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Katja Lohmann

Showing results (191-200 of 267) with videos related to

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Movement Disorders : Official Journal of the Movement Disorder Society|April 28, 2022
Nomenclature of Genetic Movement Disorders: Recommendations of the International Parkinson and Movement Disorder Society Task Force - An UpdateLara M Lange, Paulina Gonzalez-Latapi, Rajasumi Rajalingam, et al.
Annals of Neurology|April 1, 2018
Mutations in VPS13D lead to a new recessive ataxia with spasticity and mitochondrial defectsEunju Seong, Ryan Insolera, Marija Dulovic, et al.
Neurology|February 6, 2015
Short- and long-term outcome of chronic pallidal neurostimulation in monogenic isolated dystoniaNorbert Brüggemann, Andrea Kühn, Susanne A Schneider, et al.
Parkinsonism & Related Disorders|February 5, 2019
Role of ANO3 mutations in dystonia: A large-scale mutational screening studyLuisa Olschewski, Silvia Jesús, Han-Joon Kim, et al.
Parkinsonism & Related Disorders|November 15, 2018
Association of SNCA variants with α-synuclein of gastric and colonic mucosa in Parkinson's diseaseSun Ju Chung, Inke R König, Katja Lohmann, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 23, 2022
Familial Cerebellar Ataxia and Amyotrophic Lateral Sclerosis/Frontotemporal Dementia with DAB1 and C9ORF72 Repeat Expansions: An 18-Year StudyAngela Rosenbohm, Hendrik Pott, Mirja Thomsen, et al.
Genes|December 24, 2021
Validity and Prognostic Value of a Polygenic Risk Score for Parkinson's DiseaseSebastian Koch, Björn-Hergen Laabs, Meike Kasten, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|August 16, 2021
Genotype-Phenotype Relations for the Atypical Parkinsonism Genes: MDSGene Systematic ReviewChristina Wittke, Sonja Petkovic, Valerija Dobricic, et al.
Journal of the Neurological Sciences|March 22, 2017
Caffeine, creatine, GRIN2A and Parkinson's disease progressionDavid K Simon, Cai Wu, Barbara C Tilley, et al.
Brain : a Journal of Neurology|October 8, 2020
Mitochondrial damage-associated inflammation highlights biomarkers in PRKN/PINK1 parkinsonismMax Borsche, Inke R König, Sylvie Delcambre, et al.
Pageof 27

Showing results (191-200 of 267) with videos related to

Sort By:
Pageof 27
Movement Disorders : Official Journal of the Movement Disorder Society|April 28, 2022
Nomenclature of Genetic Movement Disorders: Recommendations of the International Parkinson and Movement Disorder Society Task Force - An UpdateLara M Lange, Paulina Gonzalez-Latapi, Rajasumi Rajalingam, et al.
Annals of Neurology|April 1, 2018
Mutations in VPS13D lead to a new recessive ataxia with spasticity and mitochondrial defectsEunju Seong, Ryan Insolera, Marija Dulovic, et al.
Neurology|February 6, 2015
Short- and long-term outcome of chronic pallidal neurostimulation in monogenic isolated dystoniaNorbert Brüggemann, Andrea Kühn, Susanne A Schneider, et al.
Parkinsonism & Related Disorders|February 5, 2019
Role of ANO3 mutations in dystonia: A large-scale mutational screening studyLuisa Olschewski, Silvia Jesús, Han-Joon Kim, et al.
Parkinsonism & Related Disorders|November 15, 2018
Association of SNCA variants with α-synuclein of gastric and colonic mucosa in Parkinson's diseaseSun Ju Chung, Inke R König, Katja Lohmann, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 23, 2022
Familial Cerebellar Ataxia and Amyotrophic Lateral Sclerosis/Frontotemporal Dementia with DAB1 and C9ORF72 Repeat Expansions: An 18-Year StudyAngela Rosenbohm, Hendrik Pott, Mirja Thomsen, et al.
Genes|December 24, 2021
Validity and Prognostic Value of a Polygenic Risk Score for Parkinson's DiseaseSebastian Koch, Björn-Hergen Laabs, Meike Kasten, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|August 16, 2021
Genotype-Phenotype Relations for the Atypical Parkinsonism Genes: MDSGene Systematic ReviewChristina Wittke, Sonja Petkovic, Valerija Dobricic, et al.
Journal of the Neurological Sciences|March 22, 2017
Caffeine, creatine, GRIN2A and Parkinson's disease progressionDavid K Simon, Cai Wu, Barbara C Tilley, et al.
Brain : a Journal of Neurology|October 8, 2020
Mitochondrial damage-associated inflammation highlights biomarkers in PRKN/PINK1 parkinsonismMax Borsche, Inke R König, Sylvie Delcambre, et al.
Pageof 27