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Thomas Gasser

Showing results (211-220 of 476) with videos related to

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International Journal of Oncology|July 13, 2005
High-throughput tissue microarray analysis of COX2 expression in urinary bladder cancerPeter J Wild, Leoni A Kunz-Schughart, Robert Stoehr, et al.
Journal of Neurology|January 27, 2005
Creatine supplementation lowers brain glutamate levels in Huntington's diseaseAndreas Bender, Dorothee P Auer, Thomas Merl, et al.
Neurological Research and Practice|December 16, 2020
An omics-based strategy using coenzyme Q10 in patients with Parkinson's disease: concept evaluation in a double-blind randomized placebo-controlled parallel group trialJannik Prasuhn, Norbert Brüggemann, Nicole Hessler, et al.
Neurogenetics|January 1, 2005
Epsilon-sarcoglycan is not involved in sporadic Gilles de la Tourette syndromeFriedrich Asmus, Sarah Schoenian, Peter Lichtner, et al.
Frontiers in Neuroscience|December 27, 2024
The cellular and extracellular proteomic signature of human dopaminergic neurons carrying the LRRK2 G2019S mutationFelix Knab, Giambattista Guaitoli, Mohamed Ali Jarboui, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 19, 2012
No association between NOD2 variants and Parkinson's diseaseSilke Appenzeller, Sandra Thier, Frank Papengut, et al.
Frontiers in Aging Neuroscience|September 21, 2018
Cholinergic Pathway SNPs and Postural Control in 477 Older AdultsCarina Arnold, Claudia Schulte, Mariana Moscovich, et al.
Annals of Neurology|September 3, 2002
Complex segregation analysis of restless legs syndrome provides evidence for an autosomal dominant mode of inheritance in early age at onset familiesJuliane Winkelmann, Bertram Muller-Myhsok, Hans-Ulrich Wittchen, et al.
Neurogenetics|June 27, 2003
Point mutations in exon 1 of the NR4A2 gene are not a major cause of familial Parkinson's diseaseAlexander Zimprich, Friedrich Asmus, Petra Leitner, et al.
Journal of Medical Genetics|November 5, 2014
EIF4G1 is neither a strong nor a common risk factor for Parkinson's disease: evidence from large European cohortsJohanna Huttenlocher, Rejko Krüger, Philipp Capetian, et al.
Pageof 48

Showing results (211-220 of 476) with videos related to

Sort By:
Pageof 48
International Journal of Oncology|July 13, 2005
High-throughput tissue microarray analysis of COX2 expression in urinary bladder cancerPeter J Wild, Leoni A Kunz-Schughart, Robert Stoehr, et al.
Journal of Neurology|January 27, 2005
Creatine supplementation lowers brain glutamate levels in Huntington's diseaseAndreas Bender, Dorothee P Auer, Thomas Merl, et al.
Neurological Research and Practice|December 16, 2020
An omics-based strategy using coenzyme Q10 in patients with Parkinson's disease: concept evaluation in a double-blind randomized placebo-controlled parallel group trialJannik Prasuhn, Norbert Brüggemann, Nicole Hessler, et al.
Neurogenetics|January 1, 2005
Epsilon-sarcoglycan is not involved in sporadic Gilles de la Tourette syndromeFriedrich Asmus, Sarah Schoenian, Peter Lichtner, et al.
Frontiers in Neuroscience|December 27, 2024
The cellular and extracellular proteomic signature of human dopaminergic neurons carrying the LRRK2 G2019S mutationFelix Knab, Giambattista Guaitoli, Mohamed Ali Jarboui, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 19, 2012
No association between NOD2 variants and Parkinson's diseaseSilke Appenzeller, Sandra Thier, Frank Papengut, et al.
Frontiers in Aging Neuroscience|September 21, 2018
Cholinergic Pathway SNPs and Postural Control in 477 Older AdultsCarina Arnold, Claudia Schulte, Mariana Moscovich, et al.
Annals of Neurology|September 3, 2002
Complex segregation analysis of restless legs syndrome provides evidence for an autosomal dominant mode of inheritance in early age at onset familiesJuliane Winkelmann, Bertram Muller-Myhsok, Hans-Ulrich Wittchen, et al.
Neurogenetics|June 27, 2003
Point mutations in exon 1 of the NR4A2 gene are not a major cause of familial Parkinson's diseaseAlexander Zimprich, Friedrich Asmus, Petra Leitner, et al.
Journal of Medical Genetics|November 5, 2014
EIF4G1 is neither a strong nor a common risk factor for Parkinson's disease: evidence from large European cohortsJohanna Huttenlocher, Rejko Krüger, Philipp Capetian, et al.
Pageof 48