King's College London

Research portal

Dr Elaine Hughes

  1. Phenotypic and genetic spectrum of epilepsy with myoclonic atonic seizures

    EuroEPINOMICS RES Consortium, 1 May 2020, In: Epilepsia. 61, 5, p. 995-1007 13 p.

    Research output: Contribution to journalArticlepeer-review

  2. Centromedian thalamic nuclei deep brain stimulation and Anakinra treatment for FIRES – Two different outcomes

    Sa, M., Singh, R., Pujar, S., D'arco, F., Desai, N., Eltze, C., Hughes, E., Al Obaidi, M., Eleftheriou, D., Tisdall, M., Selway, R., Cross, J. H., Kaliakatsos, M. & Valentin, A., 1 Sep 2019, In: European Journal of Paediatric Neurology. 23, 5, p. 749-754

    Research output: Contribution to journalArticlepeer-review

  3. Clinical spectrum of STX1B -related epileptic disorders

    Wolking, S., May, P., Mei, D., Møller, R. S., Balestrini, S., Helbig, K. L., Altuzarra, C. D., Chatron, N., Kaiwar, C., Stöhr, K., Widdess-Walsh, P., Mendelsohn, B. A., Numis, A., Cilio, M. R., Van Paesschen, W., Svendsen, L. L., Oates, S., Hughes, E., Goyal, S., Brown, K. & 31 others, Sifuentes Saenz, M., Dorn, T., Muhle, H., Pagnamenta, A. T., Vavoulis, D. V., Knight, S. J. L., Taylor, J. C., Canevini, M. P., Darra, F., Gavrilova, R. H., Powis, Z., Tang, S., Marquetand, J., Armstrong, M., McHale, D., Klee, E. W., Kluger, G. J., Lowenstein, D. H., Weckhuysen, S., Pal, D. K., Helbig, I., Guerrini, R., Thomas, R. H., Rees, M. I., Lesca, G., Sisodiya, S. M., Weber, Y. G., Lal, D., Marini, C., Lerche, H. & Schubert, J., 12 Mar 2019, In: Neurology. 92, 11, p. E1238-E1249

    Research output: Contribution to journalArticlepeer-review

  4. Incorporating epilepsy genetics into clinical practice: A 360° evaluation

    Oates, S., Tang, S., Rosch, R., Lear, R., Hughes, E. F., Williams, R. E., Larsen, L. H. G., Hao, Q., Dahl, H. A., Møller, R. S. & Pal, D. K., 10 May 2018, In: NPJ Genomic medicine. 3, 1

    Research output: Contribution to journalArticlepeer-review

  5. Epilepsy in patients with GRIN2A alterations: Genetics, neurodevelopment, epileptic phenotype and response to anticonvulsive drugs

    von Stülpnagel, C., Ensslen, M., Møller, R. S., Pal, D. K., Masnada, S., Veggiotti, P., Piazza, E., Dreesmann, M., Hartlieb, T., Herberhold, T., Hughes, E., Koch, M., Kutzer, C., Hoertnagel, K., Nitanda, J., Pohl, M., Rostásy, K., Haack, T. B., Stöhr, K., Kluger, G. & 1 others, Borggraefe, I., 14 Jan 2017, In: European Journal of Paediatric Neurology.

    Research output: Contribution to journalArticlepeer-review

  6. N-methyl-D-aspartate receptor antibody-associated movement disorder without encephalopathy

    Hacohen, Y., Dlamini, N., Hedderly, T., Hughes, E., Woods, M., Vincent, A. & Lim, M., Feb 2014, In: Developmental Medicine and Child Neurology. 56, 2, p. 190-193 4 p.

