Zobrazeno 1 - 10
of 290
pro vyhledávání: '"Stefan Holland"'
Autor:
Philipp Romero, Astrid Burger, Erica Wennberg, Stefanie Schmitteckert, Stefan Holland-Cunz, Constantin Schwab, Patrick Günther
Publikováno v:
Children, Vol 11, Iss 4, p 428 (2024)
Introduction: Hirschsprung disease (HD) manifests as a developmental anomaly affecting the enteric nervous system, where there is an absence of ganglion cells in the lower part of the intestine. This deficiency leads to functional blockages within th
Externí odkaz:
https://doaj.org/article/a800a25b426a4a939546ebe92050d432
Autor:
Simone Keck, Virginie Galati-Fournier, Urs Kym, Michèle Moesch, Jakob Usemann, Isabelle Müller, Ulrike Subotic, Sasha J. Tharakan, Thomas Krebs, Eleuthere Stathopoulos, Peter Schmittenbecher, Dietmar Cholewa, Philipp Romero, Bertram Reingruber, Elisabeth Bruder, NIG Study Group, Stefan Holland-Cunz
Publikováno v:
Cellular and Molecular Gastroenterology and Hepatology, Vol 12, Iss 2, Pp 507-545 (2021)
Background & Aims: Hirschsprung’s disease (HSCR) is a congenital intestinal motility disorder defined by the absence of enteric neuronal cells (ganglia) in the distal gut. The development of HSCR-associated enterocolitis remains a life-threatening
Externí odkaz:
https://doaj.org/article/a105b294e9a2478ebd7d38a65b4724b4
Cholinergic Signaling Attenuates Pro-Inflammatory Interleukin-8 Response in Colonic Epithelial Cells
Autor:
Isabelle Müller, Urs Kym, Virginie Galati, Sasha Tharakan, Ulrike Subotic, Thomas Krebs, Eleuthere Stathopoulos, Peter Schmittenbecher, Dietmar Cholewa, Philipp Romero, Bertram Reingruber, NIGStudy Group, Stefan Holland-Cunz, Simone Keck, Isabella Bielicki, Sandra Weih, Noëmi Zweifel, Kai-Uwe Kleitsch, Carole Gengler, Kiarasch Mortazawi, Milan Milosevic, Vera Otten, Lennart Homrighausen
Publikováno v:
Frontiers in Immunology, Vol 12 (2022)
Infants affected by Hirschsprung disease (HSCR), a neurodevelopmental congenital disorder, lack ganglia of the intrinsic enteric nervous system (aganglionosis) in a variable length of the colon, and are prone to developing severe Hirschsprung-associa
Externí odkaz:
https://doaj.org/article/1131af295c5f40bb80dde0fb5568addc
Autor:
Martina Frech-Dörfler, Sabrina Durand, Friederike Prüfer, Stefan Holland-Cunz, Christoph Rudin
Publikováno v:
Children, Vol 9, Iss 12, p 1890 (2022)
Background: Prenatal hydronephrosis is common and may vary in size. Although mostly unproblematic, it may be a sign of urinary tract obstruction of differing severity. Case Diagnosis/Treatment: We present a boy with prenatally detected bilateral gian
Externí odkaz:
https://doaj.org/article/9663f86c8a24443f839e9597585212aa
Autor:
Tanja Mederer, Stefanie Schmitteckert, Julia Volz, Cristina Martínez, Ralph Röth, Thomas Thumberger, Volker Eckstein, Jutta Scheuerer, Cornelia Thöni, Felix Lasitschka, Leonie Carstensen, Patrick Günther, Stefan Holland-Cunz, Robert Hofstra, Erwin Brosens, Jill A Rosenfeld, Christian P Schaaf, Duco Schriemer, Isabella Ceccherini, Marta Rusmini, Joseph Tilghman, Berta Luzón-Toro, Ana Torroglosa, Salud Borrego, Clara Sze-Man Tang, Mercè Garcia-Barceló, Paul Tam, Nagarajan Paramasivam, Melanie Bewerunge-Hudler, Carolina De La Torre, Norbert Gretz, Gudrun A Rappold, Philipp Romero, Beate Niesler
