Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Hansjoerg Schaefer"'
Autor:
Torben Kehl, Daniel Biermann, Andrea Briem-Richter, Gerhard Schoen, Jakob Olfe, Joerg S Sachweh, Lutz Fischer, Hansjoerg Schaefer, Rainer Kozlik-Feldmann, Urda Gottschalk
Publikováno v:
PLoS ONE, Vol 16, Iss 3, p e0248776 (2021)
Patients undergoing complex pediatric cardiac surgery in early infancy are at risk of postoperative secondary end-organ dysfunction. The aim of this study was to determine specific risk factors promoting the development of peri- and postoperative hep
Externí odkaz:
https://doaj.org/article/6ad7da3db425452989f694188f073aa9
Autor:
Christian Tomuschat, Stefan Mietzsch, Sebastian Dwertmann-Rico, Till Clauditz, Hansjoerg Schaefer, Konrad Reinshagen
Publikováno v:
Children, Vol 9, Iss 2, p 152 (2022)
Background: The transition zone (TZ) is defined by specific histological findings in patients with Hirschsprung Disease (HSCR). HSCR treatment includes surgical removal of the aganglionic zone (AZ). During the pull-through procedure, it is critical t
Externí odkaz:
https://doaj.org/article/09dd7d839fb240a494ca52157459c77d
Autor:
Urda Gottschalk, Joerg S. Sachweh, Torben Kehl, Andrea Briem-Richter, R. Kozlik-Feldmann, Jakob Olfe, Lutz Fischer, D. Biermann, Gerhard Schoen, Hansjoerg Schaefer
Publikováno v:
PLoS ONE
PLoS ONE, Vol 16, Iss 3, p e0248776 (2021)
PLoS ONE, Vol 16, Iss 3, p e0248776 (2021)
Patients undergoing complex pediatric cardiac surgery in early infancy are at risk of postoperative secondary end-organ dysfunction. The aim of this study was to determine specific risk factors promoting the development of peri- and postoperative hep
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::12cb96c953209c39f100fceb1cd0307f
http://europepmc.org/articles/PMC7993827
http://europepmc.org/articles/PMC7993827
Publikováno v:
Transplant International. 23:1068-1070
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7232f2d5d48bb6006b8f0199a27970a2
https://doi.org/10.1111/j.1432-2277.2010.01121.x
https://doi.org/10.1111/j.1432-2277.2010.01121.x
Autor:
Carmen Montoya, Lutz Fischer, Markus J. Kemper, Florian Brinkert, Knut Helmke, Anja Lehnhardt, Carsten Bergmann, Hansjoerg Schaefer, Bjoern Nashan, Rainer Ganschow
Publikováno v:
Transplant international : official journal of the European Society for Organ Transplantation. 26(6)
In ARPKD, mutations in the PKHD1 gene lead to remodeling of the kidneys and liver. These may result in progressive liver fibrosis with portal hypertension requiring combined liver and kidney transplantation (CLKT). There is currently no consensus on
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ed1fac5c967cfddfa20483b3ca56fbbb
https://pubmed.ncbi.nlm.nih.gov/23582048
https://pubmed.ncbi.nlm.nih.gov/23582048
Publikováno v:
Transplant international : official journal of the European Society for Organ Transplantation. 23(10)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::7237fae3d8b7021e87924ee316edaee5
https://pubmed.ncbi.nlm.nih.gov/20536793
https://pubmed.ncbi.nlm.nih.gov/20536793
Autor:
Charalampos Karadimas, René Santer, Jaya Ganesh, Antonella Spinazzola, Kostas Tsiakas, Xiaoqi Ding, Orhan H. Akman, Sara Shanske, Salvatore Di Mauro, Massimo Zeviani, Hansjoerg Schaefer
Publikováno v:
Archives of neurology. 65(8)
Background Autosomal recessive mutations in MPV17 (OMIM*137960) have been identified in the hepatocerebral form of mitochondrial DNA depletion syndrome (MDS). Objective To describe the clinical, morphologic, and genetic findings in 3 children with MP
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6007528a9901bfb6284008628510cfbd
https://pubmed.ncbi.nlm.nih.gov/18695062
https://pubmed.ncbi.nlm.nih.gov/18695062
Autor:
Paulus G. Schurr, Viacheslav Kalinin, Uta Reichelt, Robin Wachowiak, Guido Sauter, Stefan Wolter, Hansjoerg Schaefer, Tim Strate, Helge Kleinhans, Jussuf T. Kaifi, Jakob R. Izbicki, Ronald Simon, Emre F. Yekebas
Publikováno v:
Clinical cancer research : an official journal of the American Association for Cancer Research. 12(17)
Purpose: In gastrointestinal stromal tumors (GIST), loss of heterozygosity (LOH) on chromosome 22 and its presumptive biological function has been described. The prognostic value of these and other DNA regions for patient survival remains unclear.Exp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::edf1ab1b6df9b2362b87ea64a3d1b531
https://pubmed.ncbi.nlm.nih.gov/16951233
https://pubmed.ncbi.nlm.nih.gov/16951233
Autor:
Robin Wachowiak, Guido Sauter, Melitta Schachner, Hansjoerg Schaefer, Uta Reichelt, Jussuf T. Kaifi, Jakob R. Izbicki, Alexander Quaas, Emre F. Yekebas, Paulus G. Schurr, Tim Strate, Andrea Strelow
Publikováno v:
Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc. 19(3)
The treatment strategy for mesenchymal tumors of the gastrointestinal tract is based upon typing of the tumor. Especially differential diagnosis of gastrointestinal stromal tumors (GISTs) to leiomyomas is crucial for determining radicality of surgery
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3a4458f1bcd866034547709dc7c764c8
https://pubmed.ncbi.nlm.nih.gov/16400320
https://pubmed.ncbi.nlm.nih.gov/16400320
Autor:
Andreas, Block, Dragan, Milasinovic, Juergen, Mueller, Peter, Schaefer, Hansjoerg, Schaefer, Heiner, Greten
Publikováno v:
Anticancer research. 22(6A)
Mucin-1 is expressed in a variety of colon carcinomas and Muc-1/DF3 promoters have been utilized to reduce systemic toxicity through specific gene expression. To overcome weak expression, which is much lower than the widely used cytomegalovirus-promo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b2e57f4f8d8b7a8347e77de69d4be63f
https://pubmed.ncbi.nlm.nih.gov/12530077
https://pubmed.ncbi.nlm.nih.gov/12530077