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Thomas Gasser

Showing results (321-330 of 421) with videos related to

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Journal of Parkinson'S Disease|December 13, 2021
Safety, Pharmacokinetics, and Pharmacodynamics of Oral Venglustat in Patients with Parkinson's Disease and a GBA Mutation: Results from Part 1 of the Randomized, Double-Blinded, Placebo-Controlled MOVES-PD TrialM Judith Peterschmitt, Hidemoto Saiki, Taku Hatano, et al.
Neuron|November 16, 2004
Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathologyAlexander Zimprich, Saskia Biskup, Petra Leitner, et al.
Genes|October 24, 2017
Functional Characterization of Rare RAB12 Variants and Their Role in Musician's and Other DystoniasEva Hebert, Friederike Borngräber, Alexander Schmidt, et al.
Archives of Neurology|July 13, 2011
Enlarged substantia nigra hyperechogenicity and risk for Parkinson disease: a 37-month 3-center study of 1847 older personsDaniela Berg, Klaus Seppi, Stefanie Behnke, et al.
Journal of Parkinson'S Disease|July 31, 2025
Progression to Parkinson's dementia is not modulated by genetic risk variants for Alzheimer's or Parkinson's diseaseKayenat Parveen, J Alexander Ross, Hendrik van der Wurp, et al.
American Journal of Human Genetics|October 11, 2011
Absence of an orphan mitochondrial protein, c19orf12, causes a distinct clinical subtype of neurodegeneration with brain iron accumulationMonika B Hartig, Arcangela Iuso, Tobias Haack, et al.
Iscience|December 10, 2020
Human Dopaminergic Neurons Lacking PINK1 Exhibit Disrupted Dopamine Metabolism Related to Vitamin B6 Co-FactorsChristine Bus, Laimdota Zizmare, Marita Feldkaemper, et al.
Annals of Neurology|January 10, 2002
PARK6-linked parkinsonism occurs in several European familiesEnza Maria Valente, Francesco Brancati, Alessandro Ferraris, et al.
Medrxiv : the Preprint Server for Health Sciences|July 3, 2026
Large-scale functional annotation establishes a reference framework for human <i>LRRK2</i> variantsAnthea Cheung, Neringa Pratuseviciute, Kirsten Black, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|April 9, 2020
Rare Variants in Specific Lysosomal Genes Are Associated With Parkinson's DiseaseFranziska Hopfner, Stefanie H Mueller, Silke Szymczak, et al.
Pageof 43

Showing results (321-330 of 421) with videos related to

Sort By:
Pageof 43
Journal of Parkinson'S Disease|December 13, 2021
Safety, Pharmacokinetics, and Pharmacodynamics of Oral Venglustat in Patients with Parkinson's Disease and a GBA Mutation: Results from Part 1 of the Randomized, Double-Blinded, Placebo-Controlled MOVES-PD TrialM Judith Peterschmitt, Hidemoto Saiki, Taku Hatano, et al.
Neuron|November 16, 2004
Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathologyAlexander Zimprich, Saskia Biskup, Petra Leitner, et al.
Genes|October 24, 2017
Functional Characterization of Rare RAB12 Variants and Their Role in Musician's and Other DystoniasEva Hebert, Friederike Borngräber, Alexander Schmidt, et al.
Archives of Neurology|July 13, 2011
Enlarged substantia nigra hyperechogenicity and risk for Parkinson disease: a 37-month 3-center study of 1847 older personsDaniela Berg, Klaus Seppi, Stefanie Behnke, et al.
Journal of Parkinson'S Disease|July 31, 2025
Progression to Parkinson's dementia is not modulated by genetic risk variants for Alzheimer's or Parkinson's diseaseKayenat Parveen, J Alexander Ross, Hendrik van der Wurp, et al.
American Journal of Human Genetics|October 11, 2011
Absence of an orphan mitochondrial protein, c19orf12, causes a distinct clinical subtype of neurodegeneration with brain iron accumulationMonika B Hartig, Arcangela Iuso, Tobias Haack, et al.
Iscience|December 10, 2020
Human Dopaminergic Neurons Lacking PINK1 Exhibit Disrupted Dopamine Metabolism Related to Vitamin B6 Co-FactorsChristine Bus, Laimdota Zizmare, Marita Feldkaemper, et al.
Annals of Neurology|January 10, 2002
PARK6-linked parkinsonism occurs in several European familiesEnza Maria Valente, Francesco Brancati, Alessandro Ferraris, et al.
Medrxiv : the Preprint Server for Health Sciences|July 3, 2026
Large-scale functional annotation establishes a reference framework for human <i>LRRK2</i> variantsAnthea Cheung, Neringa Pratuseviciute, Kirsten Black, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|April 9, 2020
Rare Variants in Specific Lysosomal Genes Are Associated With Parkinson's DiseaseFranziska Hopfner, Stefanie H Mueller, Silke Szymczak, et al.
Pageof 43