Search Results - Hache, J.C

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  1. 1
    Autonomic and respiratory dysfunction in Charcot–Marie–Tooth disease due to Thr124Met mutation in the myelin protein zero gene

    Autonomic and respiratory dysfunction in Charcot–Marie–Tooth disease due to Thr124Met mutation in the myelin protein zero gene by Stojkovic, T, de Seze, J, Dubourg, O, Arne-Bes, M.C, Tardieu, S, Hache, J.C, Vermersch, P

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  2. 2
    Visual evoked potentials study in chronic idiopathic inflammatory demyelinating polyneuropathy

    Visual evoked potentials study in chronic idiopathic inflammatory demyelinating polyneuropathy by Stojkovic, T, de Seze, J, Hurtevent, J.F, Arndt, C, Beaume, A, Hache, J.C, Vermersch, P

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  3. 3
    Pupillary disturbances in multiple sclerosis: correlation with MRI findings

    Pupillary disturbances in multiple sclerosis: correlation with MRI findings by de Seze, J., Arndt, C., Stojkovic, T., Ayachi, M., Gauvrit, J.Y., Bughin, M., Saint Michel, T., Pruvo, J.P., Hache, J.C., Vermersch, P.

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  4. 4
    Identification of novel VMD2 gene mutations in patients with best vitelliform macular dystrophy

    Identification of novel VMD2 gene mutations in patients with best vitelliform macular dystrophy by Marchant, D., Gogat, K., Boutboul, S., Péquignot, M., Sternberg, C., Dureau, P., Roche, O., Uteza, Y., Hache, J.C., Puech, B., Puech, V., Dumur, V., Mouillon, M., Munier, F.L., Schorderet, D.F., Marsac, C., Dufier, J.L., Abitbol, M.

    Published in Human mutation
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  5. 5
    Identification of novel VMD2 gene mutations in patients with best vitelliform macular dystrophy: Mutations in Brief

    Identification of novel VMD2 gene mutations in patients with best vitelliform macular dystrophy: Mutations in Brief by Marchant, D., Gogat, K., Boutboul, S., Péquignot, M., Sternberg, C., Dureau, P., Roche, O., Uteza, Y., Hache, J.C., Puech, B., Puech, V., Dumur, V., Mouillon, M., Munier, F.L., Schorderet, D.F., Marsac, C., Dufier, J.L., Abitbol, M.

    Published in Human mutation
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  6. 6
    Use of denaturing HPLC and automated sequencing to screen the VMD2 gene for mutations associated with Best's vitelliform macular dystrophy

    Use of denaturing HPLC and automated sequencing to screen the VMD2 gene for mutations associated with Best's vitelliform macular dystrophy by Marchant, D., Gogat, K., Dureau, P., Sainton, K., Sternberg, C., Gadin, S., Dollfus, H., Brasseur, G., Hache, J.C., Dumur, V., Puech, V., Munier, F.L., Schorderet, D.F., Marsac, C., Menasche, M., Dufier, J.L., Abitbol, M.

    Published in Ophthalmic genetics
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  7. 7
    P-3-8 Eye fixations and recognition memory in schizophrenia

    P-3-8 Eye fixations and recognition memory in schizophrenia by Fleury, E., Buquet, C., Thomas, P., Goudemand, M., Hache, J.C., Charlier, J.R.

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  8. 8
    P-1-13 Eye fixations and recognition memory in depression

    P-1-13 Eye fixations and recognition memory in depression by Fleury, E., Buquet, C., Thomas, P., Goudemand, M., Hache, J.C., Charlier, J.R.

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  9. 9
    Ultrafast transient optical spectroscopy in liquid water

    Ultrafast transient optical spectroscopy in liquid water by Lascoux, N., Gallot, G., Gale, G.M., Hache, F., Bratos, S., Leicknam, J.C.

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