Zobrazeno 1 - 10
of 1 216
pro vyhledávání: '"Fiorelli, G."'
Autor:
Cappellini, MD, Fiorelli, G
Publikováno v:
In The Lancet 2008 371(9606):64-74
Autor:
Valenti, L, Dongiovanni, P, Fracanzani, A.L, Santorelli, G, Fatta, E, Bertelli, C, Taioli, E, Fiorelli, G, Fargion, S ∗
Publikováno v:
In Digestive and Liver Disease 2003 35(3):172-178
Autor:
Martinez di Montemuros, F, Di Pierro, E, Biolcati, G, Rocchi, E, Bissolotti, E, Tavazzi, D, Fiorelli, G, Cappellini, M.D
Publikováno v:
In Blood Cells, Molecules and Diseases November 2001 27(6):961-970
Autor:
Fiorelli, G.1, De Feo, T. M.1, Duca, L.1, Tavazzi, D.1, Nava, I.1, Fargion, S.1, Cappellini, M. D.1
Publikováno v:
European Journal of Clinical Investigation. Mar2002 Supplement 1, Vol. 32, p21-27. 7p.
Publikováno v:
The British Medical Journal, 1974 Mar . 1(5908), 636-636.
Externí odkaz:
https://www.jstor.org/stable/20468535
Autor:
Fargion, S, Bissoli, F, Fracanzani, A, Suigo, E, Sergi, C, Taioli, E, Ceriani, R, Dimasi, V, Sampietro, M, Fiorelli, G., PIPERNO, ALBERTO
Publikováno v:
Hepatology. 24:1161-1164
Genetic hemochromatosis and alpha1-antitrypsin (AAT) deficiency are frequent in white populations. Conflicting data on the association of the two conditions and on the severity of the disease in those in whom these disorders coexist have emerged from
Akademický článek
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Autor:
Camaschella, C., Daraio, F., Marco De Gobbi, Fiorelli, G., Kury, F., Moritz, A., Oberkanins, C.
Publikováno v:
Scopus-Elsevier
Hereditary hemochromatosis is a recessive condition characterized by iron accumulation in several organs, followed by organ damage and failure. The disorder is prevalently due to C282Y and H63D mutations in the HFE gene, but additional HFE and TFR2 m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::f34bb7019fc12d76e2c25e73218c200c