1. 2005
  2. Familial Mesial Temporal Lobe Epilepsy Associated with a Deletion Mutation in the Chorea-Acanthocytosis Gene

    Andermann, E., Jansen, A., Al-Asmi, A., Dobson-Stone, C., Monaco, A., Lang, A., Robert, F., Badhwar, A., Mercho, S., Dubeau, F., Danek, A. & Andermann, F., 2005, In : Epilepsia. 46, 26th IEC PROCEEDINGS, p. 79-79 1 p.

    Research output: Contribution to journalEditorial

  3. Familial Spastic Paraplegia and the ALS2 gene

    Jansen, A., Meijer, I., Gros-Louis, F., Macgregor, D. L., Rouleau, G. A., Andermann, F., Andermann, E. & Neurology, A. A. O. (ed.), 2005, In : Neurology. 64, p. 295-295 1 p.

    Research output: Contribution to journalMeeting abstract (Journal)

  4. Filamin A mutations cause periventricular heterotopia with Ehlers-Danlos syndrome

    Sheen, V., Jansen, A., Chen, M., Parrini, E., Morgan, T., Ravenscroft, R., Ganesh, V., Underwood, T., Wiley, J., Leventer, R., Vaid, R., Ruiz, D., Hutchins, G., Menasha, J., Willner, J., Geng, Y., Gripp, K., Nicholson, L., Berry-Kravis, E., Bodell, A. & 13 others, Apse, K., Hill, R. S., Dubeau, F., Andermann, F., Barkovich, J., Andermann, E., Shugart, Y. Y., Thomas, P., Viri, M., Veggiotti, P., Robertson, S., Guerrini, R. & Walsh, C. A., 2005, In : Neurology. 64, 2, p. 254-262 9 p.

    Research output: Contribution to journalArticle

  5. Founder effect in French-Canadian chorea-acanthocytosis

    Andermann, E., Jansen, A., Andermann, F., Dubeau, F., Chouinard, S., Robert, F., Lang, A., Danek, A., Dobson-Stone, C. & Monaco, A., 2005, In : Journal of the Neurological Sciences. 238, s1, p. 151-152 2 p.

    Research output: Contribution to journalMeeting abstract (Journal)

  6. French–Canadian Chorea–Acanthocytosis

    Andermann, E., Jansen, A., Andermann, F., Dubeau, F., Chouinard, S., Robert, F., Lang, A., Danek, A., Velayos-Baeza, A., Dobson-Stone, C. & Monaco, A., 2005, In : Movement Disorders. 20, p. 1678-1678 1 p.

    Research output: Contribution to journalMeeting abstract (Journal)

  7. Leucoeneephalopathy with Vanishing White Matter as a cause of Progressive Myodonus Epilepsy

    Jansen, A., Crevaux, I., Andermann, E. & Boespflug-Tanguy, O., 2005, In : Journal of the Neurological Sciences. 238, s1, p. 90-90 1 p.

    Research output: Contribution to journalMeeting abstract (Journal)

  8. Mild Epilepsy Phenotype in TSC2 Patients with Codon 905 Mutations

    Jansen, A., Sancak, O., D'agostino, M., Badhwar, A., Roberts, P., Gobbi, G., Wilkinson, R., Melanson, D., Koenekoop, R., Gans, M., Van Den Ouweland, A. M., Nellist, M., Pandolfo, M., Sims, K., Thiele, E., Andermann, F., Dubeau, F., Kwiatkowski, D., Halley, D. & Andermann, E., 2005, In : Epilepsia. 46, 26th IEC PROCEEDINGS, p. 52-52 1 p.

    Research output: Contribution to journalEditorial

  9. Temporal Lobe Epilepsy as the Presenting Feature of Chorea–Acanthocytosis in Two French–Canadian Families

    Jansen, A., Badhwar, A., Al-Asmi, A., Danek, A., Dobson-Stone, C., Monaco, A., Chouinard, S., Shustik, C., Mercho, S., Dubeau, F., Andermann, F. & Andermann, E., 2005, In : Movement Disorders. 20, p. 1680-1681 2 p.

    Research output: Contribution to journalMeeting abstract (Journal)

  10. Vanishing white matter disease presenting as progressive myoclonus epilepsy

    Jansen, A., Creveaux, I., Andermann, E., Boespflug-Tanguy, O. & Andermann, F., 2005, In : Epilepsia. 48, Annual Meeting of the American Epilepsy Society, p. 368-368 1 p.

    Research output: Contribution to journalEditorial

  11. 2004
  12. De novo KCNQ2 mutations in patients with benign neonatal seizures.

    Claes, L., Ceulemans, B., Audenaert, D., Deprez, L., Jansen, A., Hasaerts, D., Weckx, S., Claeys, K. G., Del-Favero, J., Van Broeckhoven, C. & De Jonghe, P., 14 Dec 2004, In : Neurology. 63, p. 2155-2158 4 p.

    Research output: Contribution to journalArticle

ID: 79216