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1دورية أكاديمية
المؤلفون: de Boer, J.N., Vingerhoets, C., Hirdes, M., McAlonan, G.M., Amelsvoort, T.V., Zinkstok, J.R.
المصدر: In Psychiatry Research August 2019 278:294-302
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2
المؤلفون: Oskarsdottir, Solveig, 1953, Boot, E., Crowley, T. B., Loo, J. C. Y., Arganbright, J. M., Armando, M., Baylis, A. L., Breetvelt, E. J., Castelein, R. M., Chadehumbe, M., Cielo, C. M., de Reuver, S., Eliez, S., Fiksinski, A. M., Forbes, B. J., Gallagher, E., Hopkins, S. E., Jackson, O. A., Levitz-Katz, L., Klingberg, G., Lambert, M. P., Marino, B., Mascarenhas, M. R., Moldenhauer, J., Moss, E. M., Nowakowska, B. A., Orchanian-Cheff, A., Putotto, C., Repetto, G. M., Schindewolf, E., Schneider, M., Solot, C. B., Sullivan, K. E., Swillen, A., Unolt, M., Van Batavia, J. P., Vingerhoets, C., Vorstman, J., Bassett, A. S., McDonald-McGinn, D. M.
المصدر: Genetics in Medicine. 25(3)
مصطلحات موضوعية: Pediatrics, Pediatrik, 22q11, 2 deletion syndrome, Children, Clinical practice guidelines, Review, Treatment, bernard-soulier-syndrome, cardio-facial-syndrome, partial, digeorge-syndrome, obstructive sleep-apnea, live viral vaccines, low-copy repeats, psychiatric-disorders, velocardiofacial syndrome, ocular findings, hearing-loss, Genetics & Heredity
URL الوصول: https://gup.ub.gu.se/publication/331591
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3
المؤلفون: Boot, E., Oskarsdottir, Solveig, 1953, Loo, J. C. Y., Crowley, T. B., Orchanian-Cheff, A., Andrade, D. M., Arganbright, J. M., Castelein, R. M., Cserti-Gazdewich, C., de Reuver, S., Fiksinski, A. M., Klingberg, G., Lang, A. E., Mascarenhas, M. R., Moss, E. M., Nowakowska, B. A., Oechslin, E., Palmer, L., Repetto, G. M., Reyes, N. G. D., Schneider, M., Silversides, C., Sullivan, K. E., Swillen, A., van Amelsvoort, Tamj, Van Batavia, J. P., Vingerhoets, C., McDonald-McGinn, D. M., Bassett, A. S.
المصدر: Genetics in Medicine. 25(3)
مصطلحات موضوعية: Clinical Medicine, Klinisk medicin, Adults, Aging, Clinical practice guidelines, DiGeorge syndrome, Treatment, bernard-soulier-syndrome, low-copy repeats, velocardiofacial syndrome, presenting symptoms, antibody deficiency, parkinsons-disease, schizophrenia, features, risk, prevalence, Genetics & Heredity
URL الوصول: https://gup.ub.gu.se/publication/330949
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4دورية أكاديمية
المؤلفون: Sylvester, A., Serrarens, C., Tse, D., Vingerhoets, C., Van Amelsvoort, T.
المصدر: In Neuroscience Applied 2023 2 Supplement 2
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5دورية أكاديمية
المؤلفون: Vingerhoets, C., Serrarens, C., Tse, D.H.Y., Steijvers-Peeters, E., Brouwers, K., Linden, D., Van Amelsvoort, T.
