Congenital Sodium Diarrhea: A Form of Intractable Diarrhea, With a Link to Inflammatory Bowel Disease von Janecke, Andreas R, Heinz-Erian, Peter, Müller, Thomas

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Loss-of-function of MYO5B is the main cause of microvillus inclusion disease: 15 novel mutations and a CaCo-2 RNAi cell model von Ruemmele, Frank M, Müller, Thomas, Schiefermeier, Natalia, Ebner, Hannes L, Lechner, Silvia, Pfaller, Kristian, Thöni, Cornelia E, Goulet, Olivier, Lacaille, Florence, Schmitz, Jacques, Colomb, Virginie, Sauvat, Frédérique, Revillon, Yann, Canioni, Danielle, Brousse, Nicole, de Saint-Basile, Genevieve, Lefebvre, Juliette, Heinz-Erian, Peter, Enninger, Axel, Utermann, Gerd, Hess, Michael W, Janecke, Andreas R, Huber, Lukas A

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Further delineation of SLC9A3‐related congenital sodium diarrhea von Bogdanic, Ema, Müller, Thomas, Heinz‐Erian, Peter, Garczarczyk‐Asim, Dorota, Janecke, Andreas R., Rückel, Aline

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Sex- and Age-Specific Reference Curves for Serum Markers of Bone Turnover in Healthy Children from 2 Months to 18 Years von Rauchenzauner, Markus, Schmid, Andrea, Heinz-Erian, Peter, Kapelari, Klaus, Falkensammer, Gerda, Griesmacher, Andrea, Finkenstedt, Gerd, Högler, Wolfgang

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Significance of Molecular Testing for Congenital Chloride Diarrhea von Lechner, Silvia, Ruemmele, Frank M, Zankl, Andreas, Lausch, Ekkehart, Huber, Wolf‐Dietrich, Mihatsch, Walter, Phillips, Alan D, Lewindon, Peter, Querfeld, Uwe, Heinz‐Erian, Peter, Müller, Thomas, Janecke, Andreas R

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MYO5B mutations cause microvillus inclusion disease and disrupt epithelial cell polarity von Partsch, Joachim, Houwen, Roderick J, Zoller, Heinz, Utermann, Gerd, Ponstingl, Hannes, Köhler, Henrik, Lechner, Silvia, Lenhartz, Henning, Ebner, Hannes L, Hess, Michael W, Schiefermeier, Natalia, Pfaller, Kristian, Röllinghoff, Barbara, Schlenck, Barbara, Goulet, Olivier, Ruemmele, Frank M, Taylor, Christopher J, Janecke, Andreas R, Berger, Thomas, Heinz-Erian, Peter, Müller, Thomas, Huber, Lukas A

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The impact of Rotavirus mass vaccination on hospitalization rates, nosocomial Rotavirus gastroenteritis and secondary blood stream infections von Zlamy, Manuela, Kofler, Sabine, Orth, Dorothea, Würzner, Reinhard, Heinz-Erian, Peter, Streng, Andrea, Prelog, Martina

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Immunohistochemical analysis of Mallory bodies in Wilsonian and non‐Wilsonian hepatic copper toxicosis von Müller, Thomas, Langner, Cord, Fuchsbichler, Andrea, Heinz‐Erian, Peter, Ellemunter, Helmut, Schlenck, Barbara, Bavdekar, Ashish R., Pradhan, Avinash M., Pandit, Anand, Müller‐Höcker, Josef, Melter, Michael, Kobayashi, Kunihiko, Nagasaka, Hironori, Kikuta, Hideaki, Müller, Wilfried, Tanner, M. Stuart, Sternlieb, Irmin, Zatloukal, Kurt, Denk, Helmut

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Gastric lactobezoar - a rare disorder? von Heinz-Erian, Peter, Gassner, Ingmar, Klein-Franke, Andreas, Jud, Veronika, Trawoeger, Rudolf, Niederwanger, Christian, Mueller, Thomas, Meister, Bernhard, Scholl-Buergi, Sabine

