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L J Ptacek

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Neurology|August 1, 1994
Autosomal dominant cerebellar ataxia with retinal degeneration: clinical, neuropathologic, and genetic analysis of a large kindredL G Gouw, K B Digre, C P Harris, et al.
American Journal of Human Genetics|October 1, 1991
Paramyotonia congenita and hyperkalemic periodic paralysis map to the same sodium-channel gene locusL J Ptacek, J S Trimmer, W S Agnew, et al.
Cell|February 24, 2001
MiRP2 forms potassium channels in skeletal muscle with Kv3.4 and is associated with periodic paralysisG W Abbott, M H Butler, S Bendahhou, et al.
Annals of Neurology|March 1, 1994
Andersen's syndrome: potassium-sensitive periodic paralysis, ventricular ectopy, and dysmorphic featuresR Tawil, L J Ptacek, S G Pavlakis, et al.
Neuropsychiatry, Neuropsychology, and Behavioral Neurology|April 30, 1998
Autosomal dominant cerebral arteriopathy: neuropsychiatric syndrome in a familyJ C Adair, B L Hart, M Kornfeld, et al.
Brain : a Journal of Neurology|October 1, 2005
The primary periodic paralyses: diagnosis, pathogenesis and treatmentS L Venance, S C Cannon, D Fialho, et al.
Annals of Neurology|March 1, 1993
Sodium channel mutations in paramyotonia congenita and hyperkalemic periodic paralysisL J Ptacek, L Gouw, H Kwieciński, et al.
Annals of Neurology|January 13, 2000
Randomized trials of dichlorphenamide in the periodic paralyses. Working Group on Periodic ParalysisR Tawil, M P McDermott, R Brown, et al.
Genome Research|October 1, 1996
An expanded CAG repeat sequence in spinocerebellar ataxia type 7K Lindblad, M L Savontaus, G Stevanin, et al.
Neurology|December 30, 2004
Clinical evaluation of idiopathic paroxysmal kinesigenic dyskinesia: new diagnostic criteriaM K Bruno, M Hallett, K Gwinn-Hardy, et al.
Pageof 2

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

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 20 results.
Neurology|August 1, 1994
Autosomal dominant cerebellar ataxia with retinal degeneration: clinical, neuropathologic, and genetic analysis of a large kindredL G Gouw, K B Digre, C P Harris, et al.
American Journal of Human Genetics|October 1, 1991
Paramyotonia congenita and hyperkalemic periodic paralysis map to the same sodium-channel gene locusL J Ptacek, J S Trimmer, W S Agnew, et al.
Cell|February 24, 2001
MiRP2 forms potassium channels in skeletal muscle with Kv3.4 and is associated with periodic paralysisG W Abbott, M H Butler, S Bendahhou, et al.
Annals of Neurology|March 1, 1994
Andersen's syndrome: potassium-sensitive periodic paralysis, ventricular ectopy, and dysmorphic featuresR Tawil, L J Ptacek, S G Pavlakis, et al.
Neuropsychiatry, Neuropsychology, and Behavioral Neurology|April 30, 1998
Autosomal dominant cerebral arteriopathy: neuropsychiatric syndrome in a familyJ C Adair, B L Hart, M Kornfeld, et al.
Brain : a Journal of Neurology|October 1, 2005
The primary periodic paralyses: diagnosis, pathogenesis and treatmentS L Venance, S C Cannon, D Fialho, et al.
Annals of Neurology|March 1, 1993
Sodium channel mutations in paramyotonia congenita and hyperkalemic periodic paralysisL J Ptacek, L Gouw, H Kwieciński, et al.
Annals of Neurology|January 13, 2000
Randomized trials of dichlorphenamide in the periodic paralyses. Working Group on Periodic ParalysisR Tawil, M P McDermott, R Brown, et al.
Genome Research|October 1, 1996
An expanded CAG repeat sequence in spinocerebellar ataxia type 7K Lindblad, M L Savontaus, G Stevanin, et al.
Neurology|December 30, 2004
Clinical evaluation of idiopathic paroxysmal kinesigenic dyskinesia: new diagnostic criteriaM K Bruno, M Hallett, K Gwinn-Hardy, et al.
Pageof 2