Detalhe da pesquisa
1.
Lessons for future clinical trials in adults with Becker muscular dystrophy: Disease progression detected by muscle magnetic resonance imaging, clinical and patient-reported outcome measures.
Eur J Neurol
; 31(7): e16282, 2024 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-38504654
2.
RFC1 repeat expansions: A recurrent cause of sensory and autonomic neuropathy with cough and ataxia.
Eur J Neurol
; 29(7): 2156-2161, 2022 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-35253317
3.
SPG43 and ALS-like syndrome in the same family due to compound heterozygous mutations of the C19orf12 gene: a case description and brief review.
Neurogenetics
; 22(1): 95-101, 2021 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-33394258
4.
Corpus callosum thinning in autosomal dominant hereditary spastic paraplegia associated with a novel TUBß4A mutation.
Clin Genet
; 98(4): 416-417, 2020 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-32720309
5.
Impact of hyponatremia on nerve conduction and muscle strength.
Eur J Clin Invest
; 46(4): 328-33, 2016 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-26835607
6.
Early-Onset Autosomal Dominant Myopathy with Vacuolated Fibers and Tubular Aggregates but No Periodic Paralysis, in a Patient with the c.1583G>A (p.R528H) mutation in the CACNA1S Gene.
J Neuromuscul Dis
; 2024 May 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-38788083
7.
A First Case of Acute Flaccid Myelitis Related to Enterovirus D68 in Belgium: Case Report.
Case Rep Neurol
; 16(1): 41-47, 2024.
Artigo
em Inglês
| MEDLINE | ID: mdl-38405019
8.
Recommendations for the management of myasthenia gravis in Belgium.
Acta Neurol Belg
; 2024 Apr 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-38649556
9.
Screening for later-onset Pompe's disease in patients with paucisymptomatic hyperCKemia.
Mol Genet Metab
; 109(2): 171-3, 2013 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-23566438
10.
A retrospective survey of patients with hereditary transthyretin-mediated (hATTR) amyloidosis treated with patisiran in real-world clinical practice in Belgium.
Acta Neurol Belg
; 123(3): 1029-1037, 2023 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-36829087
11.
A pathogenic CTBP1 variant featuring HADDTS with dystrophic myopathology.
Neuromuscul Disord
; 33(5): 410-416, 2023 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-37037050
12.
Telemedicine in Neuromuscular Diseases During Covid-19 Pandemic: ERN-NMD European Survey.
J Neuromuscul Dis
; 10(2): 173-184, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-36373291
13.
Rituximab Responsive Relapsing-Remitting IgG4 Anticontactin 1 Chronic Inflammatory Demyelinating Polyradiculoneuropathy Associated With Membranous Nephropathy: A Case Description and Brief Review.
J Clin Neuromuscul Dis
; 23(4): 219-226, 2022 Jun 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-35608646
14.
Distal acquired demyelinating symmetric neuropathy associated with anti-GM1 antibodies: is this a CIDP variant?
Acta Neurol Belg
; 110(1): 103-6, 2010 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-20514936
15.
Cerebellar ataxia, neuropathy, hearing loss, and intellectual disability due to AIFM1 mutation.
Neurol Genet
; 6(3): e420, 2020 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-32337346
16.
Acute Paraparesis after Epidural Corticosteroid Injection Revealing Spinal Dural Arteriovenous Fistula in a HIV Patient.
Eur J Case Rep Intern Med
; 7(10): 001673, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-33083349
17.
Antibodies against the node of Ranvier: a real-life evaluation of incidence, clinical features and response to treatment based on a prospective analysis of 1500 sera.
J Neurol
; 267(12): 3664-3672, 2020 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-32676765
18.
Spontaneous hydromyelic cavity in two unrelated patients with late-onset pompe disease: is this a fortuitous association?
Eur Neurol
; 70(1-2): 102-5, 2013.
Artigo
em Inglês
| MEDLINE | ID: mdl-23860444
19.
Low Prevalence Estimates of Late-Onset Glycogen Storage Disease Type II in French-Speaking Belgium are not Due to Missed Diagnoses.
J Neuromuscul Dis
; 5(4): 471-480, 2018.
Artigo
em Inglês
| MEDLINE | ID: mdl-30175981
20.
Incontinence in late-onset Pompe disease: an underdiagnosed treatable condition.
Eur Neurol
; 68(2): 75-8, 2012.
Artigo
em Inglês
| MEDLINE | ID: mdl-22760201