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المؤلفون: Barton, S.K., Magnani, D., James, O.G., Livesey, M.R., Selvaraj, B.T., James, O.T., Perkins, E.M., Gregory, J.M., Cleary, E., Ausems, C.R.M., Carter, R., Vasistha, N.A., Zhao, C., Burr, K., Story, D., Cardinali, A., Morton, N.M., Hardingham, G.E., Wyllie, D.J.A., Chandran, S.
وصف الملف: application/pdf
URL الوصول: https://explore.openaire.eu/search/publication?articleId=core_ac_uk__::16c458250344a91302504e6a2cb9a11e
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المؤلفون: Perkins, E.M., Burr, K., Banerjee, P., Mehta, A.R., Dando, O., Selvaraj, B.T., Suminaite, D., Nanda, J., Henstridge, C.M., Gillingwater, T.H., Hardingham, G.E., Wyllie, D.J.A., Chandran, S., Livesey, M.R.
المصدر: Molecular Neurodegeneration
وصف الملف: application/pdf
URL الوصول: https://explore.openaire.eu/search/publication?articleId=core_ac_uk__::e1bc6bc5783adc34768e7b84201336c8
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المؤلفون: Strehlow, V., Heyne, H.O., Vlaskamp, D.R.M., Marwick, K.F.M., Rudolf, G., Bellescize, J. de, Biskup, S., Brilstra, E.H., Brouwer, O.F., Callenbach, P.M.C., Hentschel, J., Hirsch, E., Kind, P.C., Mignot, C., Platzer, K., Rump, P., Skehel, P.A., Wyllie, D.J.A., Hardingham, G.E., Ravenswaaij-Arts, C.M.A. van, Koolen, D.A., Willemsen, M.H., Lesca, G., Lemke, J.R.
المساهمون: Clinical Cognitive Neuropsychiatry Research Program (CCNP), UCL - (MGD) Service de pédiatrie, UCL - SSS/IREC/MONT - Pôle Mont Godinne, univOAK, Archive ouverte, University Hospital Leipzig, Massachusetts General Hospital [Boston], Broad Institute of MIT and Harvard (BROAD INSTITUTE), Harvard Medical School [Boston] (HMS)-Massachusetts Institute of Technology (MIT)-Massachusetts General Hospital [Boston], University of Groningen [Groningen], University of Edinburgh, Institut de Génétique et de Biologie Moléculaire et Cellulaire (IGBMC), Université de Strasbourg (UNISTRA)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS), CHU Strasbourg, Centre Hospitalier Universitaire de Lyon (CHU Lyon), CeGaT GmbH, University Medical Center [Utrecht], Hôpital de Hautepierre [Strasbourg], Institute for Stem Cell Science and Regenerative Medicine [Bangalore, Inde] (inStem), CHU Pitié-Salpêtrière [AP-HP], Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU), Centre de référence Déficiences Intellectuelles de Causes Rares [CHU Pitié-Salpétrière], Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU), Groupe de Recherche Clinique : Déficience Intellectuelle et Autisme (GRC), Université Pierre et Marie Curie - Paris 6 (UPMC), Centre de recherche en neurosciences de Lyon - Lyon Neuroscience Research Center (CRNL), Université Claude Bernard Lyon 1 (UCBL), Université de Lyon-Université de Lyon-Université Jean Monnet - Saint-Étienne (UJM)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS), GRIN2A study group: Alexis Arzimanoglou, Paul B Augustijn, Patrick Van Bogaert, Helene Bourry, Peter Burfeind, Yoyo Chu, Brian Chung, Diane Doummar, Patrick Edery, Aviva