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    المصدر: The Journal of Headache and Pain, Vol 22, Iss 1, Pp 1-11 (2021)
    The Journal of Headache and Pain

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    المساهمون: Tampere University, Tays Research Services, Clinical Medicine, Complex Disease Genetics, Institute for Molecular Medicine Finland, Genomics of Neurological and Neuropsychiatric Disorders, Helsinki Institute of Life Science HiLIFE, Clinicum, Neurologian yksikkö, HUS Neurocenter, HUS Helsinki and Uusimaa Hospital District, University of Helsinki, Centre of Excellence in Complex Disease Genetics, Department of Public Health, Samuli Olli Ripatti / Principal Investigator, Faculty Common Matters (Faculty of Social Sciences), Biostatistics Helsinki, Helsinki Institute for Information Technology, Statistical and population genetics, Department of Mathematics and Statistics, Biosciences, Aarno Palotie / Principal Investigator, Department of Neurosciences

    المصدر: Häppölä, P, Gormley, P, Nuottamo, M E, Artto, V, Sumelahti, M L, Nissilä, M, Keski-Säntti, P, Ilmavirta, M, Kaunisto, M A, Hämäläinen, E I, Ripatti, S, Pirinen, M, Wessman, M, Palotie, A, Kallela, M, International Headache Genetics Consortium (IHGC), Hansen, T F & Olesen, J 2022, ' Polygenic risk provides biological validity for the ICHD-3 criteria among Finnish migraine families ', Cephalalgia, vol. 42, no. 4-5, pp. 345-356 . https://doi.org/10.1177/03331024211045651Test

    وصف الملف: fulltext; application/pdf