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1.
Chromosome 10q-linked FSHD identifies DUX4 as principal disease gene.
J Med Genet
; 59(2): 180-188, 2022 02.
Article
in English
| MEDLINE | ID: mdl-33436523
2.
Reduced specific force in patients with mild and severe facioscapulohumeral muscular dystrophy.
Muscle Nerve
; 63(1): 60-67, 2021 01.
Article
in English
| MEDLINE | ID: mdl-32959362
3.
Strength training and aerobic exercise training for muscle disease.
Cochrane Database Syst Rev
; 12: CD003907, 2019 12 06.
Article
in English
| MEDLINE | ID: mdl-31808555
4.
What's in a name? The clinical features of facioscapulohumeral muscular dystrophy.
Pract Neurol
; 16(3): 201-7, 2016 Jun.
Article
in English
| MEDLINE | ID: mdl-26862222
5.
The Dutch registry for facioscapulohumeral muscular dystrophy: Cohort profile and longitudinal patient reported outcomes.
Neuromuscul Disord
; 33(12): 964-971, 2023 Dec.
Article
in English
| MEDLINE | ID: mdl-38016873
6.
Causes and consequences of cerebral small vessel disease. The RUN DMC study: a prospective cohort study. Study rationale and protocol.
BMC Neurol
; 11: 29, 2011 Feb 28.
Article
in English
| MEDLINE | ID: mdl-21356112
7.
Mixed methods evaluation of a self-management group programme for patients with neuromuscular disease and chronic fatigue.
BMJ Open
; 11(8): e048890, 2021 08 25.
Article
in English
| MEDLINE | ID: mdl-34433601
8.
The neuromuscular and multisystem features of RYR1-related malignant hyperthermia and rhabdomyolysis: A study protocol.
Medicine (Baltimore)
; 100(33): e26999, 2021 Aug 20.
Article
in English
| MEDLINE | ID: mdl-34414986
9.
Strength training and aerobic exercise training for muscle disease.
Cochrane Database Syst Rev
; (1): CD003907, 2010 Jan 20.
Article
in English
| MEDLINE | ID: mdl-20091552
10.
KBTBD13 is an actin-binding protein that modulates muscle kinetics.
J Clin Invest
; 130(2): 754-767, 2020 02 03.
Article
in English
| MEDLINE | ID: mdl-31671076
11.
Facioscapulohumeral muscular dystrophy.
Curr Opin Neurol
; 22(5): 539-42, 2009 Oct.
Article
in English
| MEDLINE | ID: mdl-19724227
12.
Muscle fiber dysfunction contributes to weakness in inclusion body myositis.
Neuromuscul Disord
; 29(6): 468-476, 2019 06.
Article
in English
| MEDLINE | ID: mdl-31101463
13.
KBTBD13 is an actin-binding protein that modulates muscle kinetics.
J Clin Invest
; 134(3)2024 02 01.
Article
in English
| MEDLINE | ID: mdl-38299595
14.
MRI-Guided Biopsy as a Tool for Diagnosis and Research of Muscle Disorders.
J Neuromuscul Dis
; 5(3): 315-319, 2018.
Article
in English
| MEDLINE | ID: mdl-30103349
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