Detalhe da pesquisa
1.
MPV17 mutations in juvenile- and adult-onset axonal sensorimotor polyneuropathy.
Clin Genet
; 95(1): 182-186, 2019 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-30298599
2.
SACS variants are a relevant cause of autosomal recessive hereditary motor and sensory neuropathy.
Hum Genet
; 137(11-12): 911-919, 2018 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-30460542
3.
ANO5 gene analysis in a large cohort of patients with anoctaminopathy: confirmation of male prevalence and high occurrence of the common exon 5 gene mutation.
Hum Mutat
; 34(8): 1111-8, 2013 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-23606453
4.
Satisfaction and practicality of a prefilled glatiramer acetate pen in relapsing-remitting multiple sclerosis patients.
Neurodegener Dis Manag
; 13(5): 281-288, 2023 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-37909320
5.
Effects of Sativexâ on cognitive function in patients with multiple sclerosis: A systematic review and meta-analysis.
Mult Scler Relat Disord
; 68: 104173, 2022 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-36174323
6.
Mental symptoms in MS (MeSyMS): Development and validation of a new assessment.
Mult Scler Relat Disord
; 49: 102744, 2021 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-33517174
7.
Gaining First Insights on Secondary Progressive Multiple Sclerosis Patients Treated With Siponimod in Clinical Routine: Protocol of the Noninterventional Study AMASIA.
JMIR Res Protoc
; 9(7): e19598, 2020 Jul 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-32499214
8.
Signs of impaired selective attention in patients with amyotrophic lateral sclerosis.
J Neurol
; 255(4): 532-8, 2008 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-18274808
9.
Primary progressive aphasia accompanied by environmental sound agnosia: a neuropsychological, MRI and PET study.
Psychiatry Res
; 146(2): 191-7, 2006 Mar 31.
Artigo
em Inglês
| MEDLINE | ID: mdl-16510269
10.
Cognitive function in bulbar- and spinal-onset amyotrophic lateral sclerosis. A longitudinal study in 52 patients.
J Neurol
; 252(7): 772-81, 2005 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-15742104
11.
Is personality profile a relevant determinant of fatigue in multiple sclerosis?
Front Neurol
; 6: 2, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-25699007
12.
X-linked bulbospinal neuronopathy: Kennedy disease.
Arch Neurol
; 59(12): 1921-6, 2002 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-12470181
13.
Facioscapulohumeral muscular dystrophy. Phenotype-genotype correlation in patients with borderline D4Z4 repeat numbers.
J Neurol
; 250(8): 932-7, 2003 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-12928911
14.
Variable reduction of caveolin-3 in patients with LGMD2B/MM.
J Neurol
; 250(12): 1431-8, 2003 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-14673575
15.
Treatment of dysferlinopathy with deflazacort: a double-blind, placebo-controlled clinical trial.
Orphanet J Rare Dis
; 8: 26, 2013 Feb 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-23406536
16.
Muscle MRI findings in limb girdle muscular dystrophy type 2L.
Neuromuscul Disord
; 22 Suppl 2: S122-9, 2012 Oct 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-22980763
17.
Frontotemporal cognitive function in X-linked spinal and bulbar muscular atrophy (SBMA): a controlled neuropsychological study of 20 patients.
J Neurol
; 256(11): 1869-75, 2009 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-19572162
18.
Enhancement of chemokine expression by interferon beta therapy in patients with multiple sclerosis.
Arch Neurol
; 66(10): 1216-23, 2009 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-19667211
19.
Longitudinal effects of noninvasive positive-pressure ventilation in patients with amyotrophic lateral sclerosis.
Am J Phys Med Rehabil
; 82(8): 597-604, 2003 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-12872016