Complete hepatitis B virus genome analysis in HBsAg positive mothers and their infants with fulminant hepatitis B

por Wirth Stefan, Wintermeyer Philip, Gerner Patrick, Friedt Michael
Publicado em 2004-06-01

Complete hepatitis B virus genome analysis in HBsAg positive mothers and their infants with fulminant hepatitis B

por Friedt, Michael, Gerner, Patrick, Wintermeyer, Philip, Wirth, Stefan
Publicado em 2004

Adrenal failure followed by status epilepticus and hemolytic anemia in primary antiphospholipid syndrome

por Gerner, Patrick, Heldmann, Michael, Borusiak, Peter, Bures, Vladimir, Wirth, Stefan
Publicado em 2005

Prevalence of hepatitis B virus precore stop codon mutations in chronically infected children

por Wintermeyer, Philip, Gerner, Patrick, Gehring, Stephan, Karimi, Afshin, Wirth, Stefan
Publicado em 2006

Neonatal Cholestasis – Differential Diagnoses, Current Diagnostic Procedures, and Treatment

por Götze, Thomas, Blessing, Holger, Grillhösl, Christian, Gerner, Patrick, Hoerning, André
Publicado no Front Pediatr (2015)

Inflammatory Bowel Disease in Childhood and Adolescence: Diagnosis and Treatment

por Däbritz, Jan, Gerner, Patrick, Enninger, Axel, Claßen, Martin, Radke, Michael
Publicado no Dtsch Arztebl Int (2017)

Prevalence of autoantibodies and the risk of autoimmune thyroid disease in children with chronic hepatitis C virus infection treated with interferon-α

por Gehring, Stephan, Kullmer, Ulrike, Koeppelmann, Sabine, Gerner, Patrick, Wintermeyer, Philip, Wirth, Stefan
Publicado em 2006

Diversity of Disorders Causing Neonatal Cholestasis – The Experience of a Tertiary Pediatric Center in Germany

por Hoerning, André, Raub, Simon, Dechêne, Alexander, Brosch, Michelle N., Kathemann, Simone, Hoyer, Peter F., Gerner, Patrick
Publicado em 2014

Case Report: Hepatic Adenoma in a Child With a Congenital Extrahepatic Portosystemic Shunt

por Glonnegger, Hannah, Schulze, Maren, Kathemann, Simone, Berg, Sebastian, Füllgraf, Hannah, Tannapfel, Andrea, Gerner, Patrick, Grohmann, Jochen, Niemeyer, Charlotte, Hettmer, Simone
Publicado no Front Pediatr (2020)

Mitochondrial dysfunction in liver failure requiring transplantation

por Lane, Maria, Boczonadi, Veronika, Bachtari, Sahar, Gomez-Duran, Aurora, Langer, Thorsten, Griffiths, Alexandra, Kleinle, Stephanie, Dineiger, Christine, Abicht, Angela, Holinski-Feder, Elke, Schara, Ulrike, Gerner, Patrick, Horvath, Rita
Publicado no J Inherit Metab Dis (2016)

Vitamin E treatment for children with chronic hepatitis B: A randomized placebo controlled trial

por Gerner, Patrick, Posselt, Hans-Georg, Krahl, Andreas, Ballauff, Antje, Innerhofer, Albina, Binder, Christa, Wenzl, Tobias G, Zense, Matthias, Hector, Ariadne, Dockter, Gerhard, Adam, Rüdiger, Neubert, Jenny, Claßen, Martin, van Gemmern, Robert, Wirth, Stefan
Publicado em 2008

Phenotypic spectrum and diagnostic pitfalls of ABCB4 deficiency depending on age of onset

por Schatz, Stephanie Barbara, Jüngst, Christoph, Keitel‐Anselmo, Verena, Kubitz, Ralf, Becker, Christina, Gerner, Patrick, Pfister, Eva‐Doreen, Goldschmidt, Imeke, Junge, Norman, Wenning, Daniel, Gehring, Stephan, Arens, Stefan, Bretschneider, Dirk, Grothues, Dirk, Engelmann, Guido, Lammert, Frank, Baumann, Ulrich
Publicado no Hepatol Commun (2018)

