Hasil Pencarian - Peter Lohse

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  1. 1
    Molecular defects underlying Wolman disease appear to be more heterogeneous than those resulting in cholesteryl ester storage disease

    Molecular defects underlying Wolman disease appear to be more heterogeneous than those resulting in cholesteryl ester storage disease oleh Peter Lohse, Sylke Maas, Pia Lohse, Adrian C. Sewell, Otto P. van Diggelen, Dietrich Seidel

    Diterbitkan 1999-02-01
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  2. 2
    The cannabinoid 1 receptor (CNR1) 1359 G/A polymorphism modulates susceptibility to ulcerative colitis and the phenotype in Crohn's disease.

    The cannabinoid 1 receptor (CNR1) 1359 G/A polymorphism modulates susceptibility to ulcerative colitis and the phenotype in Crohn's disease. oleh Martin Storr, Dominik Emmerdinger, Julia Diegelmann, Simone Pfennig, Thomas Ochsenkühn, Burkhard Göke, Peter Lohse, Stephan Brand

    Diterbitkan 2010-02-01
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  3. 3
    Compound heterozygosity for a Wolman mutation is frequent among patients with cholesteryl ester storage disease

    Compound heterozygosity for a Wolman mutation is frequent among patients with cholesteryl ester storage disease oleh Peter Lohse, Sylke Maas, Pia Lohse, Milan Elleder, Jean M. Kirk, Guy T.N. Besley, Dietrich Seidel

    Diterbitkan 2000-01-01
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  4. 4
    The NOD2 p.Leu1007fsX1008 mutation (rs2066847) is a stronger predictor of the clinical course of Crohn's disease than the FOXO3A intron variant rs12212067.

    The NOD2 p.Leu1007fsX1008 mutation (rs2066847) is a stronger predictor of the clinical course of Crohn's disease than the FOXO3A intron variant rs12212067. oleh Fabian Schnitzler, Matthias Friedrich, Christiane Wolf, Marianne Angelberger, Julia Diegelmann, Torsten Olszak, Florian Beigel, Cornelia Tillack, Johannes Stallhofer, Burkhard Göke, Jürgen Glas, Peter Lohse, Stephan Brand

    Diterbitkan 2014-01-01
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  5. 5
    Development of a uniform, very aggressive disease phenotype in all homozygous carriers of the NOD2 mutation p.Leu1007fsX1008 with Crohn's disease and active smoking status resulting in ileal stenosis requiring surgery.

    Development of a uniform, very aggressive disease phenotype in all homozygous carriers of the NOD2 mutation p.Leu1007fsX1008 with Crohn's disease and active smoking status resultin... oleh Fabian Schnitzler, Matthias Friedrich, Marianne Angelberger, Julia Diegelmann, Johannes Stallhofer, Christiane Wolf, Joel Dütschler, Samuel Truniger, Torsten Olszak, Florian Beigel, Cornelia Tillack, Peter Lohse, Stephan Brand

    Diterbitkan 2020-01-01
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  6. 6
    The NOD2 Single Nucleotide Polymorphism rs72796353 (IVS4+10 A>C) Is a Predictor for Perianal Fistulas in Patients with Crohn's Disease in the Absence of Other NOD2 Mutations.

    The NOD2 Single Nucleotide Polymorphism rs72796353 (IVS4+10 A>C) Is a Predictor for Perianal Fistulas in Patients with Crohn's Disease in the Absence of Other NOD2 Mutations. oleh Fabian Schnitzler, Matthias Friedrich, Christiane Wolf, Johannes Stallhofer, Marianne Angelberger, Julia Diegelmann, Torsten Olszak, Cornelia Tillack, Florian Beigel, Burkhard Göke, Jürgen Glas, Peter Lohse, Stephan Brand

    Diterbitkan 2015-01-01
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  7. 7
    Involvement of the same TNFR1 residue in mendelian and multifactorial inflammatory disorders.

    Involvement of the same TNFR1 residue in mendelian and multifactorial inflammatory disorders. oleh Isabelle Jéru, Serge Charmion, Emmanuelle Cochet, Bruno Copin, Philippe Duquesnoy, Maria Teresa Mitjavila Garcia, Gaëlle Le Borgne, Pascal Cathebras, Jacques Gaillat, Sonia Karabina, Catherine Dodé, Peter Lohse, Véronique Hentgen, Serge Amselem

    Diterbitkan 2013-01-01
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  8. 8
    The NOD2 single nucleotide polymorphisms rs2066843 and rs2076756 are novel and common Crohn's disease susceptibility gene variants.

