Frants RR - Search Results

1

No involvement of the calcium channel gene (CACNA1A) in a family with cluster headache.

Haan J, van Vliet JA, Kors EE, Terwindt GM, Vermeulen FL, van den Maagdenberg AM, Frants RR, Ferrari MD. Haan J, et al. Among authors: frants rr. Cephalalgia. 2001 Dec;21(10):959-62. doi: 10.1046/j.1468-2982.2001.00283.x. Cephalalgia. 2001. PMID: 11843867

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

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: frants rr. Cephalalgia. 1995 Dec;15(6):477-81. doi: 10.1046/j.1468-2982.1995.1506477.x. Cephalalgia. 1995. PMID: 8706110 Clinical Trial.

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

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: frants rr. Headache. 1997 Sep;37(8):479-85. doi: 10.1046/j.1526-4610.1997.3708479.x. Headache. 1997. PMID: 9329229 Review.

6

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: frants rr. Neurologia. 1997 Dec;12 Suppl 5:31-7. Neurologia. 1997. PMID: 9436352 Review.

7

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

8

Migraine, ataxia and epilepsy: a challenging spectrum of genetically determined calcium channelopathies. Dutch Migraine Genetics Research Group.

Terwindt GM, Ophoff RA, Haan J, Sandkuijl LA, Frants RR, Ferrari MD. Terwindt GM, et al. Among authors: frants rr. Eur J Hum Genet. 1998 Jul-Aug;6(4):297-307. doi: 10.1038/sj.ejhg.5200206. Eur J Hum Genet. 1998. PMID: 9781035 Review.

9

Search for mitochondrial DNA mutations in migraine subgroups.

Haan J, Terwindt GM, Maassen JA, Hart LM, Frants RR, Ferrari MD. Haan J, et al. Among authors: frants rr. Cephalalgia. 1999 Jan;19(1):20-2. doi: 10.1111/j.1468-2982.1999.1901020.x. Cephalalgia. 1999. PMID: 10099855 Clinical Trial.

10

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

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