A case of GNE myopathy mimicking hereditary motor neuropathy-Reference-Cited by-同舟云学术

A case of GNE myopathy mimicking hereditary motor neuropathy

Published:2020-10-13 Issue:11 Volume:27 Page:2389-2391
ISSN:1351-5101
Container-title:European Journal of Neurology
language:en
Short-container-title:Eur J Neurol

Author:

Huang Y.‐N.¹,Chuang H.‐J.²,Hsueh H.‐W.¹^ORCID,Huang H.‐C.³,Lee N.‐C.⁴,Chao C.‐C.¹^ORCID,Huang P.‐H.⁵,Lee Y.‐C.⁶⁷^ORCID,Lin K.‐P.⁶⁷,Yang C.‐C.¹,Hsieh S.‐T.¹^ORCID

Affiliation:

1. Department of Neurology National Taiwan University Hospital College of Medicine National Taiwan University TaipeiTaiwan

2. Department of Physical Medicine and Rehabilitation National Taiwan University Hospital College of Medicine National Taiwan University TaipeiTaiwan

3. Department of Medical Imaging National Taiwan University Hospital College of Medicine National Taiwan University TaipeiTaiwan

4. Department of Medal Genetics National Taiwan University Hospital College of Medicine National Taiwan University TaipeiTaiwan

5. Department of Pathology National Taiwan University Hospital College of Medicine National Taiwan University TaipeiTaiwan

6. Department of Neurology Taipei Veterans General Hospital TaipeiTaiwan

7. Department of Neurology National Yang‐Ming University School of Medicine Taipei Taiwan

Publisher

Wiley

Subject

Clinical Neurology,Neurology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/ene.14489

Reference7 articles.

1. GNE myopathy: current update and future therapy

2. A new de novo missense mutation in MYH2 expands clinical and genetic findings in hereditary myosin myopathies

3. Atypical presentation of GNE myopathy with asymmetric hand weakness

4. Next-generation sequencing approaches for the diagnosis of skeletal muscle disorders

5. Muscle MRI in muscular dystrophies;Díaz‐Manera J;Acta Myol,2015

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