Zobrazeno 1 - 10
of 47
pro vyhledávání: '"Anna Elisabeth Minder"'
Publikováno v:
Acta Dermato-Venereologica, Vol 104 (2024)
Abstract is missing (Short communication)
Externí odkaz:
https://doaj.org/article/353b2c085a2344d394aba4caa719d42c
Autor:
Christine Baumgartner, Claudia Kuehni, Gisela Michel, Katharina Roser, Jörg D Leuppi, Maria M Wertli, Eva Maria Eugenia Tinner, Oezcan Dogan, Maria Boesing, Anna-Elisabeth Minder, Sabrina Maier, Marinela Bayha, Helene Affolter, Fabian Meienberg, Jochen Rössler
Publikováno v:
BMJ Open, Vol 14, Iss 7 (2024)
Objectives In our study, we aimed to characterise adult childhood cancer survivors (ACCS), assess their health issues, gauge health-related quality of life (HRQOL) and evaluate visit satisfaction.Design Prospective cohort study using data from clinic
Externí odkaz:
https://doaj.org/article/9d74f40b843b44f8997b74c72c64fc23
Autor:
Adrian Belosevic, Anna-Elisabeth Minder, Morgan Gueuning, Franziska van Breemen, Gian Andri Thun, Maja P. Mattle-Greminger, Stefan Meyer, Alessandra Baumer, Elisabeth I. Minder, Xiaoye Schneider-Yin, Jasmin Barman-Aksözen
Publikováno v:
Life, Vol 13, Iss 9, p 1889 (2023)
Acute porphyrias are a group of monogenetic inborn errors of heme biosynthesis, characterized by acute and potentially life-threatening neurovisceral attacks upon exposure to certain triggering factors. Biochemical analyses can determine the type of
Externí odkaz:
https://doaj.org/article/1aa2f4fc9c104c9db505d8c902b9f107
Autor:
Edwige Collaud, Luis Wittwer, Anna-Elisabeth Minder, Jean-Marie Annoni, Elisabeth I. Minder, Joelle N. Chabwine
Publikováno v:
Frontiers in Genetics, Vol 13 (2022)
Background and aims: Porphyrias constitute a group of rare genetic diseases due to various, mostly autosomal dominant mutations, causing enzymatic deficiency in heme biosynthesis. As a result, neurotoxic porphyrin precursors and light-sensitive porph
Externí odkaz:
https://doaj.org/article/f98a16d4673c41c694c109716c6fbe02
Autor:
Anna-Elisabeth Minder, Xiaoye Schneider-Yin, Henryk Zulewski, Christoph E. Minder, Elisabeth I. Minder
Publikováno v:
Life, Vol 13, Iss 4, p 1066 (2023)
In animal models, melanocyte-stimulating hormones (MSHs) protect the liver from various injuries. Erythropoietic protoporphyria (EPP), a metabolic disorder, leads to the accumulation of protoporphyrin (PPIX). In addition to the most prominent symptom
Externí odkaz:
https://doaj.org/article/841d190ad35344b985b32d6f0a91a8f8
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-8 (2020)
Abstract Background Erythropoietic protoporphyria (EPP) is an ultra-rare genetic disorder (prevalence 1:150`000) characterized by instant painful phototoxic burn reactions in skin exposed to visible light. Afamelanotide is the first clinically tested
Externí odkaz:
https://doaj.org/article/6b08104a96af4ca78ec05e47ca17fe7e
Autor:
Jochen A. Vielhaber, Jasmin Barman-Aksözen, Elisabeth I. Minder, Xiaoye Schneider-Yin, Henryk Zulewski, Anna-Elisabeth Minder
Publikováno v:
Obesity Surgery. 33:1600-1602
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::346e5e78a2baae81fe0d170c9de08ab0
https://doi.org/10.1007/s11695-023-06555-w
https://doi.org/10.1007/s11695-023-06555-w
Autor:
Cynthia Janine Huppermans, Anna Elisabeth Minder, Lukas Frischknecht, Eric Grouzmann, Jean-Louis Blouin, Thierry Nouspikel, Andreas Werner Jehle, Henryk Zulewski
Publikováno v:
Swiss Medical Forum ‒ Schweizerisches Medizin-Forum.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ec6b4816d74f10dd9312110951f4a38d
https://doi.org/10.4414/smf.2023.09379
https://doi.org/10.4414/smf.2023.09379
Autor:
Cynthia Janine Huppermans, Anna Elisabeth Minder, Lukas Frischknecht, Eric Grouzmann, Jean-Louis Blouin, Thierry Nouspikel, Andreas Werner Jehle, Henryk Zulewski
Publikováno v:
Forum Médical Suisse ‒ Swiss Medical Forum.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c144da9739a88e2976e753fbd102c183
https://doi.org/10.4414/fms.2023.09379
https://doi.org/10.4414/fms.2023.09379
Autor:
Jasmin Barman-Aksözen, Anna-Elisabeth Minder, Francesca Granata, Mårten Pettersson, Cornelia Dechant, Mehmet Hakan Aksözen, Rocco Falchetto
Publikováno v:
International Journal of Environmental Research and Public Health; Volume 20; Issue 7; Pages: 5296
Erythropoietic protoporphyria (EPP) is an ultra-rare inborn error of metabolism characterised by painful phototoxic burn injuries after short exposure times to visible light. Patients with EPP are highly adapted to their condition which makes the qua
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::68371d6dbba67e89820c8a17655f4d66