Search Results - Vogel, Georg‐Friedrich

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  1. 1
    Intracellular Trafficking Defects in Congenital Intestinal and Hepatic Diseases

    Intracellular Trafficking Defects in Congenital Intestinal and Hepatic Diseases by Szabó, Luca, Pollio, Adam R., Vogel, Georg Friedrich

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  2. 2
    Kinesin family member 12‐related hepatopathy: A generally indolent disorder with elevated gamma‐glutamyl‐transferase activity

    Kinesin family member 12‐related hepatopathy: A generally indolent disorder with elevated gamma‐glutamyl‐transferase activity by Vogel, Georg‐Friedrich, Podpeskar, Alexandra, Rieder, Dietmar, Salzer, Helin, Garczarczyk‐Asim, Dorota, Wang, Li, Abuduxikuer, Kuerbanjiang, Wang, Jian‐She, Scharrer, Anke, Faqeih, Eissa Ali, Aseeri, Ali T., Vodopiutz, Julia, Heilos, Andreas, Pichler, Judith, Huber, Wolf‐Dietrich, Müller, Thomas, Knisely, A. S., Janecke, Andreas R.

    Published in Clinical genetics
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  3. 3
    Co-existence of ABCB11 and DCDC2 disease: Infantile cholestasis requires both next-generation sequencing and clinical-histopathologic correlation

    Co-existence of ABCB11 and DCDC2 disease: Infantile cholestasis requires both next-generation sequencing and clinical-histopathologic correlation by Vogel, Georg-Friedrich, Maurer, Elisabeth, Entenmann, Andreas, Straub, Simon, Knisely, A S, Janecke, Andreas R, Müller, Thomas

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  4. 4
    Stereotactic radiofrequency ablation of a variety of liver masses in children

    Stereotactic radiofrequency ablation of a variety of liver masses in children by Hetzer, Benjamin, Vogel, Georg-Friedrich, Entenmann, Andreas, Heil, Michel, Schullian, Peter, Putzer, Daniel, Meister, Bernhard, Crazzolara, Roman, Kropshofer, Gabriele, Salvador, Christina, Straub, Simon, Karall, Daniela, Niederwanger, Christian, Cortina, Gérard, Janecke, Andreas, Freund-Unsinn, Karin, Maurer, Kathrin, Schweigmann, Gisela, Oberhuber, Georg, Renz, Oliver, Schneeberger, Stefan, Müller, Thomas, Bale, Reto

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  5. 5
    THU-313 - Odevixibat therapy following liver transplantation in patients with FIC1-deficient progressive familial intrahepatic cholestasis: a retrospective case series

    THU-313 - Odevixibat therapy following liver transplantation in patients with FIC1-deficient progressive familial intrahepatic cholestasis: a retrospective case series by Vogel, Georg-Friedrich, Kathemann, Simone, Pietrobattista, Andrea, Maggiore, Giuseppe, Aldrian, Denise, Sciveres, Marco, Verkade, Henkjan J., Rauschkolb, Peter, Maucksch, Christof, Valcheva, Velichka, Clemson, Christine, Lainka, Elke

    Published in Journal of hepatology
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  6. 6
    Odevixibat therapy following liver transplantation in patients with FIC1-deficient progressive familial intrahepatic cholestasis: a retrospective case series

    Odevixibat therapy following liver transplantation in patients with FIC1-deficient progressive familial intrahepatic cholestasis: a retrospective case series by Vogel, Georg-Friedrich, Kathemann, Simone, Pietrobattista, Andrea, Maggiore, Giuseppe, Aldrian, Denise, Sciveres, Marco, Verkade, Henkjan J., Rauschkolb, Peter, Maucksch, Christof, Valcheva, Velichka, Clemson, Christine, Lainka, Elke

    Published in Journal of hepatology
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  7. 7
    OS-083 Highly multiplexed spatial analysis of acute pediatric hepatitis of unknown origin indicates a characteristic immune infiltrate as a possible post-acute sequel of COVID-19

    OS-083 Highly multiplexed spatial analysis of acute pediatric hepatitis of unknown origin indicates a characteristic immune infiltrate as a possible post-acute sequel of COVID-19 by Röttele, Felix, Zollner, Andreas, Yuksel, Muhammed, Arıkan, Cigdem, Mogler, Carolin, Aberle, Judith, Aberle, Stephan, Wölfle, Lena, Maier, Felix, Lurz, Eberhart, Hasselblatt, Peter, Hofmann, Maike, Thimme, Robert, Müller, Thomas, Vogel, Georg-Friedrich, Bengsch, Bertram

    Published in Journal of hepatology
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  8. 8
    Management and outcomes after liver transplantation for progressive familial intrahepatic cholestasis: A systematic review and meta-analysis

    Management and outcomes after liver transplantation for progressive familial intrahepatic cholestasis: A systematic review and meta-analysis by Kavallar, Anna Maria, Mayerhofer, Christoph, Aldrian, Denise, Okamoto, Tatsuya, Müller, Thomas, Vogel, Georg Friedrich

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  9. 9
    Co-existence of ABCB11 and DCDC2 disease: Infantile cholestasis requires both next-generation sequencing and clinical-histopathologic correlation

    Co-existence of ABCB11 and DCDC2 disease: Infantile cholestasis requires both next-generation sequencing and clinical-histopathologic correlation by Vogel, Georg-Friedrich, Maurer, Elisabeth, Entenmann, Andreas, Straub, Simon, Knisely, A S, Janecke, Andreas R, Müller, Thomas

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