about
Homo- and heterodimerization of ROCO kinases: LRRK2 kinase inhibition by the LRRK2 ROCO fragmentA missense mutation in KCTD17 causes autosomal dominant myoclonus-dystoniaImputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studiesGenome-wide association study reveals genetic risk underlying Parkinson's diseaseTRIO amplification and abundant mRNA expression is associated with invasive tumor growth and rapid tumor cell proliferation in urinary bladder cancerNo dopamine cell loss or changes in cytoskeleton function in transgenic mice expressing physiological levels of wild type or G2019S mutant LRRK2 and in human fibroblastsTime to redefine PD? Introductory statement of the MDS Task Force on the definition of Parkinson's disease.VHL mutations and their correlation with tumour cell proliferation, microvessel density, and patient prognosis in clear cell renal cell carcinoma.Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathologyThe epsilon-sarcoglycan gene (SGCE), mutated in myoclonus-dystonia syndrome, is maternally imprintedMyoclonus-dystonia syndrome: epsilon-sarcoglycan mutations and phenotypePrognostic relevance of MAGE-A4 tumor antigen expression in transitional cell carcinoma of the urinary bladder: a tissue microarray studyLarge-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's diseaseMutations in the pantothenate kinase gene PANK2 are not associated with Parkinson diseaseThe transcription factor PITX3 is associated with sporadic Parkinson's diseaseLoss of function mutations in the gene encoding Omi/HtrA2 in Parkinson's diseaseEpsilon-sarcoglycan is not involved in sporadic Gilles de la Tourette syndromeDerivation and expansion using only small molecules of human neural progenitors for neurodegenerative disease modelingNeuroX, a fast and efficient genotyping platform for investigation of neurodegenerative diseasesPolymorphisms in the glial glutamate transporter SLC1A2 are associated with essential tremorLoss of VPS13C Function in Autosomal-Recessive Parkinsonism Causes Mitochondrial Dysfunction and Increases PINK1/Parkin-Dependent MitophagyComprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene database.GLUT1 mutations are a cause of paroxysmal exertion-induced dyskinesias and induce hemolytic anemia by a cation leak.Diagnosis of Parkinson's disease on the basis of clinical and genetic classification: a population-based modelling studyDeletions at 22q11.2 in idiopathic Parkinson's disease: a combined analysis of genome-wide association data.Data protection in biomaterial banks for Parkinson's disease research: the model of GEPARD (Gene Bank Parkinson's Disease Germany).New family with paroxysmal exercise-induced dystonia and epilepsy.Meta analysis of whole-genome linkage scans with data uncertainty: an application to Parkinson's disease.Multiple regions of alpha-synuclein are associated with Parkinson's disease.UCHL-1 gene in multiple system atrophy: a haplotype tagging approach.Type and frequency of mutations in the LRRK2 gene in familial and sporadic Parkinson's disease*.Genes associated with Parkinson syndrome.Microbial colonization and ureteral stent-associated storage lower urinary tract symptoms: the forgotten piece of the puzzle?PARK11 gene (GIGYF2) variants Asn56Ser and Asn457Thr are not pathogenic for Parkinson's disease.Enlarged hyperechogenic substantia nigra is related to motor performance and olfaction in the elderly.Additional rare variant analysis in Parkinson's disease cases with and without known pathogenic mutations: evidence for oligogenic inheritance.Single-cell expression profiling of dopaminergic neurons combined with association analysis identifies pyridoxal kinase as Parkinson's disease gene.Low field intraoperative MRI in glioma surgery.Implementation of the ultra low field intraoperative MRI PoleStar N20 during resection control of pituitary adenomas.A novel mutation in LRSAM1 causes axonal Charcot-Marie-Tooth disease with dominant inheritance
P50
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P50
name
Thomas Gasser
@ast
Thomas Gasser
@en
Thomas Gasser
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type
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Thomas Gasser
@ast
Thomas Gasser
@en
Thomas Gasser
@nl
prefLabel
Thomas Gasser
@ast
Thomas Gasser
@en
Thomas Gasser
@nl