Zobrazeno 1 - 10
of 48
pro vyhledávání: '"Antje Ballauff"'
Autor:
Jan De Laffolie, Antje Ballauff, Stefan Wirth, Carolin Blueml, Frank Risto Rommel, Martin Claßen, Martin Laaß, Thomas Lang, Almuthe Christina Hauer, the CEDATA-GPGE Study Group
Publikováno v:
Frontiers in Pediatrics, Vol 10 (2022)
ObjectiveAmong patients with inflammatory bowel disease (IBD), the risk of thromboembolism (TE) is increased, representing a relevant cause of morbidity and mortality. In contrast to other extraintestinal IBD manifestations, TE receives much less att
Externí odkaz:
https://doaj.org/article/a1ecd4ff63c545afbcf0a422d73dc258
Autor:
Antje Timmer, Jenny Peplies, Max Westphal, Birgit Kaltz, Antje Ballauff, Martin Claßen, Martin W Laass, Sibylle Koletzko
Publikováno v:
PLoS ONE, Vol 12, Iss 5, p e0177757 (2017)
BACKGROUND:Transition to adult health services is a vulnerable phase in young persons with chronic disease. We describe how young persons with inflammatory bowel disease in Germany and Austria experience care during the transitional age, focusing on
Externí odkaz:
https://doaj.org/article/f90967bf0e424e0b8a0e5d20b0e772f3
Autor:
Jürgen Heise, Christian Kreysel, Michael Blank, Philipp Euler, Ilka Melchior, Michaela Johnen, Manfred Planker, Antje Ballauff, Martina Czypull, Thomas Frieling
Publikováno v:
Zeitschrift für Gastroenterologie.
Zusammenfassung Hintergrund Die Entfernung einer Bolusobstruktion im Ösophagus ist eine Indikation zur Notfallendoskopie. In der aktuellen Leitlinie der European Society of Gastrointestinal Endoscopy (ESGE) wird u. a der Vorschub des Bolus in den Ma
Autor:
Eva‐Doreen Pfister, Carola Dröge, Roman Liebe, Amelie Stalke, Nicole Buhl, Antje Ballauff, Tobias Cantz, Eva Bueltmann, Jan Stindt, Tom Luedde, Ulrich Baumann, Verena Keitel
Publikováno v:
Liver International. 42:1084-1096
Progressive familial intrahepatic cholestasis (PFIC) is a collective term for a heterogenous group of rare, inherited cholestasis syndromes. The number of genes underlying the clinical PFIC phenotype is still increasing. While progressive liver disea
Publikováno v:
Monatsschrift Kinderheilkunde. 170:965-968
Autor:
Eva‐Doreen Pfister, Carola Dröge, Roman Liebe, Amelie Stalke, Nicole Buhl, Antje Ballauff, Tobias Cantz, Eva Bueltmann, Jan Stindt, Tom Luedde, Ulrich Baumann, Verena Keitel
Publikováno v:
Liver International. 42
Autor:
Kelly F. Meijsen, Hugo R. de Jonge, Antje Ballauff, Anke H M van Vugt, Roderick H. J. Houwen, Manuel B Bryant, Thomas Müller, Sabine Middendorp, Tanja Restin, Marcel J. C. Bijvelds, Andreas R. Janecke, Bart G. P. Koot
Publikováno v:
Clinical and Translational Gastroenterology, 12(11):e00427. Nature Publishing Group
van Vugt, A H M, Bijvelds, M J C, de Jonge, H R, Meijsen, K F, Restin, T, Bryant, M B, Ballauff, A, Koot, B, Müller, T, Houwen, R H J, Janecke, A R & Middendorp, S 2021, ' A Potential Treatment of Congenital Sodium Diarrhea in Patients With Activating GUCY2C Mutations ', CLINICAL AND TRANSLATIONAL GASTROENTEROLOGY, vol. 12, no. 11, pp. e00427 . https://doi.org/10.14309/ctg.0000000000000427
Clinical and translational gastroenterology, 12(11). Nature Publishing Group
Clinical and Translational Gastroenterology
CLINICAL AND TRANSLATIONAL GASTROENTEROLOGY, 12(11). Nature Publishing Group
van Vugt, A H M, Bijvelds, M J C, de Jonge, H R, Meijsen, K F, Restin, T, Bryant, M B, Ballauff, A, Koot, B, Müller, T, Houwen, R H J, Janecke, A R & Middendorp, S 2021, ' A Potential Treatment of Congenital Sodium Diarrhea in Patients With Activating GUCY2C Mutations ', CLINICAL AND TRANSLATIONAL GASTROENTEROLOGY, vol. 12, no. 11, pp. e00427 . https://doi.org/10.14309/ctg.0000000000000427
