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K Jurkat-Rott

Showing results (31-40 of 49) with videos related to

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Acta Neurologica Scandinavica|January 6, 2010
Whole-body high-field MRI shows no skeletal muscle degeneration in young patients with recessive myotonia congenitaC Kornblum, G G Lutterbey, B Czermin, et al.
Brain : a Journal of Neurology|May 17, 2001
Hypokalaemic periodic paralysis type 2 caused by mutations at codon 672 in the muscle sodium channel gene SCN4AD Sternberg, T Maisonobe, K Jurkat-Rott, et al.
Neurology|October 10, 2001
Generalized epilepsy with febrile seizures plus: further heterogeneity in a large familyH Lerche, Y G Weber, H Baier, et al.
Neurology|June 30, 2005
Opening of the blood-brain barrier preceding cortical edema in a severe attack of FHM type IIJ P Dreier, K Jurkat-Rott, G C Petzold, et al.
Der Nervenarzt|November 18, 2000
[Molecular diagnosis of hereditary neurologic diseases. Position paper]T Gasser, M Dichgans, K Jurkat-Rott, et al.
Neurology|May 26, 2004
Variability of familial hemiplegic migraine with novel A1A2 Na+/K+-ATPase variantsK Jurkat-Rott, T Freilinger, J P Dreier, et al.
Human Genetics|November 1, 1994
Genetic heterogeneity in hypokalemic periodic paralysis (hypoPP)E Plassart, A Elbaz, J V Santos, et al.
Nature Genetics|March 1, 1994
Mapping of the hypokalaemic periodic paralysis (HypoPP) locus to chromosome 1q31-32 in three European familiesB Fontaine, J Vale-Santos, K Jurkat-Rott, et al.
American Journal of Human Genetics|February 1, 1995
Hypokalemic periodic paralysis and the dihydropyridine receptor (CACNL1A3): genotype/phenotype correlations for two predominant mutations and evidence for the absence of a founder effect in 16 caucasian familiesA Elbaz, J Vale-Santos, K Jurkat-Rott, et al.
Human Molecular Genetics|August 1, 1994
A calcium channel mutation causing hypokalemic periodic paralysisK Jurkat-Rott, F Lehmann-Horn, A Elbaz, et al.
Pageof 5

Showing results (31-40 of 49) with videos related to

Sort By:
Pageof 5
Acta Neurologica Scandinavica|January 6, 2010
Whole-body high-field MRI shows no skeletal muscle degeneration in young patients with recessive myotonia congenitaC Kornblum, G G Lutterbey, B Czermin, et al.
Brain : a Journal of Neurology|May 17, 2001
Hypokalaemic periodic paralysis type 2 caused by mutations at codon 672 in the muscle sodium channel gene SCN4AD Sternberg, T Maisonobe, K Jurkat-Rott, et al.
Neurology|October 10, 2001
Generalized epilepsy with febrile seizures plus: further heterogeneity in a large familyH Lerche, Y G Weber, H Baier, et al.
Neurology|June 30, 2005
Opening of the blood-brain barrier preceding cortical edema in a severe attack of FHM type IIJ P Dreier, K Jurkat-Rott, G C Petzold, et al.
Der Nervenarzt|November 18, 2000
[Molecular diagnosis of hereditary neurologic diseases. Position paper]T Gasser, M Dichgans, K Jurkat-Rott, et al.
Neurology|May 26, 2004
Variability of familial hemiplegic migraine with novel A1A2 Na+/K+-ATPase variantsK Jurkat-Rott, T Freilinger, J P Dreier, et al.
Human Genetics|November 1, 1994
Genetic heterogeneity in hypokalemic periodic paralysis (hypoPP)E Plassart, A Elbaz, J V Santos, et al.
Nature Genetics|March 1, 1994
Mapping of the hypokalaemic periodic paralysis (HypoPP) locus to chromosome 1q31-32 in three European familiesB Fontaine, J Vale-Santos, K Jurkat-Rott, et al.
American Journal of Human Genetics|February 1, 1995
Hypokalemic periodic paralysis and the dihydropyridine receptor (CACNL1A3): genotype/phenotype correlations for two predominant mutations and evidence for the absence of a founder effect in 16 caucasian familiesA Elbaz, J Vale-Santos, K Jurkat-Rott, et al.
Human Molecular Genetics|August 1, 1994
A calcium channel mutation causing hypokalemic periodic paralysisK Jurkat-Rott, F Lehmann-Horn, A Elbaz, et al.
Pageof 5