Correspondence between the molecular genetic analysis and electron microscopic detection of granular osmiophilic material in CADASIL by Mykkänen, K, Ihalainen, S, Ruchoux, M.M, Baumann, M, Bergholm, R, Junna, M, Kääriäinen, H, Pöyhönen, M, Viitanen, M, Kalimo, H

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Could the pale, soft, and exudative condition be explained by distinctive histological characteristics? by Franck, M, Figwer, P, Godfraind, C, Poirel, M.T, Khazzaha, A, Ruchoux, M.M

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Outcome of children treated with preradiation chemotherapy for a high-grade glioma: Results of a French Society of Pediatric Oncology (SFOP) pilot study by Chastagner, P., Kalifa, C., Doz, F., Bouffet, E., Gentet, J.C., Ruchoux, M.M., Bracard, S., Desandes, E., Frappaz, D.

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Short stature, abnormal face, joint laxity, dislocation, hernias, delayed bone age, and severe psychomotor retardation in two brothers: Previously undescribed MCA/MR syndrome by Mégarbané, André, Ruchoux, M.M., Loeys, B., Ayoub, N., Nuytinck, L.

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Schwannome intraventriculaire : à propos d’un cas by Leveque, M., Gilliard, C., Godfraind, C., Ruchoux, M.M., Gustin, T.

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Pin1, marqueur précoce de l’agrégation des protéines tau by Maurage, C.A., Sambo, A.V., Hamdame, M., Ruchoux, M.M., Delacourte, A., Buée, L.

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New autosomal recessive cerebellar ataxia disorder in a large inbred Lebanese family by Mégarbané, A., Delague, V., Ruchoux, M.M., Rizkallah, E., Maurage, C.A., Viollet, L., Rouaix-Emery, N., Urtizberea, A.

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Dysplasie du cortex cérébelleux : aspects en IRM et signification by Soto Ares, G., Deries, B., Delmaire, C., Devisme, L., Ruchoux, M.M., Pruvo, J-P.

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