Search Results - Hallerud, M.

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  1. 1
    Molecular genetic analysis of long QT syndrome in Norway indicating a high prevalence of heterozygous mutation carriers

    Molecular genetic analysis of long QT syndrome in Norway indicating a high prevalence of heterozygous mutation carriers by Berge, K. E., Haugaa, K. H., Früh, A., Anfinsen, O.-G., Gjesdal, K., Siem, G., Øyen, N., Greve, G., Carlsson, A., Rognum, T. O., Hallerud, M., Kongsgård, E., Amlie, J. P., Leren, T. P.

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  2. 2
    Patent ductus venosus does not lead to alimentary galactosaemia in preterm infants

    Patent ductus venosus does not lead to alimentary galactosaemia in preterm infants by Fugelseth, D, Guthenberg, C, Hagenfeldt, L, Liestol, K, Hallerud, M, Lindemann, R

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    Patent ductus venosus does not lead to alimentary galactosaemia in preterm infants

    Patent ductus venosus does not lead to alimentary galactosaemia in preterm infants by Fugelseth, D, Guthenberg, C, Hagenfeldt, L, Liestøl, K, Hallerud, M, Lindemann, R

    Published in Acta Paediatrica
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