Major involvement of trunk muscles in myotonic dystrophy type 1-Reference-Cited by-同舟云学术

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Major involvement of trunk muscles in myotonic dystrophy type 1

Published:2016-02-01 Issue:6 Volume:134 Page:467-473
ISSN:0001-6314
Container-title:Acta Neurologica Scandinavica
language:en
Short-container-title:Acta Neurol Scand

Author:

Solbakken G.¹²,Ørstavik K.²,Hagen T.¹,Dietrichs E.²³,Naerland T.³⁴

Affiliation:

1. Department of Neurology; Drammen Hospital; Vestre Viken Health Trust; Drammen Norway

2. Department of Neurology; Oslo University Hospital; Oslo Norway

3. Institute of Clinical Medicine; University of Oslo; Oslo Norway

4. NevSom - Department of Rare Disorders and Disabilities; Oslo University Hospital; Oslo Norway

Funder

Norwegian Society for Neuromuscular Disorders

Norwegian Directorate of Health

Publisher

Wiley

Subject

Neurology (clinical),Neurology,General Medicine

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/ane.12565/fullpdf

Reference30 articles.

1. Molecular basis of myotonic dystrophy: expansion of a trinucleotide (CTG) repeat at the 3' end of a transcript encoding a protein kinase family member;Brook;Cell,1992

2. The myotonic dystrophies: molecular, clinical, and therapeutic challenges;Udd;Lancet Neurol,2012

3. Myotonic dystrophy: from bench to bedside;Johnson;Semin Neurol,2012

4. Assessment of a disease-specific muscular impairment rating scale in myotonic dystrophy;Mathieu;Neurology,2001

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1. Myotonic dystrophy type 1 – a multiorgan disorder;Tidsskrift for Den norske legeforening;2024-04-16

2. Walking test outcomes in adults with genetic neuromuscular diseases: a systematic literature review of their measurement properties;European Journal of Physical and Rehabilitation Medicine;2024-04

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4. Small and large fiber neuropathy in adults with myotonic dystrophy type 1;Frontiers in Neurology;2024-03-05

5. Translation, reliability, and validity of the Norwegian version of the ABILHAND-NMD and the ACTIVLIM for Myotonic Dystrophy type 1;Disability and Rehabilitation;2023-07-12

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