Search research articles
Contact Us
Filters
Showing results (1-10 of 6) with videos related to
Page
of 1
Sort By:
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.
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
|
April 30, 2004
Toward a molecular genetic classification of familial hemiplegic migraine
Joost 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 convulsions
Kaate 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 2
Tracey 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 migraine
Kaate R J Vanmolkot, Esther E Kors, Ulku Turk, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 6) with videos related to
Sort By:
Page
of 1
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.
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
|
April 30, 2004
Toward a molecular genetic classification of familial hemiplegic migraine
Joost 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 convulsions
Kaate 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 2
Tracey 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 migraine
Kaate R J Vanmolkot, Esther E Kors, Ulku Turk, et al.
Page
of 1