Specialist sinds 2015 en werkzaam bij Amsterdam UMC sinds 2019

Aandachtsgebieden

• Epilepsie
• Neuro-oncologie

• Klinische neurofysiologie

  • Algemene KNF
  • Intra-operatieve neuromonitoring
  • Epilepsiechirurgie

Opleiding

• Neurologie, Leids Universitair Medisch Centrum (2015)
• Klinische neurofysiologie, St. Antonius Ziekenhuis, Nieuwegein
• Internship The National Hospital for Neurology and Neurosurgery/Institute of Neurology, Queen Square, London, UK
• Artsexamen (cum laude), Universiteit Leiden
• Geneeskunde, Universiteit Leiden
• Biomedische Wetenschappen, Universiteit Leiden

Wetenschap - onderwijs

Gepromoveerd op onderwerp

• Genetics of migraine and related syndromes (Leiden, 2014)

Relevante beurzen/subsidies/prijzen

• ZonMw Agiko-stipendium: TREX1 in migraine and other neurovascular disorders.
• Prof. dr. P.R. Saxena Prijs van de Nederlandse Hoofdpijn Vereniging.

Wetenschappelijke publicatues

• Non-invasive measurements of ictal and interital epileptiform activity using optically pumped magnetometers.

  Hillebrand A, Holmes N, Sijsma N, O’Neil GC, Tierney TM, Liberton N, Stam AH, van Klink N, Stam CJ, Bowtell R, Brookes MJ, Barnes GR. Sci Rep. 2023 Mar 21;13(1):4623. doi: 10.1038/s41598-023-31111-y

• Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations. Stam AH, Kothari PH, Shaikh A, Gschwendter A, Jen JC, Hodgkinson S, Hardy TA, Hayes M, Kempster PA, Kotschet KE, Bajema IM, van Duinen SG, Maat-Schieman MLC, de Jong PTVM, de Smet MD, de Wolff-Rouendaal D, Dijkman G, Pelzer N, Kolar GR, Schmidt RE, Lacey J, Joseph D, Fintak DR, Grand MG, Brunt EM, Liapis H, Hajj-Ali RA, Kruit MC, van Buchem MA, Dichgans M, Frants RR, van den Maagdenberg AMJM, Haan J, Baloh RW, Atkinson JP, Terwindt GM, Ferrari MD. Brain. 2016 Nov 1;139(11):2909-2922. doi: 10.1093/brain/aww217.
• Early seizures and cerebral oedema after trivial head trauma associated with the CACNA1A S218L mutation. Stam AH, Luijckx GJ, Poll-Thé BT, Ginjaar IB, Frants RR, Haan J, Ferrari MD, Terwindt GM, van den Maagdenberg AM. J Neurol Neurosurg Psychiatry. 2009;80:1125-9. J Neurol Neurosurg Psychiatry. 2009 Oct;80(10):1125-9. doi: 10.1136/jnnp.2009.177279. Epub 2009 Jun 10. Review.
• Familial hemiplegic migraine is associated with febrile seizures in an FHM2 family with a novel de novo ATP1A2 mutation. 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. Epilepsia. 2009 Nov;50(11):2503-4. doi: 10.1111/j.1528-1167.2009.02186.x.
• Shared genetic factors in migraine and depression: evidence from a genetic isolate. Stam AH, de Vries B, Janssens AC, Vanmolkot KR, Aulchenko YS, Henneman P, Oostra BA, Frants RR, van den Maagdenberg AM, Ferrari MD, van Duijn CM, Terwindt GM. Neurology. 2010 Jan 26;74(4):288-94. doi: 10.1212/WNL.0b013e3181cbcd19. Epub 2010 Jan 13.
• RVCL-S and CADASIL display distinct impaired vascular function. de Boer I, Stam AH, Buntinx L, Zielman R, van der Steen I, van den Maagdenberg AMJM, de Koning EJP, Ferrari MD, de Hoon JN, Terwindt GM. Neurology. 2018 Sep 4;91(10):e956-e963. doi: 10.1212/WNL.0000000000006119. Epub 2018 Aug 3.
• Clinical spectrum of hemiplegic migraine and chances of finding a pathogenic mutation. Pelzer N, Haan J, Stam AH, Vijfhuizen LS, Koelewijn SC, Smagge A, de Vries B, Ferrari MD, van den Maagdenberg AMJM, Terwindt GM. Neurology. 2018 Feb 13;90(7):e575-e582. doi: 10.1212/WNL.0000000000004966. Epub 2018 Jan 17.
• Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine. Gormley P, Anttila V, Winsvold BS, Palta P, Esko T, Pers TH, Farh KH, Cuenca-Leon E, Muona M, Furlotte NA, Kurth T, Ingason A, McMahon G, Ligthart L, Terwindt GM, Kallela M, Freilinger TM, Ran C, Gordon SG, Stam AH, Steinberg S, Borck G, Koiranen M, Quaye L, Adams HH, Lehtimäki T, Sarin AP, Wedenoja J, Hinds DA, Buring JE, Schürks M, Ridker PM, Hrafnsdottir MG, Stefansson H, Ring SM, Hottenga JJ, Penninx BW, Färkkilä M, Artto V, Kaunisto M, Vepsäläinen S, Malik R, Heath AC, Madden PA, Martin NG, Montgomery GW, Kurki MI, Kals M, Mägi R, Pärn K, Hämäläinen E, Huang H, Byrnes AE, Franke L, Huang J, Stergiakouli E, Lee PH, Sandor C, Webber C, Cader Z, Muller-Myhsok B, Schreiber S, Meitinger T, Eriksson JG, Salomaa V, Heikkilä K, Loehrer E, Uitterlinden AG, Hofman A, van Duijn CM, Cherkas L, Pedersen LM, Stubhaug A, Nielsen CS, Männikkö M, Mihailov E, Milani L, Göbel H, Esserlind AL, Christensen AF, Hansen TF, Werge T; International Headache Genetics Consortium, Kaprio J, Aromaa AJ, Raitakari O, Ikram MA, Spector T, Järvelin MR, Metspalu A, Kubisch C, Strachan DP, Ferrari MD, Belin AC, Dichgans M, Wessman M, van den Maagdenberg AM, Zwart JA, Boomsma DI, Smith GD, Stefansson K, Eriksson N, Daly MJ, Neale BM, Olesen J, Chasman DI, Nyholt DR, Palotie A. Nat Genet. 2016 Aug;48(8):856-66. doi: 10.1038/ng.3598. Epub 2016 Jun 20.