Detalhe da pesquisa
1.
Early onset collagen VI myopathies: Genetic and clinical correlations.
Ann Neurol
; 68(4): 511-20, 2010 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-20976770
2.
Long-term patterns of gender imbalance in an industry without ability or level of interest differences.
PLoS One
; 15(4): e0229662, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-32236126
3.
[Myasthenia gravis: treatments and remissions]. / Myasthénie grave, traitements et rémissions.
Rev Med Suisse
; 3(110): 1185-6, 1188-90, 2007 May 09.
Artigo
em Francês
| MEDLINE | ID: mdl-17564346
4.
[The role of pathology in neuromuscular diseases]. / Le rôle du pathologiste dans la prise en charge des maladies neuromusculaires.
Rev Med Suisse
; 3(119): 1733-6, 2007 Jul 18.
Artigo
em Francês
| MEDLINE | ID: mdl-17727093
5.
Phenotypic expression of a Pro 87 to Leu mutation in the connexin 32 gene in a large Swiss family with Charcot-Marie-Tooth neuropathy.
J Neurol Sci
; 207(1-2): 77-86, 2003 Mar 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-12614935
6.
Creutzfeldt-Jakob disease: evolution from nonconvulsive status epilepticus, through SIRPIDs, to generalized periodic discharges.
Clin Neurophysiol
; 118(11): 2533-6, 2007 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-17890150
7.
High cardiovascular morbidity and mortality in myofibrillar myopathies due to DES gene mutations: a 10-year longitudinal study.
Neuromuscul Disord
; 22(3): 211-8, 2012 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-22153487
8.
Unsatisfactory outcomes in myasthenia gravis: influence by care providers.
J Neurol
; 257(3): 338-43, 2010 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-19760347
9.
Marked hemiatrophy in carriers of Duchenne muscular dystrophy.
Arch Neurol
; 67(4): 497-500, 2010 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-20385919
10.
Comparative efficacy of repetitive nerve stimulation, exercise, and cold in differentiating myotonic disorders.
Muscle Nerve
; 36(5): 643-50, 2007 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-17654559
11.
Eosinophilic perimyositis as the presenting feature of a monoclonal T-cell expansion.
Muscle Nerve
; 31(5): 646-51, 2005 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-15770667
12.
Confirmation that abnormal desmin accumulation and migration are due to a desmin gene mutation in a familial cardiomyopathy and distal myopathy.
Neuromuscul Disord
; 19(11): 802, 2009 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-19716701