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L J Ptacek

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Italian Journal of Neurological Sciences|December 1, 1994
Mutation in the S4 segment of the adult skeletal sodium channel gene in an Italian paramyotonia congenita (PC) familyV Sansone, G Rotondo, L J Ptacek, et al.
Muscle & Nerve|July 1, 1994
Paramyotonia congenita: abnormal short exercise test, and improvement after mexiletine therapyC E Jackson, R J Barohn, L J Ptacek
Neurology|December 31, 1997
A new locus for hemiplegic migraine maps to chromosome 1q31K Gardner, M M Barmada, L J Ptacek, et al.
Neurology|February 1, 1992
Linkage of atypical myotonia congenita to a sodium channel locusL J Ptacek, R Tawil, R C Griggs, et al.
American Journal of Diseases of Children (1960)|May 1, 1977
Immunological studies on an aberrant form of ataxia telangiectasiaR L Hansen, J J Marx, L J Ptacek, et al.
Journal of Clinical Neuro-Ophthalmology|December 1, 1988
Trochlear nerve palsy following minor head trauma. A sign of structural disorderD M Jacobson, J J Warner, A K Choucair, et al.
Neurology|May 1, 1992
Evidence of genetic heterogeneity among the nondystrophic myotoniasL J Ptacek, F A Ziter, J W Roberts, et al.
American Journal of Human Genetics|August 1, 1991
Analysis in a large hyperkalemic periodic paralysis pedigree supports tight linkage to a sodium channel locusL J Ptacek, F Tyler, J S Trimmer, et al.
Neurogenetics|March 25, 2000
Genomic structure of human anion exchanger 3 and its potential role in hereditary neurological diseaseD D Einum, J Zhang, P J Arneson, et al.
Genomics|April 12, 2005
The Mass1frings mutation underlies early onset hearing impairment in BUB/BnJ mice, a model for the auditory pathology of Usher syndrome IICK R Johnson, Q Y Zheng, M D Weston, et al.
Pageof 2

Showing results (1-10 of 20) with videos related to

Sort By:
Pageof 2
Italian Journal of Neurological Sciences|December 1, 1994
Mutation in the S4 segment of the adult skeletal sodium channel gene in an Italian paramyotonia congenita (PC) familyV Sansone, G Rotondo, L J Ptacek, et al.
Muscle & Nerve|July 1, 1994
Paramyotonia congenita: abnormal short exercise test, and improvement after mexiletine therapyC E Jackson, R J Barohn, L J Ptacek
Neurology|December 31, 1997
A new locus for hemiplegic migraine maps to chromosome 1q31K Gardner, M M Barmada, L J Ptacek, et al.
Neurology|February 1, 1992
Linkage of atypical myotonia congenita to a sodium channel locusL J Ptacek, R Tawil, R C Griggs, et al.
American Journal of Diseases of Children (1960)|May 1, 1977
Immunological studies on an aberrant form of ataxia telangiectasiaR L Hansen, J J Marx, L J Ptacek, et al.
Journal of Clinical Neuro-Ophthalmology|December 1, 1988
Trochlear nerve palsy following minor head trauma. A sign of structural disorderD M Jacobson, J J Warner, A K Choucair, et al.
Neurology|May 1, 1992
Evidence of genetic heterogeneity among the nondystrophic myotoniasL J Ptacek, F A Ziter, J W Roberts, et al.
American Journal of Human Genetics|August 1, 1991
Analysis in a large hyperkalemic periodic paralysis pedigree supports tight linkage to a sodium channel locusL J Ptacek, F Tyler, J S Trimmer, et al.
Neurogenetics|March 25, 2000
Genomic structure of human anion exchanger 3 and its potential role in hereditary neurological diseaseD D Einum, J Zhang, P J Arneson, et al.
Genomics|April 12, 2005
The Mass1frings mutation underlies early onset hearing impairment in BUB/BnJ mice, a model for the auditory pathology of Usher syndrome IICK R Johnson, Q Y Zheng, M D Weston, et al.
Pageof 2