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Respiratory Medicine
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March 21, 2008
Alpha-1 antitrypsin Null mutations and severity of emphysema
Laura Fregonese, Jan Stolk, Rune R Frants, et al.
Biochimica Et Biophysica Acta
|
July 14, 2006
Facioscapulohumeral muscular dystrophy
Silvère M van der Maarel, Rune R Frants, George W Padberg
Mutation Research
|
August 30, 2008
Epigenetic mechanisms of facioscapulohumeral muscular dystrophy
Jessica 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 hyperekplexia
Ruth Rea, Marina A Tijssen, Colin Herd, et al.
Expert Review of Neurotherapeutics
|
September 16, 2005
Migraine: new treatment options from molecular biology
Anine H Stam, Joost Haan, Rune R Frants, et al.
Advances in Genetics
|
February 3, 2009
Familial hemiplegic migraine
Curtis F Barrett, Arn M J M van den Maagdenberg, Rune R Frants, et al.
Human Genetics
|
May 21, 2009
Molecular genetics of migraine
Boukje 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 childhood
Petra 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 parents
Dorret I Boomsma, Hans M Princen, Rune R Frants, et al.
Headache
|
July 27, 2006
Genetic biomarkers for migraine
Boukje De Vries, Joost Haan, Rune R Frants, et al.
Page
of 11
Search research articles
Search
Showing results (1-10 of 104) with videos related to
Sort By:
Page
of 11
Respiratory Medicine
|
March 21, 2008
Alpha-1 antitrypsin Null mutations and severity of emphysema
Laura Fregonese, Jan Stolk, Rune R Frants, et al.
Biochimica Et Biophysica Acta
|
July 14, 2006
Facioscapulohumeral muscular dystrophy
Silvère M van der Maarel, Rune R Frants, George W Padberg
Mutation Research
|
August 30, 2008
Epigenetic mechanisms of facioscapulohumeral muscular dystrophy
Jessica 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 hyperekplexia
Ruth Rea, Marina A Tijssen, Colin Herd, et al.
Expert Review of Neurotherapeutics
|
September 16, 2005
Migraine: new treatment options from molecular biology
Anine H Stam, Joost Haan, Rune R Frants, et al.
Advances in Genetics
|
February 3, 2009
Familial hemiplegic migraine
Curtis F Barrett, Arn M J M van den Maagdenberg, Rune R Frants, et al.
Human Genetics
|
May 21, 2009
Molecular genetics of migraine
Boukje 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 childhood
Petra 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 parents
Dorret I Boomsma, Hans M Princen, Rune R Frants, et al.
Headache
|
July 27, 2006
Genetic biomarkers for migraine
Boukje De Vries, Joost Haan, Rune R Frants, et al.
Page
of 11