Detalhe da pesquisa
1.
KCNN2 mutation in autosomal-dominant tremulous myoclonus-dystonia.
Eur J Neurol
; 27(8): 1471-1477, 2020 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-32212350
2.
Mitochondrial complex I NUBPL mutations cause combined dystonia with bilateral striatal necrosis and cerebellar atrophy.
Eur J Neurol
; 26(9): 1240-1243, 2019 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-30897263
3.
Tremor in motor neuron disease may be central rather than peripheral in origin.
Eur J Neurol
; 26(3): 394-e31, 2019 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-29953699
4.
Non-invasive brain stimulation for dystonia: therapeutic implications.
Eur J Neurol
; 24(10): 1228-e64, 2017 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-28782903
5.
Mind the gap: temporal discrimination and dystonia.
Eur J Neurol
; 24(6): 796-806, 2017 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-28544409
6.
Abnormal movement-related suppression of sensory evoked potentials in upper limb dystonia.
Eur J Neurol
; 23(3): 562-8, 2016 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-26757449
7.
Management of dystonia in Europe: a survey of the European network for the study of the dystonia syndromes.
Eur J Neurol
; 23(4): 772-9, 2016 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-26826067
8.
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
9.
Isolated and combined dystonia syndromes - an update on new genes and their phenotypes.
Eur J Neurol
; 22(4): 610-7, 2015 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-25643588
10.
A positive diagnosis of functional (psychogenic) tics.
Eur J Neurol
; 22(3): 527-e36, 2015 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-25487253
11.
All in the blink of an eye: new insight into cerebellar and brainstem function in DYT1 and DYT6 dystonia.
Eur J Neurol
; 22(5): 762-7, 2015 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-25039324
12.
Evaluation of cerebrospinal fluid alpha-synuclein seed amplification assay in PSP and CBS.
medRxiv
; 2024 Feb 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-38529496
13.
Cerebellum-dependent associative learning deficits in primary dystonia are normalized by rTMS and practice.
Eur J Neurosci
; 38(1): 2166-71, 2013 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-23551802
14.
EFNS guidelines on diagnosis and treatment of primary dystonias.
Eur J Neurol
; 18(1): 5-18, 2011 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-20482602
15.
C2orf37 mutational spectrum in Woodhouse-Sakati syndrome patients.
Clin Genet
; 78(6): 585-90, 2010 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-20507343
16.
The role of DAT-SPECT in movement disorders.
J Neurol Neurosurg Psychiatry
; 81(1): 5-12, 2010 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-20019219
17.
Using reaction time and co-contraction to differentiate acquired (secondary) from functional 'fixed' dystonia.
J Neurol Neurosurg Psychiatry
; 86(8): 933-4, 2015 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-25433034
18.
Secondary dystonia--clinical clues and syndromic associations.
Eur J Neurol
; 17 Suppl 1: 52-7, 2010 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-20590809
19.
Abnormal sensorimotor plasticity in organic but not in psychogenic dystonia.
Brain
; 132(Pt 10): 2871-7, 2009 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-19690095
20.
Genotype-phenotype interactions in primary dystonias revealed by differential changes in brain structure.
Neuroimage
; 47(4): 1141-7, 2009 Oct 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-19344776