Vergouwe MN - 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. Among authors: vergouwe mn. Eur J Hum Genet. 1996;4(6):321-8. Eur J Hum Genet. 1996. PMID: 9043864

2

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. Among authors: vergouwe mn. Cell. 1996 Nov 1;87(3):543-52. doi: 10.1016/s0092-8674(00)81373-2. Cell. 1996. PMID: 8898206 Free article.

3

Wolff Award 1997. Involvement of a Ca2+ channel gene in familial hemiplegic migraine and migraine with and without aura. Dutch Migraine Genetics Research Group.

Ophoff RA, Terwindt GM, Vergouwe MN, Frants RR, Ferrari MD. Ophoff RA, et al. Among authors: vergouwe mn. Headache. 1997 Sep;37(8):479-85. doi: 10.1046/j.1526-4610.1997.3708479.x. Headache. 1997. PMID: 9329229 Review.

4

Familial hemiplegic migraine: involvement of a calcium neuronal channel.

Ophoff RA, Terwindt GM, Vergouwe MN, Frants RR, Ferrari MD. Ophoff RA, et al. Among authors: vergouwe mn. Neurologia. 1997 Dec;12 Suppl 5:31-7. Neurologia. 1997. PMID: 9436352 Review.

5

Variable clinical expression of mutations in the P/Q-type calcium channel gene in familial hemiplegic migraine. Dutch Migraine Genetics Research Group.

Terwindt GM, Ophoff RA, Haan J, Vergouwe MN, van Eijk R, Frants RR, Ferrari MD. Terwindt GM, et al. Among authors: vergouwe mn. Neurology. 1998 Apr;50(4):1105-10. doi: 10.1212/wnl.50.4.1105. Neurology. 1998. PMID: 9566402

6

Alternating hemiplegia of childhood: no mutations in the familial hemiplegic migraine CACNA1A gene.

Haan J, Kors EE, Terwindt GM, Vermeulen FL, Vergouwe MN, van den Maagdenberg AM, Gill DS, Pascual J, Ophoff RA, Frants RR, Ferrari. Haan J, et al. Among authors: vergouwe mn. Cephalalgia. 2000 Oct;20(8):696-700. doi: 10.1046/j.0333-1024.2000.00095.x. Cephalalgia. 2000. PMID: 11167897

7

Involvement of the CACNA1A gene containing region on 19p13 in migraine with and without aura.

Terwindt GM, Ophoff RA, van Eijk R, Vergouwe MN, Haan J, Frants RR, Sandkuijl LA, Ferrari MD; Dutch Migraine Genetics Research Group. Terwindt GM, et al. Among authors: vergouwe mn. Neurology. 2001 Apr 24;56(8):1028-32. doi: 10.1212/wnl.56.8.1028. Neurology. 2001. PMID: 11320173

8

Hyperekplexia-like syndromes without mutations in the GLRA1 gene.

Vergouwe MN, Tijssen MA, Shiang R, van Dijk JG, al Shahwan S, Ophoff RA, Frants RR. Vergouwe MN, et al. Clin Neurol Neurosurg. 1997 Aug;99(3):172-8. doi: 10.1016/s0303-8467(97)00022-x. Clin Neurol Neurosurg. 1997. PMID: 9350397

9

Chromosomal localization of the 5-HT1F receptor gene: no evidence for involvement in response to sumatriptan in migraine patients.

Maassen VanDenBrink A, Vergouwe MN, Ophoff RA, Naylor SL, Dauwerse HG, Saxena PR, Ferrari MD, Frants RR. Maassen VanDenBrink A, et al. Among authors: vergouwe mn. Am J Med Genet. 1998 Jun 5;77(5):415-20. Am J Med Genet. 1998. PMID: 9632173

10

5-HT1B receptor polymorphism and clinical response to sumatriptan.

MaassenVanDenBrink A, Vergouwe MN, Ophoff RA, Saxena PR, Ferrari MD, Frants RR. MaassenVanDenBrink A, et al. Among authors: vergouwe mn. Headache. 1998 Apr;38(4):288-91. doi: 10.1046/j.1526-4610.1998.3804288.x. Headache. 1998. PMID: 9595868

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