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J Haan

Showing results (171-180 of 223) with videos related to

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Archives of Neurology|January 1, 1996
White matter lesions and cognitive deterioration in presymptomatic carriers of the amyloid precursor protein gene codon 693 mutationM Bornebroek, J Haan, M A van Buchem, et al.
Archives of Neurology|February 1, 1995
Cerebral blood flow during migraine attacks without aura and effect of sumatriptanM D Ferrari, J Haan, J A Blokland, et al.
Neurology|June 17, 1999
Diagnostic Notch3 sequence analysis in CADASIL: three new mutations in Dutch patients. Dutch CADASIL Research GroupS A Oberstein, M D Ferrari, E Bakker, et al.
Cephalalgia : an International Journal of Headache|April 11, 2008
A gene for a new monogenic neurovascular migraine syndrome: a next step in unravelling molecular pathways for migraine?K R J Vanmolkot, G M Terwindt, R R Frants, et al.
Nederlands Tijdschrift Voor Geneeskunde|October 22, 2004
[From gene to disease; familial hemiplegic migraine as a result of mutations in a sodium-potassium pump gene]E E Kors, K R J Vanmolkot, J Haan, et al.
Current Pain and Headache Reports|May 24, 2005
Migraine genetics: an updateJ Haan, E E Kors, Kaate R J Vanmolkot, et al.
Neurology|April 26, 2001
Involvement of the CACNA1A gene containing region on 19p13 in migraine with and without auraG M Terwindt, R A Ophoff, R van Eijk, et al.
Archives of Neurology|November 1, 1989
Single photon emission computed tomography in Alzheimer's diseaseJ Haan, H C Weinstein, M J van Kroonenburgh, et al.
Frontiers in Rehabilitation Sciences|October 3, 2022
The Usability of the Preliminary ICF Core Set for Hospitalized Patients After a Hematopoietic Stem Cell Transplantation From the Perspective of Nurses: A Feasibility StudyHillegonda A Stallinga, Janita Bakker, Sylvia J Haan, et al.
Science (New York, N.Y.)|June 1, 1990
Amyloid beta protein precursor gene and hereditary cerebral hemorrhage with amyloidosis (Dutch)C Van Broeckhoven, J Haan, E Bakker, et al.
Pageof 23

Showing results (171-180 of 223) with videos related to

Sort By:
Pageof 23
Archives of Neurology|January 1, 1996
White matter lesions and cognitive deterioration in presymptomatic carriers of the amyloid precursor protein gene codon 693 mutationM Bornebroek, J Haan, M A van Buchem, et al.
Archives of Neurology|February 1, 1995
Cerebral blood flow during migraine attacks without aura and effect of sumatriptanM D Ferrari, J Haan, J A Blokland, et al.
Neurology|June 17, 1999
Diagnostic Notch3 sequence analysis in CADASIL: three new mutations in Dutch patients. Dutch CADASIL Research GroupS A Oberstein, M D Ferrari, E Bakker, et al.
Cephalalgia : an International Journal of Headache|April 11, 2008
A gene for a new monogenic neurovascular migraine syndrome: a next step in unravelling molecular pathways for migraine?K R J Vanmolkot, G M Terwindt, R R Frants, et al.
Nederlands Tijdschrift Voor Geneeskunde|October 22, 2004
[From gene to disease; familial hemiplegic migraine as a result of mutations in a sodium-potassium pump gene]E E Kors, K R J Vanmolkot, J Haan, et al.
Current Pain and Headache Reports|May 24, 2005
Migraine genetics: an updateJ Haan, E E Kors, Kaate R J Vanmolkot, et al.
Neurology|April 26, 2001
Involvement of the CACNA1A gene containing region on 19p13 in migraine with and without auraG M Terwindt, R A Ophoff, R van Eijk, et al.
Archives of Neurology|November 1, 1989
Single photon emission computed tomography in Alzheimer's diseaseJ Haan, H C Weinstein, M J van Kroonenburgh, et al.
Frontiers in Rehabilitation Sciences|October 3, 2022
The Usability of the Preliminary ICF Core Set for Hospitalized Patients After a Hematopoietic Stem Cell Transplantation From the Perspective of Nurses: A Feasibility StudyHillegonda A Stallinga, Janita Bakker, Sylvia J Haan, et al.
Science (New York, N.Y.)|June 1, 1990
Amyloid beta protein precursor gene and hereditary cerebral hemorrhage with amyloidosis (Dutch)C Van Broeckhoven, J Haan, E Bakker, et al.
Pageof 23