    Research output: Contribution to journalArticlepeer-review

  7. Mutations in GRIN2A cause idiopathic focal epilepsy with rolandic spikes

    Lemke, J. R., Lal, D., Reinthaler, E. M., Steiner, I., Nothnagel, M., Alber, M., Geider, K., Laube, B., Schwake, M., Finsterwalder, K., Franke, A., Schilhabel, M., Jähn, J. A., Muhle, H., Boor, R., Van Paesschen, W., Caraballo, R., Fejerman, N., Weckhuysen, S., De Jonghe, P. & 51 others, Larsen, J., Møller, R. S., Hjalgrim, H., Addis, L., Tang, S., Hughes, E., Pal, D. K., Veri, K., Vaher, U., Talvik, T., Dimova, P., Guerrero López, R., Serratosa, J. M., Linnankivi, T., Lehesjoki, A-E., Ruf, S., Wolff, M., Buerki, S., Wohlrab, G., Kroell, J., Datta, A. N., Fiedler, B., Kurlemann, G., Kluger, G., Hahn, A., Haberlandt, D. E., Kutzer, C., Sperner, J., Becker, F., Weber, Y. G., Feucht, M., Steinböck, H., Neophythou, B., Ronen, G. M., Gruber-Sedlmayr, U., Geldner, J., Harvey, R. J., Hoffmann, P., Herms, S., Altmüller, J., Toliat, M. R., Thiele, H., Nürnberg, P., Wilhelm, C., Stephani, U., Helbig, I., Lerche, H., Zimprich, F., Neubauer, B. A., Biskup, S. & von Spiczak, S., Sep 2013, In: Nature Genetics. 45, 9, p. 1067-1072 6 p.

    Research output: Contribution to journalArticlepeer-review

  8. Paediatric autoimmune encephalopathies: clinical features, laboratory investigations and outcomes in patients with or without antibodies to known central nervous system autoantigens

    Hacohen, Y., Wright, S., Waters, P., Agrawal, S., Carr, L., Cross, H., De Sousa, C., DeVile, C., Fallon, P., Gupta, R., Hedderly, T., Hughes, E., Kerr, T., Lascelles, K., Lin, J-P., Philip, S., Pohl, K., Prabahkar, P., Smith, M., Williams, R. & 5 others, Clarke, A., Hemingway, C., Wassmer, E., Vincent, A. & Lim, M., Jul 2013, In: Journal of Neurology, Neurosurgery and Psychiatry. 84, 7, p. 748-755 8 p.

    Research output: Contribution to journalArticlepeer-review

  9. Migrating partial seizures of infancy: expansion of the electroclinical, radiological and pathological disease spectrum

    McTague, A., Appleton, R., Avula, S., Cross, J. H., King, M. D., Jacques, T. S., Bhate, S., Cronin, A., Curran, A., Desurkar, A., Farrell, M. A., Hughes, E., Jefferson, R., Lascelles, K., Livingston, J., Meyer, E., McLellan, A., Poduri, A., Scheffer, I. E., Spinty, S. & 2 others, Kurian, M. A. & Kneen, R., May 2013, In: Brain. 136, 5, p. 1578-1591 14 p.

    Research output: Contribution to journalArticlepeer-review

  10. Molybdenum cofactor deficiency presenting with a parkinsonism-dystonia syndrome

    Alkufri, F., Harrower, T., Rahman, Y., Hughes, E., Mundy, H., Knibb, J. A., Moriarty, J., Connor, S. & Samuel, M., Mar 2013, In: Movement Disorders. 28, 3, p. 399-401 3 p.

    Research output: Contribution to journalLetterpeer-review

  11. Mortality Rates and Causes of Death in Children with Epilepsy Prescribed Antiepileptic Drugs A Retrospective Cohort Study using the UK General Practice Research Database

    Ackers, R., Besag, F. M. C., Hughes, E., Squier, W., Murray, M. L. & Wong, I. C. K., May 2011, In: Drug Safety. 34, 5, p. 403-413 11 p.

    Research output: Contribution to journalArticlepeer-review

  12. Encephalopathy and SCN1A mutations

    Tang, S., Lin, J-P., Hughes, E., Siddiqui, A., Lim, M. & Lascelles, K., Apr 2011, In: Epilepsia. 52, 4, p. E26-E30 5 p.

    Research output: Contribution to journalArticlepeer-review

  13. Paroxysmal disorders in infancy: a diagnostic challenge

    Besag, F. M. C. & Hughes, E., Nov 2010, In: Developmental Medicine and Child Neurology. 52, 11, p. 980-981 2 p.

    Research output: Contribution to journalEditorialpeer-review

  14. Trihexyphenidyl for Acute Life-Threatening Episodes Due to a Dystonic Movement Disorder in Rett Syndrome

    Gika, A. D., Hughes, E., Goyal, S., Sparkes, M. & Lin, J-P., 15 Feb 2010, In: Movement Disorders. 25, 3, p. 385-389 5 p.

    Research output: Contribution to journalArticlepeer-review

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