1 – 34 of 34
- show: 250
- |
- sort: year (new to old)
Close
Embed this list
<iframe src=" "
width=" "
height=" "
allowtransparency="true"
frameborder="0">
</iframe>
- 2024
-
Mark
Basal activity of PINK1 and PRKN in cell models and rodent brain
(
- Contribution to journal › Article
- 2023
-
Mark
Substitution of PINK1 Gly411 modulates substrate receptivity and turnover
(
- Contribution to journal › Article
- 2022
-
Mark
Tau and neurofilament light-chain as fluid biomarkers in spinocerebellar ataxia type 3
(
- Contribution to journal › Article
- 2020
-
Mark
Toward allele-specific targeting therapy and pharmacodynamic marker for spinocerebellar ataxia type 3
(
- Contribution to journal › Article
- 2018
-
Mark
Slowly progressive dementia caused by MAPT R406W mutations : Longitudinal report on a new kindred and systematic review
(
- Contribution to journal › Article
- 2017
-
Mark
PBB3 imaging in Parkinsonian disorders : Evidence for binding to tau and other proteins
(
- Contribution to journal › Article
-
Mark
Reply: Heterozygous PINK1 p.G411S in rapid eye movement sleep behaviour disorder
(
- Contribution to journal › Letter
-
Mark
Heterozygous PINK1 p.G411S increases risk of Parkinson's disease via a dominant-negative mechanism
(
- Contribution to journal › Article
- 2016
-
Mark
Autosomal dominant Parkinson's disease caused by SNCA duplications.
(
- Contribution to journal › Article
- 2015
-
Mark
CHCHD2 and Parkinson's disease
(
- Contribution to journal › Letter
-
Mark
Mitochondrial targeting sequence variants of the CHCHD2 gene are a risk for Lewy body disorders.
2015) In Neurology(
- Contribution to journal › Article
-
Mark
Role for the microtubule-associated protein tau variant p.A152T in risk of α-synucleinopathies.
(
- Contribution to journal › Article
-
Mark
Clinical Correlations With Lewy Body Pathology in LRRK2-Related Parkinson Disease.
(
- Contribution to journal › Article
- 2014
-
Mark
Genotype-Phenotype Correlations in Parkinson Disease
2014) p.259-285(
- Chapter in Book/Report/Conference proceeding › Book chapter
-
Mark
Alpha-Synuclein Repeat Variants and Survival in Parkinson's Disease
(
- Contribution to journal › Article
- 2013
-
Mark
Olfactory Dysfunction.
2013) p.335-348(
- Chapter in Book/Report/Conference proceeding › Book chapter
-
Mark
GNAL mutations cause adult-onset primary dystonia
(
- Contribution to journal › Published meeting abstract
-
Mark
Role of Gα(olf) in Familial and Sporadic Adult-Onset Primary Dystonia.
(
- Contribution to journal › Article
-
Mark
Population-specific Frequencies for LRRK2 Susceptibility Variants in the Genetic Epidemiology of Parkinson's Disease (GEO-PD) Consortium
(
- Contribution to journal › Article
- 2012
-
Mark
First neuropathological description of a patient with Parkinson's disease and LRRK2 p.N1437H mutation.
(
- Contribution to journal › Article
-
Mark
Creation of an Open-Access, Mutation-Defined Fibroblast Resource for Neurological Disease Research
(
- Contribution to journal › Article
-
Mark
Large-scale replication and heterogeneity in Parkinson disease genetic loci
(
- Contribution to journal › Article
- 2011
-
Mark
Diagnosis and Treatment of Common Forms of Tremor
(
- Contribution to journal › Article
-
Mark
An African-American family with dystonia.
(
- Contribution to journal › Article
-
Mark
Human leukocyte antigen variation and Parkinson's disease.
(
- Contribution to journal › Article
-
Mark
VPS35 Mutations in Parkinson Disease
(
- Contribution to journal › Article
-
Mark
A large-scale genetic association study to evaluate the contribution of Omi/HtrA2 (PARK13) to Parkinson's disease
(
- Contribution to journal › Article
-
Mark
Independent and Joint Effects of the MAPT and SNCA Genes in Parkinson Disease
(
- Contribution to journal › Article
-
Mark
Association of LRRK2 exonic variants with susceptibility to Parkinson's disease: a case-control study
(
- Contribution to journal › Article
- 2010
-
Mark
Familial late-onset focal dystonia in an African American family
(
- Contribution to journal › Published meeting abstract
-
Mark
LRRK2 variation and Parkinson's disease in African Americans
(
- Contribution to journal › Article
- 2009
-
Mark
Alpha-synuclein multiplications with parkinsonism, dementia or progressive myoclonus?
(
- Contribution to journal › Article
-
Mark
A Swedish family with de novo alpha-synuclein A53T mutation: Evidence for early cortical dysfunction.
(
- Contribution to journal › Article
- 2007
-
Mark
The "Lister family": An extended pedigree with alpha-synuclein multiplications and Parkinson's disease.
2007) XVII WFN World Congress on Parkinson's Disease and Related Disorders, 2007 In Parkinsonism & Related Disorders 13(supplement 2). p.95-96(
- Contribution to journal › Published meeting abstract