Detalhe da pesquisa
1.
Cytosolic 5'-nucleotidase 1A autoantibody profile and clinical characteristics in inclusion body myositis.
Ann Rheum Dis
; 76(5): 862-868, 2017 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-28122761
2.
The wrong end of the telescope: neuromuscular mimics of movement disorders (and vice versa).
Pract Neurol
; 16(4): 264-9, 2016 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-26965497
3.
RYR1-related myopathies: a wide spectrum of phenotypes throughout life.
Eur J Neurol
; 22(7): 1094-112, 2015 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-25960145
4.
Facioscapulohumeral Disease as a myodevelopmental disease: Applying Ockham's razor to its various features.
J Neuromuscul Dis
; 10(3): 411-425, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-36872787
5.
Establishing the role of muscle ultrasound as an imaging biomarker in facioscapulohumeral muscular dystrophy.
Neuromuscul Disord
; 33(12): 936-944, 2023 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-37968164
6.
Having an eye for myotonic dystrophy: A qualitative study on experiences and support needs in myotonic dystrophy type 1 patients with a diagnostic delay after early-onset cataract.
Neuromuscul Disord
; 32(10): 829-835, 2022 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-36192279
7.
Speech pathology interventions in patients with neuromuscular diseases: a systematic review.
Folia Phoniatr Logop
; 63(1): 15-20, 2011.
Artigo
em Inglês
| MEDLINE | ID: mdl-20689305
8.
Characterizing the face in facioscapulohumeral muscular dystrophy.
J Neurol
; 268(4): 1342-1350, 2021 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-33113021
9.
Only fat infiltrated muscles in resting lower leg of FSHD patients show disturbed energy metabolism.
NMR Biomed
; 23(6): 563-8, 2010 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-20175146
10.
New cases of adult-onset Sandhoff disease with a cerebellar or lower motor neuron phenotype.
J Neurol Neurosurg Psychiatry
; 81(9): 968-72, 2010 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-20798201
11.
[Facioscapulohumeral muscular dystrophy]. / Facioscapulohumerale spierdystrofie.
Ned Tijdschr Tandheelkd
; 117(1): 11-4, 2010 Jan.
Artigo
em Holandês
| MEDLINE | ID: mdl-20180344
12.
Evaluation of blood gene expression levels in facioscapulohumeral muscular dystrophy patients.
Sci Rep
; 10(1): 17547, 2020 10 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-33067535
13.
Strong association between myotonic dystrophy type 2 and autoimmune diseases.
J Neurol Neurosurg Psychiatry
; 80(11): 1293-5, 2009 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-19864666
14.
Trunk sway analysis to quantify the warm-up phenomenon in myotonia congenita patients.
J Neurol Neurosurg Psychiatry
; 80(2): 207-12, 2009 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-18550628
15.
Redefining the clinical phenotypes of non-dystrophic myotonic syndromes.
J Neurol Neurosurg Psychiatry
; 80(6): 647-52, 2009 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-19211598
16.
Evaluation of prednisolone treatment in the acute phase of neuralgic amyotrophy: an observational study.
J Neurol Neurosurg Psychiatry
; 80(10): 1120-4, 2009 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-19321467
17.
Epidemiology and pathophysiology of falls in facioscapulohumeral disease.
J Neurol Neurosurg Psychiatry
; 80(12): 1357-63, 2009 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-19546106
18.
Optimizing referral of patients with neuromuscular disorders to allied health care.
Eur J Neurol
; 16(5): 562-8, 2009 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-19405198
19.
Clinical neurophysiology of fatigue.
Clin Neurophysiol
; 119(1): 2-10, 2008 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-18039594
20.
Identifying deficits in balance control following vestibular or proprioceptive loss using posturographic analysis of stance tasks.
Clin Neurophysiol
; 119(10): 2338-46, 2008 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-18782677