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Isolated choanal and gut atresias: pathogenetic role of serine protease inhibitor type 2 (SPINT2) gene mutations unlikely von Niederwanger, Christian, Lechner, Silvia, König, Lisa, Janecke, Andreas R, Pototschnig, Claus, Häussler, Beatrice, Scholl-Bürgi, Sabine, Müller, Thomas, Heinz-Erian, Peter

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Amino Acid Cerebrospinal Fluid/Plasma Ratios in Children: Influence of Age, Gender, and Antiepileptic Medication von Scholl-Burgi, Sabine, Haberlandt, Edda, Heinz-Erian, Peter, Deisenhammer, Florian, Albrecht, Ursula, Sigl, Sara Baumgartner, Rauchenzauner, Markus, Ulmer, Hanno, Karall, Daniela

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Disintegration of Large Gastric Lactobezoars by N‐acetylcysteine von Heinz‐Erian, Peter, Klein‐Franke, Andreas, Gassner, Ingmar, Kropshofer, Gabriele, Salvador, Christina, Meister, Bernhard, Müller, Thomas, Scholl‐Buergi, Sabine

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A Novel Homozygous SLC26A3 Nonsense Mutation in a Tyrolean Girl With Congenital Chloride Diarrhea von Heinz‐Erian, Peter, Oberauer, Michaela, Neu, Nikolaus, Müller, Thomas, Scholl‐Bürgi, Sabine, Hager, Josef, Pittschieler, Klaus, Janecke, Andreas R

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Congenital sodium diarrhea is an autosomal recessive disorder of sodium/proton exchange but unrelated to known candidate genes von Müller, Thomas, Wijmenga, Cisca, Phillips, Alan D., Janecke, Andreas, Houwen, Roderick H.J., Fischer, Helmut, Ellemunter, Helmut, Frühwirth, Martin, Offner, Felix, Hofer, Sabine, Müller, Wilfried, Booth, Ian W., Heinz–Erian, Peter

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Reduced sodium/proton exchanger NHE3 activity causes congenital sodium diarrhea von 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

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Universal Mass Vaccination Against Rotavirus: Indirect Effects on Rotavirus Infections in Neonates and Unvaccinated Young Infants Not Eligible for Vaccination von Prelog, Martina, Gorth, Peter, Zwazl, Ines, Kleines, Michael, Streng, Andrea, Zlamy, Manuela, Heinz-Erian, Peter, Wiedermann, Ursula

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Congenital secretory diarrhoea caused by activating germline mutations in GUCY2C von Müller, Thomas, Rasool, Insha, Heinz-Erian, Peter, Mildenberger, Eva, Hülstrunk, Christian, Müller, Andreas, Michaud, Laurent, Koot, Bart G P, Ballauff, Antje, Vodopiutz, Julia, Rosipal, Stefan, Petersen, Britt-Sabina, Franke, Andre, Fuchs, Irene, Witt, Heiko, Zoller, Heinz, Janecke, Andreas R, Visweswariah, Sandhya S

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SPINT2 (HAI-2) missense variants identified in congenital sodium diarrhea/tufting enteropathy affect the ability of HAI-2 to inhibit prostasin but not matriptase von Holt-Danborg, Lasse, Vodopiutz, Julia, Nonboe, Annika W, De Laffolie, Jan, Skovbjerg, Signe, Wolters, Victorien M, Müller, Thomas, Hetzer, Benjamin, Querfurt, Alexander, Zimmer, Klaus-Peter, Jensen, Jan K, Entenmann, Andreas, Heinz-Erian, Peter, Vogel, Lotte K, Janecke, Andreas R

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AP1S1 missense mutations cause a congenital enteropathy via an epithelial barrier defect von Klee, Katharina M. C., Janecke, Andreas R., Civan, Hasret A., Rosipal, Štefan, Heinz-Erian, Peter, Huber, Lukas A., Müller, Thomas, Vogel, Georg F.

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Reduced NHE3 activity results in congenital diarrhea and can predispose to inflammatory bowel disease von Janecke, Andreas R, Heinz-Erian, Peter, Müller, Thomas

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