van den Maagdenberg AMJM - Search Results

1

Rapid Prototyping of Organ-on-a-Chip Devices Using Maskless Photolithography.

Kasi DG, de Graaf MNS, Motreuil-Ragot PA, Frimat JMS, Ferrari MD, Sarro PM, Mastrangeli M, van den Maagdenberg AMJM, Mummery CL, Orlova VV. Kasi DG, et al. Among authors: van den maagdenberg amjm. Micromachines (Basel). 2021 Dec 29;13(1):49. doi: 10.3390/mi13010049. Micromachines (Basel). 2021. PMID: 35056214 Free PMC article.

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

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.

4

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

5

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.

6

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

7

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.

8

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

9

Transmitter release deficits at the neuromuscular synapse of mice with mutations in the Cav2.1 (alpha1A) subunit of the P/Q-type Ca2+ channel.

Plomp JJ, van den Maagdenberg AM, Ferrari MD, Frants RR, Molenaar PC. Plomp JJ, et al. Ann N Y Acad Sci. 2003 Sep;998:29-32. doi: 10.1196/annals.1254.005. Ann N Y Acad Sci. 2003. PMID: 14592860 No abstract available.

10

New discoveries about the second gene for familial hemiplegic migraine, ATP1A2.

Vanmolkot KR, van den Maagdenberg AM, Haan J, Ferrari MD. Vanmolkot KR, et al. Lancet Neurol. 2003 Dec;2(12):721. doi: 10.1016/s1474-4422(03)00591-x. Lancet Neurol. 2003. PMID: 14636773 No abstract available.

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