Clinical and translational gastroenterology, 12(11). Nature Publishing Group
Clinical and Translational Gastroenterology
CLINICAL AND TRANSLATIONAL GASTROENTEROLOGY, 12(11). Nature Publishing Group
INTRODUCTION: Gain-of-function mutations in guanylyl cyclase C (GCC) result in persistent diarrhea with perinatal onset. We investigated a specific GCC inhibitor, SSP2518, for its potential to treat this disorder. METHODS: We investigated the effect
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::75d3192ebcfb634acea304772d3b318e
https://pure.eur.nl/en/publications/476a3967-0cd2-4270-92cc-95c7bcb17260
https://pure.eur.nl/en/publications/476a3967-0cd2-4270-92cc-95c7bcb17260
Autor:
Henry Taylor, Marta C. Cohen, Stephan Buderus, Charis Eng, Isabel Rojas, Kevin Sweet, Peter Dale, Natalia Nedelkopoulou, Victor L. Fox, Claudia Phen, Inés Loverdos, Holm H. Uhlig, Tim G. J. de Meij, Jürgen Heise, Isabel Spier, Dilay Yerlioglu, Stefan Aretz, Emmanuel Mas, Veronica Busoni, Mike Thomson, Antje Ballauff
Publikováno v:
Taylor, H, Yerlioglu, D, Phen, C, Ballauff, A, Nedelkopoulou, N, Spier, I, Loverdos, I, Busoni, V B, Heise, J R, Dale, P, de Meij, T, Sweet, K, Cohen, M C, Fox, V L, Mas, E, Aretz, S, Eng, C, Buderus, S, Thomson, M, Rojas, I & Uhlig, H H 2021, ' MTOR inhibitors reduce enteropathy, intestinal bleeding and colectomy rate in patients with juvenile polyposis of infancy with PTEN-BMPR1A deletion ', Human Molecular Genetics, vol. 30, no. 14, pp. 1273-1282 . https://doi.org/10.1093/hmg/ddab094
Human Molecular Genetics
Human Molecular Genetics, Oxford University Press (OUP), 2021, 30 (14), pp.1273-1282. ⟨10.1093/hmg/ddab094⟩
Human Molecular Genetics, 30(14), 1273-1282. Oxford University Press
Human Molecular Genetics
Human Molecular Genetics, Oxford University Press (OUP), 2021, 30 (14), pp.1273-1282. ⟨10.1093/hmg/ddab094⟩
Human Molecular Genetics, 30(14), 1273-1282. Oxford University Press
Ultra-rare genetic disorders can provide proof of concept for efficacy of targeted therapeutics and reveal pathogenic mechanisms relevant to more common conditions. Juvenile polyposis of infancy (JPI) is caused by microdeletions in chromosome 10 that
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3ad8ad5ebb805fcf1e7837b1bca16fa2
https://research.vumc.nl/en/publications/cf26bd78-6a65-4fc8-8f7a-97b617db5510
https://research.vumc.nl/en/publications/cf26bd78-6a65-4fc8-8f7a-97b617db5510
Publikováno v:
Klinische Pädiatrie. 231:21-27
The number of inconspicuous results of esophagogastroduodenoscopies (EGDs) in childhood appears to be disturbingly high. The aim of this study was to analyze the diagnostic yield of EGD and to determine its relevance of specific clinical indications.
Autor:
Andreas R. Janecke, Insha Rasool, Eva Mildenberger, Sandhya S. Visweswariah, Antje Ballauff, Heiko Witt, Laurent Michaud, Peter Heinz-Erian, Andreas Müller, Christian Hülstrunk, Bart G. P. Koot, Irene Fuchs, Heinz Zoller, Britt-Sabina Petersen, Štefan Rosipal, Thomas Müller, Andre Franke, Julia Vodopiutz
Publikováno v:
Gut, 65(8), 1306-1313. BMJ Publishing Group
Gut
Gut
Objective Congenital sodium diarrhoea (CSD) refers to a form of secretory diarrhoea with intrauterine onset and high faecal losses of sodium without congenital malformations. The molecular basis for CSD remains unknown. We clinically characterised a