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Items: 36

1.

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.

PMID:
30076273
2.

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.

PMID:
29343472
3.

Corrigendum: 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 Sep 28;48(10):1296. doi: 10.1038/ng1016-1296c. No abstract available.

PMID:
27681292
4.

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. No abstract available.

5.

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. Erratum in: Nat Genet. 2016 Sep 28;48(10 ):1296.

6.

Recurrent coma and fever in familial hemiplegic migraine type 2. A prospective 15-year follow-up of a large family with a novel ATP1A2 mutation.

Pelzer N, Blom DE, Stam AH, Vijfhuizen LS, Hageman A, van Vliet JA, Ferrari MD, van den Maagdenberg A, Haan J, Terwindt GM.

Cephalalgia. 2017 Jul;37(8):737-755. doi: 10.1177/0333102416651284. Epub 2016 May 24.

PMID:
27226003
7.

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

Zhao H, Eising E, de Vries B, Vijfhuizen LS; International Headache Genetics Consortium, Anttila V, Winsvold BS, Kurth T, Stefansson H, Kallela M, Malik R, Stam AH, Ikram MA, Ligthart L, Freilinger T, Alexander M, Müller-Myhsok B, Schreiber S, Meitinger T, Aromas A, Eriksson JG, Boomsma DI, van Duijn CM, Zwart JA, Quaye L, Kubisch C, Dichgans M, Wessman M, Stefansson K, Chasman DI, Palotie A, Martin NG, Montgomery GW, Ferrari MD, Terwindt GM, van den Maagdenberg AM, Nyholt DR.

Cephalalgia. 2016 Jun;36(7):648-57. doi: 10.1177/0333102415591497. Epub 2015 Dec 8.

8.

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

Nyholt DR; International Headache Genetics Consortium, Anttila V, Winsvold BS, Kurth T, Stefansson H, Kallela M, Malik R, Vries Bd, Terwindt GM, Ikram MA, Stam AH, Ligthart L, Freilinger T, Alexander M, Muller-Myhsok B, Schreiber S, Meitinger T, Aromaa A, Eriksson JG, Kaprio J, Boomsma DI, Duijn Cv, Raitakari O, Järvelin MR, Zwart JA, Quaye L, Strachan DP, Kubisch C, Ferrari MD, van den Maagdenberg AM, Dichgans M, Wessman M, Smith GD, Stefansson K, Chasman DI, Palotie A.

Cephalalgia. 2015 May;35(6):489-99. doi: 10.1177/0333102414547784. Epub 2014 Sep 1.

PMID:
25179292
9.

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

Weller CM, Pelzer N, de Vries B, López MA, De Fàbregues O, Pascual J, Arroyo MA, Koelewijn SC, Stam AH, Haan J, Ferrari MD, Terwindt GM, van den Maagdenberg AM.

Cephalalgia. 2014 Nov;34(13):1062-9. doi: 10.1177/0333102414529195. Epub 2014 Apr 4.

PMID:
24707016
10.

Familial hemiplegic migraine treated by sodium valproate and lamotrigine.

Pelzer N, Stam AH, Carpay JA, Vries BD, van den Maagdenberg AM, Ferrari MD, Haan J, Terwindt GM.

Cephalalgia. 2014 Aug;34(9):708-711. Epub 2014 Jan 17.

PMID:
24443394
11.

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

Anttila V, Winsvold BS, Gormley P, Kurth T, Bettella F, McMahon G, Kallela M, Malik R, de Vries B, Terwindt G, Medland SE, Todt U, McArdle WL, Quaye L, Koiranen M, Ikram MA, Lehtimäki T, Stam AH, Ligthart L, Wedenoja J, Dunham I, Neale BM, Palta P, Hamalainen E, Schürks M, Rose LM, Buring JE, Ridker PM, Steinberg S, Stefansson H, Jakobsson F, Lawlor DA, Evans DM, Ring SM, Färkkilä M, Artto V, Kaunisto MA, Freilinger T, Schoenen J, Frants RR, Pelzer N, Weller CM, Zielman R, Heath AC, Madden PAF, Montgomery GW, Martin NG, Borck G, Göbel H, Heinze A, Heinze-Kuhn K, Williams FMK, Hartikainen AL, Pouta A, van den Ende J, Uitterlinden AG, Hofman A, Amin N, Hottenga JJ, Vink JM, Heikkilä K, Alexander M, Muller-Myhsok B, Schreiber S, Meitinger T, Wichmann HE, Aromaa A, Eriksson JG, Traynor B, Trabzuni D; North American Brain Expression Consortium; UK Brain Expression Consortium, Rossin E, Lage K, Jacobs SBR, Gibbs JR, Birney E, Kaprio J, Penninx BW, Boomsma DI, van Duijn C, Raitakari O, Jarvelin MR, Zwart JA, Cherkas L, Strachan DP, Kubisch C, Ferrari MD, van den Maagdenberg AMJM, Dichgans M, Wessman M, Smith GD, Stefansson K, Daly MJ, Nyholt DR, Chasman D, Palotie A.

