Vanmolkot KR - Search Results

1

CACNA1A mutation linking hemiplegic migraine and alternating hemiplegia of childhood.

de Vries B, Stam AH, Beker F, van den Maagdenberg AM, Vanmolkot KR, Laan L, Ginjaar IB, Frants RR, Lauffer H, Haan J, Haas JP, Terwindt GM, Ferrari MD. de Vries B, et al. Among authors: vanmolkot kr. Cephalalgia. 2008 Aug;28(8):887-91. doi: 10.1111/j.1468-2982.2008.01596.x. Epub 2008 May 21. Cephalalgia. 2008. PMID: 18498393

2

Novel mutations in the Na+, K+-ATPase pump gene ATP1A2 associated with familial hemiplegic migraine and benign familial infantile convulsions.

Vanmolkot KR, Kors EE, Hottenga JJ, Terwindt GM, Haan J, Hoefnagels WA, Black DF, Sandkuijl LA, Frants RR, Ferrari MD, van den Maagdenberg AM. Vanmolkot KR, et al. Ann Neurol. 2003 Sep;54(3):360-6. doi: 10.1002/ana.10674. Ann Neurol. 2003. PMID: 12953268

3

Toward a molecular genetic classification of familial hemiplegic migraine.

Haan J, Kors EE, van den Maagdenberg AM, Vanmolkot KR, Terwindt GM, Frants RR, Ferrari MD. Haan J, et al. Among authors: vanmolkot kr. Curr Pain Headache Rep. 2004 Jun;8(3):238-43. doi: 10.1007/s11916-004-0058-0. Curr Pain Headache Rep. 2004. PMID: 15115644 Review.

4

Migraine genetics: an update.

Haan J, Kors EE, Vanmolkot KR, van den Maagdenberg AM, Frants RR, Ferrari MD. Haan J, et al. Among authors: vanmolkot kr. Curr Pain Headache Rep. 2005 Jun;9(3):213-20. doi: 10.1007/s11916-005-0065-9. Curr Pain Headache Rep. 2005. PMID: 15907261 Review.

5

The novel p.L1649Q mutation in the SCN1A epilepsy gene is associated with familial hemiplegic migraine: genetic and functional studies. Mutation in brief #957. Online.

Vanmolkot KR, Babini E, de Vries B, Stam AH, Freilinger T, Terwindt GM, Norris L, Haan J, Frants RR, Ramadan NM, Ferrari MD, Pusch M, van den Maagdenberg AM, Dichgans M. Vanmolkot KR, et al. Hum Mutat. 2007 May;28(5):522. doi: 10.1002/humu.9486. Hum Mutat. 2007. PMID: 17397047

6

First case of compound heterozygosity in Na,K-ATPase gene ATP1A2 in familial hemiplegic migraine.

Vanmolkot KR, Stam AH, Raman A, Koenderink JB, de Vries B, van den Boogerd EH, van Vark J, van den Heuvel JJ, Bajaj N, Terwindt GM, Haan J, Frants RR, Ferrari MD, van den Maagdenberg AM. Vanmolkot KR, et al. Eur J Hum Genet. 2007 Aug;15(8):884-8. doi: 10.1038/sj.ejhg.5201841. Epub 2007 May 2. Eur J Hum Genet. 2007. PMID: 17473835

7

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: vanmolkot kr. Arch Neurol. 2009 Jan;66(1):97-101. doi: 10.1001/archneurol.2008.535. Arch Neurol. 2009. PMID: 19139306

8

Episodic ataxia type 2. Three novel truncating mutations and one novel missense mutation in the CACNA1A gene.

van den Maagdenberg AM, Kors EE, Brunt ER, van Paesschen W, Pascual J, Ravine D, Keeling S, Vanmolkot KR, Vermeulen FL, Terwindt GM, Haan J, Frants RR, Ferrari MD. van den Maagdenberg AM, et al. Among authors: vanmolkot kr. J Neurol. 2002 Nov;249(11):1515-9. doi: 10.1007/s00415-002-0860-8. J Neurol. 2002. PMID: 12420090

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: vanmolkot kr. Neurology. 2004 Sep 28;63(6):1136-7. doi: 10.1212/01.wnl.0000138571.48593.fc. Neurology. 2004. PMID: 15452324 No abstract available.

10

[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: vanmolkot kr. Ned Tijdschr Geneeskd. 2004 Sep 25;148(39):1919-20. Ned Tijdschr Geneeskd. 2004. PMID: 15495990 Review. Dutch.

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