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Katja Lohmann

Showing results (121-130 of 267) with videos related to

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Cerebellum (London, England)|April 21, 2023
POLG2-Linked Mitochondrial Disease: Functional Insights from New Mutation Carriers and Review of the LiteratureMax Borsche, Marija Dulovic-Mahlow, Hauke Baumann, et al.
Archives of Neurology|October 15, 2008
Myoclonus-dystonia due to maternal uniparental disomyEmilie Guettard, Marie-France Portnoi, Katja Lohmann-Hedrich, et al.
Neurology|September 3, 2020
Clinical spectrum of the pentanucleotide repeat expansion in the <i>RFC1</i> gene in ataxia syndromesMaria Gisatulin, Valerija Dobricic, Christine Zühlke, et al.
Archives of Neurology|July 12, 2012
Two faces of the same coin: benign familial infantile seizures and paroxysmal kinesigenic dyskinesia caused by PRRT2 mutationsAlexander Schmidt, Kishore R Kumar, Katharina Redyk, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|January 25, 2021
Parkin Deficiency Appears Not to Be Associated with Cardiac Damage in Parkinson's DiseaseMichaela Trilck-Winkler, Max Borsche, Inke R König, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|February 6, 2021
Linking Penetrance and Transcription in DYT-THAP1: Insights From a Human iPSC-Derived Cortical ModelHauke Baumann, Fabian Ott, Joachim Weber, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|June 4, 2011
No evidence for THAP1/DYT6 variants as disease modifiers in DYT1 dystoniaChristoph Kamm, Nils Uflacker, Friedrich Asmus, et al.
Biochimica Et Biophysica Acta|August 5, 2014
THAP1, the gene mutated in DYT6 dystonia, autoregulates its own expressionAlev Erogullari, Ronja Hollstein, Philip Seibler, et al.
Movement Disorders Clinical Practice|March 15, 2024
RFC1 and FGF14 Repeat Expansions in Serbian Patients with Cerebellar AtaxiaAndona Milovanović, Nataša Dragaševic-Mišković, Mirja Thomsen, et al.
Parkinsonism & Related Disorders|June 29, 2017
Screening study of TUBB4A in isolated dystoniaFranca Vulinovic, Susen Schaake, Aloysius Domingo, et al.
Pageof 27

Showing results (121-130 of 267) with videos related to

Sort By:
Pageof 27
Cerebellum (London, England)|April 21, 2023
POLG2-Linked Mitochondrial Disease: Functional Insights from New Mutation Carriers and Review of the LiteratureMax Borsche, Marija Dulovic-Mahlow, Hauke Baumann, et al.
Archives of Neurology|October 15, 2008
Myoclonus-dystonia due to maternal uniparental disomyEmilie Guettard, Marie-France Portnoi, Katja Lohmann-Hedrich, et al.
Neurology|September 3, 2020
Clinical spectrum of the pentanucleotide repeat expansion in the <i>RFC1</i> gene in ataxia syndromesMaria Gisatulin, Valerija Dobricic, Christine Zühlke, et al.
Archives of Neurology|July 12, 2012
Two faces of the same coin: benign familial infantile seizures and paroxysmal kinesigenic dyskinesia caused by PRRT2 mutationsAlexander Schmidt, Kishore R Kumar, Katharina Redyk, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|January 25, 2021
Parkin Deficiency Appears Not to Be Associated with Cardiac Damage in Parkinson's DiseaseMichaela Trilck-Winkler, Max Borsche, Inke R König, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|February 6, 2021
Linking Penetrance and Transcription in DYT-THAP1: Insights From a Human iPSC-Derived Cortical ModelHauke Baumann, Fabian Ott, Joachim Weber, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|June 4, 2011
No evidence for THAP1/DYT6 variants as disease modifiers in DYT1 dystoniaChristoph Kamm, Nils Uflacker, Friedrich Asmus, et al.
Biochimica Et Biophysica Acta|August 5, 2014
THAP1, the gene mutated in DYT6 dystonia, autoregulates its own expressionAlev Erogullari, Ronja Hollstein, Philip Seibler, et al.
Movement Disorders Clinical Practice|March 15, 2024
RFC1 and FGF14 Repeat Expansions in Serbian Patients with Cerebellar AtaxiaAndona Milovanović, Nataša Dragaševic-Mišković, Mirja Thomsen, et al.
Parkinsonism & Related Disorders|June 29, 2017
Screening study of TUBB4A in isolated dystoniaFranca Vulinovic, Susen Schaake, Aloysius Domingo, et al.
Pageof 27