Nat Genet. 2013 Aug;45(8):912-917. doi: 10.1038/ng.2676. Epub 2013 Jun 23.

12.

Familial and sporadic hemiplegic migraine: diagnosis and treatment.

Pelzer N, Stam AH, Haan J, Ferrari MD, Terwindt GM.

Curr Treat Options Neurol. 2013 Feb;15(1):13-27. doi: 10.1007/s11940-012-0208-3.

PMID:
23203776
13.

Migraine is not associated with enhanced atherosclerosis.

Stam AH, Weller CM, Janssens AC, Aulchenko YS, Oostra BA, Frants RR, van den Maagdenberg AM, Ferrari MD, van Duijn CM, Terwindt GM.

Cephalalgia. 2013 Mar;33(4):228-35. doi: 10.1177/0333102412466966. Epub 2012 Nov 12.

PMID:
23147163
14.

Validation of the web-based LUMINA questionnaire for recruiting large cohorts of migraineurs.

van Oosterhout WP, Weller CM, Stam AH, Bakels F, Stijnen T, Ferrari MD, Terwindt GM.

Cephalalgia. 2011 Oct;31(13):1359-67. doi: 10.1177/0333102411418846. Epub 2011 Sep 13.

PMID:
21914734
15.

Head tremor related to CACNA1A mutations.

Geerlings RP, Koehler PJ, Haane DY, Stam AH, de Vries B, Boon EM, Haan J.

Cephalalgia. 2011 Sep;31(12):1315-9. doi: 10.1177/0333102411414442. Epub 2011 Jul 18.

PMID:
21768184
16.

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

Stam AH, Louter MA, Haan J, de Vries B, van den Maagdenberg AM, Frants RR, Ferrari MD, Terwindt GM.

Cephalalgia. 2011 Jan;31(2):199-205. doi: 10.1177/0333102410375629. Epub 2010 Jul 2.

PMID:
20974584
17.

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

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.

Nat Genet. 2010 Oct;42(10):869-73. doi: 10.1038/ng.652. Epub 2010 Aug 29.

18.

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.

19.

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. No abstract available.

20.

Migraine and genetic and acquired vasculopathies.

Stam AH, Haan J, van den Maagdenberg AM, Ferrari MD, Terwindt GM.

Cephalalgia. 2009 Sep;29(9):1006-17. doi: 10.1111/j.1468-2982.2009.01940.x. Review.

PMID:
19689610
21.

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 Oct;80(10):1125-9. doi: 10.1136/jnnp.2009.177279. Epub 2009 Jun 10. Review.

PMID:
19520699
22.

First mutation in the voltage-gated Nav1.1 subunit gene SCN1A with co-occurring familial hemiplegic migraine and epilepsy.

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.

Cephalalgia. 2009 Mar;29(3):308-13. doi: 10.1111/j.1468-2982.2008.01721.x.

PMID:
19220312
23.

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.

Arch Neurol. 2009 Jan;66(1):97-101. doi: 10.1001/archneurol.2008.535. Erratum in: Arch Neurol. 2009 Apr;66(4):497. Arch Neurol. 2009 Jun;66(6):772.

PMID:
19139306
24.

CACNA1A mutation linking hemiplegic migraine and alternating hemiplegia of childhood.

de Vries B, Stam AH, Beker F, van den Maagdenberg AM, Vanmolkot KR, Laan L, Ginjaar IB, Frants RR, Lauffer H, Haan J, Haas JP, Terwindt GM, Ferrari MD.

Cephalalgia. 2008 Aug;28(8):887-91. doi: 10.1111/j.1468-2982.2008.01596.x. Epub 2008 May 21.

PMID:
18498393
25.

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

Stam AH, van den Maagdenberg AM, Haan J, Terwindt GM, Ferrari MD.

