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M D Ferrari

Showing results (221-230 of 246) with videos related to

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Neurology|January 14, 2009
MRI correlates of cognitive decline in CADASIL: a 7-year follow-up studyM K Liem, S A J Lesnik Oberstein, J Haan, et al.
The Journal of Headache and Pain|February 10, 2016
European Headache Federation consensus on technical investigation for primary headache disordersD D Mitsikostas, M Ashina, A Craven, 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.
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.
Neurology|September 29, 2004
Childhood epilepsy, familial hemiplegic migraine, cerebellar ataxia, and a new CACNA1A mutationE E Kors, A Melberg, K R J Vanmolkot, et al.
Cephalalgia : an International Journal of Headache|April 12, 2012
Aortic root pathology in Marfan syndrome increases the risk of migraine with auraH Koppen, J C Vis, D J Gooiker, et al.
Cephalalgia : an International Journal of Headache|February 13, 2001
Guidelines for controlled trials of drugs in migraine: second editionP Tfelt-Hansen, G Block, C Dahlöf, 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.
Neuropediatrics|November 10, 2004
Alternating hemiplegia of childhood: no mutations in the second familial hemiplegic migraine gene ATP1A2E E Kors, K R J Vanmolkot, J Haan, et al.
Pageof 25

Showing results (221-230 of 246) with videos related to

Sort By:
Pageof 25
Neurology|January 14, 2009
MRI correlates of cognitive decline in CADASIL: a 7-year follow-up studyM K Liem, S A J Lesnik Oberstein, J Haan, et al.
The Journal of Headache and Pain|February 10, 2016
European Headache Federation consensus on technical investigation for primary headache disordersD D Mitsikostas, M Ashina, A Craven, 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.
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.
Neurology|September 29, 2004
Childhood epilepsy, familial hemiplegic migraine, cerebellar ataxia, and a new CACNA1A mutationE E Kors, A Melberg, K R J Vanmolkot, et al.
Cephalalgia : an International Journal of Headache|April 12, 2012
Aortic root pathology in Marfan syndrome increases the risk of migraine with auraH Koppen, J C Vis, D J Gooiker, et al.
Cephalalgia : an International Journal of Headache|February 13, 2001
Guidelines for controlled trials of drugs in migraine: second editionP Tfelt-Hansen, G Block, C Dahlöf, 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.
Neuropediatrics|November 10, 2004
Alternating hemiplegia of childhood: no mutations in the second familial hemiplegic migraine gene ATP1A2E E Kors, K R J Vanmolkot, J Haan, et al.
Pageof 25