Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Katja Lohmann

Showing results (161-170 of 267) with videos related to

Pageof 27
Sort By:
Cellular and Molecular Life Sciences : CMLS|February 17, 2016
Evidence of TAF1 dysfunction in peripheral models of X-linked dystonia-parkinsonismAloysius Domingo, David Amar, Karen Grütz, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|May 18, 2017
Nomenclature of genetic movement disorders: Recommendations of the International Parkinson and Movement Disorder Society task forceConnie Marras, Anthony Lang, Bart P van de Warrenburg, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|December 15, 2021
Relationship of Genotype, Phenotype, and Treatment in Dopa-Responsive Dystonia: MDSGene ReviewAnne Weissbach, Martje G Pauly, Rebecca Herzog, et al.
Genes|April 28, 2023
The Expanding Phenotypical Spectrum of <i>WARS2</i>-Related Disorder: Four Novel Cases with a Common Recurrent VariantMartje G Pauly, G Christoph Korenke, Sokhna Haissatou Diaw, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|February 10, 2025
Classification and Genotype-Phenotype Relationships of GBA1 Variants: MDSGene Systematic ReviewMalco Rossi, Susen Schaake, Tatiana Usnich, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|December 12, 2018
Utility and implications of exome sequencing in early-onset Parkinson's diseaseJoanne Trinh, Katja Lohmann, Hauke Baumann, et al.
Medrxiv : the Preprint Server for Health Sciences|January 2, 2026
How many do we miss? - Evaluation of age at onset and family history as selection criteria for genetic testing in Parkinson's diseaseAlexander Balck, Eva-Juliane Vollstedt, Ana Westenberger, et al.
JAMA Neurology|May 11, 2026
Genetic Testing by Age at Onset in Parkinson DiseaseAlexander Balck, Eva-Juliane Vollstedt, Ana Westenberger, et al.
Journal of Clinical Medicine|December 11, 2019
Pallidal Deep Brain Stimulation in DYT6 Dystonia: Clinical Outcome and Predictive Factors for Motor ImprovementAnnika Danielsson, Miryam Carecchio, Laura Cif, et al.
Journal of Neurology|November 9, 2013
Recessive dystonia-ataxia syndrome in a Turkish family caused by a COX20 (FAM36A) mutationSarah Doss, Katja Lohmann, Philip Seibler, et al.
Pageof 27

Showing results (161-170 of 267) with videos related to

Sort By:
Pageof 27
Cellular and Molecular Life Sciences : CMLS|February 17, 2016
Evidence of TAF1 dysfunction in peripheral models of X-linked dystonia-parkinsonismAloysius Domingo, David Amar, Karen Grütz, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|May 18, 2017
Nomenclature of genetic movement disorders: Recommendations of the International Parkinson and Movement Disorder Society task forceConnie Marras, Anthony Lang, Bart P van de Warrenburg, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|December 15, 2021
Relationship of Genotype, Phenotype, and Treatment in Dopa-Responsive Dystonia: MDSGene ReviewAnne Weissbach, Martje G Pauly, Rebecca Herzog, et al.
Genes|April 28, 2023
The Expanding Phenotypical Spectrum of <i>WARS2</i>-Related Disorder: Four Novel Cases with a Common Recurrent VariantMartje G Pauly, G Christoph Korenke, Sokhna Haissatou Diaw, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|February 10, 2025
Classification and Genotype-Phenotype Relationships of GBA1 Variants: MDSGene Systematic ReviewMalco Rossi, Susen Schaake, Tatiana Usnich, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|December 12, 2018
Utility and implications of exome sequencing in early-onset Parkinson's diseaseJoanne Trinh, Katja Lohmann, Hauke Baumann, et al.
Medrxiv : the Preprint Server for Health Sciences|January 2, 2026
How many do we miss? - Evaluation of age at onset and family history as selection criteria for genetic testing in Parkinson's diseaseAlexander Balck, Eva-Juliane Vollstedt, Ana Westenberger, et al.
JAMA Neurology|May 11, 2026
Genetic Testing by Age at Onset in Parkinson DiseaseAlexander Balck, Eva-Juliane Vollstedt, Ana Westenberger, et al.
Journal of Clinical Medicine|December 11, 2019
Pallidal Deep Brain Stimulation in DYT6 Dystonia: Clinical Outcome and Predictive Factors for Motor ImprovementAnnika Danielsson, Miryam Carecchio, Laura Cif, et al.
Journal of Neurology|November 9, 2013
Recessive dystonia-ataxia syndrome in a Turkish family caused by a COX20 (FAM36A) mutationSarah Doss, Katja Lohmann, Philip Seibler, et al.
Pageof 27