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C Kamm

Showing results (21-30 of 36) with videos related to

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Biochemical Medicine|July 1, 1975
Electrophoretic characterization of plasma RNAL W Guin, K E Griswold, S Patton, et al.
Journal of Neurology|January 22, 2008
Primary central nervous system vasculitis in a child mimicking parasitosisC Kamm, T Nägele, M Mittelbronn, et al.
Neurology|April 17, 2008
Novel ATP1A3 mutation in a sporadic RDP patient with minimal benefit from deep brain stimulationC Kamm, W Fogel, T Wächter, et al.
Journal of Neuroimmunology|December 31, 1997
Highly purified oligo-His tagged human recombinant alpha(1)-AChR is immunogenic in vivo and suitable for T cell stimulation in vitro in experimental and human myasthenia gravisR Voltz, C Kamm, F Padberg, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|August 6, 1999
GAG deletion in the DYT1 gene in early limb-onset idiopathic torsion dystonia in GermanyC Kamm, E Castelon-Konkiewitz, M Naumann, et al.
Neuroepidemiology|June 18, 2002
Service-based survey of dystonia in munichE Castelon Konkiewitz, I Trender-Gerhard, C Kamm, et al.
Neurology|June 28, 2006
Possible gender-dependent association of vascular endothelial growth factor (VEGF) gene and ALSR Fernández-Santiago, M Sharma, J C Mueller, et al.
Neurology|June 4, 2008
Susceptibility to DYT1 dystonia in European patients is modified by the D216H polymorphismC Kamm, H Fischer, B Garavaglia, et al.
European Journal of Neurology|March 13, 2018
A novel heterozygous variant in ERLIN2 causes autosomal dominant pure hereditary spastic paraplegiaS L Rydning, A Dudesek, F Rimmele, et al.
Neurology|November 30, 2006
Strong genetic evidence for association of TOR1A/TOR1B with idiopathic dystoniaC Kamm, F Asmus, J Mueller, et al.
Pageof 4

Showing results (21-30 of 36) with videos related to

Sort By:
Pageof 4
Biochemical Medicine|July 1, 1975
Electrophoretic characterization of plasma RNAL W Guin, K E Griswold, S Patton, et al.
Journal of Neurology|January 22, 2008
Primary central nervous system vasculitis in a child mimicking parasitosisC Kamm, T Nägele, M Mittelbronn, et al.
Neurology|April 17, 2008
Novel ATP1A3 mutation in a sporadic RDP patient with minimal benefit from deep brain stimulationC Kamm, W Fogel, T Wächter, et al.
Journal of Neuroimmunology|December 31, 1997
Highly purified oligo-His tagged human recombinant alpha(1)-AChR is immunogenic in vivo and suitable for T cell stimulation in vitro in experimental and human myasthenia gravisR Voltz, C Kamm, F Padberg, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|August 6, 1999
GAG deletion in the DYT1 gene in early limb-onset idiopathic torsion dystonia in GermanyC Kamm, E Castelon-Konkiewitz, M Naumann, et al.
Neuroepidemiology|June 18, 2002
Service-based survey of dystonia in munichE Castelon Konkiewitz, I Trender-Gerhard, C Kamm, et al.
Neurology|June 28, 2006
Possible gender-dependent association of vascular endothelial growth factor (VEGF) gene and ALSR Fernández-Santiago, M Sharma, J C Mueller, et al.
Neurology|June 4, 2008
Susceptibility to DYT1 dystonia in European patients is modified by the D216H polymorphismC Kamm, H Fischer, B Garavaglia, et al.
European Journal of Neurology|March 13, 2018
A novel heterozygous variant in ERLIN2 causes autosomal dominant pure hereditary spastic paraplegiaS L Rydning, A Dudesek, F Rimmele, et al.
Neurology|November 30, 2006
Strong genetic evidence for association of TOR1A/TOR1B with idiopathic dystoniaC Kamm, F Asmus, J Mueller, et al.
Pageof 4