Curr Opin Neurol. 2008 Jun;21(3):288-93. doi: 10.1097/WCO.0b013e3282fd171a. Review.

PMID:
18451712
26.

CACNA1A R1347Q: a frequent recurrent mutation in hemiplegic migraine.

Stam AH, Vanmolkot KR, Kremer HP, Gärtner J, Brown J, Leshinsky-Silver E, Gilad R, Kors EE, Frankhuizen WS, Ginjaar HB, Haan J, Frants RR, Ferrari MD, van den Maagdenberg AM, Terwindt GM.

Clin Genet. 2008 Nov;74(5):481-5. doi: 10.1111/j.1399-0004.2008.00996.x. Epub 2008 Apr 8.

PMID:
18400034
27.

A review of the genetic relation between migraine and epilepsy.

Haan J, Terwindt GM, van den Maagdenberg AM, Stam AH, Ferrari MD.

Cephalalgia. 2008 Feb;28(2):105-13. doi: 10.1111/j.1468-2982.2007.01460.x. Review.

PMID:
18197881
28.

Systematic analysis of three FHM genes in 39 sporadic patients with hemiplegic migraine.

de Vries B, Freilinger T, Vanmolkot KR, Koenderink JB, Stam AH, Terwindt GM, Babini E, van den Boogerd EH, van den Heuvel JJ, Frants RR, Haan J, Pusch M, van den Maagdenberg AM, Ferrari MD, Dichgans M.

Neurology. 2007 Dec 4;69(23):2170-6.

PMID:
18056581
29.

Recurrent ATP1A2 mutations in Portuguese families with familial hemiplegic migraine.

Castro MJ, Stam AH, Lemos C, Barros J, Gouveia RG, Martins IP, Koenderink JB, Vanmolkot KR, Mendes AP, Frants RR, Ferrari MD, Sequeiros J, Pereira-Monteiro JM, van den Maagdenberg AM.

J Hum Genet. 2007;52(12):990-8. Epub 2007 Oct 19.

PMID:
17952365
30.

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

Richards A, van den Maagdenberg AM, Jen JC, Kavanagh D, Bertram P, Spitzer D, Liszewski MK, Barilla-Labarca ML, Terwindt GM, Kasai Y, McLellan M, Grand MG, Vanmolkot KR, de Vries B, Wan J, Kane MJ, Mamsa H, Schäfer R, Stam AH, Haan J, de Jong PT, Storimans CW, van Schooneveld MJ, Oosterhuis JA, Gschwendter A, Dichgans M, Kotschet KE, Hodgkinson S, Hardy TA, Delatycki MB, Hajj-Ali RA, Kothari PH, Nelson SF, Frants RR, Baloh RW, Ferrari MD, Atkinson JP.

Nat Genet. 2007 Sep;39(9):1068-70. Epub 2007 Jul 29.

PMID:
17660820
31.

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.

Eur J Hum Genet. 2007 Aug;15(8):884-8. Epub 2007 May 2.

32.

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.

Hum Mutat. 2007 May;28(5):522.

PMID:
17397047
33.

Alternating hemiplegia of childhood: no mutations in the glutamate transporter EAAT1.

de Vries B, Haan J, Stam AH, Vanmolkot KR, Stroink H, Laan LA, Gill DS, Pascual J, Frants RR, van den Maagdenberg AM, Ferrari MD.

Neuropediatrics. 2006 Oct;37(5):302-4.

PMID:
17236110
34.

Severe episodic neurological deficits and permanent mental retardation in a child with a novel FHM2 ATP1A2 mutation.

Vanmolkot KR, Stroink H, Koenderink JB, Kors EE, van den Heuvel JJ, van den Boogerd EH, Stam AH, Haan J, De Vries BB, Terwindt GM, Frants RR, Ferrari MD, van den Maagdenberg AM.

Ann Neurol. 2006 Feb;59(2):310-4.

PMID:
16437583
35.

Alternating hemiplegia of childhood successfully treated with topiramate: 18 months of follow-up.

Di Rosa G, Spanò M, Pustorino G, Ferrari MD, Stam AH, Sgrò DL, Mannarino E, Bonsignore M, Tortorella G.

Neurology. 2006 Jan 10;66(1):146. No abstract available.

PMID:
16401872
36.

Migraine: new treatment options from molecular biology.

Stam AH, Haan J, Frants RR, Ferrari MD, van den Maagdenberg AM.

Expert Rev Neurother. 2005 Sep;5(5):653-61. Review.

PMID:
16162089

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