Wetenschappelijke publicaties

Meest recente publicaties

2017

2016

2015

2014

2013

  • Louter MA, Bosker JE, Van Oosterhout WPJ, Van Zwet EW, Zitman FG, Ferrari MD, Terwindt GM. Cutaneous allodynia as a predictor of migraine chronification. Brain, September 2013
  • Eising E, de Vries B, Ferrari MD, Terwindt GM, van den Maagdenberg AM.Pearls and pitfalls in genetic studies of migraine. Cephalalgia. June 2013.
  • Wilbrink LA, Weller CM, Cheung C, Stijnen T, Haan J, Ferrari MD, Terwindt GM.Stepwise web-based questionnaires for diagnosing cluster headache: LUCA and QATCH. Cephalalgia. April 2013.
  • Kruit MC, Thijs RD, Ferrari MD, Launer LJ, van Buchem MA, van Dijk JG.Syncope and orthostatic intolerance increase risk of brain lesions in migraineurs and controls. Neurology. May 2013
  • Van Oosterhout WP, van der Plas AA, van Zwet EW, Zielman R, Ferrari MD, Terwindt GM. Postdural puncture headache in migraineurs and nonheadache subjects: a prospective study. Neurology. March 2013
  • Eising E, A Datson N, van den Maagdenberg AM, Ferrari MD. Epigenetic mechanisms in migraine: a promising avenue? BMC Med. February 2013
  • Pelzer N, Stam AH, Haan J, Ferrari MD, Terwindt GM. Familial and sporadic hemiplegic migraine: diagnosis and treatment. Curr Treat Options Neurol. February 2013.
  • L.A. Wilbrink, Carlo Cheung, Claudia M. Weller, Michel D. Ferrari en Joost Haan. Aurasymptomen bij clusterhoofdpijn: Resultaten van een deelonderzoek in de LUCA-studie Ned Tijdschr Geneeskd. 2013;157:A5306

2012

  • Palm-Meinders IH, Koppen H, Terwindt GM, et al. Structural brain changes in migraine. JAMA: the journal of the American Medical Association. 2012;308(18):1889–97.
  • Freilinger T, Anttila V, de Vries B, et al. Genome-wide association analysis identifies susceptibility loci for migraine without aura. Nature genetics. 2012;44(7):777–82.
  • Stam AH, Weller CM, Janssens AC, Aulchenko YS, Oostra BA, Frants RR, van den Maagdenberg AM, Ferrari MD, van Duijn CM, Gisela MT. Migraine is not associated with enhanced atherosclerosis. Cephalalgia. 2012 Nov 12.
  • Pelzer N, Stam AH, Haan J, Ferrari MD, Terwindt GM. Familial and Sporadic Hemiplegic Migraine: Diagnosis and Treatment. Curr Treat Options Neurol 2012 Dec 1.
  • de Vries B, Callenbach PM, Kamphorst JT, Weller CM, Koelewijn SC, ten Houten R, de Coo IF, Brouwer OF, van den Maagdenberg AM. PRRT2 mutation causes benign familial infantile convulsions. Neurology. 2012 Nov 20;79(21):2154-5.

2011

  • van Oosterhout WP, Weller CM, Stam AH, Bakels F, Stijnen T, Ferrari MD, Terwindt GM. Validation of the web-based LUMINA questionnaire for recruiting large cohorts of migraineurs. Cephalalgia. 2011 Oct;31(13):1359-67.

2010

  • Anttila V, Stefansson H, Kallela M, Todt U, Terwindt GM, Calafato MS, Nyholt DR, Dimas AS, Freilinger T, Müller-Myhsok B, Artto V, Inouye M, Alakurtti K, Kaunisto MA, Hämäläinen E, de Vries B, Stam AH, Weller CM, Heinze A, Heinze-Kuhn K, Goebel I, Borck G, Göbel H, Steinberg S, Wolf C, Björnsson A, Gudmundsson G, Kirchmann M, Hauge A, Werge T, Schoenen J, Eriksson JG, Hagen K, Stovner L, Wichmann HE, Meitinger T, Alexander M, Moebus S, Schreiber S, Aulchenko YS, Breteler MM, Uitterlinden AG, Hofman A, van Duijn CM, Tikka-Kleemola P, Vepsäläinen S, Lucae S, Tozzi F, Muglia P, Barrett J, Kaprio J, Färkkilä M, Peltonen L, Stefansson K, Zwart JA, Ferrari MD, Olesen J, Daly M, Wessman M, van  den Maagdenberg AM, Dichgans M, Kubisch C, Dermitzakis ET, Frants RR, Palotie A;  International Headache Genetics Consortium. Genome-wide association study of migraine implicates a common susceptibility variant on 8q22.1. Nat Genet. 2010 Oct;42(10):869-73. doi: 10.1038/ng.652.
  • Mark A. Louter, Gerthe Veen, Michel D. Ferrari, Frans G. Zitman en Gisela M. Terwindt Stand van zaken: Migraine en depressie verdienen gezamenlijke zorg Ned Tijdschr Geneeskd. 2010;154:A1044