An inducible mouse model for microvillus inclusion disease reveals a role for myosin Vb in apical and basolateral trafficking

por Schneeberger, Kerstin, Vogel, Georg F., Teunissen, Hans, van Ommen, Domenique D., Begthel, Harry, El Bouazzaoui, Layla, van Vugt, Anke H. M., Beekman, Jeffrey M., Klumperman, Judith, Müller, Thomas, Janecke, Andreas, Gerner, Patrick, Huber, Lukas A., Hess, Michael W., Clevers, Hans, van Es, Johan H., Nieuwenhuis, Edward E. S., Middendorp, Sabine
Publicado no Proc Natl Acad Sci U S A (2015)

Reduced sodium/proton exchanger NHE3 activity causes congenital sodium diarrhea

por Janecke, Andreas R., Heinz-Erian, Peter, Yin, Jianyi, Petersen, Britt-Sabina, Franke, Andre, Lechner, Silvia, Fuchs, Irene, Melancon, Serge, Uhlig, Holm H., Travis, Simon, Marinier, Evelyne, Perisic, Vojislav, Ristic, Nina, Gerner, Patrick, Booth, Ian W., Wedenoja, Satu, Baumgartner, Nadja, Vodopiutz, Julia, Frechette-Duval, Marie-Christine, De Lafollie, Jan, Persad, Rabindranath, Warner, Neil, Tse, C. Ming, Sud, Karan, Zachos, Nicholas C., Sarker, Rafiquel, Zhu, Xinjun, Muise, Aleixo M., Zimmer, Klaus-Peter, Witt, Heiko, Zoller, Heinz, Donowitz, Mark, Müller, Thomas
Publicado no Hum Mol Genet (2015)

Congenital Diarrhea and Cholestatic Liver Disease: Phenotypic Spectrum Associated with MYO5B Mutations

por Aldrian, Denise, Vogel, Georg F., Frey, Teresa K., Ayyıldız Civan, Hasret, Aksu, Aysel Ünlüsoy, Avitzur, Yaron, Ramos Boluda, Esther, Çakır, Murat, Demir, Arzu Meltem, Deppisch, Caroline, Duba, Hans-Christoph, Düker, Gesche, Gerner, Patrick, Hertecant, Jozef, Hornová, Jarmila, Kathemann, Simone, Koeglmeier, Jutta, Koutroumpa, Arsinoi, Lanzersdorfer, Roland, Lev-Tzion, Raffi, Lima, Rosa, Mansour, Sahar, Meissl, Manfred, Melek, Jan, Miqdady, Mohamad, Montoya, Jorge Hernan, Posovszky, Carsten, Rachman, Yelena, Siahanidou, Tania, Tabbers, Merit, Uhlig, Holm H., Ünal, Sevim, Wirth, Stefan, Ruemmele, Frank M., Hess, Michael W., Huber, Lukas A., Müller, Thomas, Sturm, Ekkehard, Janecke, Andreas R.
Publicado no J Clin Med (2021)

CCDC115 Deficiency Causes a Disorder of Golgi Homeostasis with Abnormal Protein Glycosylation

por Jansen, Jos C., Cirak, Sebahattin, van Scherpenzeel, Monique, Timal, Sharita, Reunert, Janine, Rust, Stephan, Pérez, Belén, Vicogne, Dorothée, Krawitz, Peter, Wada, Yoshinao, Ashikov, Angel, Pérez-Cerdá, Celia, Medrano, Celia, Arnoldy, Andrea, Hoischen, Alexander, Huijben, Karin, Steenbergen, Gerry, Quelhas, Dulce, Diogo, Luisa, Rymen, Daisy, Jaeken, Jaak, Guffon, Nathalie, Cheillan, David, van den Heuvel, Lambertus P., Maeda, Yusuke, Kaiser, Olaf, Schara, Ulrike, Gerner, Patrick, van den Boogert, Marjolein A.W., Holleboom, Adriaan G., Nassogne, Marie-Cécile, Sokal, Etienne, Salomon, Jody, van den Bogaart, Geert, Drenth, Joost P.H., Huynen, Martijn A., Veltman, Joris A., Wevers, Ron A., Morava, Eva, Matthijs, Gert, Foulquier, François, Marquardt, Thorsten, Lefeber, Dirk J.
Publicado no Am J Hum Genet (2016)