Zobrazeno 1 - 10
of 41
pro vyhledávání: '"Schuster, Georg"'
Autor:
Zegota, Maksymilian M., Schuster, Georg, De Pra, Mauro, Müllner, Tibor, Menzen, Tim, Steiner, Frank, Hawe, Andrea
Publikováno v:
In Journal of Chromatography A 12 April 2024 1720
Thisreport about a study with H63D syndrome p:i s about the relationship between diabetes and iron metabolism disorders, focusing on the underlying mechanisms and potential therapeutic approaches. The association between iron metabolism disorders and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d4a3efd9809dc1164b5ad6e8f4be4c2e
H63D Syndrome is a genetic disorder characterized by iron accumulation in the body, which has been historically associated with hereditary hemochromatosis (HH). However, recent research has provided evidence that this syndrome, particularly type-1 H6
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8289b3f5b150b6db8be20b542011bd88
Autor:
Park, Soo Hyun, Shellie, Robert A., Dicinoski, Greg W., Schuster, Georg, Talebi, Mohammad, Haddad, Paul R., Szucs, Roman, Dolan, John W., Pohl, Christopher A.
Publikováno v:
In Journal of Chromatography A 4 March 2016 1436:59-63
The kynurenine pathway (KP) plays a crucial role in the metabolism of tryptophan, an essential amino acid. Accumulating evidence suggests that the KP and its intermediates, as well as the kynurenine/tryptophan (K/T) ratio, are closely associated with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cbad07f8146b866da33382f9168dfc41
Nach Auswertung von 1082 Patientenfällen hatdie Internationale Arbeitsgemeinschaft für die HFE-Gen-H63D-Forschung (International HFE Gene H63D Mutation Research Consortium) nun eine weitere klinische Variante des klassischen H63D-Syndroms (im Folge
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::55334b31c6e47cca52124ca7ab65bd5e
Publikováno v:
In Journal of Chromatography A 11 December 2015 1424:69-76
Autor:
Lazar, Marius, Seideman, David, Smith, Lucas, Makri, Sofia, Steinberg, Benjamin, Tudor, Adrian, Dimitrikova, Tamara, Ivanova, Olga, Wagner, Marianne, Louw, Alexander, Pistorius, Margaret, Honda, Riku, Cohen, Boris, Strelkov, Alexander, Tudor, Susan, Schuster, Georg, Diamandis, Carolina
Since H63D syndrome was first described, the authors of this paper systematically investigated for the first time to what extent the adrenal glands, as an integral part of the HPA and SAM axes, are also affected by damage caused by non-transferrin bo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0e0dc0ad7426cc41439bacf7586d2b62
The medical literature was systematically reviewed to answer the medical ethics question of whether patients with chronic cataplexy and a history of dangerous falls should be cared for by permanent use of custom-built wheelchairs with postural suppor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a8514a593de3574745674ad968b45d1d
Autor:
Lazar, Marius, Smith, Lucas, Seideman, David, Kaufmann, Marianne, Papadopoulou, Sophia, Tudor, Adrian, Feldman, Jonathan, Schuster, Georg, Honda, Riku, Adams, Jacob, Olga, Ivanova, Diamandis, Carolina
Evidence-based medicine has shown for many years that homozygous mutations of the HFE gene H63D are by no means negligible. Not only can it cause, usually after a second hit, rather mild classical hemochromatosis, but it can also cause numerous other
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::79afb4a23deccb787a06e8931e5536df
https://doi.org/10.22541/au.165271249.94667689/v1
https://doi.org/10.22541/au.165271249.94667689/v1