Zobrazeno 1 - 6
of 6
pro vyhledávání: '"hemochromatosis, iron overload"'
Autor:
Pierre Brissot, Ioav Cabantchik, Fabiana Busti, Domenico Girelli, Martina U. Muckenthaler, Graça Porto
Publikováno v:
Blood
Blood, 2022, 139 (20), pp.3018-3029. ⟨10.1182/blood.2021011338⟩
Blood, American Society of Hematology, 2021, ⟨10.1182/blood.2021011338⟩
Blood, 2022, 139 (20), pp.3018-3029. ⟨10.1182/blood.2021011338⟩
Blood, American Society of Hematology, 2021, ⟨10.1182/blood.2021011338⟩
Hemochromatosis (HC) is a genetically heterogeneous disorder in which uncontrolled intestinal iron absorption may lead to progressive iron overload (IO) responsible for disabling and life-threatening complications such as arthritis, diabetes, heart f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::416d5dcdc653ae0cf8a7c0ae40fc56d9
https://hal.science/hal-03418911/document
https://hal.science/hal-03418911/document
Autor:
GRENI, FEDERICO, MARIANI, RAFFAELLA, RAVASI, GIULIA, GALIMBERTI, STEFANIA, PIPERNO, ALBERTO, PELUCCHI, SARA, Valenti, L, Pelloni, I, Rametta, R, Busti, F, Girelli, D, Fargion, S
Publikováno v:
Annals of Hepatology, Vol 16, Iss 3, Pp 451-456 (2017)
Background and Aim: HFE-related Hemochromatosis (HH) is characterized by marked phenotype heterogeneity, probably due to the combined action of acquired and genetic factors. Among them, GNPAT rs11558492 was proposed as genetic modifier of iron status
Autor:
Barton, James C, Chen, Wen-Pin, Emond, Mary J, Phatak, Pradyumna D, Subramaniam, V Nathan, Adams, Paul C, Gurrin, Lyle C, Anderson, Gregory J, Ramm, Grant A, Powell, Lawrie W, Allen, Katrina J, Phillips, John D, Parker, Charles J, McLaren, Gordon D, McLaren, Christine E
BackgroundGNPAT p.D519G positivity is significantly increased in HFE p.C282Y homozygotes with markedly increased iron stores. We sought to determine associations of p.D519G and iron-related variables with iron stores in p.C282Y homozygotes.MethodsWe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______325::b9627cf30ad7c819ca1ad01e8ea499f6
https://escholarship.org/uc/item/8h0504v7
https://escholarship.org/uc/item/8h0504v7
Autor:
Barton, James C a, f1f1Reprint request to: Dr. James C. Barton, Southern Iron Disorders Center, G-105, 2022 Brookwood Medical Center Drive, Birmingham, Alabama 35209, telephone (205) 877-2888, fax (205) 877-2039, email: ironmd@dnamail.com., Sawada-Hirai, Ritsuko b, Rothenberg, Barry E c, Acton, Ronald T c
Publikováno v:
In Blood Cells, Molecules and Diseases June 1999 25(3):147-155
Autor:
Phatak, P, Brissot, P, Wurster, M, Adams, P, Bonkovsky, H, Gross, J, Malfertheiner, P, Mclaren, G, Niederau, C, Powell, L, Russo, M, Stoelzel, U, Stremmel, W, Griffel, L, Lynch, N, Zhang, Y, Pietrangelo, A., PIPERNO, ALBERTO
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______1299::7ecc0cbc9fb1787fc9cd9613044aed40
http://hdl.handle.net/10281/77166
http://hdl.handle.net/10281/77166
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