A new mechanism of dominance in hypophosphatasia: the mutated protein can disturb the cell localization of the wild-type protein von Lia-Baldini, A. S., Brun-Heath, I., Carrion, C., Simon-Bouy, B., Serre, J. L., Nunes, M. E., Mornet, E.

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Treatment Response and Outcomes in Post-transplantation Lymphoproliferative Disease vs Lymphoma in Immunocompetent Patients von Trusson, R, Serre, J.E, Szwarc, I, Brunot, V, Garrigue, V, Delmas, S, Kanouni, T, Cartron, G, Mourad, G

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A molecular approach to dominance in hypophosphatasia von Lia-Baldini, A S, Muller, F, Taillandier, A, Gibrat, J F, Mouchard, M, Robin, B, Simon-Bouy, B, Serre, J L, Aylsworth, A S, Bieth, E, Delanote, S, Freisinger, P, Hu, J C, Krohn, H P, Nunes, M E, Mornet, E

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A novel locus for autosomal recessive primary torsion dystonia (DYT17) maps to 20p11.22–q13.12 von Chouery, E., Kfoury, J., Delague, V., Jalkh, N., Bejjani, P., Serre, J. L., Mégarbané, A.

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Hasse principle for $ G$-trace forms von Bayer-Fluckiger, Eva, Parimala, Raman, Serre, Jean-Pierre

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Childhood Hypophosphatasia Due to a de Novo Missense Mutation in the Tissue-Nonspecific Alkaline Phosphatase Gene von Taillandier, A., Sallinen, S.-L., Brun-Heath, I., De Mazancourt, P., Serre, J.-L., Mornet, E.

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Severe hypophosphatasia: Characterization of fifteen novel mutations in the ALPL gene von Spentchian, M., Merrien, Y., Herasse, M., Dobbie, Z., Gläser, D., Holder, S. E., Ivarsson, S-A., Kostiner, D., Mansour, S., Norman, A., Roth, J., Stipoljev, F., Taillemite, J-L., van der Smagt, J. J., Serre, J-L., Simon-Bouy, B., Taillandier, A., Mornet, E.

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Guide to good practices to ensure privacy protection in secondary use of medical records von Riou, C., Fresson, J., Serre, J.L., Avillach, P., Leneveut, L., Quantin, C.

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Le diagnostic prénatal n’est pas de l’eugénisme von Simon-Bouy, B., Serre, J.-L.

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Correlations of Genotype and Phenotype in Hypophosphatasia von Zurutuza, L., Muller, F., Gibrat, J.F., Taillandier, A., Simon-Bouy, B., Serre, L., Mornet, E.

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A mini-invasive approach to renal autotransplantation in the management of loin pain hematuria syndrome von Almaiman, H, Serre, J E, Abid, N, Fouque, D, Martin, X

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A Course in Arithmetic von Serre, J-P

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A case of lethal hypophosphatasia providing new insights into the perinatal benign form of hypophosphatasia and expression of the ALPL gene von Brun-Heath, I, Chabrol, E, Fox, M, Drexler, K, Petit, C, Taillandier, A, De Mazancourt, P, Serre, J-L, Mornet, E

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The prenatal diagnosis is not the eugenics von Simon-Bouy, B, Serre, J-L

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Modular Functions of One Variable III: Proceedings International Summer School, University of Antwerp, RUCA, July 17 - August 3, 1972 von Kuyk, Willem, Serre, J.-P

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Existence of a genetic risk factor on chromosome 5q in Italian Coeliac Disease families von GRECO, L., BABRON, M. C., CORAZZA, G. R., PERCOPO, S., SICA, R., CLOT, F., FULCHIGNONI-LATAUD, M. C., ZAVATTARI, P., MOMIGLIANO-RICHIARDI, P., CASARI, G., GASPARINI, P., TOSI, R., MANTOVANI, V., DE VIRGILIIS, S., IACONO, G., D'ALFONSO, A., SELINGER-LENEMAN, H., LEMAINQUE, A., SERRE, J. L., CLERGET-DARPOUX, F.

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Amélioration de la couverture vaccinale antipneumococcique chez les patients pris en charge pour une maladie systémique grâce à un programme de vaccination mené par les infirmières... von Serre, J., Goulenok, T., Francois, C., Vanderhaegen, M.C., Alexandra, J.F., Papo, T., Sacré, K.

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Characterization of 11 novel mutations in the tissue non-specific alkaline phosphatase gene responsible for hypophosphatasia and genotype–phenotype correlations von Brun-Heath, Isabelle, Taillandier, Agnes, Serre, Jean-Louis, Mornet, Etienne

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Screening of the C677T mutation on the methylenetetrahydrofolate reductase gene in French patients with neural tube defects von MORNET, E, MULLER, F, LENVOISE-FURET, A, DELEZOIDE, A.-L, COL, J.-Y, SIMON-BOUY, B, SERRE, J.-L

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Epidémiologie du syndrome néphrotique idiopathique de l’enfant en Indre et Loire : étude rétrospective sur 30 ans von Serre, J., Prat, L., Merieau, E., Cloarec, S., Benoit, S., Halimi, J.-M.

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