Detalhe da pesquisa
1.
ANO10 mutational screening in recessive ataxia: genetic findings and refinement of the clinical phenotype.
J Neurol
; 266(2): 378-385, 2019 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-30515630
2.
Clinical expression of facioscapulohumeral muscular dystrophy in carriers of 1-3 D4Z4 reduced alleles: experience of the FSHD Italian National Registry.
BMJ Open
; 6(1): e007798, 2016 Jan 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-26733561
3.
A novel clinical tool to classify facioscapulohumeral muscular dystrophy phenotypes.
J Neurol
; 263(6): 1204-14, 2016 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-27126453
4.
Updates on Somatoform Disorders (SFMD) in Parkinson's Disease and Dementia with Lewy Bodies and discussion of phenomenology.
J Neurol Sci
; 310(1-2): 166-71, 2011 Nov 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-21813140
5.
Holmes-Like Tremor in Ataxia With Oculomotor Apraxia Type 2.
Mov Disord Clin Pract
; 1(3): 261-262, 2014 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-30713863