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1دورية أكاديمية
المؤلفون: Beekman, M, Heijmans, BT, Martin, NG, Whitfield, JB, Pedersen, NL, DeFaire, U, Snieder, H, Lakenberg, N, Eka, H, Suchiman, D, de Knijff, P, Frants, RR, van Ommen, GJB, Kluft, C, Vogler, GP, Boomsma, DI, Slagboom, PE
المصدر: European journal of human genetics : EJHG. 11(11):845-850
مصطلحات موضوعية: Medicin och hälsovetenskap
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2دورية أكاديمية
المؤلفون: Kogelman, LJA, Esserlind, AL, Christensen, AF, Awasthi, S, Ripke, S, Ingason, A, Davidsson, OB, Erikstrup, C, Hjalgrim, H, Ullum, H, Olesen, J, Hansen, TF, Gudbjartsson, D, Gastafsson, O, Stefansson, K, Stefansson, H, Porsteinsdottir, U, Andersen, S, Banasik, K, Brunak, S, Buil, A, Burgdorf, K, Gregor, J, Jennum, P, Nielsen, KR, Nyegaard, M, Paarup, HM, Pedersen, OB, Sorensen, E, Werge, T, Anttila, V, Artto, V, Belin, AC, de Boer, I, Boomsma, DI, Borte, S, Chasman, DI, Cherkas, L, Cormand, B, Cuenca-Leon, E, Davey-Smith, G, Dichgans, M, van Duijn, C, Esko, T, Ferrari, M, Frants, RR, Freilinger, T, Furlotte, N, Gormley, P, Griffiths, L, Hamalainen, E, Hiekkala, M, Ikram, MA, Jarvelin, MR, Kajanne, R, Kallela, M, Kaprio, J, Kaunisto, M, Kubisch, C, Kurki, M, Kurth, T, Launer, L, Lehtimaki, T, Lessel, D, Ligthart, L, Litterman, N, van den Maagdenberg, A, Macaya, A, Malik, R, Mangino, M, McMahon, G, Muller-Myhsok, B, Neale, BM, Northover, C, Nyholt, DR, Palotie, A, Palta, P, Pedersen, L, Pedersen, N, Posthuma, D, Pozo-Rosich, P, Pressman, A, Raitakari, O, Schurks, M, Sintas, C, Steinberg, S, Strachan, D, Terwindt, G, Vila-Pueyo, M, Wessman, M, Winsvold, BS, Zhao, HY, Zwart, JA
المصدر: Neurology. Genetics. 5(6):e364
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3دورية أكاديمية
المؤلفون: Beekman, M, Heijmans, BT, Martin, NG, Whitfield, JB, Pedersen, NL, DeFaire, U, Snieder, H, Lakenberg, N, Knijff, PC, Frants, RR, van Ommen, GJB, Kluft, C, Vogler, GR, Slagboom, RE, Boomsma, DI
المصدر: Twin research : the official journal of the International Society for Twin Studies. 6(4):322-324
مصطلحات موضوعية: Medicin och hälsovetenskap
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4دورية أكاديمية
المؤلفون: De Vries, B Loci, Freilinger, T, Anttila, V, Malik, R, Terwindt, GM, Pozo-Rosich, P, Winsvold, B, Nyholt, D, van Oosterhout, WPJ, Artto, V, Todt, M, Hämäläinen, E, Fernandez-Moralez, J, Louter, M, Kaunisto, MA, Schoenen, J, Raitakari, O, Lehtimäki, T, Ville-Pueyo, M, Göbel, H, Wichman, E, Sintas, C, Uitterlinden, A, Hofman, A, Rivadeneira, F, Heinze, A, Tronvik, E, van Duin, CM, Kaprio, J, Cormand, B, Wessman, M, Frants, RR, Meitinger, T, Müller-Myhsok, B, Zwart, JA, Färkkilä, M, Macaya, A, Ferrari, MD, Kubisch, C, Palotie, A, Dichgans, M, van den Maagdenberg, AMJ
المصدر: The Journal of Headache and Pain. February 2013 14(1):1-2
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المؤلفون: Frants Rr, RA Ophoff, EE Kors, Flmg Vermeulen, J Pascual, Amjm van den Maagdenberg, Ferrari, D S Gill, J Haan, M N Vergouwe, GM Terwindt
المصدر: Cephalalgia. 20:696-700
مصطلحات موضوعية: Adult, Male, Candidate gene, medicine.medical_specialty, Migraine Disorders, Hemiplegia, Chromosome 19, medicine, Humans, Amino Acid Sequence, Child, Gene, Polymorphism, Single-Stranded Conformational, Familial hemiplegic migraine, Genetics, Polymorphism, Genetic, Base Sequence, business.industry, Alternating hemiplegia of childhood, Single-strand conformation polymorphism, General Medicine, medicine.disease, Migraine, Child, Preschool, Mutation, Mutation testing, Physical therapy, Female, Calcium Channels, Neurology (clinical), business
