Detalhe da pesquisa
1.
The Use of the Voice Trainer App for Vocal Control in People with a Degenerative Ataxia: A Pilot Intervention Study.
Cerebellum
; 2024 Jan 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-38285133
2.
Management of rare movement disorders in Europe: outcome of surveys of the European Reference Network for Rare Neurological Diseases.
Eur J Neurol
; 27(8): 1493-1500, 2020 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-32386078
3.
The Personalized Parkinson Project: examining disease progression through broad biomarkers in early Parkinson's disease.
BMC Neurol
; 19(1): 160, 2019 Jul 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-31315608
4.
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
5.
A gait paradigm reveals different patterns of abnormal cerebellar motor learning in primary focal dystonias.
Cerebellum
; 13(6): 760-6, 2014 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-25182695
6.
The clinical utility of botulinum toxin injections targeted at the motor endplate zone in cervical dystonia.
Eur J Neurol
; 21(12): 1486-e98, 2014 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-25060697
7.
EFNS/ENS Consensus on the diagnosis and management of chronic ataxias in adulthood.
Eur J Neurol
; 21(4): 552-62, 2014 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-24418350
8.
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
9.
Inventory of Non-Ataxia Signs (INAS): validation of a new clinical assessment instrument.
Cerebellum
; 12(3): 418-28, 2013 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-23090211
10.
Prospective analysis of falls in dominant ataxias.
Eur Neurol
; 69(1): 53-7, 2013.
Artigo
em Inglês
| MEDLINE | ID: mdl-23146840
11.
Autosomal recessive cerebellar ataxias: the current state of affairs.
J Med Genet
; 48(10): 651-9, 2011 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-21856962
12.
Neurofilament light chain: A novel blood biomarker in patients with ataxia telangiectasia.
Eur J Paediatr Neurol
; 32: 93-97, 2021 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-33878608
13.
New cases of adult-onset Sandhoff disease with a cerebellar or lower motor neuron phenotype.
J Neurol Neurosurg Psychiatry
; 81(9): 968-72, 2010 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-20798201
14.
Hereditary spastic paraplegia due to SPAST mutations in 151 Dutch patients: new clinical aspects and 27 novel mutations.
J Neurol Neurosurg Psychiatry
; 81(10): 1073-8, 2010 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-20562464
15.
Postural instability in cerebellar ataxia: correlations of knee, arm and trunk movements to center of mass velocity.
Neuroscience
; 159(1): 390-404, 2009 Mar 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-19136042
16.
Neurophysiological evidence for cerebellar dysfunction in primary focal dystonia.
J Neurol Neurosurg Psychiatry
; 80(1): 80-3, 2009 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-19091711
17.
Excessive short-latency stretch reflexes in the calf muscles do not cause postural instability in patients with hereditary spastic paraplegia.
Clin Neurophysiol
; 130(8): 1188-1195, 2019 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-31163363
18.
"Ears of the Lynx" MRI Sign Is Associated with SPG11 and SPG15 Hereditary Spastic Paraplegia.
AJNR Am J Neuroradiol
; 40(1): 199-203, 2019 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-30606727
19.
SPG10 is a rare cause of spastic paraplegia in European families.
J Neurol Neurosurg Psychiatry
; 79(5): 584-7, 2008 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-18245137
20.
[From psychiatric symptoms to paraneoplastic syndrome]. / Van psychiatrisch symptoom tot paraneoplastisch syndroom.
Tijdschr Psychiatr
; 50(9): 603-9, 2008.
Artigo
em Holandês
| MEDLINE | ID: mdl-18785107