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151 results

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Page 1
Aktualisierte S2k-Leitlinie nicht-alkoholische Fettlebererkrankung der Deutschen Gesellschaft für Gastroenterologie, Verdauungs- und Stoffwechselkrankheiten (DGVS) – April 2022 – AWMF-Registernummer: 021–025.
Roeb E, Canbay A, Bantel H, Bojunga J, de Laffolie J, Demir M, Denzer UW, Geier A, Hofmann WP, Hudert C, Karlas T, Krawczyk M, Longerich T, Luedde T, Roden M, Schattenberg J, Sterneck M, Tannapfel A, Lorenz P, Tacke F; Collaborators:. Roeb E, et al. Z Gastroenterol. 2022 Sep;60(9):1346-1421. doi: 10.1055/a-1880-2283. Epub 2022 Sep 13. Z Gastroenterol. 2022. PMID: 36100202 Free article. German. No abstract available.
Amendment „Neue Nomenklatur zur MASLD (Metabolic Dysfunction Associated Steatotic Liver Disease; metabolische Dysfunktion assoziierte steatotische Lebererkrankung)“ zur S2k-Leitlinie „Nicht-alkoholische Fettlebererkrankung“ (v.2.0/April 2022) der Deutschen Gesellschaft für Gastroenterologie, Verdauungs- und Stoffwechselkrankheiten (DGVS).
Roeb E, Canbay A, Bantel H, Bojunga J, de Laffolie J, Demir M, Denzer UW, Geier A, Hofmann WP, Hudert C, Karlas T, Krawczyk M, Longerich T, Lüdde T, Roden M, Schattenberg JM, Sterneck M, Tannapfel A, Lorenz P, Tacke F; Collaborators. Roeb E, et al. Z Gastroenterol. 2024 Jul;62(7):1077-1087. doi: 10.1055/a-2309-6052. Epub 2024 Jul 8. Z Gastroenterol. 2024. PMID: 38976985 German. No abstract available.
Everolimus in pediatric transplantation.
Pape L, Ganschow R, Ahlenstiel T. Pape L, et al. Among authors: ganschow r. Curr Opin Organ Transplant. 2012 Oct;17(5):515-9. doi: 10.1097/MOT.0b013e328356b080. Curr Opin Organ Transplant. 2012. PMID: 22890040 Review.
The role of everolimus in liver transplantation.
Ganschow R, Pollok JM, Jankofsky M, Junge G. Ganschow R, et al. Clin Exp Gastroenterol. 2014 Sep 2;7:329-43. doi: 10.2147/CEG.S41780. eCollection 2014. Clin Exp Gastroenterol. 2014. PMID: 25214801 Free PMC article. Review.
Murine catalase phenotypes.
Ganschow RE, Schimke RT. Ganschow RE, et al. Biochem Genet. 1970 Feb;4(1):157-67. doi: 10.1007/BF00484027. Biochem Genet. 1970. PMID: 5462766 No abstract available.
Paediatric acute liver failure: A prospective, nationwide, population-based surveillance study in Germany.
Lenz D, Abdulaziz M, Peters B, Wagner M, Schlieben LD, Corman VM, Baumann U, Bufler P, Dattner T, Ganschow R, Genzel K, Hammann N, Hartleif S, Hegen B, Henning S, Hoerning A, Jankofsky M, Junge N, Kathemann S, Knoppke B, Kohl-Sobania M, Laass M, Lainka E, Lurz E, Melter M, Müller H, Pilic D, Ries M, Schiefele L, Schwerd T, Sturm E, Wegner M, Urschitz MS, Garbade SF, Wenning D, Drosten C, Fichtner A, Kölker S, Hoffmann GF, Prokisch H, Staufner C. Lenz D, et al. Among authors: ganschow r. J Pediatr Gastroenterol Nutr. 2025 Sep;81(3):653-662. doi: 10.1002/jpn3.70149. Epub 2025 Jul 7. J Pediatr Gastroenterol Nutr. 2025. PMID: 40621689 Free PMC article.
Mutations in CRLF1 cause familial achalasia.
Busch A, Žarković M, Lowe C, Jankofsky M, Ganschow R, Buers I, Kurth I, Reutter H, Rutsch F, Hübner CA. Busch A, et al. Among authors: ganschow r. Clin Genet. 2017 Jul;92(1):104-108. doi: 10.1111/cge.12953. Epub 2017 Mar 15. Clin Genet. 2017. PMID: 27976805
151 results