Found: 17

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  • Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations.

    Published in:
    2016
    By:
    • Stam, Anine H.;
    • Kothari, Parul H.;
    • Shaikh, Aisha;
    • Gschwendter, Andreas;
    • Jen, Joanna C.;
    • Hodgkinson, Suzanne;
    • Hardy, Todd A.;
    • Hayes, Michael;
    • Kempster, Peter A.;
    • Kotschet, Katya E.;
    • Bajema, Ingeborg M.;
    • van Duinen, Sjoerd G.;
    • Maat-Schieman, Marion L. C.;
    • de Jong, Paulus T. V. M.;
    • de Smet, Marc D.;
    • de Wolff-Rouendaal, Didi;
    • Dijkman, Greet;
    • Pelzer, Nadine;
    • Kolar, Grant R.;
    • Schmidt, Robert E.
    Publication type:
    journal article

  • Familial hemiplegic migraine is associated with febrile seizures in an FHM2 family with a novel de novo ATP1A2 mutation.

    Published in:
    2009
    By:
    • de Vries, Boukje;
    • Stam, Anine H.;
    • Kirkpatrick, Martin;
    • Vanmolkot, Kaate R.J.;
    • Koenderink, Jan B.;
    • van den Heuvel, Jeroen J.M.W.;
    • Stunnenberg, Bas;
    • Goudie, David;
    • Shetty, Jay;
    • Jain, Vivek;
    • van Vark, Judith;
    • Terwindt, Gisela M.;
    • Frants, Rune R.;
    • Haan, Joost;
    • van den Maagdenberg, Arn M.J.M.;
    • Ferrari, Michel D.
    Publication type:
    Letter

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

    Published in:
    Scientific Reports, 2023, v. 13, n. 1, p. 1, doi. 10.1038/s41598-023-31111-y
    By:
    • Hillebrand, Arjan;
    • Holmes, Niall;
    • Sijsma, Ndedi;
    • O'Neill, George C.;
    • Tierney, Tim M.;
    • Liberton, Niels;
    • Stam, Anine H.;
    • van Klink, Nicole;
    • Stam, Cornelis J.;
    • Bowtell, Richard;
    • Brookes, Matthew J.;
    • Barnes, Gareth R.
    Publication type:
    Article

  • Gene-based pleiotropy across migraine with aura and migraine without aura patient groups.

    Published in:
    2016
    By:
    • Zhao, Huiying;
    • Eising, Else;
    • de Vries, Boukje;
    • Vijfhuizen, Lisanne S.;
    • Anttila, Verneri;
    • Winsvold, Bendik S.;
    • Kurth, Tobias;
    • Stefansson, Hreinn;
    • Kallela, Mikko;
    • Malik, Rainer;
    • Stam, Anine H.;
    • Ikram, M. Arfan;
    • Ligthart, Lannie;
    • Freilinger, Tobias;
    • Alexander, Michael;
    • Müller-Myhsok, Bertram;
    • Schreiber, Stefan;
    • Meitinger, Thomas;
    • Aromas, Arpo;
    • Eriksson, Johan G.
    Publication type:
    journal article

  • Concordance of genetic risk across migraine subgroups: Impact on current and future genetic association studies.

    Published in:
    Cephalalgia, 2015, v. 35, n. 6, p. 489, doi. 10.1177/0333102414547784
    By:
    • Nyholt, Dale R;
    • Anttila, Verneri;
    • Winsvold, Bendik S;
    • Kurth, Tobias;
    • Stefansson, Hreinn;
    • Kallela, Mikko;
    • Malik, Rainer;
    • Vries, Boukje de;
    • Terwindt, Gisela M;
    • Ikram, M Arfan;
    • Stam, Anine H;
    • Ligthart, Lannie;
    • Freilinger, Tobias;
    • Alexander, Michael;
    • Muller-Myhsok, Bertram;
    • Schreiber, Stefan;
    • Meitinger, Thomas;
    • Aromaa, Arpo;
    • Eriksson, Johan G;
    • Kaprio, Jaakko
    Publication type:
    Article

  • Familial hemiplegic migraine treated by sodium valproate and lamotrigine.

