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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: terwindt gm. 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
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: terwindt gm. 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.
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. Among authors: terwindt gm. Hum Mutat. 2007 May;28(5):522. doi: 10.1002/humu.9486. Hum Mutat. 2007. PMID: 17397047
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. Among authors: terwindt gm. 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
Migraine: gene mutations and functional consequences.
van den Maagdenberg AM, Haan J, Terwindt GM, Ferrari MD. van den Maagdenberg AM, et al. Among authors: terwindt gm. Curr Opin Neurol. 2007 Jun;20(3):299-305. doi: 10.1097/WCO.0b013e3281338d1f. Curr Opin Neurol. 2007. PMID: 17495624 Review.
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
Genetics of headaches.
Van Den Maagdenberg AM, Terwindt GM, Haan J, Frants RR, Ferrari MD. Van Den Maagdenberg AM, et al. Among authors: terwindt gm. Handb Clin Neurol. 2010;97:85-97. doi: 10.1016/S0072-9752(10)97006-1. Handb Clin Neurol. 2010. PMID: 20816412
344 results