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Displaying 4 results.
    • Journal article
    Myopathy and phosphorylase kinase deficiency caused by a mutation in the PHKA1 gene
    Wuyts, W. Reyniers, E Ceuterick, C. Storm, K. de Barsy, Thierry[UCL] Martin, JJ. (2005) American Journal of Medical Genetics. Part A — Vol. 133A, no. 1, p. 82-4 (2005)
    • Journal article
    Intact satellite cells lead to remarkable protection against Smn gene defect in differentiated skeletal muscle
    Nicole, S Desforges, B Millet, G Lesbordes, J Cifuentes-Diaz, C Vertes, D Cao, ML. De Backer, Fabienne[UCL] Languille, L Roblot, N Joshi, V Gillis, Jean-Marie[UCL] Melki, J. (2003) The Journal of Cell Biology — Vol. 161, no. 3, p. 571-82 (2003)
    • Journal article
    Duane anomaly, congenital myopathy and severe scoliosis in sibs: new AR syndrome?
    Verloes, A. Misson, JP. Gillet, P Baumann, C Spiritus, Micheline[UCL] Deprez, M (2003) Annales de génétique — Vol. 46, no. 4, p. 449-452 (2003)
    • Journal article
    Prise en charge anesthésique d'un enfant atteint de deltasarcoglycanopathie
    Moro, C. Dangelser, G. Veyckemans, Francis[UCL] (2007) Annales françaises d'anesthésie et de réanimation - AFAR — Vol. 26, no. 4, p. 359-62 (2007)