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Kaate R J Vanmolkot

Showing results (1-10 of 14) with videos related to

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Headache|September 24, 2005
Familial hemiplegic migraine presenting as recurrent encephalopathy in a Native Indian familySian D Spacey, Kaate R J Vanmolkot, Colleen Murphy, et al.
Current Opinion in Neurology|May 29, 2004
Recent findings in headache geneticsEsther E Kors, Kaate R J Vanmolkot, Joost Haan, 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 sumatriptanSuneet Mehrotra, Kaate R J Vanmolkot, Rune R Frants, et al.
Current Pain and Headache Reports|May 24, 2005
Migraine genetics: an updateJ Haan, E E Kors, Kaate R J Vanmolkot, et al.
Human Molecular Genetics|April 4, 2002
Gain-of-function mutation in ADULT syndrome reveals the presence of a second transactivation domain in p63Pascal H G Duijf, Kaate R J Vanmolkot, Peter Propping, et al.
Current Pain and Headache Reports|April 30, 2004
Toward a molecular genetic classification of familial hemiplegic migraineJoost Haan, Esther E Kors, Arn M J M van den Maagdenberg, et al.
Arquivos De Neuro-Psiquiatria|November 23, 2006
Mutation analysis of CACNA1A and ATP1A2 genes in Brazilian FHM familiesLuciana R Lopes, Mario Fernando Prieto Peres, Kaate R J Vanmolkot, 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.
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.
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 2

Showing results (1-10 of 14) with videos related to

Sort By:
Pageof 2
Headache|September 24, 2005
Familial hemiplegic migraine presenting as recurrent encephalopathy in a Native Indian familySian D Spacey, Kaate R J Vanmolkot, Colleen Murphy, et al.
Current Opinion in Neurology|May 29, 2004
Recent findings in headache geneticsEsther E Kors, Kaate R J Vanmolkot, Joost Haan, 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 sumatriptanSuneet Mehrotra, Kaate R J Vanmolkot, Rune R Frants, et al.
Current Pain and Headache Reports|May 24, 2005
Migraine genetics: an updateJ Haan, E E Kors, Kaate R J Vanmolkot, et al.
Human Molecular Genetics|April 4, 2002
Gain-of-function mutation in ADULT syndrome reveals the presence of a second transactivation domain in p63Pascal H G Duijf, Kaate R J Vanmolkot, Peter Propping, et al.
Current Pain and Headache Reports|April 30, 2004
Toward a molecular genetic classification of familial hemiplegic migraineJoost Haan, Esther E Kors, Arn M J M van den Maagdenberg, et al.
Arquivos De Neuro-Psiquiatria|November 23, 2006
Mutation analysis of CACNA1A and ATP1A2 genes in Brazilian FHM familiesLuciana R Lopes, Mario Fernando Prieto Peres, Kaate R J Vanmolkot, 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.
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.
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 2