نتائج البحث - P J Willems

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  1. 1
    Evaluation of the Association Between Gastric Acid Suppression and Risk of Intestinal Colonization With Multidrug-Resistant Microorganisms

    Evaluation of the Association Between Gastric Acid Suppression and Risk of Intestinal Colonization With Multidrug-Resistant Microorganisms حسب Roel P J Willems, Karin van Dijk, Johannes C. F. Ket, Christina M. J. E. Vandenbroucke‐Grauls

    منشور في 2020
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    Revisão
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  2. 2
    Homocysteine lowering by B vitamins and the secondary prevention of deep vein thrombosis and pulmonary embolism: a randomized, placebo-controlled, double-blind trial

    Homocysteine lowering by B vitamins and the secondary prevention of deep vein thrombosis and pulmonary embolism: a randomized, placebo-controlled, double-blind trial حسب Martin den Heijer, Huub P J Willems, Henk J. Blom, W.B.J. Gerrits, Marco Cattaneo, Sabine Eichinger, Frits R. Rosendaal, Gerard M.J. Bos

    منشور في 2006
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    Artigo
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  3. 3
    Paget's Disease of Bone: Evidence for a Susceptibility Locus on Chromosome 18q and for Genetic Heterogeneity

    Paget's Disease of Bone: Evidence for a Susceptibility Locus on Chromosome 18q and for Genetic Heterogeneity حسب Sonya I. Haslam, Wim Van Hul, Antonio Morales‐Piga, Wendy Balemans, J. L. San-Millan, Kiyoshi Nakatsuka, P J Willems, Neva E. Haites, Stuart H. Ralston

    منشور في 1998
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    Artigo
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  4. 4
    Gut colonisation by extended-spectrum β-lactamase-producing Escherichia coli and its association with the gut microbiome and metabolome in Dutch adults: a matched case-control study

    Gut colonisation by extended-spectrum β-lactamase-producing Escherichia coli and its association with the gut microbiome and metabolome in Dutch adults: a matched case-control stud... حسب Quinten R. Ducarmon, Romy D. Zwittink, Roel P J Willems, Aswin Verhoeven, Sam Nooij, Fiona van der Klis, Eelco Franz, Jolanda Kool, Martin Giera, Christina M. J. E. Vandenbroucke‐Grauls, Susana Fuentes, Ed J. Kuijper

    منشور في 2022
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    Artigo
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  5. 5
    Mutations in the EXT1 and EXT2 Genes in Hereditary Multiple Exostoses

    Mutations in the EXT1 and EXT2 Genes in Hereditary Multiple Exostoses حسب Wim Wuyts, Wim Van Hul, Kristel De Boulle, Jan Hendrickx, Egbert Bakker, Filip Vanhoenacker, Florindo Mollica, Hermann‐Josef Lüdecke, Bekir Sıtkı Şayli, Ugo E. Pazzaglia, Geert Mortier, B Hamel, Ernest U. Conrad, Mark Matsushita, W H Raskind, P J Willems

    منشور في 1998
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    Artigo
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  6. 6
    Adult-onset autoinflammation caused by somatic mutations in UBA1: A Dutch case series of patients with VEXAS

    Adult-onset autoinflammation caused by somatic mutations in UBA1: A Dutch case series of patients with VEXAS حسب Caspar I. van der Made, Judith Potjewijd, Annemiek Hoogstins, Huub P J Willems, Arjan J. Kwakernaak, Ruud G.L. de Sévaux, Paul Van Daele, Annet Simons, Marloes W Heijstek, David B. Beck, Mihai G. Netea, Pieter van Paassen, A. Elizabeth Hak, Lars T. van der Veken, Mariëlle van Gijn, Alexander Hoischen, Frank L. van de Veerdonk, Helen L. Leavis, Abraham Rutgers

    منشور في 2021
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    Artigo
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  7. 7
    Novel Mutations Including Deletions of the Entire<i>OFD1</i>Gene in 30 Families with Type 1 Orofaciodigital Syndrome: A Study of the Extensive Clinical Variability

    Novel Mutations Including Deletions of the Entire<i>OFD1</i>Gene in 30 Families with Type 1 Orofaciodigital Syndrome: A Study of the Extensive Clinical Variability حسب Izak Johannes Bisschoff, Christine Zeschnigk, Denise Horn, Brigitte Wellek, Angelika Rieß, M.W. Wessels, P J Willems, Peter Bjødstrup Jensen, Andreas Busche, Jens Bekkebraten, Maya Chopra, Hanne Hove, Christina Evers, Ketil Heimdal, Ann-Sophie Kaiser, Erdmut Kunstmann, Kristina Lagerstedt‐Robinson, Maja Linné, Patricia Martín, James McGrath, Winnie Pradel, Katrina Prescott, Bernd Roesler, Goražd Rudolf, Ulrike Siebers‐Renelt, Nataliya Tyshchenko, Dagmar Wieczorek, G. Wolff, William B. Dobyns, Deborah Morris‐Rosendahl

    منشور في 2012
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    Artigo
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  8. 8
    Sporadic Imprinting Defects in Prader-Willi Syndrome and Angelman Syndrome: Implications for Imprint-Switch Models, Genetic Counseling, and Prenatal Diagnosis

    Sporadic Imprinting Defects in Prader-Willi Syndrome and Angelman Syndrome: Implications for Imprint-Switch Models, Genetic Counseling, and Prenatal Diagnosis حسب Karin Buiting, Bärbel Dittrich, Stephanie Groß, Christina Lich, Claudia Färber, Tina Buchholz, Ellie Smith, André Reis, Joachim Bürger, Markus M. Nöthen, U. Barth-Witte, Bart Janssen, Dvorah Abeliovich, Israela Lerer, Ans M.W. van den Ouweland, Dicky Halley, Connie Schrander‐Stumpel, H.J.M. Smeets, Peter Meinecke, Sue Malcolm, Anne Gardner, Marc Lalande, Robert D. Nicholls, K. Friend, Astrid Schulze, Gert Matthijs, Hannaleena Kokkonen, P Hilbert, Lionel Van Maldergem, G. Glóver, Pablo Carbonell, P J Willems, Gabriele Gillessen-Kaesbach, Bernhard Horsthemke

    منشور في 1998
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    Artigo
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