المصدر: In Neuroscience Applied 2023 2 Supplement 2
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6دورية أكاديمية
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7دورية أكاديمية
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8
المؤلفون: Oenema A, de Ruijter D, Vingerhoets C, Ism, Wurff, Dj, Bos, Mary Nicolaou, Bot M, Ej, Giltay, Rjt, Mocking
المصدر: Europe PubMed Central
مصطلحات موضوعية: Adult, Mental Health, Adolescent, Attention Deficit Disorder with Hyperactivity, Dietary Supplements, Fatty Acids, Omega-3, Longevity, Humans, Child
URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::90c480f4176e3a500a4f106c92647dc3
https://pubmed.ncbi.nlm.nih.gov/33443742 -
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المؤلفون: Davies, R. W., Fiksinski, A. M., Breetvelt, E. J., Williams, N. M., Hooper, S. R., Monfeuga, T., Bassett, A. S., Owen, M. J., Gur, R. E., Morrow, B. E., McDonald-McGinn, D. M., Swillen, A., Chow, E. W. C., van den Bree, M., Emanuel, B. S., Vermeesch, J. R., van Amelsvoort, T., Arango, C., Armando, M., Campbell, L. E., Cubells, J. F., Eliez, S., Garcia-Minaur, S., Gothelf, D., Kates, W. R., Murphy, K. C., Murphy, C. M., Murphy, D. G., Philip, N., Repetto, G. M., Shashi, V., Simon, T. J., Suner, D. H., Vicari, Stefano, Scherer, S. W., Epstein, M. P., Warren, S. T., Morrison, S., Chawner, S., Vingerhoets, C., Breckpot, J., Vergaelen, E., Vogels, A., Monks, S., Prasad, S. E., Sandini, C., Schneider, M., Maeder, J., Fraguas, D., Evers, R., Tassone, F., Morey-Canyelles, J., Ousley, O. Y., Antshel, K. M., Fremont, W., Fritsch, R., Ornstein, C., Daly, E. M., Costain, G. A., Boot, E., Heung, T., Crowley, T. B., Zackai, E. H., Calkins, M. E., Gur, R. C., Mccabe, K. L., Busa, T., Schoch, K., Pontillo, M., Duijff, S. N., Kahn, R. S., Houben, Mariasofia, Kushan, L., Jalbrzikowski, M., Carmel, M., Mekori-Domachevsky, E., Michaelovsky, E., Weinberger, R., Bearden, C. E., Vorstman, J. A. S.
المساهمون: Marseille medical genetics - Centre de génétique médicale de Marseille (MMG), Aix Marseille Université (AMU)-Institut National de la Santé et de la Recherche Médicale (INSERM), Département de génétique médicale [Hôpital de la Timone - APHM], Institut National de la Santé et de la Recherche Médicale (INSERM)- Hôpital de la Timone [CHU - APHM] (TIMONE)-Assistance Publique - Hôpitaux de Marseille (APHM)-Aix Marseille Université (AMU), RS: MHeNs - R2 - Mental Health, Psychiatrie & Neuropsychologie, MUMC+: MA Med Staf Spec Psychiatrie (9)
المصدر: Nature Medicine
Nature Medicine, Nature Publishing Group, 2020, 26 (12), pp.1912-1918. ⟨10.1038/s41591-020-1103-1⟩
Nature Medicine, Vol. 26, No 12 (2020) pp. 1912-1918
Nat Med
Nature medicine, vol 26, iss 12
Nature Medicine, 26(12), 1912-1918. Nature Publishing Groupمصطلحات موضوعية: 0301 basic medicine, Male, Multifactorial Inheritance, [SDV]Life Sciences [q-bio], INTELLIGENCE, Medical and Health Sciences, Cohort Studies, ddc:616.89, 0302 clinical medicine, Borderline intellectual functioning, Risk Factors, Intellectual disability, 2.1 Biological and endogenous factors, PREMORBID IQ, Cognitive decline, Aetiology, Child, ComputingMilieux_MISCELLANEOUS, Intelligence quotient, ABNORMALITIES, General Medicine, Middle Aged, Serious Mental Illness, Mental Health, Phenotype, Schizophrenia, 030220 oncology & carcinogenesis, Child, Preschool, Cohort, Female, Clinical psychology, Adult, Psychosis, Adolescent, Immunology, behavioral disciplines and activities, General Biochemistry, Genetics and Molecular Biology, Article, 03 medical and health sciences, Young Adult, Settore MED/39 - NEUROPSICHIATRIA INFANTILE, PSYCHOSIS, Clinical Research, Intellectual Disability, Genetic variation, Behavioral and Social Science, mental disorders, medicine, Genetics, DiGeorge Syndrome, Humans, Cognitive Dysfunction, Preschool, METAANALYSIS, International 22q11.2 Brain and Behavior Consortium, Aged, DECLINE, reliability, business.industry, Prevention, cognitive-development, Genetic Variation, PERFORMANCE, medicine.disease, Brain Disorders, schizophrenia, 030104 developmental biology, [SDV.GEN.GH]Life Sciences [q-bio]/Genetics/Human genetics, business
وصف الملف: application/pdf
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10دورية أكاديمية
لا يتم عرض هذه النتيجة على الضيوف.
تسجيل الدخول للوصول الكامل.