Detalhe da pesquisa
1.
Clinical phenotype heterogeneity in a family with ε-sarcoglycan gene mutation.
Neurol Neurochir Pol
; 54(1): 33-38, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-31956970
2.
The relation between plasma α-synuclein level and clinical symptoms or signs of Parkinson's disease.
Neurol Neurochir Pol
; 52(2): 243-251, 2018 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-29342421
3.
Cognitive impairment in carriers of glucocerebrosidase gene mutation in Parkinson disease patients.
Neurol Neurochir Pol
; 48(4): 258-61, 2014.
Artigo
em Inglês
| MEDLINE | ID: mdl-25168325
4.
Factors affecting the quality of life in hemifacial spasm patients.
Neurol Neurochir Pol
; 46(2): 121-9, 2012.
Artigo
em Inglês
| MEDLINE | ID: mdl-22581593
5.
A novel conserved mutation in SGCE gene in 3 unrelated patients with classical phenotype myoclonus-dystonia syndrome.
Neurol Res
; 35(6): 659-62, 2013 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-23561547