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G M Terwindt

Showing results (71-80 of 96) with videos related to

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Cephalalgia : an International Journal of Headache|May 27, 2016
Recurrent coma and fever in familial hemiplegic migraine type 2. A prospective 15-year follow-up of a large family with a novel ATP1A2 mutationN Pelzer, D E Blom, A H Stam, et al.
European Journal of Neurology|May 2, 2020
Cold extremities in migraine: a marker for vascular dysfunction in womenK M Linstra, M J L Perenboom, E W van Zwet, et al.
International Journal of Stroke : Official Journal of the International Stroke Society|August 24, 2021
Cerebellar hemorrhages in patients with Dutch-type hereditary cerebral amyloid angiopathyS Voigt, P C de Kruijff, E A Koemans, et al.
Brain : a Journal of Neurology|April 29, 1998
Clinical and genetic analysis of a large Dutch family with autosomal dominant vascular retinopathy, migraine and Raynaud's phenomenonG M Terwindt, J Haan, R A Ophoff, et al.
Cephalalgia : an International Journal of Headache|February 13, 2001
Alternating hemiplegia of childhood: no mutations in the familial hemiplegic migraine CACNA1A geneJ Haan, E E Kors, G M Terwindt, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|June 13, 2009
Early seizures and cerebral oedema after trivial head trauma associated with the CACNA1A S218L mutationA H Stam, G-J Luijckx, B T Poll-Thé, et al.
Annals of Neurology|June 21, 2001
Delayed cerebral edema and fatal coma after minor head trauma: role of the CACNA1A calcium channel subunit gene and relationship with familial hemiplegic migraineE E Kors, G M Terwindt, F L Vermeulen, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|June 11, 2024
Quantitative electroencephalography in cerebral amyloid angiopathyM C van der Plas, I Rasing, V J Geraedts, et al.
Archives of Neurology|May 21, 2003
Expanding the phenotypic spectrum of the CACNA1A gene T666M mutation: a description of 5 families with familial hemiplegic migraineE E Kors, J Haan, N J Giffin, et al.
Cephalalgia : an International Journal of Headache|November 25, 2005
The 3p21.1-p21.3 hereditary vascular retinopathy locus increases the risk for Raynaud's phenomenon and migraineJ J Hottenga, K R J Vanmolkot, E E Kors, et al.
Pageof 10

Showing results (71-80 of 96) with videos related to

Sort By:
Pageof 10
Cephalalgia : an International Journal of Headache|May 27, 2016
Recurrent coma and fever in familial hemiplegic migraine type 2. A prospective 15-year follow-up of a large family with a novel ATP1A2 mutationN Pelzer, D E Blom, A H Stam, et al.
European Journal of Neurology|May 2, 2020
Cold extremities in migraine: a marker for vascular dysfunction in womenK M Linstra, M J L Perenboom, E W van Zwet, et al.
International Journal of Stroke : Official Journal of the International Stroke Society|August 24, 2021
Cerebellar hemorrhages in patients with Dutch-type hereditary cerebral amyloid angiopathyS Voigt, P C de Kruijff, E A Koemans, et al.
Brain : a Journal of Neurology|April 29, 1998
Clinical and genetic analysis of a large Dutch family with autosomal dominant vascular retinopathy, migraine and Raynaud's phenomenonG M Terwindt, J Haan, R A Ophoff, et al.
Cephalalgia : an International Journal of Headache|February 13, 2001
Alternating hemiplegia of childhood: no mutations in the familial hemiplegic migraine CACNA1A geneJ Haan, E E Kors, G M Terwindt, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|June 13, 2009
Early seizures and cerebral oedema after trivial head trauma associated with the CACNA1A S218L mutationA H Stam, G-J Luijckx, B T Poll-Thé, et al.
Annals of Neurology|June 21, 2001
Delayed cerebral edema and fatal coma after minor head trauma: role of the CACNA1A calcium channel subunit gene and relationship with familial hemiplegic migraineE E Kors, G M Terwindt, F L Vermeulen, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|June 11, 2024
Quantitative electroencephalography in cerebral amyloid angiopathyM C van der Plas, I Rasing, V J Geraedts, et al.
Archives of Neurology|May 21, 2003
Expanding the phenotypic spectrum of the CACNA1A gene T666M mutation: a description of 5 families with familial hemiplegic migraineE E Kors, J Haan, N J Giffin, et al.
Cephalalgia : an International Journal of Headache|November 25, 2005
The 3p21.1-p21.3 hereditary vascular retinopathy locus increases the risk for Raynaud's phenomenon and migraineJ J Hottenga, K R J Vanmolkot, E E Kors, et al.
Pageof 10