    The NOD2 single nucleotide polymorphisms rs2066843 and rs2076756 are novel and common Crohn's disease susceptibility gene variants. oleh Jürgen Glas, Julia Seiderer, Cornelia Tillack, Simone Pfennig, Florian Beigel, Matthias Jürgens, Torsten Olszak, Rüdiger P Laubender, Maria Weidinger, Bertram Müller-Myhsok, Burkhard Göke, Thomas Ochsenkühn, Peter Lohse, Julia Diegelmann, Darina Czamara, Stephan Brand

    Diterbitkan 2010-01-01
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  9. 9
    CEACAM6 gene variants in inflammatory bowel disease.

    CEACAM6 gene variants in inflammatory bowel disease. oleh Jürgen Glas, Julia Seiderer, Christoph Fries, Cornelia Tillack, Simone Pfennig, Maria Weidinger, Florian Beigel, Torsten Olszak, Ulrich Lass, Burkhard Göke, Thomas Ochsenkühn, Christiane Wolf, Peter Lohse, Bertram Müller-Myhsok, Julia Diegelmann, Darina Czamara, Stephan Brand

    Diterbitkan 2011-01-01
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  10. 10
    Evidence for STAT4 as a common autoimmune gene: rs7574865 is associated with colonic Crohn's disease and early disease onset.

    Evidence for STAT4 as a common autoimmune gene: rs7574865 is associated with colonic Crohn's disease and early disease onset. oleh Jürgen Glas, Julia Seiderer, Melinda Nagy, Christoph Fries, Florian Beigel, Maria Weidinger, Simone Pfennig, Wolfram Klein, Jörg T Epplen, Peter Lohse, Matthias Folwaczny, Burkhard Göke, Thomas Ochsenkühn, Julia Diegelmann, Bertram Müller-Myhsok, Darina Roeske, Stephan Brand

    Diterbitkan 2010-01-01
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  11. 11
    Increased Risk of Interstitial Lung Disease in Children with a Single R288K Variant of ABCA3

    Increased Risk of Interstitial Lung Disease in Children with a Single R288K Variant of ABCA3 oleh Thomas Wittmann, Sabrina Frixel, Stefanie Höppner, Ulrike Schindlbeck, Andrea Schams, Matthias Kappler, Jan Hegermann, Christoph Wrede, Gerhard Liebisch, Anne Vierzig, Angela Zacharasiewicz, Matthias Volkmar Kopp, Christian F Poets, Winfried Baden, Dominik Hartl, Anton H van Kaam, Peter Lohse, Charalampos Aslanidis, Ralf Zarbock, Matthias Griese

    Diterbitkan 2016-02-01
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  12. 12
    rs1004819 is the main disease-associated IL23R variant in German Crohn's disease patients: combined analysis of IL23R, CARD15, and OCTN1/2 variants.

    rs1004819 is the main disease-associated IL23R variant in German Crohn's disease patients: combined analysis of IL23R, CARD15, and OCTN1/2 variants. oleh Jürgen Glas, Julia Seiderer, Martin Wetzke, Astrid Konrad, Helga-Paula Török, Silke Schmechel, Laurian Tonenchi, Christine Grassl, Julia Dambacher, Simone Pfennig, Kerstin Maier, Thomas Griga, Wolfram Klein, Jörg T Epplen, Uwe Schiemann, Christian Folwaczny, Peter Lohse, Burkhard Göke, Thomas Ochsenkühn, Bertram Müller-Myhsok, Matthias Folwaczny, Thomas Mussack, Stephan Brand

    Diterbitkan 2007-01-01
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  13. 13
    Analysis of Plasminogen Genetic Variants in Multiple Sclerosis Patients

    Analysis of Plasminogen Genetic Variants in Multiple Sclerosis Patients oleh A. Dessa Sadovnick, Anthony L. Traboulsee, Cecily Q. Bernales, Jay P. Ross, Amanda L. Forwell, Irene M. Yee, Lena Guillot-Noel, Bertrand Fontaine, Isabelle Cournu-Rebeix, Antonio Alcina, Maria Fedetz, Guillermo Izquierdo, Fuencisla Matesanz, Kelly Hilven, Bénédicte Dubois, An Goris, Ianire Astobiza, Iraide Alloza, Alfredo Antigüedad, Koen Vandenbroeck, Denis A. Akkad, Orhan Aktas, Paul Blaschke, Mathias Buttmann, Andrew Chan, Joerg T. Epplen, Lisa-Ann Gerdes, Antje Kroner, Christian Kubisch, Tania Kümpfel, Peter Lohse, Peter Rieckmann, Uwe K. Zettl, Frauke Zipp, Lars Bertram, Christina M Lill, Oscar Fernandez, Patricia Urbaneja, Laura Leyva, Jose Carlos Alvarez-Cermeño, Rafael Arroyo, Aroa M. Garagorri, Angel García-Martínez, Luisa M. Villar, Elena Urcelay, Sunny Malhotra, Xavier Montalban, Manuel Comabella, Thomas Berger, Franz Fazekas, Markus Reindl, Mascha C. Schmied, Alexander Zimprich, Carles Vilariño-Güell

    Diterbitkan 2016-07-01
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