2009

  • Koek MM, Bakel F, Engel W, van den Maagdenberg A, Ferrari MD, Coulier L, Hankemeier T. Metabolic Profiling of Ultrasmall Sample Volumes with GC/MS: From Microliter to Nanoliter Samples. Anal Chem. 2009  Nov 30.
  • de Vries B, Stam AH, Kirkpatrick M,Vanmolkot KR, Koenderink JB, van den Heuvel JJ, Stunnenberg B, Goudie D, Shetty J, Jain V, van Vark J, Terwindt GM, Frants RR, Haan J, van den Maagdenberg AM, Ferrari MD. Familial hemiplegic migraine is associated with febrile seizures in an FHM2 family with a novel de novo ATP1A2 mutation. Epilepsia. 2009 Nov;50(11):2503-4. 
  • de Vries B, Steup-Beekman G, Haan J, Bollen E, Luyendijk J, Frants R, Terwindt G, van Buchem M, Huizinga T, van den Maagdenberg A, Ferrari M.TREX1 Gene Variant in Neuropsychiatric Systemic Lupus Erythematosus. Ann Rheum Dis. 2009 Oct 28. [Epub ahead of print] 
  • Eikermann-Haerter K, Baum MJ, Ferrari MD, van den Maagdenberg AM, Moskowitz MA, Ayata C. Androgenic suppression of spreading depression in familial hemiplegic migraine type 1 mutant mice. Ann Neurol. 2009 Oct;66(4):564-8. 
  • Schoonman GG, van Oosterhout WR, Ferrari MD, van der Grond J.Anatomical Variations in the Circle of Willis and Migraine Susceptibility: Is There an Association? Headache. 2009 Oct 21.
  • Koppen H, Terwindt GM, Haan J, de Bruijn SF, Bax JJ, Ferrari MD. No indication for patent foramen ovale closure in migraine. Neth Heart J. 2009 Sep;17(9):320-1.
  • Stam AH, Haan J, van den Maagdenberg AM, Ferrari MD, Terwindt GM.Migraine and genetic and acquired vasculopathies. Cephalalgia 2009;29:1006-17.
  • Stam AH, Luijckx GJ, Poll-The BT, Ginjaar I, Frants RR, Haan J, Ferrari MD, Terwindt GM, van den Maagdenberg AM. Early seizures and cerebral edema after trivial head trauma associated with the CACNA1A S218L mutation. J Neurol Neurosurg Psychiatry 2009.
  • Kruit M, van Buchem M, Launer L, Terwindt G, Ferrari M. Migraine is associated with an increased risk of deep white matter lesions, subclinical posterior circulation infarcts and brain iron accumulation: the population-based MRI CAMERA study. Cephalalgia 2009.
  • Vein AA, Koppen H, Haan J, Terwindt GM, Ferrari MD. Space headache: a new secondary headache. Cephalalgia 2009.
  • De Vries B, Frants RR, Ferrari MD, van den Maagdenberg AM. Molecular genetics of migraine. Hum Genet. 2009.
  • Wilbrink LA, Ferrari MD, Kruit MC, Haan J: Neuroimaging in trigeminal autonomic cephalgias: when, how, and of what? Curr.Opin.Neurol. 2009, 22:247-253.
  • Castro MJ, Stam AH, Lemos C, de Vries B, Vanmolkot KR, Barros J, Terwindt GM, Frants RR, Sequeiros J, Ferrari MD, Pereira-Monteiro JM, van den Maagdenberg AM. First mutation in the voltage-gated Nav1.1 subunit gene SCN1A with co-occurring familial hemiplegic migraine and epilepsy. Cephalalgia. 2009 29(3):308-313.