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Kathrin Grundmann

Showing results (1-10 of 40) with videos related to

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Archives of Neurology|April 13, 2005
Primary torsion dystoniaKathrin Grundmann
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 19, 2005
The IRF6 p.274V polymorphism is not a risk factor for isolated cleft lipRobert Hering, Kathrin Grundmann
Frontiers in Neurology|February 15, 2017
Needs and Requirements of Modern Biobanks on the Example of Dystonia SyndromesEbba Lohmann, Thomas Gasser, Kathrin Grundmann
Trends in Neurosciences|October 23, 2013
New genetic insights highlight 'old' ideas on motor dysfunction in dystoniaRose E Goodchild, Kathrin Grundmann, Antonio Pisani
Neuroreport|October 16, 2009
Adult neural precursor cells unaffected in animal models of DYT1 dystoniaMartin Regensburger, Zacharias Kohl, Kathrin Grundmann, et al.
Movement Disorders Clinical Practice|August 18, 2021
Compound Heterozygous <i>DARS2</i> Mutations as a Mimic of Hereditary Spastic ParaplegiaMartje G Pauly, Yorck Hellenbroich, Kathrin Grundmann-Hauser, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|January 11, 2014
Screening of mutations in GNAL in sporadic dystonia patientsClaudia Dufke, Marc Sturm, Christopher Schroeder, et al.
Neurogenetics|March 3, 2026
Novel genetic and nerve imaging characterization of Charcot-Marie-Tooth disease type 4FHanna Küpper, Lara G Stühn, Kathrin Grundmann-Hauser, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|May 28, 2014
Combined occurrence of a novel TOR1A and a THAP1 mutation in primary dystoniaFu-Bo Cheng, Jia-Chun Feng, Ling-Yan Ma, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|November 14, 2020
Tetraparesis and sensorimotor axonal polyneuropathy due to co-occurrence of Pompe disease and hereditary ATTR amyloidosisMilan Zimmermann, Natalie Deininger, Sophia Willikens, et al.
Pageof 4

Showing results (1-10 of 40) with videos related to

Sort By:
Pageof 4
Archives of Neurology|April 13, 2005
Primary torsion dystoniaKathrin Grundmann
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 19, 2005
The IRF6 p.274V polymorphism is not a risk factor for isolated cleft lipRobert Hering, Kathrin Grundmann
Frontiers in Neurology|February 15, 2017
Needs and Requirements of Modern Biobanks on the Example of Dystonia SyndromesEbba Lohmann, Thomas Gasser, Kathrin Grundmann
Trends in Neurosciences|October 23, 2013
New genetic insights highlight 'old' ideas on motor dysfunction in dystoniaRose E Goodchild, Kathrin Grundmann, Antonio Pisani
Neuroreport|October 16, 2009
Adult neural precursor cells unaffected in animal models of DYT1 dystoniaMartin Regensburger, Zacharias Kohl, Kathrin Grundmann, et al.
Movement Disorders Clinical Practice|August 18, 2021
Compound Heterozygous <i>DARS2</i> Mutations as a Mimic of Hereditary Spastic ParaplegiaMartje G Pauly, Yorck Hellenbroich, Kathrin Grundmann-Hauser, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|January 11, 2014
Screening of mutations in GNAL in sporadic dystonia patientsClaudia Dufke, Marc Sturm, Christopher Schroeder, et al.
Neurogenetics|March 3, 2026
Novel genetic and nerve imaging characterization of Charcot-Marie-Tooth disease type 4FHanna Küpper, Lara G Stühn, Kathrin Grundmann-Hauser, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|May 28, 2014
Combined occurrence of a novel TOR1A and a THAP1 mutation in primary dystoniaFu-Bo Cheng, Jia-Chun Feng, Ling-Yan Ma, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|November 14, 2020
Tetraparesis and sensorimotor axonal polyneuropathy due to co-occurrence of Pompe disease and hereditary ATTR amyloidosisMilan Zimmermann, Natalie Deininger, Sophia Willikens, et al.
Pageof 4