    Published in:
    2014
    By:
    • Pelzer, Nadine;
    • Stam, Anine H;
    • Carpay, Johannes A;
    • Vries, Boukje de;
    • van den Maagdenberg, Arn MJM;
    • Ferrari, Michel D;
    • Haan, Joost;
    • Terwindt, Gisela M
    Publication type:
    journal article

  • Two novel SCN1A mutations identified in families with familial hemiplegic migraine.

    Published in:
    Cephalalgia, 2014, v. 34, n. 13, p. 1062, doi. 10.1177/0333102414529195
    By:
    • Weller, Claudia M;
    • Pelzer, Nadine;
    • de Vries, Boukje;
    • López, Mercè Artigas;
    • De Fàbregues, Oriol;
    • Pascual, Julio;
    • Arroyo, María A Ramos;
    • Koelewijn, Stephany C;
    • Stam, Anine H;
    • Haan, Joost;
    • Ferrari, Michel D;
    • Terwindt, Gisela M;
    • van den Maagdenberg, Arn MJM
    Publication type:
    Article

  • Migraine is not associated with enhanced atherosclerosis.

    Published in:
    Cephalalgia, 2013, v. 33, n. 4, p. 228, doi. 10.1177/0333102412466966
    By:
    • Stam, Anine H;
    • Weller, Claudia M;
    • Janssens, A Cecile JW;
    • Aulchenko, Yurii S;
    • Oostra, Ben A;
    • Frants, Rune R;
    • van den Maagdenberg, Arn MJM;
    • Ferrari, Michel D;
    • van Duijn, Cornelia M;
    • Gisela, M Terwindt
    Publication type:
    Article

  • Head tremor related to CACNA1A mutations.

    Published in:
    Cephalalgia, 2011, v. 31, n. 12, p. 1315, doi. 10.1177/0333102411414442
    By:
    • Geerlings, Rianne PJ;
    • Koehler, Peter J;
    • Haane, Danielle YP;
    • Stam, Anine H;
    • de Vries, Boukje;
    • Boon, Elles MJ;
    • Haan, Joost
    Publication type:
    Article

  • Head tremor related to CACNA1A mutations.

    Published in:
    Cephalalgia, 2011, v. 31, n. 12, p. 1315, doi. 10.1177/0333102411414442
    By:
    • Geerlings, Rianne PJ;
    • Koehler, Peter J;
    • Haane, Danielle YP;
    • Stam, Anine H;
    • de Vries, Boukje;
    • Boon, Elles MJ;
    • Haan, Joost
    Publication type:
    Article

  • A long-term follow-up study of 18 patients with sporadic hemiplegic migraine.

    Published in:
    Cephalalgia, 2011, v. 31, n. 2, p. 199, doi. 10.1177/0333102410375629
    By:
    • Stam, Anine H;
    • Louter, Mark A;
    • Haan, Joost;
    • de Vries, Boukje;
    • van den Maagdenberg, Arn MJM;
    • Frants, Rune R;
    • Ferrari, Michel D;
    • Terwindt, Gisela M
    Publication type:
    Article

  • Recurrent ATP1A2 mutations in Portuguese families with familial hemiplegic migraine.

    Published in:
    Journal of Human Genetics, 2007, v. 52, n. 12, p. 990, doi. 10.1007/s10038-007-0205-7
    By:
    • Castro, Maria-José;
    • Stam, Anine H.;
    • Lemos, Carolina;
    • Barros, José;
    • Gouveia, Raquel G.;
    • Martins, Isabel Pavão;
    • Koenderink, Jan B.;
    • Vanmolkot, Kaate R. J.;
    • Mendes, Alexandre P.;
    • Frants, Rune R.;
    • Ferrari, Michel D.;
    • Sequeiros, Jorge;
    • Pereira-Monteiro, José M.;
    • van den Maagdenberg, Arn M. J. M.
    Publication type:
    Article

  • Genome-wide meta-analysis identifies new susceptibility loci for migraine.

