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

od Wirth Stefan, Wintermeyer Philip, Gerner Patrick, Friedt Michael
Izdano 2004-06-01

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

od Friedt, Michael, Gerner, Patrick, Wintermeyer, Philip, Wirth, Stefan
Izdano 2004

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

od Gerner, Patrick, Heldmann, Michael, Borusiak, Peter, Bures, Vladimir, Wirth, Stefan
Izdano 2005

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

od Wintermeyer, Philip, Gerner, Patrick, Gehring, Stephan, Karimi, Afshin, Wirth, Stefan
Izdano 2006

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

od Götze, Thomas, Blessing, Holger, Grillhösl, Christian, Gerner, Patrick, Hoerning, André
izdano v Front Pediatr (2015)

Inflammatory Bowel Disease in Childhood and Adolescence: Diagnosis and Treatment

od Däbritz, Jan, Gerner, Patrick, Enninger, Axel, Claßen, Martin, Radke, Michael
izdano v 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

od Gehring, Stephan, Kullmer, Ulrike, Koeppelmann, Sabine, Gerner, Patrick, Wintermeyer, Philip, Wirth, Stefan
Izdano 2006

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

od Hoerning, André, Raub, Simon, Dechêne, Alexander, Brosch, Michelle N., Kathemann, Simone, Hoyer, Peter F., Gerner, Patrick
Izdano 2014

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

od Glonnegger, Hannah, Schulze, Maren, Kathemann, Simone, Berg, Sebastian, Füllgraf, Hannah, Tannapfel, Andrea, Gerner, Patrick, Grohmann, Jochen, Niemeyer, Charlotte, Hettmer, Simone
izdano v Front Pediatr (2020)

Mitochondrial dysfunction in liver failure requiring transplantation

od 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
izdano v J Inherit Metab Dis (2016)

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

od 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
Izdano 2008

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

od 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
izdano v Hepatol Commun (2018)

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

od 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
izdano v Proc Natl Acad Sci U S A (2015)

Reduced sodium/proton exchanger NHE3 activity causes congenital sodium diarrhea

od 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
izdano v Hum Mol Genet (2015)

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

od 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.
izdano v J Clin Med (2021)

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

od 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.
izdano v Am J Hum Genet (2016)