Publikováno v:
PLoS Genetics, Vol 16, Iss 11, p e1009106 (2020)
Hirschsprung disease (HSCR, OMIM 142623) involves congenital intestinal obstruction caused by dysfunction of neural crest cells and their progeny during enteric nervous system (ENS) development. HSCR is a multifactorial disorder; pathogenetic variant
Externí odkaz:
https://doaj.org/article/454318530f204fd59d5a4e5139fe2ded
Autor:
Rong Zhang, Jan Gehlen, Amit Kawalia, Maria-Theodora Melissari, Tikam Chand Dakal, Athira M Menon, Julia Höfele, Korbinian Riedhammer, Lea Waffenschmidt, Julia Fabian, Katinka Breuer, Jeshurun Kalanithy, Alina Christine Hilger, Amit Sharma, Alice Hölscher, Thomas M Boemers, Markus Pauly, Andreas Leutner, Jörg Fuchs, Guido Seitz, Barbara M Ludwikowski, Barbara Gomez, Jochen Hubertus, Andreas Heydweiller, Ralf Kurz, Johannes Leonhardt, Ferdinand Kosch, Stefan Holland-Cunz, Oliver Münsterer, Beno Ure, Eberhard Schmiedeke, Jörg Neser, Petra Degenhardt, Stefanie Märzheuser, Katharina Kleine, Mattias Schäfer, Nicole Spychalski, Oliver J Deffaa, Jan-Hendrik Gosemann, Martin Lacher, Stefanie Heilmann-Heimbach, Nadine Zwink, Ekkehart Jenetzky, Michael Ludwig, Phillip Grote, Johannes Schumacher, Holger Thiele, Heiko Reutter
Publikováno v:
PLoS ONE, Vol 15, Iss 6, p e0234246 (2020)
INTRODUCTION:Esophageal atresia with or without tracheoesophageal fistula (EA/TEF) occurs approximately 1 in 3.500 live births representing the most common malformation of the upper digestive tract. Only half a century ago, EA/TEF was fatal among aff
Externí odkaz:
https://doaj.org/article/e65c671b393f40a3941b948d3cfe6051
Autor:
Thomas Menter, Stefan Holland-Cunz
Publikováno v:
Fetal and Pediatric Pathology. :1-3
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ede5933e9fb701f1d2f487b517b5eac8
https://doi.org/10.1080/15513815.2023.2193847
https://doi.org/10.1080/15513815.2023.2193847
Publikováno v:
Children, Vol 8, Iss 9, p 784 (2021)
Neuroblastoma, like other cancer types, has an increased need for energy. This results in an increased thermogenic profile of the cells. How tumor cells optimize their energy efficiency has been discussed since Warburg described the fact that tumor c
Externí odkaz:
https://doaj.org/article/74ea9ecfd9e34abba08c07152fddaf75
Autor:
Nora Manz, Claudia Höfele-Behrendt, Julia Bielicki, Hanna Schmid, Matthias S. Matter, Isabella Bielicki, Stefan Holland-Cunz, Stephanie J. Gros
Publikováno v:
Children, Vol 8, Iss 8, p 712 (2021)
Background: multisystem inflammatory syndrome in children (MIS-C) is a new disease associated with a recent infection with severe acute respiratory syndrome coronavirus type 2 (SARS-CoV-2). Affected children can present predominantly with abdominal s
Externí odkaz:
https://doaj.org/article/16f7063ca864423c98f014cec00ba9f0
Publikováno v:
Journal of Pediatric Surgery Case Reports, Vol 25, Iss C, Pp 52-55 (2017)
Introduction: Necrotizing fasciitis is a soft tissue infection that can rapidly progress and end lethally if not treated early and radically. With an extremely low prevalence (0.02% of all pediatric in hospital cases), most physicians will probably o
Externí odkaz:
https://doaj.org/article/8163708ef45c4235b249052441c876af