Detalhe da pesquisa
1.
Myasthenia gravis: descriptive analysis of life-threatening events in a recent nationwide registry.
Eur J Neurol
; 22(7): 1056-61, 2015 Jul.
Artigo
Inglês
| MEDLINE | ID: mdl-25847221
2.
Does ALS-FUS without FUS mutation represent ALS-FET? Report of three cases.
Neuropathol Appl Neurobiol
; 45(4): 421-426, 2019 06.
Artigo
Inglês
| MEDLINE | ID: mdl-30375034
3.
Clinical practice guidelines for the diagnosis and management of Charcot-Marie-Tooth disease.
Neurologia (Engl Ed)
; 2024 Mar 01.
Artigo
Inglês
| MEDLINE | ID: mdl-38431252
4.
Anti-ganglioside antibodies in patients with systemic lupus erythematosus and neurological manifestations.
Lupus
; 21(6): 611-5, 2012 May.
Artigo
Inglês
| MEDLINE | ID: mdl-22323340
5.
Differential levels of Neurofilament Light protein in cerebrospinal fluid in patients with a wide range of neurodegenerative disorders.
Sci Rep
; 10(1): 9161, 2020 06 08.
Artigo
Inglês
| MEDLINE | ID: mdl-32514050
6.
Cranial, axial and proximal myopathy and hypertrophic cardiomyopathy caused by a mutation in the globular head region of the MYH7 gene.
Eur J Neurol
; 21(6): e51-2, 2014 Jun.
Artigo
Inglês
| MEDLINE | ID: mdl-24805292
7.
Dysferlin expression in monocytes: a source of mRNA for mutation analysis.
Neuromuscul Disord
; 17(1): 69-76, 2007 Jan.
Artigo
Inglês
| MEDLINE | ID: mdl-17070050
8.
SMN2 copy number predicts acute or chronic spinal muscular atrophy but does not account for intrafamilial variability in siblings.
J Neurol
; 253(1): 21-5, 2006 Jan.
Artigo
Inglês
| MEDLINE | ID: mdl-15981080
9.
Inflammation in dysferlin myopathy: immunohistochemical characterization of 13 patients.
Neurology
; 57(11): 2136-8, 2001 Dec 11.
Artigo
Inglês
| MEDLINE | ID: mdl-11739845
10.
Antidisialosyl antibodies in chronic idiopathic ataxic neuropathy.
J Neurol
; 249(11): 1525-8, 2002 Nov.
Artigo
Inglês
| MEDLINE | ID: mdl-12420092
11.
[Anti-GQ1b antibodies: usefulness of its detection for the diagnosis of Miller-Fisher syndrome]. / Anticuerpos anti-GQ1b: utilidad de su determinación en el diagnóstico del síndrome de Miller-Fisher.
Med Clin (Barc)
; 116(20): 761-4, 2001 Jun 02.
Artigo
Espanhol
| MEDLINE | ID: mdl-11440679
12.
Long-lasting treatment effect of rituximab in MuSK myasthenia.
Neurology
; 78(3): 189-93, 2012 Jan 17.
Artigo
Inglês
| MEDLINE | ID: mdl-22218276
13.
Redefining dysferlinopathy phenotypes based on clinical findings and muscle imaging studies.
Neurology
; 75(4): 316-23, 2010 Jul 27.
Artigo
Inglês
| MEDLINE | ID: mdl-20574037
14.
The absence of survival motor neuron 2 gene may play a role in multifocal motor neuropathy.
Neurology
; 59(7): 1112-3, 2002 Oct 08.
Artigo
Inglês
| MEDLINE | ID: mdl-12370479
15.
Symptomatic dysferlin gene mutation carriers: characterization of two cases.
Neurology
; 68(16): 1284-9, 2007 Apr 17.
Artigo
Inglês
| MEDLINE | ID: mdl-17287450
16.
[Antiganglioside antibodies: when, which and for what]. / Anticuerpos antigangliósido: cuándo, cuál y para qué
Neurologia
; 16(7): 293-7, 2001.
Artigo
Espanhol
| MEDLINE | ID: mdl-11485721
17.
Chronic neuropathy with IgM anti-ganglioside antibodies: lack of long term response to rituximab.
Neurology
; 61(12): 1814-6, 2003 Dec 23.
Artigo
Inglês
| MEDLINE | ID: mdl-14694058
18.
Distal anterior compartment myopathy: a dysferlin mutation causing a new muscular dystrophy phenotype.
Ann Neurol
; 49(1): 130-4, 2001 Jan.
Artigo
Inglês
| MEDLINE | ID: mdl-11198284
19.
Anticuerpos antigangliósido: cuándo, cuál y para qué / Antiganglioside antibodies: when, which and for what
Neurología (Barc., Ed. impr.)
; 16(7): 293-297, ago. 2001.
Artigo
Es
| IBECS (Espanha) | ID: ibc-3349