Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Eleuthere Stathopoulos"'
Autor:
Christelle Sommer, Paola Andrea Rouge Elton, Nermin Halkic, Meriam Koob, Leonor Alamo, Sylvain Mauron, Eleuthere Stathopoulos
Publikováno v:
Journal of Pediatric Surgery Case Reports, Vol 110, Iss , Pp 102877- (2024)
Introduction: Recurrence of splenic volvulus after splenopexy in children is rare. A consensus on the optimal surgical strategy in splenic volvulus is lacking. Case Presentation: An 11-year-old female presented left upper quadrant abdominal pain for
Externí odkaz:
https://doaj.org/article/3d97ef9b3f9740bd9a9de8acee70dfbf
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:
Christelle Sommer, Eleuthere Stathopoulos, Maria Christina Antoniou, Kanetee Busiah, Michael Hauschild, Oliver Sanchez
Publikováno v:
Journal of Pediatric Surgery Case Reports, Vol 59, Iss , Pp 101532- (2020)
Externí odkaz:
https://doaj.org/article/b808d11e422449a0a5bd90914b37e943
Autor:
Elisabeth Bruder, Virginie Galati-Fournier, Michèle Moesch, Jakob Usemann, Eleuthere Stathopoulos, Dietmar Cholewa, Peter Schmittenbecher, Thomas Krebs, Bertram Reingruber, Sasha J. Tharakan, Simone Keck, Urs Kym, Ulrike Subotic, Philipp Romero, Stefan Holland-Cunz
Background & AimsHirschsprung’s disease (HSCR) is a congenital intestinal motility disorder defined by the absence of enteric nervous cells (ganglia). The development of HSCR-associated enterocolitis remains a life-threatening complication. Absence
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1da626cb85ee7ec8120b59a9f7b84673
https://doi.org/10.1101/2020.06.15.151621
https://doi.org/10.1101/2020.06.15.151621
Autor:
Maria Christina Antoniou, Kanetee Busiah, Christelle Sommer, Oliver Sanchez, Eleuthere Stathopoulos, Michael Hauschild
Publikováno v:
Journal of Pediatric Surgery Case Reports, Vol 59, Iss, Pp 101532-(2020)
Publikováno v:
Journal of Pediatric Surgery Case Reports, Vol 3, Iss 6, Pp 242-244 (2015)
Journal of Pediatric Surgery Case Reports, vol. 3, pp. 242-244
Journal of Pediatric Surgery Case Reports, vol. 3, pp. 242-244
We describe a unique case of anorectal malformation (ARM) with a non-terminal colovesical fistula. While some aspects are similar to the congenital pouch colon (CPC), the differences make it a distinct form.
Publikováno v:
Journal of Pediatric Surgery Case Reports, Vol 3, Iss 6, Pp 242-244 (2015)
We describe a unique case of anorectal malformation (ARM) with a non-terminal colovesical fistula. While some aspects are similar to the congenital pouch colon (CPC), the differences make it a distinct form.
Externí odkaz:
https://doaj.org/article/d49d724f38914885941abb936cc15423