Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Denise Aldrian"'
Autor:
Barbara E Wildhaber, Wei Zhang, Martin de Santibañes, Victoria Ardiles, Xueli Bai, Mukesh Kumar, Mohamed Rela, Reinoud P H Bokkers, Ekkehard Sturm, Simon McGuirk, Girish Gupte, Esteban Frauca, Francisco Hernández-Oliveros, Winita Hardikar, Helen Evans, Khalid Sharif, Jiří Froněk, David Duncan, Emmanuel Gonzales, Carl Jorns, Alessandro Parente, Ulrich Baumann, Lidia Monti, Marco Spada, Denise Aldrian, Hubert P J van der Doef, Thomas Casswall, Martin Delle, Georg F Vogel, Adam Kolesnik, Mauricio Larrarte K, Paolo Marra, Michela Bravi, Domenico Pinelli, Hajime Uchida, Vidyadhar Mali, Marion Aw, Stéphanie Franchi-Abella, Florent Guérin, Julia Minetto, Sergio Sierre, Jimmy Walker Uno, Steffen Hartleif, Cristina T Ferreira, Luiza S Nader, Catalina Jaramillo, Amit A Shah, Michael R Acord, Tommaso Alterio, Marisa Beretta, Haritha Rajakrishnan, Sudhindran Surendran, Weihao Li, Marcelo Dip, Sue Bates, Lynette Goh, Jonathan Seisenbacher, Joao Seda Neto, Eduardo Antunes da Fonseca, Carolina Magalhães Costa, Marco A Farina, Khaled Z Dajani, David L Bigam, Ting-Bo Liang, Lucie Gonsorčíková, Šimon Bohuš, Norman Junge, Nicolas Richter, Muthukumarassamy Rajakannu, Kumar Palaniappan, Arti Pawaria, Shaleen Agarwal, Subhash Gupta, Sonal Asthana, Vaishnavi Bandewar, Karthik Raichurkar, Yusuke Yanagi, Ryuji Komine, Peter Carr-Boyd, Marek Stefanowicz, Julita Latka-Grot, Dieter C Broering, Dimitri A Raptis, Kris Ann H Marquez, Francisca Van der Schyff, Jesús Quintero-Bernabeu, Maria Mercadal-Hally, Ane M Andres, Riccardo Superina, Juan Carlos Caicedo, Leandra Bitterfeld, Zachary Kastenberg, Bryanna Domenick, George V Mazariegos, Kyle Soltys, Joseph DiNorcia, Swanti Antala, Sander S Florman, Bettina M Buchholz, Uta Herden, Lutz Fischer, Rudi A J O Dierckx, Hermien Hartog
Publikováno v:
BMJ Open, Vol 14, Iss 6 (2024)
Introduction Hepatic artery complications (HACs), such as a thrombosis or stenosis, are serious causes of morbidity and mortality after paediatric liver transplantation (LT). This study will investigate the incidence, current management practices and
Externí odkaz:
https://doaj.org/article/b5c519cf55df4801870085b52149e12e
Autor:
Barbara E Wildhaber, Martin de Santibañes, Victoria Ardiles, Ruben H J de Kleine, Raj Prasad, Bhargava Mullapudi, Jai Patel, Reinoud P H Bokkers, Ekkehard Sturm, Simon McGuirk, Girish Gupte, John McCall, Richard J Hendrickson, Winita Hardikar, Helen Evans, Khalid Sharif, Marumbo Mtegha, Amar Mukund, David Duncan, Emmanuel Gonzales, Marco Spada, Mureo Kasahara, Denise Aldrian, Bader A Alfares, Hubert P J van der Doef, Thomas Casswall, Greg Nowak, Martin Delle, Valeria Berchtold, Georg F Vogel, Piotr Kaliciński, Malgorzata Markiewicz-Kijewska, Adam Kolesnik, Jesús Q Bernabeu, María Mercadal Hally, Mauricio Larrarte K, Paolo Marra, Michela Bravi, Domenico Pinelli, Seisuke Sakamoto, Hajime Uchida, Vidyadhar Mali, Marion Aw, Stéphanie Franchi-Abella, Florent Guérin, Guillermo Cervio, Julia Minetto, Sergio Sierre, Jimmy Walker Uno, Steffen Hartleif, Cristina T Ferreira, Luiza S Nader, Marco Farina, Catalina Jaramillo, Manuel I Rodriguez-Davalos, Peter Feola, Amit A Shah, Phoebe M Wood, Michael R Acord, Ryan T Fischer, Rajeev Khanna, Viniyendra Pamecha, Gilda Porta, Tommaso Alterio, Giuseppe Maggiore, Marisa Beretta, Rudi Dierckx
Publikováno v:
BMJ Open, Vol 13, Iss 7 (2023)
Introduction Portal vein obstruction (PVO) consists of anastomotic stenosis and thrombosis, which occurs due to a progression of the former. The aim of this large-scale international study is to assess the prevalence, current management practices and
Externí odkaz:
https://doaj.org/article/0bed8fe8879b4abe89157619e252beb9
Autor:
Murat Cakir, Elif Sag, Burcu Guven, Ulas Emre Akbulut, Fatma Issi, Alper Han Cebi, Thomas Müller, Denise Aldrian, Andreas R. Janecke
Publikováno v:
Pediatrics and Neonatology, Vol 62, Iss 6, Pp 612-619 (2021)
Background: Congenital diarrheal disorders (CDDs) are a rare group of enteropathies that typically present in the early few months of life and pose a diagnostic challenge. We aimed to analyze the clinical findings and outcome of infants with CDDs and
Externí odkaz:
https://doaj.org/article/4f1f67007e0342319775497790907672
Autor:
Anna M. Kavallar, Franka Messner, Stefan Scheidl, Rupert Oberhuber, Stefan Schneeberger, Denise Aldrian, Valeria Berchtold, Murat Sanal, Andreas Entenmann, Simon Straub, Anna Gasser, Andreas R. Janecke, Thomas Müller, Georg F. Vogel
Publikováno v:
Children, Vol 9, Iss 12, p 1964 (2022)
Background: Progressive Familial Intrahepatic cholestasis type I (PFIC1) is a rare congenital hepatopathy causing cholestasis with progressive liver disease. Surgical interruption of the enterohepatic circulation, e.g., surgical biliary diversion (SB
Externí odkaz:
https://doaj.org/article/3f6935a47f1e4c8bb488a1303a8fa774
Autor:
Christoph Mayerhofer, Anna Maria Kavallar, Denise Aldrian, Andrea Katharina Lindner, Thomas Müller, Georg Friedrich Vogel
Publikováno v:
Clinical Gastroenterology and Hepatology.
