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1دورية أكاديمية
المؤلفون: Catarino, C. B., Liu, J. Y. W., Liagkouras, I., Gibbons, V. S., Labrum, R. W., Ellis, R., Woodward, C., Davis, M. B., Smith, S. J., Cross, J. H., Appleton, R. E., Yendle, S. C., McMahon, J. M., Bellows, S. T., Jacques, T. S., Zuberi, S. M., Koepp, M. J., Martinian, L., Scheffer, I. E., Thom, M., Sisodiya, S. M.
المصدر: Brain ; volume 134, issue 10, page 2982-3010 ; ISSN 0006-8950 1460-2156
الإتاحة: https://doi.org/10.1093/brain/awr129Test
http://academic.oup.com/brain/article-pdf/134/10/2982/17345548/awr129.pdfTest -
2دورية أكاديمية
المؤلفون: Møller, R., Heron, S., Larsen, L., Lim, C., Ricos, M., Bayly, M., Van Kempen, M., Klinkenberg, S., Andrews, I., Kelley, K., Ronen, G., Callen, D., McMahon, J., Yendle, S., Carvill, G., Mefford, H., Nabbout, R., Poduri, A., Striano, P., Baglietto, M.
مصطلحات موضوعية: KCNT1, Autosomal dominant nocturnal frontal lobe epilepsy, Epileptic encephalopathy, Cardiac arrhythmia, Sudden unexpected death in epilepsy
العلاقة: http://purl.org/au-research/grants/nhmrc/1016715Test; http://purl.org/au-research/grants/nhmrc/1032603Test; http://purl.org/au-research/grants/nhmrc/628952Test; Epilepsia, 2015; 56(9):e114-e120; http://hdl.handle.net/2440/99797Test; Heron, S. [0000-0001-8759-6748]; Smith, N. [0000-0003-2409-9239]
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3دورية أكاديمية
المؤلفون: Grinton, B., Heron, S., Pelekanos, J., Zuberi, S., Kivity, S., Afawi, Z., Williams, T., Casalaz, D., Yendle, S., Linder, I., Lev, D., Lerman-Sagie, T., Malone, S., Bassan, H., Goldberg-Stern, H., Stanley, T., Hayman, M., Calvert, S., Korczyn, A., Shevell, M.
مصطلحات موضوعية: Epilepsy, Genetics, Ion channels, Neonatal seizures, Clinical neurology
العلاقة: http://purl.org/au-research/grants/nhmrc/628952Test; http://purl.org/au-research/grants/nhmrc/466671Test; http://purl.org/au-research/grants/nhmrc/1006110Test; http://purl.org/au-research/grants/nhmrc/1016715Test; Epilepsia, 2015; 56(7):1071-1080; http://hdl.handle.net/2440/99798Test; Heron, S. [0000-0001-8759-6748]
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4مؤتمر
المؤلفون: Carvill, G. L., Heavin, S. B., Yendle, S. C., O'Roak, B. J., Cook, J., Khan, A., Dorschner, M. O., Weaver, M. A., Calvert, S., Malone, S., Wallace, G., Stanley, T., Bye, A. M., Bleasel, A., Howell, K. B., Kivity, S., Mackay, M. T., Rodriguez-Casero, V, Webster, R., Korczyn, A., Zelnick, N., Lerman-Sagie, T., Lev, D., Møller, Steensbjerre R., Andrade, D. M., Freeman, J. L., Sadleir, L. G., Shendure, J., Berkovic, S. F., Scheffer, I. E., Mefford, H. C.
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5دورية أكاديمية
المؤلفون: Heron, S., Ong, Y., Yendle, S., McMahon, J., Berkovic, S., Scheffer, I., Dibbens, L.
