Search Results - Triki, C., Dr

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  1. 1
    Exploration de la cause génétique des myopathies mitochondriales par l’étude moléculaire des gènes candidats mitochondriaux

    Exploration de la cause génétique des myopathies mitochondriales par l’étude moléculaire des gènes candidats mitochondriaux by Ghorbel, R, Triki, C., Dr, Hachicha, M., Dr, Keskes-Ammar, L., Pr, Fakhfakh, F., Pr

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  2. 2
    Phenotypic variability in a Tunisian family with X-linked adrenoleukodystrophy caused by the p.Gln316Pro novel mutation

    Phenotypic variability in a Tunisian family with X-linked adrenoleukodystrophy caused by the p.Gln316Pro novel mutation by Kallabi, F., Dr, Ellouz, E., Dr, Kaabechi, N., Pr, Keskes, L., Pr, Triki, C., Pr, Kamoun, H., Pr

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  3. 3
    Interest of early management of children with cerebral palsy within a specialized network

    Interest of early management of children with cerebral palsy within a specialized network by Ghroubi, S., Prof, Elleuch, W., Dr, Alila, S., Dr, Kammoun, F., Prof, Hmida, N., Prof, Triki, C., Prof, Elleuch, M.H., Prof

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  4. 4
    Interest of neuromotor assessment in early screening of children at high risk for cerebral palsy within a specialized network

    Interest of neuromotor assessment in early screening of children at high risk for cerebral palsy within a specialized network by Ghroubi, S., Prof, Elleuch, W., Dr, Mahersi, S., Dr, Kammoun, F., Prof, Hmida, N., Prof, Triki, C., Prof, Elleuch, M.H., Prof

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