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Rune R Frants

Showing results (11-20 of 104) with videos related to

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Movement Disorders : Official Journal of the Movement Disorder Society|September 5, 2002
Major and minor form of hereditary hyperekplexiaMarina A J Tijssen, Monique N Vergouwe, J Gert van Dijk, et al.
Handbook of Clinical Neurology|September 7, 2010
Genetics of headachesArn M J M Van Den Maagdenberg, Gisela M Terwindt, Joost Haan, et al.
Current Opinion in Neurology|June 5, 2002
Calcium channel mutations and migraineEsther E Kors, Arn M J M van den Maagdenberg, Jaap J Plomp, et al.
American Journal of Human Genetics|October 7, 2004
Contractions of D4Z4 on 4qB subtelomeres do not cause facioscapulohumeral muscular dystrophyRichard J F L Lemmers, Mariëlle Wohlgemuth, Rune R Frants, et al.
Headache|May 16, 2007
The phe-124-Cys and A-161T variants of the human 5-HT1B receptor gene are not major determinants of the clinical response to sumatriptanSuneet Mehrotra, Kaate R J Vanmolkot, Rune R Frants, et al.
Current Opinion in Neurology|May 29, 2004
Recent findings in headache geneticsEsther E Kors, Kaate R J Vanmolkot, Joost Haan, et al.
Current Pain and Headache Reports|May 24, 2005
Migraine genetics: an updateJ Haan, E E Kors, Kaate R J Vanmolkot, et al.
Chromosoma|November 15, 2006
FRG1P-mediated aggregation of proteins involved in pre-mRNA processingSilvana van Koningsbruggen, Kirsten R Straasheijm, Ellen Sterrenburg, et al.
Human Molecular Genetics|March 13, 2008
Calpain 3 is a modulator of the dysferlin protein complex in skeletal muscleYanchao Huang, Antoine de Morrée, Alexandra van Remoortere, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|September 24, 2011
Self-regulated alternative splicing at the AHNAK locusAntoine de Morrée, Marjolein Droog, Laure Grand Moursel, et al.
Pageof 11

Showing results (11-20 of 104) with videos related to

Sort By:
Pageof 11
Movement Disorders : Official Journal of the Movement Disorder Society|September 5, 2002
Major and minor form of hereditary hyperekplexiaMarina A J Tijssen, Monique N Vergouwe, J Gert van Dijk, et al.
Handbook of Clinical Neurology|September 7, 2010
Genetics of headachesArn M J M Van Den Maagdenberg, Gisela M Terwindt, Joost Haan, et al.
Current Opinion in Neurology|June 5, 2002
Calcium channel mutations and migraineEsther E Kors, Arn M J M van den Maagdenberg, Jaap J Plomp, et al.
American Journal of Human Genetics|October 7, 2004
Contractions of D4Z4 on 4qB subtelomeres do not cause facioscapulohumeral muscular dystrophyRichard J F L Lemmers, Mariëlle Wohlgemuth, Rune R Frants, et al.
Headache|May 16, 2007
The phe-124-Cys and A-161T variants of the human 5-HT1B receptor gene are not major determinants of the clinical response to sumatriptanSuneet Mehrotra, Kaate R J Vanmolkot, Rune R Frants, et al.
Current Opinion in Neurology|May 29, 2004
Recent findings in headache geneticsEsther E Kors, Kaate R J Vanmolkot, Joost Haan, et al.
Current Pain and Headache Reports|May 24, 2005
Migraine genetics: an updateJ Haan, E E Kors, Kaate R J Vanmolkot, et al.
Chromosoma|November 15, 2006
FRG1P-mediated aggregation of proteins involved in pre-mRNA processingSilvana van Koningsbruggen, Kirsten R Straasheijm, Ellen Sterrenburg, et al.
Human Molecular Genetics|March 13, 2008
Calpain 3 is a modulator of the dysferlin protein complex in skeletal muscleYanchao Huang, Antoine de Morrée, Alexandra van Remoortere, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|September 24, 2011
Self-regulated alternative splicing at the AHNAK locusAntoine de Morrée, Marjolein Droog, Laure Grand Moursel, et al.
Pageof 11