Detalhe da pesquisa
1.
Frequency and phenotypic spectrum of spinocerebellar ataxia 27B and other genetic ataxias in a Spanish cohort of late-onset cerebellar ataxia.
Eur J Neurol
; 30(12): 3828-3833, 2023 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-37578187
2.
R1441G but not G2019S mutation enhances LRRK2 mediated Rab10 phosphorylation in human peripheral blood neutrophils.
Acta Neuropathol
; 142(3): 475-494, 2021 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-34125248
3.
The Genetic Architecture of Parkinson Disease in Spain: Characterizing Population-Specific Risk, Differential Haplotype Structures, and Providing Etiologic Insight.
Mov Disord
; 34(12): 1851-1863, 2019 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-31660654
4.
A potential patient stratification biomarker for Parkinson´s disease based on LRRK2 kinase-mediated centrosomal alterations in peripheral blood-derived cells.
NPJ Parkinsons Dis
; 10(1): 12, 2024 Jan 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-38191886
5.
Elevated urine BMP phospholipids in LRRK2 and VPS35 mutation carriers with and without Parkinson's disease.
NPJ Parkinsons Dis
; 9(1): 52, 2023 Apr 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-37015928
6.
Falls Predict Acute Hospitalization in Parkinson's Disease.
J Parkinsons Dis
; 13(1): 105-124, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-33843696
7.
A More Homogeneous Phenotype in Parkinson's Disease Related to R1441G Mutation in the LRRK2 Gene.
Front Neurol
; 12: 635396, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-33763016