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Rune R Frants

Showing results (61-70 of 104) with videos related to

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Magnetic Resonance in Medicine|July 27, 2007
T(1) relaxation in in vivo mouse brain at ultra-high fieldRob C G van de Ven, Bianca Hogers, Arn M J M van den Maagdenberg, et al.
Nature Genetics|November 25, 2003
Hypomethylation of D4Z4 in 4q-linked and non-4q-linked facioscapulohumeral muscular dystrophyPetra G M van Overveld, Richard J F L Lemmers, Lodewijk A Sandkuijl, et al.
European Journal of Human Genetics : EJHG|April 14, 2005
Protein studies in dysferlinopathy patients using llama-derived antibody fragments selected by phage displayYanchao Huang, Peter Verheesen, Andreas Roussis, et al.
American Journal of Human Genetics|October 10, 2007
Specific sequence variations within the 4q35 region are associated with facioscapulohumeral muscular dystrophyRichard J L F Lemmers, Marielle Wohlgemuth, Kristiaan J van der Gaag, et al.
Genetic Epidemiology|April 20, 2004
Combined association and linkage analysis applied to the APOE locusMarian Beekman, Daniëlle Posthuma, Bastiaan T Heijmans, et al.
Annals of Neurology|December 21, 2005
Migraine and MTHFR C677T genotype in a population-based sampleAnn I Scher, Gisela M Terwindt, W M Monique Verschuren, et al.
Plos One|August 10, 2010
Calpain 3 is a rapid-action, unidirectional proteolytic switch central to muscle remodelingAntoine de Morrée, David Lutje Hulsik, Antonietta Impagliazzo, et al.
Neurobiology of Disease|July 9, 2008
Premature stop codons in a facilitating EF-hand splice variant of CaV2.1 cause episodic ataxia type 2Tracey D Graves, Paola Imbrici, Esther E Kors, et al.
Annals of Neurology|September 4, 2003
Novel mutations in the Na+, K+-ATPase pump gene ATP1A2 associated with familial hemiplegic migraine and benign familial infantile convulsionsKaate R J Vanmolkot, Esther E Kors, Jouke-Jan Hottenga, et al.
Journal of the American Academy of Dermatology|February 6, 2007
From sporadic atypical nevi to familial melanoma: risk analysis for melanoma in sporadic atypical nevus patientsFemke A de Snoo, Marije W Kroon, Wilma Bergman, et al.
Pageof 11

Showing results (61-70 of 104) with videos related to

Sort By:
Pageof 11
Magnetic Resonance in Medicine|July 27, 2007
T(1) relaxation in in vivo mouse brain at ultra-high fieldRob C G van de Ven, Bianca Hogers, Arn M J M van den Maagdenberg, et al.
Nature Genetics|November 25, 2003
Hypomethylation of D4Z4 in 4q-linked and non-4q-linked facioscapulohumeral muscular dystrophyPetra G M van Overveld, Richard J F L Lemmers, Lodewijk A Sandkuijl, et al.
European Journal of Human Genetics : EJHG|April 14, 2005
Protein studies in dysferlinopathy patients using llama-derived antibody fragments selected by phage displayYanchao Huang, Peter Verheesen, Andreas Roussis, et al.
American Journal of Human Genetics|October 10, 2007
Specific sequence variations within the 4q35 region are associated with facioscapulohumeral muscular dystrophyRichard J L F Lemmers, Marielle Wohlgemuth, Kristiaan J van der Gaag, et al.
Genetic Epidemiology|April 20, 2004
Combined association and linkage analysis applied to the APOE locusMarian Beekman, Daniëlle Posthuma, Bastiaan T Heijmans, et al.
Annals of Neurology|December 21, 2005
Migraine and MTHFR C677T genotype in a population-based sampleAnn I Scher, Gisela M Terwindt, W M Monique Verschuren, et al.
Plos One|August 10, 2010
Calpain 3 is a rapid-action, unidirectional proteolytic switch central to muscle remodelingAntoine de Morrée, David Lutje Hulsik, Antonietta Impagliazzo, et al.
Neurobiology of Disease|July 9, 2008
Premature stop codons in a facilitating EF-hand splice variant of CaV2.1 cause episodic ataxia type 2Tracey D Graves, Paola Imbrici, Esther E Kors, et al.
Annals of Neurology|September 4, 2003
Novel mutations in the Na+, K+-ATPase pump gene ATP1A2 associated with familial hemiplegic migraine and benign familial infantile convulsionsKaate R J Vanmolkot, Esther E Kors, Jouke-Jan Hottenga, et al.
Journal of the American Academy of Dermatology|February 6, 2007
From sporadic atypical nevi to familial melanoma: risk analysis for melanoma in sporadic atypical nevus patientsFemke A de Snoo, Marije W Kroon, Wilma Bergman, et al.
Pageof 11