مصطلحات موضوعية: PRRT2, Epilepsy, Encephalopathy, Mutation
العلاقة: http://purl.org/au-research/grants/nhmrc/628952Test; http://purl.org/au-research/grants/nhmrc/1006110Test; http://purl.org/au-research/grants/nhmrc/1016715Test; http://purl.org/au-research/grants/nhmrc/1032603Test; Epilepsia, 2013; 54(5):e86-e89; http://hdl.handle.net/2440/93382Test; Heron, S. [0000-0001-8759-6748]
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6دورية أكاديمية
المؤلفون: Weckhuysen, S., Mandelstam, S., Suls, A., Audenaert, D., Deconinck, T., Claes, L., Deprez, L., Smets, K., Hristova, D., Yordanova, I., Jordanova, A., Ceulemans, B., Jansen, A., Hasaerts, D., Roelens, F., Lagae, L., Yendle, S., Stanley, T., Heron, S., Mulley, J.
مصطلحات موضوعية: Humans, Epilepsy, Benign Neonatal, Phenotype, Mutation, Child, Preschool, Female, Male, KCNQ2 Potassium Channel
العلاقة: Annals of Neurology, 2012; 71(1):15-25; http://hdl.handle.net/2440/70198Test; Heron, S. [0000-0001-8759-6748]
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7دورية أكاديمية
المؤلفون: Carranza Rojo, D., Hamiwka, L., Mcmahon, J., Dibbens, L., Arsov, T., Suls, A., Stodberg, T., Kelley, K., Wirrell, E., Appleton, B., Mackay, M., Freeman, J., Yendle, S., Berkovic, S., Bienvenu, Thierry, de Jonghe, P., Thorburn, D., Mulley, J., Mefford, H., Scheffer, I.
المساهمون: Institut Cochin (IC UM3 (UMR 8104 / U1016)), Université Paris Descartes - Paris 5 (UPD5)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)
المصدر: ISSN: 0028-3878.
مصطلحات موضوعية: [SDV.BDD]Life Sciences [q-bio]/Development Biology
العلاقة: hal-04029866; https://hal.science/hal-04029866Test
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8دورية أكاديمية
المؤلفون: Deprez, L, Weckhuysen, S, Holmgren, P, Suls, A, Van Dyck, T, Goossens, D, Del-Favero, J, Jansen, A, Verhaert, K, Lagae, Lieven, Jordanova, A, Van Coster, R, Yendle, S, Berkovic, S F, Scheffer, I, Ceulemans, Berten, De Jonghe, P
مصطلحات موضوعية: Anticonvulsants, Child, Cohort Studies, Electroencephalography, Epilepsies, Myoclonic, Female, Genome-Wide Association Study, Humans, Male, Munc18 Proteins, Mutation
العلاقة: Neurology vol:75 issue:13 pages:1159-65; https://lirias.kuleuven.be/handle/123456789/286006Test
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9دورية أكاديمية
المؤلفون: Deprez, Liesbet, Weckhuysen, Sarah, Holmgren, Philip, Suls, Arvid, Van Dyck, Tine, Goossens, Dirk, Del-Favero, Jurgen, Jansen, Anna, Verhaert, K., Lagae, L., Jordanova, Albena, van Coster, R., Yendle, S., Berkovic, S.F., Scheffer, I., Ceulemans, Berten, De Jonghe, Peter
المصدر: 0028-3878 ; Neurology
مصطلحات موضوعية: Human medicine
العلاقة: info:eu-repo/semantics/altIdentifier/isi/000282219300011
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10دورية أكاديمية
المؤلفون: White, R., Ho, G., Schmidt, S., Scheffer, I., Fischer, A., Yendle, S., Bienvenu, T., Nectoux, J., Ellaway, C., Darmanian, A., Tong, X., Cloosterman, D., Bennetts, B., Kalra, V., Fullston, T., Gecz, J., Cox, T., Christodoulou, J.
مصطلحات موضوعية: CDKL5, Rett syndrome, infantile spasms, epileptic encephalopathy, intellectual disability, mutation
العلاقة: Twin Research and Human Genetics, 2010; 13(2):168-178; http://hdl.handle.net/2440/59971Test; Fullston, T. [0000-0003-1314-3038]; Gecz, J. [0000-0002-7884-6861]
النص الكامل