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Unexplained isolated hyperferritinemia without iron overload.
Ravasi G, Pelucchi S, Mariani R, Casati M, Greni F, Arosio C, Pelloni I, Majore S, Santambrogio P, Levi S, Piperno A. Ravasi G, et al. Among authors: arosio c. Am J Hematol. 2017 Apr;92(4):338-343. doi: 10.1002/ajh.24641. Epub 2017 Feb 7. Am J Hematol. 2017. PMID: 28052375 Free article.
Transferrin receptor 2 mutations in patients with juvenile hemochromatosis phenotype.
Ravasi G, Rausa M, Pelucchi S, Arosio C, Greni F, Mariani R, Pelloni I, Silvestri L, Pineda P, Camaschella C, Piperno A. Ravasi G, et al. Among authors: arosio c. Am J Hematol. 2015 Dec;90(12):E226-7. doi: 10.1002/ajh.24202. Epub 2015 Nov 17. Am J Hematol. 2015. PMID: 26408288 Free article. No abstract available.
HIF1A: A Putative Modifier of Hemochromatosis.
Pelucchi S, Ravasi G, Arosio C, Mauri M, Piazza R, Mariani R, Piperno A. Pelucchi S, et al. Among authors: arosio c. Int J Mol Sci. 2021 Jan 27;22(3):1245. doi: 10.3390/ijms22031245. Int J Mol Sci. 2021. PMID: 33513852 Free PMC article.
Type 3 hemochromatosis and beta-thalassemia trait.
Riva A, Mariani R, Bovo G, Pelucchi S, Arosio C, Salvioni A, Vergani A, Piperno A. Riva A, et al. Among authors: arosio c. Eur J Haematol. 2004 May;72(5):370-4. doi: 10.1111/j.1600-0609.2004.00230.x. Eur J Haematol. 2004. PMID: 15059075
Movement disorders and brain iron overload in a new subtype of aceruloplasminemia.
Melgari JM, Marano M, Quattrocchi CC, Piperno A, Arosio C, Frontali M, Nuovo S, Siotto M, Salomone G, Altavilla R, di Biase L, Scrascia F, Squitti R, Vernieri F. Melgari JM, et al. Among authors: arosio c. Parkinsonism Relat Disord. 2015 Jun;21(6):658-60. doi: 10.1016/j.parkreldis.2015.03.014. Epub 2015 Mar 19. Parkinsonism Relat Disord. 2015. PMID: 25864092 No abstract available.
43 results