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Esther E Kors

Showing results (1-10 of 6) with videos related to

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Current Opinion in Neurology|June 5, 2002
Calcium channel mutations and migraineEsther E Kors, Arn M J M van den Maagdenberg, Jaap J Plomp, et al.
Current Opinion in Neurology|May 29, 2004
Recent findings in headache geneticsEsther E Kors, Kaate R J Vanmolkot, Joost Haan, 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.
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.
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.
European Journal of Human Genetics : EJHG|March 16, 2006
Two de novo mutations in the Na,K-ATPase gene ATP1A2 associated with pure familial hemiplegic migraineKaate R J Vanmolkot, Esther E Kors, Ulku Turk, et al.
Pageof 1

Showing results (1-10 of 6) with videos related to

Sort By:
Pageof 1
Current Opinion in Neurology|June 5, 2002
Calcium channel mutations and migraineEsther E Kors, Arn M J M van den Maagdenberg, Jaap J Plomp, et al.
Current Opinion in Neurology|May 29, 2004
Recent findings in headache geneticsEsther E Kors, Kaate R J Vanmolkot, Joost Haan, 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.
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.
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.
European Journal of Human Genetics : EJHG|March 16, 2006
Two de novo mutations in the Na,K-ATPase gene ATP1A2 associated with pure familial hemiplegic migraineKaate R J Vanmolkot, Esther E Kors, Ulku Turk, et al.
Pageof 1