    Published in:
    Nature Genetics, 2013, v. 45, n. 8, p. 912, doi. 10.1038/ng.2676
    By:
    • Anttila, Verneri;
    • Winsvold, Bendik S;
    • Gormley, Padhraig;
    • Kurth, Tobias;
    • Bettella, Francesco;
    • McMahon, George;
    • Kallela, Mikko;
    • Malik, Rainer;
    • de Vries, Boukje;
    • Terwindt, Gisela;
    • Medland, Sarah E;
    • Todt, Unda;
    • McArdle, Wendy L;
    • Quaye, Lydia;
    • Koiranen, Markku;
    • Ikram, M Arfan;
    • Lehtimäki, Terho;
    • Stam, Anine H;
    • Ligthart, Lannie;
    • Wedenoja, Juho
    Publication type:
    Article

  • Genome-wide association study of migraine implicates a common susceptibility variant on 8q22.1.

    Published in:
    Nature Genetics, 2010, v. 42, n. 10, p. 869, doi. 10.1038/ng.652
    By:
    • Anttila, Verneri;
    • Stefansson, Hreinn;
    • Kallela, Mikko;
    • Todt, Unda;
    • Terwindt, Gisela M.;
    • Calafato, M. Stella;
    • Nyholt, Dale R.;
    • Dimas, Antigone S.;
    • Freilinger, Tobias;
    • Müller-Myhsok, Bertram;
    • Artto, Ville;
    • Inouye, Michael;
    • Alakurtti, Kirsi;
    • Kaunisto, Mari A.;
    • Hämäläinen, Eija;
    • de Vries, Boukje;
    • Stam, Anine H.;
    • Weller, Claudia M.;
    • Heinze, Axel;
    • Heinze-Kuhn, Katja
    Publication type:
    Article

  • C-terminal truncations in human 3′-5′ DNA exonuclease TREX1 cause autosomal dominant retinal vasculopathy with cerebral leukodystrophy.

    Published in:
    Nature Genetics, 2007, v. 39, n. 9, p. 1068, doi. 10.1038/ng2082
    By:
    • Richards, Anna;
    • van den Maagdenberg, Arn M. J. M.;
    • Jen, Joanna C.;
    • Kavanagh, David;
    • Bertram, Paula;
    • Spitzer, Dirk;
    • Liszewski, M. Kathryn;
    • Barilla-LaBarca, Maria-Louise;
    • Terwindt, Gisela M.;
    • Kasai, Yumi;
    • McLellan, Mike;
    • Grand, Mark Gilbert;
    • Vanmolkot, Kaate R. J.;
    • de Vries, Boukje;
    • Jijun Wan;
    • Kane, Michael J.;
    • Mamsa, Hafsa;
    • Schäfer, Ruth;
    • Stam, Anine H.;
    • Haan, Joost
    Publication type:
    Article

  • First case of compound heterozygosity in Na,K-ATPase gene ATP1A2 in familial hemiplegic migraine.

    Published in:
    European Journal of Human Genetics, 2007, v. 15, n. 8, p. 884, doi. 10.1038/sj.ejhg.5201841
    By:
    • Vanmolkot, Kaate R. J.;
    • Stam, Anine H.;
    • Raman, Ashok;
    • Koenderink, Jan B.;
    • de Vries, Boukje;
    • van den Boogerd, Eelke H.;
    • van Vark, Judith;
    • van den Heuvel, Jeroen J. M. W.;
    • Bajaj, Nin;
    • Terwindt, Gisela M.;
    • Haan, Joost;
    • Frants, Rune R.;
    • Ferrari, Michel D.;
    • van den Maagdenberg, Arn M. J. M.
    Publication type:
    Article

  • The novel p.L1649Q mutation in the SCN1A epilepsy gene is associated with familial hemiplegic migraine: genetic and functional studies.

    Published in:
    Human Mutation, 2007, v. 28, n. 5, p. 522, doi. 10.1002/humu.9486
    By:
    • Vanmolkot, Kaate R.J.;
    • Babini, Elena;
    • de Vries, Boukje;
    • Stam, Anine H.;
    • Freilinger, Tobias;
    • Terwindt, Gisela M.;
    • Norris, Lisa;
    • Haan, Joost;
    • Frants, Rune R.;
    • Ramadan, Nabih M.;
    • Ferrari, Michel D.;
    • Pusch, Michael;
    • van den Maagdenberg, Arn M.J.M.;
    • Dichgans, Martin
    Publication type:
    Article