Detalhe da pesquisa
1.
Candidate variants in TUB are associated with familial tremor.
PLoS Genet
; 16(9): e1009010, 2020 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-32956375
2.
Common Variants Near ZIC1 and ZIC4 in Autopsy-Confirmed Multiple System Atrophy.
Mov Disord
; 37(10): 2110-2121, 2022 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-35997131
3.
Evidence for pathogenicity of variant ATM Val1729Leu in a family with ataxia telangiectasia.
Neurogenetics
; 22(2): 143-147, 2021 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-33779842
4.
Validation of α-Synuclein in L1CAM-Immunocaptured Exosomes as a Biomarker for the Stratification of Parkinsonian Syndromes.
Mov Disord
; 36(11): 2663-2669, 2021 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-33826157
5.
Serum neuronal exosomes predict and differentiate Parkinson's disease from atypical parkinsonism.
J Neurol Neurosurg Psychiatry
; 91(7): 720-729, 2020 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-32273329
6.
Multiomics Analyses Identify Genes and Pathways Relevant to Essential Tremor.
Mov Disord
; 35(7): 1153-1162, 2020 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-32249994
7.
Rare Variants in Specific Lysosomal Genes Are Associated With Parkinson's Disease.
Mov Disord
; 35(7): 1245-1248, 2020 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-32267580
8.
Biomarkers of Parkinson's disease: 20 years later.
J Neural Transm (Vienna)
; 126(7): 803-813, 2019 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-30949837
9.
HOMER-3 Antibodies Were Not Detected in Two German Cohorts of Patients with Multiple System Atrophy.
Mov Disord
; 37(10): 2165-2166, 2022 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-35975882
10.
Genome-wide association study in essential tremor identifies three new loci.
Brain
; 139(Pt 12): 3163-3169, 2016 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-27797806
11.
Early- and late-onset essential tremor patients represent clinically distinct subgroups.
Mov Disord
; 31(10): 1560-1566, 2016 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-27384030
12.
Outcomes of SARS-CoV-2 Infections in Patients with Neurodegenerative Diseases in the LEOSS Cohort.
Mov Disord
; 36(4): 791-793, 2021 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-33638915
13.
Validation of the QUEST for German-speaking countries.
Int J Neurosci
; 126(2): 127-34, 2016.
Artigo
em Inglês
| MEDLINE | ID: mdl-26327253
14.
The impact of rare variants in FUS in essential tremor.
Mov Disord
; 30(5): 721-4, 2015 Apr 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-25631824
15.
Whole-Genome Sequencing Analysis Reveals New Susceptibility Loci and Structural Variants Associated with Progressive Supranuclear Palsy.
medRxiv
; 2024 Jan 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-38234807
16.
Association of Structural Forms of 17q21.31 with the Risk of Progressive Supranuclear Palsy and MAPT Sub-haplotypes.
medRxiv
; 2024 Feb 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-38464214
17.
Co-aggregate formation of CADASIL-mutant NOTCH3: a single-particle analysis.
Hum Mol Genet
; 20(16): 3256-65, 2011 Aug 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-21628316
18.
The role of SCARB2 as susceptibility factor in Parkinson's disease.
Mov Disord
; 28(4): 538-40, 2013 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-23408458
19.
A new paradigm for diagnosis of neurodegenerative diseases: peripheral exosomes of brain origin.
Transl Neurodegener
; 11(1): 28, 2022 05 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-35527262
20.
Transcriptome and Proteome Analysis in LUHMES Cells Overexpressing Alpha-Synuclein.
Front Neurol
; 13: 787059, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35481270