van den Maagdenberg AMJM - Search Results

1

Metabolomics Profile in Depression: A Pooled Analysis of 230 Metabolic Markers in 5283 Cases With Depression and 10,145 Controls.

Bot M, Milaneschi Y, Al-Shehri T, Amin N, Garmaeva S, Onderwater GLJ, Pool R, Thesing CS, Vijfhuizen LS, Vogelzangs N, Arts ICW, Demirkan A, van Duijn C, van Greevenbroek M, van der Kallen CJH, Köhler S, Ligthart L, van den Maagdenberg AMJM, Mook-Kanamori DO, de Mutsert R, Tiemeier H, Schram MT, Stehouwer CDA, Terwindt GM, Willems van Dijk K, Fu J, Zhernakova A, Beekman M, Slagboom PE, Boomsma DI, Penninx BWJH; BBMRI-NL Metabolomics Consortium. Bot M, et al. Among authors: van greevenbroek m, van den maagdenberg amjm, van der kallen cjh, van duijn c. Biol Psychiatry. 2020 Mar 1;87(5):409-418. doi: 10.1016/j.biopsych.2019.08.016. Epub 2019 Aug 29. Biol Psychiatry. 2020. PMID: 31635762

2

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

3

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

4

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. 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.

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

Migraine: gene mutations and functional consequences.

van den Maagdenberg AM, Haan J, Terwindt GM, Ferrari MD. van den Maagdenberg AM, et al. Curr Opin Neurol. 2007 Jun;20(3):299-305. doi: 10.1097/WCO.0b013e3281338d1f. Curr Opin Neurol. 2007. PMID: 17495624 Review.

8

Genetics of migraine: an update with special attention to genetic comorbidity.

Stam AH, van den Maagdenberg AM, Haan J, Terwindt GM, Ferrari MD. Stam AH, et al. Curr Opin Neurol. 2008 Jun;21(3):288-93. doi: 10.1097/WCO.0b013e3282fd171a. Curr Opin Neurol. 2008. PMID: 18451712 Review.

9

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

10

Genetics of headaches.

Van Den Maagdenberg AM, Terwindt GM, Haan J, Frants RR, Ferrari MD. Van Den Maagdenberg AM, et al. Handb Clin Neurol. 2010;97:85-97. doi: 10.1016/S0072-9752(10)97006-1. Handb Clin Neurol. 2010. PMID: 20816412

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