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Dagmar Nolte

Showing results (11-20 of 17) with videos related to

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Archives of Neurology|December 15, 2004
Phenotypic and molecular analyses of X-linked dystonia-parkinsonism ("lubag") in womenVirgilio Gerald H Evidente, Dagmar Nolte, Stephan Niemann, et al.
Archives of Neurology|May 12, 2010
The N141I mutation in PSEN2: implications for the quintessential case of Alzheimer diseaseChang-En Yu, Elizabeth Marchani, Georg Nikisch, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|February 1, 2007
Subthalamic-thalamic DBS in a case with spinocerebellar ataxia type 2 and severe tremor-A unusual clinical benefitHans-Joachim Freund, Utako B Barnikol, Dagmar Nolte, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|June 21, 2007
First case of X-linked dystonia-parkinsonism ("Lubag") to demonstrate a response to bilateral pallidal stimulationVirgilio Gerald H Evidente, Mark K Lyons, Mark Wheeler, et al.
Neuropathology and Applied Neurobiology|February 6, 2026
Myopathy With Exercise-Induced Intolerance due to Novel Biallelic Variants in OBSCN-A Clinical, Morphological and Molecular AnalysisHeidrun H Krämer-Best, Marlen C Reis, Andreas Hentschel, et al.
Journal of Medical Genetics|March 27, 2019
Pathogenic variants in the AFG3L2 proteolytic domain cause SCA28 through haploinsufficiency and proteostatic stress-driven OMA1 activationSusanna Tulli, Andrea Del Bondio, Valentina Baderna, et al.
Nature Genetics|February 28, 2006
Mutations in voltage-gated potassium channel KCNC3 cause degenerative and developmental central nervous system phenotypesMichael F Waters, Natali A Minassian, Giovanni Stevanin, et al.
Pageof 2

Showing results (11-20 of 17) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 17 results.
Archives of Neurology|December 15, 2004
Phenotypic and molecular analyses of X-linked dystonia-parkinsonism ("lubag") in womenVirgilio Gerald H Evidente, Dagmar Nolte, Stephan Niemann, et al.
Archives of Neurology|May 12, 2010
The N141I mutation in PSEN2: implications for the quintessential case of Alzheimer diseaseChang-En Yu, Elizabeth Marchani, Georg Nikisch, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|February 1, 2007
Subthalamic-thalamic DBS in a case with spinocerebellar ataxia type 2 and severe tremor-A unusual clinical benefitHans-Joachim Freund, Utako B Barnikol, Dagmar Nolte, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|June 21, 2007
First case of X-linked dystonia-parkinsonism ("Lubag") to demonstrate a response to bilateral pallidal stimulationVirgilio Gerald H Evidente, Mark K Lyons, Mark Wheeler, et al.
Neuropathology and Applied Neurobiology|February 6, 2026
Myopathy With Exercise-Induced Intolerance due to Novel Biallelic Variants in OBSCN-A Clinical, Morphological and Molecular AnalysisHeidrun H Krämer-Best, Marlen C Reis, Andreas Hentschel, et al.
Journal of Medical Genetics|March 27, 2019
Pathogenic variants in the AFG3L2 proteolytic domain cause SCA28 through haploinsufficiency and proteostatic stress-driven OMA1 activationSusanna Tulli, Andrea Del Bondio, Valentina Baderna, et al.
Nature Genetics|February 28, 2006
Mutations in voltage-gated potassium channel KCNC3 cause degenerative and developmental central nervous system phenotypesMichael F Waters, Natali A Minassian, Giovanni Stevanin, et al.
Pageof 2