Autor:
Andreas Entenmann, Stefan Schneeberger, Dietmar Öfner, Hanno Ulmer, Christian Margreiter, Franka Messner, Georg F. Vogel, Johanna Krapf, Thomas Müller, Denise Aldrian, Raimund Margreiter, Rupert Oberhuber, Valeria Berchtold, Benno Cardini, Annemarie Weissenbacher, Hans J. Schlitt
Publikováno v:
Pediatric transplantationREFERENCES. 25(7)
BACKGROUND Early biliary complications (EBC) constitute a burden after pediatric liver transplantation frequently requiring immediate therapy. We aimed to assess the impact of EBC on short- and long-term patient and graft survival as well as post-tra
Autor:
Przemyslaw A. Filipek, Iris M. Krainer, Ilja Vietor, Andreas R. Janecke, Michael W. Hess, Karin Gutleben, Heinz Zoller, James R. Goldenring, Georg F. Vogel, Thomas Müller, Denise Aldrian, Lukas A. Huber, Barbara Witting, Ekkehard Sturm
Publikováno v:
Journal of Clinical Medicine
Journal of Clinical Medicine, Vol 10, Iss 1901, p 1901 (2021)
Volume 10
Issue 9
Journal of Clinical Medicine, Vol 10, Iss 1901, p 1901 (2021)
Volume 10
Issue 9
Mutations in the actin motor protein myosinVb (myo5b) cause aberrant apical cargo transport and the congenital enteropathy microvillus inclusion disease (MVID). Recently, missense mutations in myo5b were also associated with progressive familial intr
Autor:
S Ünal, J Koeglmeier, M Meissl, H Ayyıldız Civan, J Melek, T Siahanidou, A M Demir, Patrick Gerner, J H Montoya, Duba H-C., Denise Aldrian, A Koutroumpa, Sahar Mansour, Michael W. Hess, Murat Cakir, Georg F. Vogel, Thomas Müller, J Hornova, T K Frey, Aysel Ünlüsoy Aksu, Y Rachman, Ekkehard Sturm, Andreas R. Janecke, G Düker, M Miqdady, Lukas A. Huber, R Lima, Frank M. Ruemmele, Carsten Posovszky, J Hertecant, Holm H. Uhlig, E Ramos Boluda, Stefan Wirth, Raffi Lev-Tzion, C Deppisch, R Lanzersdorfer, Merit M. Tabbers, Simone Kathemann, Yaron Avitzur
Publikováno v:
Journal of Clinical Medicine, Vol 10, Iss 481, p 481 (2021)
Journal of clinical medicine, 10(3):481, 1-15. Multidisciplinary Digital Publishing Institute (MDPI)
Journal of Clinical Medicine
Volume 10
Issue 3
Journal of clinical medicine, 10(3):481, 1-15. Multidisciplinary Digital Publishing Institute (MDPI)
Journal of Clinical Medicine
Volume 10
Issue 3
Myosin Vb (MYO5B) is a motor protein that facilitates protein trafficking and recycling in polarized cells by RAB11- and RAB8-dependent mechanisms. Biallelic MYO5B mutations are identified in the majority of patients with microvillus inclusion diseas
Autor:
Georg Oberhuber, Thomas Müller, Denise Aldrian, Nikolaus Neu, Gabriele Kropshofer, Georg-Friedrich Vogel
Publikováno v:
Journal of pediatric hematology/oncology. 44(1)
Malignant peritoneal mesothelioma (MPM) is an extremely rare entity with a poor prognosis. We report on a 16-year-old boy with ascites and abdominal distension. A computed tomography scan showed peritoneal thickening and a mass adjacent to the transv