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المؤلفون: Rana, Js, Monraats, Ps, Zwinderman, Ah, Maat, Mpm, Kastelein, Jjp, Agema, Wrp, Doevendons, Paf, Winter, Rj, Tio, Ra, Waltenberger, J., Frants, Rr, Laarse, A., Wall, Ee, J. Wouter Jukema
المساهمون: Hematology, Vascular Ageing Programme (VAP), Amsterdam Public Health, Epidemiology and Data Science, Amsterdam Cardiovascular Sciences, Vascular Medicine, Cardiology
المصدر: Thrombosis and Haemostasis, 94(4), 892-894. Georg Thieme Verlag
Thrombosis and Haemostasis, 94(4), 892-894. GEORG THIEME VERLAG KG
Publons
Thrombosis and haemostasis, 94(4), 892-894. Schattauer GmbHمصطلحات موضوعية: EVENTS, ACUTE-PHASE RESPONSE, MYOCARDIAL-INFARCTION, INFLAMMATION, HEART-DISEASE, IMPLANTATION, ASSOCIATION, Hematology, PLASMA-LEVELS, ANGIOPLASTY, C-REACTIVE PROTEIN
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::20cf154dc3679509dd5d0c3956e180c9
https://doi.org/10.1055/s-0037-1615586 -
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المؤلفون: Stam, AH, de Vries, B, Janssens, Cecile, Vanmolkot, KRJ, Aulchenko, YS, Henneman, Peter, Oostra, Ben, Frants, RR, Maagdenberg, AMJM, Ferrari, MD, Duijn, Cornelia, Terwindt, GM
المساهمون: Epidemiology, Clinical Genetics
المصدر: Neurology, 74(4), 288-294. Lippincott Williams & Wilkins
URL الوصول: https://explore.openaire.eu/search/publication?articleId=narcis______::ce1af22b6c8f0cc8d2043bda7cc82f29
https://pure.eur.nl/en/publications/c288de1d-5a55-4dce-a15d-a8efe71abae2 -
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المؤلفون: 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.
المصدر: Human mutation 28 (2007): 522–522.
info:cnr-pdr/source/autori: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./titolo:The novel p.L1649Q mutation in the SCN1A epilepsy gene is associated with familial hemiplegic migraine: genetic and functional studies. Mutation in brief #957./doi:/rivista:Human mutation/anno:2007/pagina_da:522/pagina_a:522/intervallo_pagine:522–522/volume:28URL الوصول: https://explore.openaire.eu/search/publication?articleId=cnr_________::ea0e28c18646165f7c2a45fb0a71b000
http://www.cnr.it/prodotto/i/9605 -
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المؤلفون: Callenbach, PMC, van den Boogerd, EH, Coo, IFM, ten Houten, R, Oosterwijk, JC, Hageman, G, Frants, RR, Brouwer, OF, Maagdenberg, AMJM
المساهمون: Damage and Repair in Cancer Development and Cancer Treatment (DARE), Targeted Gynaecologic Oncology (TARGON), Neurology
المصدر: Clinical Genetics, 67(6), 517-525. Wiley
Clinical Genetics, 67(6), 517-525. Wiley-Blackwell Publishing Ltdمصطلحات موضوعية: MODULE, CONFIRMATION, benign familial infantile convulsions, DOMAINS, epilepsy, PROTEIN, linkage analysis, MULTILOCUS LINKAGE ANALYSIS, 16P12-Q12, ALGORITHM, INHERITANCE, chromosome 16p, CHOREOATHETOSIS
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المؤلفون: Callenbach, PMC, van den Maagdenberg, AMJM, Hottenga, JJ, van den Boogerd, EH, de Coo, RFM, Lindhout, D, Frants, RR, Sandkuijl, LA, Brouwer, OF
المساهمون: Epidemiology, Neurology, Clinical Genetics
المصدر: Epilepsia, 44, 1298-1305. Wiley-Blackwell Publishing Ltd
Epilepsia, 44(10), 1298-1305. Wileyمصطلحات موضوعية: NORWEGIAN FAMILY, ELECTROCLINICAL PICTURE, FPEVF, CHRNA4 GENE, LATERAL TEMPORAL EPILEPSY, chromosome 22q, SUBUNIT, DOMINANT PARTIAL EPILEPSY, ADNFLE, genetics, AUDITORY FEATURES, LGI1, clinical characteristics, MUTATION, FRONTAL-LOBE EPILEPSY
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