van den Maagdenberg AMJM - Search Results

1

Ferrari MD, Goadsby PJ, Burstein R, Kurth T, Ayata C, Charles A, Ashina M, van den Maagdenberg AMJM, Dodick DW. Ferrari MD, et al. Among authors: van den maagdenberg amjm. Nat Rev Dis Primers. 2022 Jan 13;8(1):2. doi: 10.1038/s41572-021-00328-4. Nat Rev Dis Primers. 2022. PMID: 35027572 Review.

2

Abnormal transmitter release at neuromuscular junctions of mice carrying the tottering alpha(1A) Ca(2+) channel mutation.

Plomp JJ, Vergouwe MN, Van den Maagdenberg AM, Ferrari MD, Frants RR, Molenaar PC. Plomp JJ, et al. Brain. 2000 Mar;123 Pt 3:463-71. doi: 10.1093/brain/123.3.463. Brain. 2000. PMID: 10686170

3

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

4

The impact of pharmacogenetics for migraine.

Ophoff RA, van den Maagdenberg AM, Roon KI, Ferrari MD, Frants RR. Ophoff RA, et al. Eur J Pharmacol. 2001 Feb 9;413(1):1-10. doi: 10.1016/s0014-2999(00)00949-3. Eur J Pharmacol. 2001. PMID: 11173058 Review.

5

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. Ann Neurol. 2001 Jun;49(6):753-60. doi: 10.1002/ana.1031. Ann Neurol. 2001. PMID: 11409427

6

Hereditary vascular retinopathy, cerebroretinal vasculopathy, and hereditary endotheliopathy with retinopathy, nephropathy, and stroke map to a single locus on chromosome 3p21.1-p21.3.

Ophoff RA, DeYoung J, Service SK, Joosse M, Caffo NA, Sandkuijl LA, Terwindt GM, Haan J, van den Maagdenberg AM, Jen J, Baloh RW, Barilla-LaBarca ML, Saccone NL, Atkinson JP, Ferrari MD, Freimer NB, Frants RR. Ophoff RA, et al. Am J Hum Genet. 2001 Aug;69(2):447-53. doi: 10.1086/321975. Epub 2001 Jun 28. Am J Hum Genet. 2001. PMID: 11438888 Free PMC article.

7

Mutant P/Q-type calcium channel electrophysiology and migraine.

Plomp JJ, van den Maagdenberg AM, Molenaar PC, Frants RR, Ferrari MD. Plomp JJ, et al. Curr Opin Investig Drugs. 2001 Sep;2(9):1250-60. Curr Opin Investig Drugs. 2001. PMID: 11717812 Review.

8

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. Cephalalgia. 2001 Dec;21(10):959-62. doi: 10.1046/j.1468-2982.2001.00283.x. Cephalalgia. 2001. PMID: 11843867

9

Calcium channel mutations and migraine.

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

10

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

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