Ophoff RA - Search Results

1

A 3-Mb region for the familial hemiplegic migraine locus on 19p13.1-p13.2: exclusion of PRKCSH as a candidate gene. Dutch Migraine Genetic Research Group.

Ophoff RA, Terwindt GM, Vergouwe MN, van Eijk R, Mohrenweiser H, Litt M, Hofker MH, Haan J, Ferrari MD, Frants RR. Ophoff RA, et al. Eur J Hum Genet. 1996;4(6):321-8. Eur J Hum Genet. 1996. PMID: 9043864

2

Mutation in DHP receptor alpha 1 subunit (CACLN1A3) gene in a Dutch family with hypokalaemic periodic paralysis.

Boerman RH, Ophoff RA, Links TP, van Eijk R, Sandkuijl LA, Elbaz A, Vale-Santos JE, Wintzen AR, van Deutekom JC, Isles DE, et al. Boerman RH, et al. Among authors: ophoff ra. J Med Genet. 1995 Jan;32(1):44-7. doi: 10.1136/jmg.32.1.44. J Med Genet. 1995. PMID: 7897626 Free PMC article.

3

Genetic heterogeneity of familial hemiplegic migraine.

Ophoff RA, van Eijk R, Sandkuijl LA, Terwindt GM, Grubben CP, Haan J, Lindhout D, Ferrari MD, Frants RR. Ophoff RA, et al. Genomics. 1994 Jul 1;22(1):21-6. doi: 10.1006/geno.1994.1340. Genomics. 1994. PMID: 7959770

4

Familial hemiplegic migraine in The Netherlands. Dutch Migraine Genetics Research Group.

Haan J, Terwindt GM, Bos PL, Ophoff RA, Frants RR, Ferrari MD. Haan J, et al. Among authors: ophoff ra. Clin Neurol Neurosurg. 1994 Aug;96(3):244-9. doi: 10.1016/0303-8467(94)90076-0. Clin Neurol Neurosurg. 1994. PMID: 7988094

5

Familial hemiplegic migraine locus on 19p13 is involved in the common forms of migraine with and without aura.

May A, Ophoff RA, Terwindt GM, Urban C, van Eijk R, Haan J, Diener HC, Lindhout D, Frants RR, Sandkuijl LA, et al. May A, et al. Among authors: ophoff ra. Hum Genet. 1995 Nov;96(5):604-8. doi: 10.1007/BF00197420. Hum Genet. 1995. PMID: 8530012

6

A four-generation Dutch family with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL), linked to chromosome 19p13.

Wielaard R, Bornebroek M, Ophoff RA, Winter-Warnars HA, Scheltens P, Frants RR, Ferrari MD, Haan J. Wielaard R, et al. Among authors: ophoff ra. Clin Neurol Neurosurg. 1995 Nov;97(4):307-13. doi: 10.1016/0303-8467(95)00068-u. Clin Neurol Neurosurg. 1995. PMID: 8599897

7

Is familial hemiplegic migraine a hereditary form of basilar migraine?

Haan J, Terwindt GM, Ophoff RA, Bos PL, Frants RR, Ferrari MD, Krommenhoek T, Lindhout DL, Sandkuyl LA, Van Eyk R. Haan J, et al. Among authors: ophoff ra. Cephalalgia. 1995 Dec;15(6):477-81. doi: 10.1046/j.1468-2982.1995.1506477.x. Cephalalgia. 1995. PMID: 8706110 Clinical Trial.

8

Familial hemiplegic migraine: a clinical comparison of families linked and unlinked to chromosome 19.DMG RG.

Terwindt GM, Ophoff RA, Haan J, Frants RR, Ferrari MD. Terwindt GM, et al. Among authors: ophoff ra. Cephalalgia. 1996 May;16(3):153-5. doi: 10.1046/j.1468-2982.1996.1603153.x. Cephalalgia. 1996. PMID: 8734765 Clinical Trial.

9

Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2+ channel gene CACNL1A4.

Ophoff RA, Terwindt GM, Vergouwe MN, van Eijk R, Oefner PJ, Hoffman SM, Lamerdin JE, Mohrenweiser HW, Bulman DE, Ferrari M, Haan J, Lindhout D, van Ommen GJ, Hofker MH, Ferrari MD, Frants RR. Ophoff RA, et al. Cell. 1996 Nov 1;87(3):543-52. doi: 10.1016/s0092-8674(00)81373-2. Cell. 1996. PMID: 8898206 Free article.

10

The quest for migraine genes.

Terwindt GM, Haan J, Ophoff RA, Frants RR, Ferrari MD. Terwindt GM, et al. Among authors: ophoff ra. Curr Opin Neurol. 1997 Jun;10(3):221-5. doi: 10.1097/00019052-199706000-00009. Curr Opin Neurol. 1997. PMID: 9229129 Review.

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