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G M Terwindt

Showing results (81-90 of 96) with videos related to

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International Journal of Stroke : Official Journal of the International Stroke Society|March 6, 2024
Sensitivity of the Boston criteria version 2.0 in Dutch-type hereditary cerebral amyloid angiopathyRgj van der Zwet, E A Koemans, S Voigt, et al.
Neurology|December 16, 2014
Reduced trigeminovascular cyclicity in patients with menstrually related migraineKhatera Ibrahimi, Willebrordus Petrus Johannes van Oosterhout, Wendy van Dorp, et al.
Annals of the Rheumatic Diseases|October 31, 2009
TREX1 gene variant in neuropsychiatric systemic lupus erythematosusB de Vries, G M Steup-Beekman, J Haan, 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.
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 Neurology|November 7, 2002
Episodic ataxia type 2. Three novel truncating mutations and one novel missense mutation in the CACNA1A geneA M J M van den Maagdenberg, E E Kors, E R Brunt, et al.
Journal of Internal Medicine|November 10, 2018
Systemic features of retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations: a monogenic small vessel diseaseN Pelzer, E S Hoogeveen, J Haan, et al.
Cell|November 1, 1996
Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2+ channel gene CACNL1A4R A Ophoff, G M Terwindt, M N Vergouwe, et al.
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.
Pageof 10

Showing results (81-90 of 96) with videos related to

Sort By:
Pageof 10
International Journal of Stroke : Official Journal of the International Stroke Society|March 6, 2024
Sensitivity of the Boston criteria version 2.0 in Dutch-type hereditary cerebral amyloid angiopathyRgj van der Zwet, E A Koemans, S Voigt, et al.
Neurology|December 16, 2014
Reduced trigeminovascular cyclicity in patients with menstrually related migraineKhatera Ibrahimi, Willebrordus Petrus Johannes van Oosterhout, Wendy van Dorp, et al.
Annals of the Rheumatic Diseases|October 31, 2009
TREX1 gene variant in neuropsychiatric systemic lupus erythematosusB de Vries, G M Steup-Beekman, J Haan, 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.
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 Neurology|November 7, 2002
Episodic ataxia type 2. Three novel truncating mutations and one novel missense mutation in the CACNA1A geneA M J M van den Maagdenberg, E E Kors, E R Brunt, et al.
Journal of Internal Medicine|November 10, 2018
Systemic features of retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations: a monogenic small vessel diseaseN Pelzer, E S Hoogeveen, J Haan, et al.
Cell|November 1, 1996
Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2+ channel gene CACNL1A4R A Ophoff, G M Terwindt, M N Vergouwe, et al.
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.
Pageof 10