Hasil Pencarian - Kathelijn Keymolen

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  1. 1
    Pancreas and gallbladder agenesis in a newborn with semilobar holoprosencephaly, a case report

    Pancreas and gallbladder agenesis in a newborn with semilobar holoprosencephaly, a case report oleh Robert Hilbrands, Kathelijn Keymolen, Alex Michotte, Miriam Marichal, Filip Cools, Anieta Goossens, Peter In’t Veld, Jean De Schepper, Andrew Hattersley, Harry Heimberg

    Diterbitkan 2017-05-01
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  2. 2
    Cleavage-stage or blastocyst-stage embryo biopsy has no impact on growth and health in children up to 2 years of age

    Cleavage-stage or blastocyst-stage embryo biopsy has no impact on growth and health in children up to 2 years of age oleh Florence Belva, Fiskani Kondowe, Anick De Vos, Kathelijn Keymolen, Andrea Buysse, Frederik Hes, Veerle Berckmoes, Pieter Verdyck, Willem Verpoest, Martine De Rycke

    Diterbitkan 2023-09-01
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  3. 3
    A prenatal case of lissencephaly with cerebellar hypoplasia: New mutation in RELN gene

    A prenatal case of lissencephaly with cerebellar hypoplasia: New mutation in RELN gene oleh Claire Balza, Giulia Garofalo, Teresa Cos, Julie Désir, Xin Kang, Kathelijn Keymolen, Julie Soblet, Kim Van Berkel, Catheline Vilain, Wafa Ben Abbou, Marie Cassart

    Diterbitkan 2021-12-01
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  4. 4
    A focused 35-minute whole body MRI screening protocol for patients with von Hippel-Lindau disease

    A focused 35-minute whole body MRI screening protocol for patients with von Hippel-Lindau disease oleh Anne-Marie Vanbinst, Carola Brussaard, Evelynn Vergauwen, Vera Van Velthoven, Robert Kuijpers, Olaf Michel, Ina Foulon, Anna C. Jansen, Bieke Lefevere, Susanne Bohler, Kathelijn Keymolen, Johan de Mey, Dirk Michielsen, Corina E. Andreescu, Sven Gläsker

    Diterbitkan 2019-07-01
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  5. 5
    Central nervous system gadolinium accumulation in patients undergoing periodical contrast MRI screening for hereditary tumor syndromes

    Central nervous system gadolinium accumulation in patients undergoing periodical contrast MRI screening for hereditary tumor syndromes oleh Evelynn Vergauwen, Anne-Marie Vanbinst, Carola Brussaard, Peter Janssens, Dieter De Clerck, Michel Van Lint, Anne C. Houtman, Olaf Michel, Kathelijn Keymolen, Bieke Lefevere, Susanne Bohler, Dirk Michielsen, Anna C. Jansen, Vera Van Velthoven, Sven Gläsker

    Diterbitkan 2018-01-01
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  6. 6
    Congenital hydrocephalus: new Mendelian mutations and evidence for oligogenic inheritance

    Congenital hydrocephalus: new Mendelian mutations and evidence for oligogenic inheritance oleh Valerie Jacquemin, Nassim Versbraegen, Sarah Duerinckx, Annick Massart, Julie Soblet, Camille Perazzolo, Nicolas Deconinck, Elise Brischoux-Boucher, Anne De Leener, Nicole Revencu, Sandra Janssens, Stèphanie Moorgat, Bettina Blaumeiser, Kristiina Avela, Renaud Touraine, Imad Abou Jaoude, Kathelijn Keymolen, Pascale Saugier-Veber, Tom Lenaerts, Marc Abramowicz, Isabelle Pirson

    Diterbitkan 2023-03-01
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  7. 7
    Phenotypes and genotypes in non‐consanguineous and consanguineous primary microcephaly: High incidence of epilepsy

    Phenotypes and genotypes in non‐consanguineous and consanguineous primary microcephaly: High incidence of epilepsy oleh Sarah Duerinckx, Julie Désir, Camille Perazzolo, Cindy Badoer, Valérie Jacquemin, Julie Soblet, Isabelle Maystadt, Yusuf Tunca, Bettina Blaumeiser, Berten Ceulemans, Winnie Courtens, François‐Guillaume Debray, Anne Destree, Koenraad Devriendt, Anna Jansen, Kathelijn Keymolen, Damien Lederer, Bart Loeys, Marije Meuwissen, Stéphanie Moortgat, Geert Mortier, Marie‐Cécile Nassogne, Tayeb Sekhara, Rudy Van Coster, Jenny Van Den Ende, Nathalie Van der Aa, Hilde Van Esch, Olivier Vanakker, Helene Verhelst, Catheline Vilain, Sarah Weckhuysen, Sandrine Passemard, Alain Verloes, Alec Aeby, Nicolas Deconinck, Patrick Van Bogaert, Isabelle Pirson, Marc Abramowicz

    Diterbitkan 2021-09-01
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