Frants RR - Search Results

1

[From gene to disease; familial hemiplegic migraine as a result of mutations in a sodium-potassium pump gene].

Kors EE, Vanmolkot KR, Haan J, van den Maagdenberg AM, Frants RR, Ferrari MD. Kors EE, et al. Among authors: frants rr. Ned Tijdschr Geneeskd. 2004 Sep 25;148(39):1919-20. Ned Tijdschr Geneeskd. 2004. PMID: 15495990 Review. Dutch.

2

Calcium channel mutations and migraine.

Kors EE, van den Maagdenberg AM, Plomp JJ, Frants RR, Ferrari MD. Kors EE, et al. Among authors: frants rr. Curr Opin Neurol. 2002 Jun;15(3):311-6. doi: 10.1097/00019052-200206000-00014. Curr Opin Neurol. 2002. PMID: 12045730 Review.

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. Among authors: frants rr. Genomics. 1994 Jul 1;22(1):21-6. doi: 10.1006/geno.1994.1340. Genomics. 1994. PMID: 7959770

4

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: frants rr. Cephalalgia. 1996 May;16(3):153-5. doi: 10.1046/j.1468-2982.1996.1603153.x. Cephalalgia. 1996. PMID: 8734765 Clinical Trial.

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: frants rr. Neurology. 1998 Apr;50(4):1105-10. doi: 10.1212/wnl.50.4.1105. Neurology. 1998. PMID: 9566402

6

Partial cosegregation of familial hemiplegic migraine and a benign familial infantile epileptic syndrome.

Terwindt GM, Ophoff RA, Lindhout D, Haan J, Halley DJ, Sandkuijl LA, Brouwer OF, Frants RR, Ferrari MD. Terwindt GM, et al. Among authors: frants rr. Epilepsia. 1997 Aug;38(8):915-21. doi: 10.1111/j.1528-1157.1997.tb01257.x. Epilepsia. 1997. PMID: 9579893 Free article.

7

[Channelopathies: a genetic explanation of migraine and other paroxysmal neurologic disorders].

Terwindt GM, Ophoff RA, Haan J, Frants RR, Ferrari MD. Terwindt GM, et al. Among authors: frants rr. Ned Tijdschr Geneeskd. 1998 May 2;142(18):1015-9. Ned Tijdschr Geneeskd. 1998. PMID: 9623202 Review. Dutch.

8

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: frants rr. Cephalalgia. 2000 Oct;20(8):696-700. doi: 10.1046/j.0333-1024.2000.00095.x. Cephalalgia. 2000. PMID: 11167897

9

[From gene to disease; from CACNA1A to migraine].

Kors EE, Haan J, Frants RR, Ferrari MD. Kors EE, et al. Among authors: frants rr. Ned Tijdschr Geneeskd. 2001 Feb 10;145(6):266-7. Ned Tijdschr Geneeskd. 2001. PMID: 11236374 Review. Dutch.

10

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: frants rr. Neurology. 2001 Apr 24;56(8):1028-32. doi: 10.1212/wnl.56.8.1028. Neurology. 2001. PMID: 11320173

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