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H Stam

Showing results (131-140 of 144) with videos related to

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Clinical Genetics|April 11, 2008
CACNA1A R1347Q: a frequent recurrent mutation in hemiplegic migraineA H Stam, K R J Vanmolkot, H P H Kremer, et al.
Archives of Neurology|January 14, 2009
Episodic ataxia associated with EAAT1 mutation C186S affecting glutamate reuptakeBoukje de Vries, Hafsa Mamsa, Anine H Stam, et al.
Epilepsia|October 31, 2009
Familial hemiplegic migraine is associated with febrile seizures in an FHM2 family with a novel de novo ATP1A2 mutationBoukje de Vries, Anine H Stam, Martin Kirkpatrick, et al.
Annals of Neurology|January 27, 2006
Severe episodic neurological deficits and permanent mental retardation in a child with a novel FHM2 ATP1A2 mutationK R J Vanmolkot, H Stroink, J B Koenderink, et al.
Neurology|December 7, 2007
Systematic analysis of three FHM genes in 39 sporadic patients with hemiplegic migraineB de Vries, T Freilinger, K R J Vanmolkot, et al.
European Journal of Human Genetics : EJHG|May 3, 2007
First case of compound heterozygosity in Na,K-ATPase gene ATP1A2 in familial hemiplegic migraineKaate R J Vanmolkot, Anine H Stam, Ashok Raman, et al.
Cephalalgia : an International Journal of Headache|September 3, 2014
Concordance of genetic risk across migraine subgroups: Impact on current and future genetic association studiesDale R Nyholt, , Verneri Anttila, et al.
Cephalalgia : an International Journal of Headache|December 15, 2015
Gene-based pleiotropy across migraine with aura and migraine without aura patient groupsHuiying Zhao, Else Eising, Boukje de Vries, et al.
Nature Genetics|July 31, 2007
C-terminal truncations in human 3'-5' DNA exonuclease TREX1 cause autosomal dominant retinal vasculopathy with cerebral leukodystrophyAnna Richards, Arn M J M van den Maagdenberg, Joanna C Jen, et al.
Brain : a Journal of Neurology|September 9, 2016
Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestationsAnine H Stam, Parul H Kothari, Aisha Shaikh, et al.
Pageof 15

Showing results (131-140 of 144) with videos related to

Sort By:
Pageof 15
Clinical Genetics|April 11, 2008
CACNA1A R1347Q: a frequent recurrent mutation in hemiplegic migraineA H Stam, K R J Vanmolkot, H P H Kremer, et al.
Archives of Neurology|January 14, 2009
Episodic ataxia associated with EAAT1 mutation C186S affecting glutamate reuptakeBoukje de Vries, Hafsa Mamsa, Anine H Stam, et al.
Epilepsia|October 31, 2009
Familial hemiplegic migraine is associated with febrile seizures in an FHM2 family with a novel de novo ATP1A2 mutationBoukje de Vries, Anine H Stam, Martin Kirkpatrick, et al.
Annals of Neurology|January 27, 2006
Severe episodic neurological deficits and permanent mental retardation in a child with a novel FHM2 ATP1A2 mutationK R J Vanmolkot, H Stroink, J B Koenderink, et al.
Neurology|December 7, 2007
Systematic analysis of three FHM genes in 39 sporadic patients with hemiplegic migraineB de Vries, T Freilinger, K R J Vanmolkot, et al.
European Journal of Human Genetics : EJHG|May 3, 2007
First case of compound heterozygosity in Na,K-ATPase gene ATP1A2 in familial hemiplegic migraineKaate R J Vanmolkot, Anine H Stam, Ashok Raman, et al.
Cephalalgia : an International Journal of Headache|September 3, 2014
Concordance of genetic risk across migraine subgroups: Impact on current and future genetic association studiesDale R Nyholt, , Verneri Anttila, et al.
Cephalalgia : an International Journal of Headache|December 15, 2015
Gene-based pleiotropy across migraine with aura and migraine without aura patient groupsHuiying Zhao, Else Eising, Boukje de Vries, et al.
Nature Genetics|July 31, 2007
C-terminal truncations in human 3'-5' DNA exonuclease TREX1 cause autosomal dominant retinal vasculopathy with cerebral leukodystrophyAnna Richards, Arn M J M van den Maagdenberg, Joanna C Jen, et al.
Brain : a Journal of Neurology|September 9, 2016
Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestationsAnine H Stam, Parul H Kothari, Aisha Shaikh, et al.
Pageof 15