Participations à des congrès et colloques internationaux (7)

1. Naeije, G., Goldman, S., Pandolfo, M., & De Tiege, X. (2017). Cortical processing of tactile novelty detection in Friedreich ataxia (P2. 203). Neurology. Vol. 88 (p. P2. 203) Abstract session presented at American Academy of Neurology(Boston).
2. Naeije, G., Pandolfo, M., & De Tiege, X. (2017). Corticokinematic coherence is decreased in patients with Friedreich Ataxia and correlates with GAA1 expansion (S5. 002). Neurology. Vol. 88 (p. S5. 002) Abstract session presented at American Academy of Neurology(Boston).
3. Naeije, G., Mavroudakis, N., & Pandolfo, M. (2016). Evoked motor potentials in genetically proven Friedreich’s ataxia patients. frontiers in aging neuroscience Abstract session presented at Belgian Brain Council(Mons)
4. Remiche, G., Abramowicz, M., & Pandolfo, M. (2016). Is late-onset type II glycogenosis underdiagnosed in Brussels and Wallonia (Belgium)? Neuromuscular disorders,(26), P.62.
5. Igoillo Esteve, M., Serroukh, Y., Rai, M., Depondt, C., Musuaya, A., Ladrière, L., Marhfour, I., Marchetti, P., Koeppen, A., Pandolfo, M., Eizirik, D. L., & Fery, F. (2011). Pancreatic beta-cell dysfunction and death cause diabetes in Friedreich’s ataxia. Paper session presented at 21st Meeting of the Belgian Endocrine Society (2011: Leuven. Belgium).
6. Remiche, G., Kentos, A., Pandolfo, M., & Mavroudakis, N. (2006). DADS syndrome associated with anti-GM1 antibodies.(13), 232 Abstract session presented at European Federation of Neurological Societies (EFNS)(10: 2-5 septembre 2006: Glasgow, Royaume-Uni).
7. Pandolfo, M., Manto, M., & Lubicz, B. (2002). Cerebellar atrophy with hypercupremia: a new recessive ataxia. Paper session presented at American Academy of Neurology 2002.

Divers (5)

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