopharyngodistal myopathy: a distinct phenotypical, histological, and genetic entity

5. The clinical and myopathological features of oculopharyngodistal myopathy in a Chinese family;Lu H;Neuromuscul Disord.,2008

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