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Movement Disorders : Official Journal of the Movement Disorder Society
|
September 5, 2002
Major and minor form of hereditary hyperekplexia
Marina A J Tijssen, Monique N Vergouwe, J Gert van Dijk, et al.
Handbook of Clinical Neurology
|
September 7, 2010
Genetics of headaches
Arn M J M Van Den Maagdenberg, Gisela M Terwindt, Joost Haan, et al.
Current Opinion in Neurology
|
June 5, 2002
Calcium channel mutations and migraine
Esther 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 dystrophy
Richard 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 sumatriptan
Suneet Mehrotra, Kaate R J Vanmolkot, Rune R Frants, et al.
Current Opinion in Neurology
|
May 29, 2004
Recent findings in headache genetics
Esther E Kors, Kaate R J Vanmolkot, Joost Haan, et al.
Current Pain and Headache Reports
|
May 24, 2005
Migraine genetics: an update
J Haan, E E Kors, Kaate R J Vanmolkot, et al.
Chromosoma
|
November 15, 2006
FRG1P-mediated aggregation of proteins involved in pre-mRNA processing
Silvana 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 muscle
Yanchao 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 locus
Antoine de Morrée, Marjolein Droog, Laure Grand Moursel, et al.
Page
of 11
Search research articles
Search
Showing results (11-20 of 104) with videos related to
Sort By:
Page
of 11
Movement Disorders : Official Journal of the Movement Disorder Society
|
September 5, 2002
Major and minor form of hereditary hyperekplexia
Marina A J Tijssen, Monique N Vergouwe, J Gert van Dijk, et al.
Handbook of Clinical Neurology
|
September 7, 2010
Genetics of headaches
Arn M J M Van Den Maagdenberg, Gisela M Terwindt, Joost Haan, et al.
Current Opinion in Neurology
|
June 5, 2002
Calcium channel mutations and migraine
Esther 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 dystrophy
Richard 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 sumatriptan
Suneet Mehrotra, Kaate R J Vanmolkot, Rune R Frants, et al.
Current Opinion in Neurology
|
May 29, 2004
Recent findings in headache genetics
Esther E Kors, Kaate R J Vanmolkot, Joost Haan, et al.
Current Pain and Headache Reports
|
May 24, 2005
Migraine genetics: an update
J Haan, E E Kors, Kaate R J Vanmolkot, et al.
Chromosoma
|
November 15, 2006
FRG1P-mediated aggregation of proteins involved in pre-mRNA processing
Silvana 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 muscle
Yanchao 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 locus
Antoine de Morrée, Marjolein Droog, Laure Grand Moursel, et al.
Page
of 11