1. 2005
  2. 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)

  3. 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

  4. 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)

  5. 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

  6. 2004
  7. 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

  8. Striking intra-familial phenotypic variability and spastic paraplegia in the presence of similar homozygous expansions of the FRDA1 gene.

    Badhwar, A., Jansen, A., Andermann, F., Pandolfo, M. & Andermann, E., 1 Dec 2004, In : Movement Disorders. 19, p. 1424-1431 8 p.

    Research output: Contribution to journalArticle

  9. Neuropathological basis of polymicrogyria

    Jansen, A., Andermann, F., Valerio, R., Guerrini, R., Leventer, R., Robitaille, Y., Meencke, H. J., Dubeau, F. & Andermann, E., Dec 2004, In : Epilepsia. 45, p. 33-33 1 p.

    Research output: Contribution to journalMeeting abstract (Journal)

  10. Biparental inheritance in idiopathic generalized epilepsy

    Jansen, A., Andermann, E. & Andermann, F., 1 Oct 2004, In : Epilepsia. 45, p. 1294-1295 2 p.

    Research output: Contribution to journalArticle

  11. COGNITIVE FUNCTIONING IN BILATERAL PERISYLVIAN POLYMICROGYRIA

    Jansen, A., Leonard, G., Bastos, A., Tampieri, D., Watkins, K., Andermann, F. & Andermann, E., 2004, In : Epilepsia. 45, s7, p. 180-181 2 p.

    Research output: Contribution to journalMeeting abstract (Journal)

  12. DELETION MUTATION IN THE CHAC GENE CAUSING FAMILIAL TEMPORAL LOBE EPILEPSY

    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., 2004, In : Epilepsia. 45, s7, p. 357-358 2 p.

    Research output: Contribution to journalMeeting abstract (Journal)

ID: 79216