Fattal-Valevski, Mélanie Fradin, Marion Gerard, Christa de Geus, Boudewijn Gunning, Danielle Hasaerts, Ingo Helbig, Katherine L Helbig, Rami Jamra, Mélanie Jennesson Lyver, Jolien S Klein Wassink-Ruiter, David A Koolen, Damien Lederer, Roelineke J Lunsing, Mikaël Mathot, Hélène Maurey, Shay Menascu, Anne Michel, Ghayda Mirzaa, Diana Mitter, Hiltrud Muhle, Rikke S Møller, Caroline Nava, Margaret O'Brien, Evelyn van Pinxteren-Nagler, Anne van Riesen, Christelle Rougeot, Damien Sanlaville, Jolanda H Schieving, Steffen Syrbe, Hermine E Veenstra-Knol, Nienke Verbeek, Dorothée Ville, Yvonne J Vos, Pascal Vrielynck, Sabrina Wagner, Sarah Weckhuysen, Marjolein H Willemsen
المصدر: Brain : a journal of neurology, 142(1), 80. Oxford University Press
Brain, 142(1), 80-92. Oxford University Press
Brain : a journal of neurology, Vol. 142, no. 1, p. 80-92 (2019)
Strehlow, V, Heyne, H O, Vlaskamp, D R M, Marwick, K F M, Rudolf, G, de Bellescize, J, Biskup, S, Brilstra, E H, Brouwer, O F, Callenbach, P M C, Hentschel, J, Hirsch, E, Kind, P C, Mignot, C, Platzer, K, Rump, P, Skehel, P A, Wyllie, D J A, Hardingham, G E, van Ravenswaaij-Arts, C M A & Lesca, G & Lemke, J R 2019, ' GRIN2A-related disorders : genotype and functional consequence predict phenotype ', Brain, vol. 142, no. 1, pp. 80–92 . https://doi.org/10.1093/brain/awy304
Brain-A Journal of Neurology
Brain-A Journal of Neurology, 2019, 142 (1), pp.80-92. ⟨10.1093/brain/awy304⟩
Brain, 142, 80-92
Strehlow, V, Heyne, H O, Vlaskamp, D R M, Marwick, K F M, Rudolf, G, de Bellescize, J, Biskup, S, Brilstra, E H, Brouwer, O F, Callenbach, P M C, Hentschel, J, Hirsch, E, Kind, P C, Mignot, C, Platzer, K, Rump, P, Skehel, P A, Wyllie, D J A, Hardingham, G E, van Ravenswaaij-Arts, C M A, Lesca, G, Lemke, J R, GRIN2A study group & Møller, R S 2019, ' GRIN2A-related disorders : genotype and functional consequence predict phenotype ', Brain, vol. 142, no. 1, pp. 80-92 . https://doi.org/10.1093/brain/awy304
Brain
Brain, 142, 1, pp. 80-92مصطلحات موضوعية: GLUN2A, Adult, Male, Adolescent, Genotype, [SDV.GEN] Life Sciences [q-bio]/Genetics, VARIANTS, Neurodevelopmental Disorders/genetics, Receptors, N-Methyl-D-Aspartate, Epilepsy/genetics, Cerebellar Cortex, Young Adult, channelopathy, GRIN2A MUTATIONS, Research Support, N.I.H., Extramural, Journal Article, Animals, Humans, Child, EPILEPSY, Cells, Cultured, Aged, [SDV.GEN]Life Sciences [q-bio]/Genetics, SPECTRUM, learning disability, Receptors, N-Methyl-D-Aspartate/genetics, Research Support, Non-U.S. Gov't, childhood epilepsy, Cerebellar Cortex/metabolism, Infant, ENCEPHALOPATHY, Original Articles, Middle Aged, spike-wave EEG, Rats, Editor's Choice, Phenotype, NMDA, Neurodevelopmental Disorders, Child, Preschool, molecular genetics, SUBUNIT, Mutation, Female, APHASIA, Rare cancers Radboud Institute for Health Sciences [Radboudumc 9]
وصف الملف: image/pdf; application/pdf
URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::c7c4221de5d2b36826e39f9bd5d115e2
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