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Katja Lohmann

Showing results (141-150 of 267) with videos related to

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Human Mutation|August 7, 2018
Motor protein binding and mitochondrial transport are altered by pathogenic TUBB4A variantsFranca Vulinovic, Victor Krajka, Torben J Hausrat, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|November 30, 2012
Exome sequencing in a family with restless legs syndromeAnne Weissbach, Katharina Siegesmund, Norbert Brüggemann, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|December 20, 2008
Genetic association study of the P-type ATPase ATP13A2 in late-onset Parkinson's diseaseAleksandar Rakovic, Barbara Stiller, Ana Djarmati, et al.
Clinical and Translational Medicine|January 28, 2022
Multi-omic landscaping of human midbrains identifies disease-relevant molecular targets and pathways in advanced-stage Parkinson's diseaseLucas Caldi Gomes, Ana Galhoz, Gaurav Jain, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|October 26, 2018
Genotype-phenotype relations for the Parkinson's disease genes SNCA, LRRK2, VPS35: MDSGene systematic reviewJoanne Trinh, Florentine M J Zeldenrust, Jana Huang, et al.
JAMA Neurology|May 24, 2013
A novel OPA3 mutation revealed by exome sequencing: an example of reverse phenotypingBeenish Arif, Kishore R Kumar, Philip Seibler, et al.
Parkinsonism & Related Disorders|October 12, 2010
Association of Parkinson disease to PARK16 in a Chilean sampleAlfredo Ramirez, Andreas Ziegler, Susen Winkler, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|March 23, 2011
Homozygous THAP1 mutations as cause of early-onset generalized dystoniaSusanne A Schneider, Alfredo Ramirez, Kaveh Shafiee, et al.
Neuro-Degenerative Diseases|June 25, 2020
Clinical Phenotype of LRRK2 R1441C in 2 Chinese SistersShen-Yang Lim, Jia Lun Lim, Azlina Ahmad-Annuar, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|August 6, 2010
Clinical neuroimaging and electrophysiological assessment of three DYT6 dystonia familiesSimone Zittel, Christian K E Moll, Norbert Brüggemann, et al.
Pageof 27

Showing results (141-150 of 267) with videos related to

Sort By:
Pageof 27
Human Mutation|August 7, 2018
Motor protein binding and mitochondrial transport are altered by pathogenic TUBB4A variantsFranca Vulinovic, Victor Krajka, Torben J Hausrat, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|November 30, 2012
Exome sequencing in a family with restless legs syndromeAnne Weissbach, Katharina Siegesmund, Norbert Brüggemann, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|December 20, 2008
Genetic association study of the P-type ATPase ATP13A2 in late-onset Parkinson's diseaseAleksandar Rakovic, Barbara Stiller, Ana Djarmati, et al.
Clinical and Translational Medicine|January 28, 2022
Multi-omic landscaping of human midbrains identifies disease-relevant molecular targets and pathways in advanced-stage Parkinson's diseaseLucas Caldi Gomes, Ana Galhoz, Gaurav Jain, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|October 26, 2018
Genotype-phenotype relations for the Parkinson's disease genes SNCA, LRRK2, VPS35: MDSGene systematic reviewJoanne Trinh, Florentine M J Zeldenrust, Jana Huang, et al.
JAMA Neurology|May 24, 2013
A novel OPA3 mutation revealed by exome sequencing: an example of reverse phenotypingBeenish Arif, Kishore R Kumar, Philip Seibler, et al.
Parkinsonism & Related Disorders|October 12, 2010
Association of Parkinson disease to PARK16 in a Chilean sampleAlfredo Ramirez, Andreas Ziegler, Susen Winkler, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|March 23, 2011
Homozygous THAP1 mutations as cause of early-onset generalized dystoniaSusanne A Schneider, Alfredo Ramirez, Kaveh Shafiee, et al.
Neuro-Degenerative Diseases|June 25, 2020
Clinical Phenotype of LRRK2 R1441C in 2 Chinese SistersShen-Yang Lim, Jia Lun Lim, Azlina Ahmad-Annuar, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|August 6, 2010
Clinical neuroimaging and electrophysiological assessment of three DYT6 dystonia familiesSimone Zittel, Christian K E Moll, Norbert Brüggemann, et al.
Pageof 27