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Claudia Funke

Showing results (1-10 of 12) with videos related to

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Journal of Movement Disorders|October 30, 2020
New Nonsense Variant c.2983G>T; p.Glu995* in the CACNA1A Gene Causes Progressive Autosomal Dominant AtaxiaYannic Saathoff, Saskia Biskup, Claudia Funke, et al.
Neurochemistry International|December 11, 2012
Genetics and iron in the systems biology of Parkinson's disease and some related disordersClaudia Funke, Susanne A Schneider, Daniela Berg, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)|May 29, 2009
Genetic analysis of heme oxygenase-1 (HO-1) in German Parkinson's disease patientsClaudia Funke, Juergen Tomiuk, Olaf Riess, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)|March 4, 2009
Genetic analysis of coding SNPs in blood-brain barrier transporter MDR1 in European Parkinson's disease patientsClaudia Funke, Anne S Soehn, Juergen Tomiuk, et al.
Parkinsonism & Related Disorders|October 18, 2019
IRF2BPL mutations cause autosomal dominant dystonia with anarthria, slow saccades and seizuresChristos Ganos, Simone Zittel, Ute Hidding, et al.
The American Journal of Pathology|June 5, 2010
Progressive secondary neurodegeneration and microcalcification co-occur in osteopontin-deficient miceWalter Maetzler, Daniela Berg, Claudia Funke, et al.
Journal of Applied Crystallography|July 21, 2020
X-ray diffraction using focused-ion-beam-prepared single crystalsTina Weigel, Claudia Funke, Matthias Zschornak, et al.
Tremor and Other Hyperkinetic Movements (New York, N.Y.)|October 31, 2017
A Case of Beta-propeller Protein-associated Neurodegeneration due to a Heterozygous Deletion of <i>WDR45</i>Andreas Hermann, Hagen H Kitzler, Tobias Pollack, et al.
Neuropediatrics|June 26, 2015
SYNGAP1 Mutation in Focal and Generalized Epilepsy: A Literature Overview and A Case Report with Special Aspects of the EEGCelina von Stülpnagel, Claudia Funke, Caroline Haberl, et al.
Frontiers in Neuroscience|January 11, 2021
Case Report: Association of a Variant of Unknown Significance in the <i>FIG4</i> Gene With Frontotemporal Dementia and Slowly Progressing Motoneuron Disease: A Case Report Depicting Common Challenges in Clinical and Genetic Diagnostics of Rare Neuropsychiatric and Neurologic DisordersCaroline Gertrud Bergner, Christiane Michaela Neuhofer, Claudia Funke, et al.
Pageof 2

Showing results (1-10 of 12) with videos related to

Sort By:
Pageof 2
Journal of Movement Disorders|October 30, 2020
New Nonsense Variant c.2983G>T; p.Glu995* in the CACNA1A Gene Causes Progressive Autosomal Dominant AtaxiaYannic Saathoff, Saskia Biskup, Claudia Funke, et al.
Neurochemistry International|December 11, 2012
Genetics and iron in the systems biology of Parkinson's disease and some related disordersClaudia Funke, Susanne A Schneider, Daniela Berg, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)|May 29, 2009
Genetic analysis of heme oxygenase-1 (HO-1) in German Parkinson's disease patientsClaudia Funke, Juergen Tomiuk, Olaf Riess, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)|March 4, 2009
Genetic analysis of coding SNPs in blood-brain barrier transporter MDR1 in European Parkinson's disease patientsClaudia Funke, Anne S Soehn, Juergen Tomiuk, et al.
Parkinsonism & Related Disorders|October 18, 2019
IRF2BPL mutations cause autosomal dominant dystonia with anarthria, slow saccades and seizuresChristos Ganos, Simone Zittel, Ute Hidding, et al.
The American Journal of Pathology|June 5, 2010
Progressive secondary neurodegeneration and microcalcification co-occur in osteopontin-deficient miceWalter Maetzler, Daniela Berg, Claudia Funke, et al.
Journal of Applied Crystallography|July 21, 2020
X-ray diffraction using focused-ion-beam-prepared single crystalsTina Weigel, Claudia Funke, Matthias Zschornak, et al.
Tremor and Other Hyperkinetic Movements (New York, N.Y.)|October 31, 2017
A Case of Beta-propeller Protein-associated Neurodegeneration due to a Heterozygous Deletion of <i>WDR45</i>Andreas Hermann, Hagen H Kitzler, Tobias Pollack, et al.
Neuropediatrics|June 26, 2015
SYNGAP1 Mutation in Focal and Generalized Epilepsy: A Literature Overview and A Case Report with Special Aspects of the EEGCelina von Stülpnagel, Claudia Funke, Caroline Haberl, et al.
Frontiers in Neuroscience|January 11, 2021
Case Report: Association of a Variant of Unknown Significance in the <i>FIG4</i> Gene With Frontotemporal Dementia and Slowly Progressing Motoneuron Disease: A Case Report Depicting Common Challenges in Clinical and Genetic Diagnostics of Rare Neuropsychiatric and Neurologic DisordersCaroline Gertrud Bergner, Christiane Michaela Neuhofer, Claudia Funke, et al.
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