Frants RR - Search Results

1

Shared genetic factors in migraine and depression: evidence from a genetic isolate.

Stam AH, de Vries B, Janssens AC, Vanmolkot KR, Aulchenko YS, Henneman P, Oostra BA, Frants RR, van den Maagdenberg AM, Ferrari MD, van Duijn CM, Terwindt GM. Stam AH, et al. Among authors: frants rr. Neurology. 2010 Jan 26;74(4):288-94. doi: 10.1212/WNL.0b013e3181cbcd19. Epub 2010 Jan 13. Neurology. 2010. PMID: 20071666 Free PMC article.

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

The quest for migraine genes.

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

4

Clinical and genetic analysis of a large Dutch family with autosomal dominant vascular retinopathy, migraine and Raynaud's phenomenon.

Terwindt GM, Haan J, Ophoff RA, Groenen SM, Storimans CW, Lanser JB, Roos RA, Bleeker-Wagemakers EM, Frants RR, Ferrari MD. Terwindt GM, et al. Among authors: frants rr. Brain. 1998 Feb;121 ( Pt 2):303-16. doi: 10.1093/brain/121.2.303. Brain. 1998. PMID: 9549508

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

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

7

Delayed cerebral edema and fatal coma after minor head trauma: role of the CACNA1A calcium channel subunit gene and relationship with familial hemiplegic migraine.

Kors EE, Terwindt GM, Vermeulen FL, Fitzsimons RB, Jardine PE, Heywood P, Love S, van den Maagdenberg AM, Haan J, Frants RR, Ferrari MD. Kors EE, et al. Among authors: frants rr. Ann Neurol. 2001 Jun;49(6):753-60. doi: 10.1002/ana.1031. Ann Neurol. 2001. PMID: 11409427

8

Expanding the phenotypic spectrum of the CACNA1A gene T666M mutation: a description of 5 families with familial hemiplegic migraine.

Kors EE, Haan J, Giffin NJ, Pazdera L, Schnittger C, Lennox GG, Terwindt GM, Vermeulen FL, Van den Maagdenberg AM, Frants RR, Ferrari MD. Kors EE, et al. Among authors: frants rr. Arch Neurol. 2003 May;60(5):684-8. doi: 10.1001/archneur.60.5.684. Arch Neurol. 2003. PMID: 12756131

9

Childhood epilepsy, familial hemiplegic migraine, cerebellar ataxia, and a new CACNA1A mutation.

Kors EE, Melberg A, Vanmolkot KR, Kumlien E, Haan J, Raininko R, Flink R, Ginjaar HB, Frants RR, Ferrari MD, van den Maagdenberg AM. Kors EE, et al. Among authors: frants rr. Neurology. 2004 Sep 28;63(6):1136-7. doi: 10.1212/01.wnl.0000138571.48593.fc. Neurology. 2004. PMID: 15452324 No abstract available.

10

Severe episodic neurological deficits and permanent mental retardation in a child with a novel FHM2 ATP1A2 mutation.

Vanmolkot KR, Stroink H, Koenderink JB, Kors EE, van den Heuvel JJ, van den Boogerd EH, Stam AH, Haan J, De Vries BB, Terwindt GM, Frants RR, Ferrari MD, van den Maagdenberg AM. Vanmolkot KR, et al. Among authors: frants rr. Ann Neurol. 2006 Feb;59(2):310-4. doi: 10.1002/ana.20760. Ann Neurol. 2006. PMID: 16437583

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