Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

H Stam

Showing results (121-130 of 144) with videos related to

Pageof 15
Sort By:
Cephalalgia : an International Journal of Headache|November 14, 2012
Migraine is not associated with enhanced atherosclerosisAnine H Stam, Claudia M Weller, A Cecile Jw Janssens, et al.
Neurology|August 5, 2018
RVCL-S and CADASIL display distinct impaired vascular functionIrene de Boer, Anine H Stam, Linde Buntinx, et al.
Neuropediatrics|January 20, 2007
Alternating hemiplegia of childhood: no mutations in the glutamate transporter EAAT1B de Vries, J Haan, A H Stam, et al.
Cephalalgia : an International Journal of Headache|February 18, 2009
First mutation in the voltage-gated Nav1.1 subunit gene SCN1A with co-occurring familial hemiplegic migraine and epilepsyM-J Castro, A H Stam, C Lemos, et al.
Human Mutation|April 3, 2007
The novel p.L1649Q mutation in the SCN1A epilepsy gene is associated with familial hemiplegic migraine: genetic and functional studies. Mutation in brief #957. OnlineKaate R J Vanmolkot, Elena Babini, Boukje de Vries, et al.
Molecular Genetics and Metabolism|July 19, 2011
Rate of progression and predictive factors for pulmonary outcome in children and adults with Pompe diseaseN A M E van der Beek, C I van Capelle, K I van der Velden-van Etten, et al.
Cephalalgia : an International Journal of Headache|April 8, 2014
Two novel SCN1A mutations identified in families with familial hemiplegic migraineClaudia M Weller, Nadine Pelzer, Boukje de Vries, et al.
Cephalalgia : an International Journal of Headache|May 24, 2008
CACNA1A mutation linking hemiplegic migraine and alternating hemiplegia of childhoodB de Vries, A H Stam, F Beker, et al.
Neurology|January 15, 2010
Shared genetic factors in migraine and depression: evidence from a genetic isolateA H Stam, B de Vries, A C J W Janssens, et al.
Journal of Human Genetics|October 24, 2007
Recurrent ATP1A2 mutations in Portuguese families with familial hemiplegic migraineMaria-José Castro, Anine H Stam, Carolina Lemos, et al.
Pageof 15

Showing results (121-130 of 144) with videos related to

Sort By:
Pageof 15
Cephalalgia : an International Journal of Headache|November 14, 2012
Migraine is not associated with enhanced atherosclerosisAnine H Stam, Claudia M Weller, A Cecile Jw Janssens, et al.
Neurology|August 5, 2018
RVCL-S and CADASIL display distinct impaired vascular functionIrene de Boer, Anine H Stam, Linde Buntinx, et al.
Neuropediatrics|January 20, 2007
Alternating hemiplegia of childhood: no mutations in the glutamate transporter EAAT1B de Vries, J Haan, A H Stam, et al.
Cephalalgia : an International Journal of Headache|February 18, 2009
First mutation in the voltage-gated Nav1.1 subunit gene SCN1A with co-occurring familial hemiplegic migraine and epilepsyM-J Castro, A H Stam, C Lemos, et al.
Human Mutation|April 3, 2007
The novel p.L1649Q mutation in the SCN1A epilepsy gene is associated with familial hemiplegic migraine: genetic and functional studies. Mutation in brief #957. OnlineKaate R J Vanmolkot, Elena Babini, Boukje de Vries, et al.
Molecular Genetics and Metabolism|July 19, 2011
Rate of progression and predictive factors for pulmonary outcome in children and adults with Pompe diseaseN A M E van der Beek, C I van Capelle, K I van der Velden-van Etten, et al.
Cephalalgia : an International Journal of Headache|April 8, 2014
Two novel SCN1A mutations identified in families with familial hemiplegic migraineClaudia M Weller, Nadine Pelzer, Boukje de Vries, et al.
Cephalalgia : an International Journal of Headache|May 24, 2008
CACNA1A mutation linking hemiplegic migraine and alternating hemiplegia of childhoodB de Vries, A H Stam, F Beker, et al.
Neurology|January 15, 2010
Shared genetic factors in migraine and depression: evidence from a genetic isolateA H Stam, B de Vries, A C J W Janssens, et al.
Journal of Human Genetics|October 24, 2007
Recurrent ATP1A2 mutations in Portuguese families with familial hemiplegic migraineMaria-José Castro, Anine H Stam, Carolina Lemos, et al.
Pageof 15