Pelucchi S - Search Results

1

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: pelucchi s. Eur J Haematol. 2004 May;72(5):370-4. doi: 10.1111/j.1600-0609.2004.00230.x. Eur J Haematol. 2004. PMID: 15059075

2

Prevalence of C282Y and E168X HFE mutations in an Italian population of Northern European ancestry.

Salvioni A, Mariani R, Oberkanins C, Moritz A, Mauri V, Pelucchi S, Riva A, Arosio C, Cerutti P, Piperno A. Salvioni A, et al. Among authors: pelucchi s. Haematologica. 2003 Mar;88(3):250-5. Haematologica. 2003. PMID: 12651261

3

Homozygosity for transferrin receptor-2 Y250X mutation induces early iron overload.

Piperno A, Roetto A, Mariani R, Pelucchi S, Corengia C, Daraio F, Piga A, Garozzo G, Camaschella C. Piperno A, et al. Among authors: pelucchi s. Haematologica. 2004 Mar;89(3):359-60. Haematologica. 2004. PMID: 15020277

4

Gene symbol: FTL. Disease: Hyperferritinemia-cataract syndrome.

Piperno A, Pelucchi S. Piperno A, et al. Among authors: pelucchi s. Hum Genet. 2004 Mar;114(4):406. Hum Genet. 2004. PMID: 15046083 No abstract available.

5

Iron chelation therapy in aceruloplasminaemia: study of a patient with a novel missense mutation.

Mariani R, Arosio C, Pelucchi S, Grisoli M, Piga A, Trombini P, Piperno A. Mariani R, et al. Among authors: pelucchi s. Gut. 2004 May;53(5):756-8. doi: 10.1136/gut.2003.030429. Gut. 2004. PMID: 15082597 Free PMC article.

6

Erythrocytapheresis plus erythropoietin: an alternative therapy for selected patients with hemochromatosis and severe organ damage.

Mariani R, Pelucchi S, Perseghin P, Corengia C, Piperno A. Mariani R, et al. Among authors: pelucchi s. Haematologica. 2005 May;90(5):717-8. Haematologica. 2005. PMID: 15921401

7

Novel mutations of the ferroportin gene (SLC40A1): analysis of 56 consecutive patients with unexplained iron overload.

Pelucchi S, Mariani R, Salvioni A, Bonfadini S, Riva A, Bertola F, Trombini P, Piperno A. Pelucchi S, et al. Clin Genet. 2008 Feb;73(2):171-8. doi: 10.1111/j.1399-0004.2007.00950.x. Epub 2007 Dec 27. Clin Genet. 2008. PMID: 18177470

8

Hepcidin and iron-related gene expression in subjects with Dysmetabolic Hepatic Iron Overload.

Barisani D, Pelucchi S, Mariani R, Galimberti S, Trombini P, Fumagalli D, Meneveri R, Nemeth E, Ganz T, Piperno A. Barisani D, et al. Among authors: pelucchi s. J Hepatol. 2008 Jul;49(1):123-33. doi: 10.1016/j.jhep.2008.03.011. Epub 2008 Apr 10. J Hepatol. 2008. PMID: 18462824

9

Reduced expression of hepcidin in patients with myelodysplastic syndrome and myelofibrosis: the causes might be more heterogeneous than in thalassaemia.

Mariani R, Pelucchi S, Pozzi M, Paolini V, Piperno A. Mariani R, et al. Among authors: pelucchi s. Br J Haematol. 2008 Dec;143(5):746-7. doi: 10.1111/j.1365-2141.2008.07397.x. Br J Haematol. 2008. PMID: 19036019 Free article. No abstract available.

10

Expression of hepcidin and other iron-related genes in type 3 hemochromatosis due to a novel mutation in transferrin receptor-2.

Pelucchi S, Mariani R, Trombini P, Coletti S, Pozzi M, Paolini V, Barisani D, Piperno A. Pelucchi S, et al. Haematologica. 2009 Feb;94(2):276-9. doi: 10.3324/haematol.13576. Epub 2009 Jan 14. Haematologica. 2009. PMID: 19144662 Free PMC article.

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