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Rune R Frants

Showing results (1-10 of 104) with videos related to

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Respiratory Medicine|March 21, 2008
Alpha-1 antitrypsin Null mutations and severity of emphysemaLaura Fregonese, Jan Stolk, Rune R Frants, et al.
Biochimica Et Biophysica Acta|July 14, 2006
Facioscapulohumeral muscular dystrophySilvère M van der Maarel, Rune R Frants, George W Padberg
Mutation Research|August 30, 2008
Epigenetic mechanisms of facioscapulohumeral muscular dystrophyJessica C de Greef, Rune R Frants, Silvère M van der Maarel
The European Journal of Neuroscience|August 10, 2002
Functional characterization of compound heterozygosity for GlyRalpha1 mutations in the startle disease hyperekplexiaRuth Rea, Marina A Tijssen, Colin Herd, et al.
Expert Review of Neurotherapeutics|September 16, 2005
Migraine: new treatment options from molecular biologyAnine H Stam, Joost Haan, Rune R Frants, et al.
Advances in Genetics|February 3, 2009
Familial hemiplegic migraineCurtis F Barrett, Arn M J M van den Maagdenberg, Rune R Frants, et al.
Human Genetics|May 21, 2009
Molecular genetics of migraineBoukje de Vries, Rune R Frants, Michel D Ferrari, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|April 22, 2005
Clinical and genetic aspects of idiopathic epilepsies in childhoodPetra M C Callenbach, Arn M J M van den Maagdenberg, Rune R Frants, et al.
Twin Research : the Official Journal of the International Society for Twin Studies|September 27, 2003
Genetic analysis of indicators of cholesterol synthesis and absorption: lathosterol and phytosterols in Dutch twins and their parentsDorret I Boomsma, Hans M Princen, Rune R Frants, et al.
Headache|July 27, 2006
Genetic biomarkers for migraineBoukje De Vries, Joost Haan, Rune R Frants, et al.
Pageof 11

Showing results (1-10 of 104) with videos related to

Sort By:
Pageof 11
Respiratory Medicine|March 21, 2008
Alpha-1 antitrypsin Null mutations and severity of emphysemaLaura Fregonese, Jan Stolk, Rune R Frants, et al.
Biochimica Et Biophysica Acta|July 14, 2006
Facioscapulohumeral muscular dystrophySilvère M van der Maarel, Rune R Frants, George W Padberg
Mutation Research|August 30, 2008
Epigenetic mechanisms of facioscapulohumeral muscular dystrophyJessica C de Greef, Rune R Frants, Silvère M van der Maarel
The European Journal of Neuroscience|August 10, 2002
Functional characterization of compound heterozygosity for GlyRalpha1 mutations in the startle disease hyperekplexiaRuth Rea, Marina A Tijssen, Colin Herd, et al.
Expert Review of Neurotherapeutics|September 16, 2005
Migraine: new treatment options from molecular biologyAnine H Stam, Joost Haan, Rune R Frants, et al.
Advances in Genetics|February 3, 2009
Familial hemiplegic migraineCurtis F Barrett, Arn M J M van den Maagdenberg, Rune R Frants, et al.
Human Genetics|May 21, 2009
Molecular genetics of migraineBoukje de Vries, Rune R Frants, Michel D Ferrari, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|April 22, 2005
Clinical and genetic aspects of idiopathic epilepsies in childhoodPetra M C Callenbach, Arn M J M van den Maagdenberg, Rune R Frants, et al.
Twin Research : the Official Journal of the International Society for Twin Studies|September 27, 2003
Genetic analysis of indicators of cholesterol synthesis and absorption: lathosterol and phytosterols in Dutch twins and their parentsDorret I Boomsma, Hans M Princen, Rune R Frants, et al.
Headache|July 27, 2006
Genetic biomarkers for migraineBoukje De Vries, Joost Haan, Rune R Frants, et al.
Pageof 11