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J Haan

Showing results (181-190 of 223) with videos related to

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Annals of Neurology|May 1, 1997
Dutch hereditary cerebral amyloid angiopathy: structural lesions and apolipoprotein E genotypeM Bornebroek, J Haan, S G Van Duinen, et al.
Annals of Neurology|July 1, 1997
Presenilin-1 polymorphism and hereditary cerebral hemorrhage with amyloidosis, Dutch typeM Bornebroek, J Haan, H Backhovens, et al.
Acta Neuropathologica|May 30, 1998
Secondary microvascular degeneration in amyloid angiopathy of patients with hereditary cerebral hemorrhage with amyloidosis, Dutch type (HCHWA-D)H V Vinters, R Natté, M L Maat-Schieman, et al.
AJNR. American Journal of Neuroradiology|February 18, 2006
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy: structural MR imaging changes and apolipoprotein E genotypeR van den Boom, S A J Lesnick Oberstein, A A van den Berg-Huysmans, et al.
American Journal of Human Genetics|September 1, 1991
DNA diagnosis for hereditary cerebral hemorrhage with amyloidosis (Dutch type)E Bakker, C van Broeckhoven, J Haan, et al.
Epilepsia|August 1, 1997
Partial cosegregation of familial hemiplegic migraine and a benign familial infantile epileptic syndromeG M Terwindt, R A Ophoff, D Lindhout, et al.
Genomics|July 1, 1994
Genetic heterogeneity of familial hemiplegic migraineR A Ophoff, R van Eijk, L A Sandkuijl, et al.
AJNR. American Journal of Neuroradiology|March 10, 2009
Cerebrovascular reactivity is a main determinant of white matter hyperintensity progression in CADASILM K Liem, S A J Lesnik Oberstein, J Haan, et al.
Human Genetics|November 1, 1995
Familial hemiplegic migraine locus on 19p13 is involved in the common forms of migraine with and without auraA May, R A Ophoff, G M Terwindt, et al.
Cephalalgia : an International Journal of Headache|February 15, 2002
No involvement of the calcium channel gene (CACNA1A) in a family with cluster headacheJ Haan, J A van Vliet, E E Kors, et al.
Pageof 23

Showing results (181-190 of 223) with videos related to

Sort By:
Pageof 23
Annals of Neurology|May 1, 1997
Dutch hereditary cerebral amyloid angiopathy: structural lesions and apolipoprotein E genotypeM Bornebroek, J Haan, S G Van Duinen, et al.
Annals of Neurology|July 1, 1997
Presenilin-1 polymorphism and hereditary cerebral hemorrhage with amyloidosis, Dutch typeM Bornebroek, J Haan, H Backhovens, et al.
Acta Neuropathologica|May 30, 1998
Secondary microvascular degeneration in amyloid angiopathy of patients with hereditary cerebral hemorrhage with amyloidosis, Dutch type (HCHWA-D)H V Vinters, R Natté, M L Maat-Schieman, et al.
AJNR. American Journal of Neuroradiology|February 18, 2006
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy: structural MR imaging changes and apolipoprotein E genotypeR van den Boom, S A J Lesnick Oberstein, A A van den Berg-Huysmans, et al.
American Journal of Human Genetics|September 1, 1991
DNA diagnosis for hereditary cerebral hemorrhage with amyloidosis (Dutch type)E Bakker, C van Broeckhoven, J Haan, et al.
Epilepsia|August 1, 1997
Partial cosegregation of familial hemiplegic migraine and a benign familial infantile epileptic syndromeG M Terwindt, R A Ophoff, D Lindhout, et al.
Genomics|July 1, 1994
Genetic heterogeneity of familial hemiplegic migraineR A Ophoff, R van Eijk, L A Sandkuijl, et al.
AJNR. American Journal of Neuroradiology|March 10, 2009
Cerebrovascular reactivity is a main determinant of white matter hyperintensity progression in CADASILM K Liem, S A J Lesnik Oberstein, J Haan, et al.
Human Genetics|November 1, 1995
Familial hemiplegic migraine locus on 19p13 is involved in the common forms of migraine with and without auraA May, R A Ophoff, G M Terwindt, et al.
Cephalalgia : an International Journal of Headache|February 15, 2002
No involvement of the calcium channel gene (CACNA1A) in a family with cluster headacheJ Haan, J A van Vliet, E E Kors, et al.
Pageof 23