Search Results - Heuvel, Bernadette Van Den

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  1. 1
    Facilitating cooperation through promotion of good practices

    Facilitating cooperation through promotion of good practices by De Nutte, Hilde, Van Den Heuvel, Bernadette, De Vuyst, Karen, Leenders, Jo, Peeters, Mathias, Viaene, Mineke, Taerwe, Timothy

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  2. 2
    Health and Social Care Policy for the Elderly in Belgium

    Health and Social Care Policy for the Elderly in Belgium by Arnaert, Antonia, Heuvel, Bernadette Van Den, Windey, Tarsi

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  3. 3
    A novel mutation in COQ2 leading to fatal infantile multisystem disease

    A novel mutation in COQ2 leading to fatal infantile multisystem disease by Jakobs, Bernadette S, van den Heuvel, Lambert P, Smeets, Roel J.P, de Vries, Maaike C, Hien, Steffen, Schaible, Thomas, Smeitink, Jan A.M, Wevers, Ron A, Wortmann, Saskia B, Rodenburg, Richard J.T

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    Differential effects of 670 and 830 nm red near infrared irradiation therapy: a comparative study of optic nerve injury, retinal degeneration, traumatic brain and spinal cord injury

    Differential effects of 670 and 830 nm red near infrared irradiation therapy: a comparative study of optic nerve injury, retinal degeneration, traumatic brain and spinal cord injur... by Giacci, Marcus K, Wheeler, Lachlan, Lovett, Sarah, Dishington, Emma, Majda, Bernadette, Bartlett, Carole A, Thornton, Emma, Harford-Wright, Elizabeth, Leonard, Anna, Vink, Robert, Harvey, Alan R, Provis, Jan, Dunlop, Sarah A, Hart, Nathan S, Hodgetts, Stuart, Natoli, Riccardo, Van Den Heuvel, Corinna, Fitzgerald, Melinda

    Published in PloS one
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  5. 5
    A common point mutation in the tyrosine hydroxylase gene in autosomal recessive L-DOPA-responsive dystonia in the Dutch population

    A common point mutation in the tyrosine hydroxylase gene in autosomal recessive L-DOPA-responsive dystonia in the Dutch population by VAN DEN HEUVEL, L. P. W. J, LUITEN, B, SMEITINK, J. A. M, DE RIJK-VAN ANDEL, J. F, HYLAND, K, STEENBERGEN-SPANJERS, G. C. H, JANSSEN, R. J. T, WEVERS, R. A

    Published in Human genetics
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