Terwindt GM - Search Results

1

Acute disseminating encephalomyelitis following legionnaires disease.

de Lau LM, Siepman DA, Remmers MJ, Terwindt GM, Hintzen RQ. de Lau LM, et al. Among authors: terwindt gm. Arch Neurol. 2010 May;67(5):623-6. doi: 10.1001/archneurol.2010.75. Arch Neurol. 2010. PMID: 20457963

2

Rizatriptan vs sumatriptan in the acute treatment of migraine. A placebo-controlled, dose-ranging study. Dutch/US Rizatriptan Study Group.

Visser WH, Terwindt GM, Reines SA, Jiang K, Lines CR, Ferrari MD. Visser WH, et al. Among authors: terwindt gm. Arch Neurol. 1996 Nov;53(11):1132-7. doi: 10.1001/archneur.1996.00550110072014. Arch Neurol. 1996. PMID: 8912486 Clinical Trial.

3

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. Brain. 1998 Feb;121 ( Pt 2):303-16. doi: 10.1093/brain/121.2.303. Brain. 1998. PMID: 9549508

4

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

5

The impact of migraine on quality of life in the general population: the GEM study.

Terwindt GM, Ferrari MD, Tijhuis M, Groenen SM, Picavet HS, Launer LJ. Terwindt GM, et al. Neurology. 2000 Sep 12;55(5):624-9. doi: 10.1212/wnl.55.5.624. Neurology. 2000. PMID: 10980723 Clinical Trial.

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

7

Mutation analysis of the CACNA1A calcium channel subunit gene in 27 patients with sporadic hemiplegic migraine.

Terwindt G, Kors E, Haan J, Vermeulen F, Van den Maagdenberg A, Frants R, Ferrari M. Terwindt G, et al. Arch Neurol. 2002 Jun;59(6):1016-8. doi: 10.1001/archneur.59.6.1016. Arch Neurol. 2002. PMID: 12056940 Review.

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: terwindt gm. Arch Neurol. 2003 May;60(5):684-8. doi: 10.1001/archneur.60.5.684. Arch Neurol. 2003. PMID: 12756131

9

Single-fiber EMG in familial hemiplegic migraine.

Terwindt GM, Kors EE, Vein AA, Ferrari MD, van Dijk JG. Terwindt GM, et al. Neurology. 2004 Nov 23;63(10):1942-3. doi: 10.1212/01.wnl.0000144342.35011.54. Neurology. 2004. PMID: 15557518

10

Episodic ataxia associated with EAAT1 mutation C186S affecting glutamate reuptake.

de Vries B, Mamsa H, Stam AH, Wan J, Bakker SL, Vanmolkot KR, Haan J, Terwindt GM, Boon EM, Howard BD, Frants RR, Baloh RW, Ferrari MD, Jen JC, van den Maagdenberg AM. de Vries B, et al. Among authors: terwindt gm. Arch Neurol. 2009 Jan;66(1):97-101. doi: 10.1001/archneurol.2008.535. Arch Neurol. 2009. PMID: 19139306

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