Ravasi G - Search Results

1

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. 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.

2

A severe hemojuvelin mutation leading to late onset of HFE2-hemochromatosis.

Ravasi G, Pelucchi S, Mariani R, Silvestri L, Camaschella C, Piperno A. Ravasi G, et al. Dig Liver Dis. 2018 Aug;50(8):859-862. doi: 10.1016/j.dld.2018.04.018. Epub 2018 Apr 27. Dig Liver Dis. 2018. PMID: 29764732 No abstract available.

3

Proprotein convertase 7 rs236918 associated with liver fibrosis in Italian patients with HFE-related hemochromatosis.

Pelucchi S, Galimberti S, Greni F, Rametta R, Mariani R, Pelloni I, Girelli D, Busti F, Ravasi G, Valsecchi MG, Valenti L, Piperno A. Pelucchi S, et al. Among authors: ravasi g. J Gastroenterol Hepatol. 2016 Jul;31(7):1342-8. doi: 10.1111/jgh.13315. J Gastroenterol Hepatol. 2016. PMID: 26868056

4

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. 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.

5

GNPAT rs11558492 is not a Major Modifier of Iron Status: Study of Italian Hemochromatosis Patients and Blood Donors.

Greni F, Valenti L, Mariani R, Pelloni I, Rametta R, Busti F, Ravasi G, Girelli D, Fargion S, Galimberti S, Piperno A, Pelucchi S. Greni F, et al. Among authors: ravasi g. Ann Hepatol. 2017 May-Jun;16(3):451-456. doi: 10.5604/16652681.1235489. Ann Hepatol. 2017. PMID: 28425416 Free article.

6

Ferroportin disease: A novel SLC40A1 mutation.

Ravasi G, Pelucchi S, Russo A, Mariani R, Piperno A. Ravasi G, et al. Dig Liver Dis. 2020 Jun;52(6):688-690. doi: 10.1016/j.dld.2020.03.013. Epub 2020 Apr 29. Dig Liver Dis. 2020. PMID: 32360131 No abstract available.

7

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: ravasi g. Int J Mol Sci. 2021 Jan 27;22(3):1245. doi: 10.3390/ijms22031245. Int J Mol Sci. 2021. PMID: 33513852 Free PMC article.

8

Ceruloplasmin variants might have different effects in different iron overload disorders.

Pelucchi S, Ravasi G, Piperno A. Pelucchi S, et al. Among authors: ravasi g. J Hepatol. 2021 Oct;75(4):1003-1004. doi: 10.1016/j.jhep.2021.05.005. Epub 2021 May 21. J Hepatol. 2021. PMID: 34023349 No abstract available.

9

Identification of Novel Mutations by Targeted NGS Panel in Patients with Hyperferritinemia.

Ravasi G, Pelucchi S, Bertola F, Capelletti MM, Mariani R, Piperno A. Ravasi G, et al. Genes (Basel). 2021 Nov 9;12(11):1778. doi: 10.3390/genes12111778. Genes (Basel). 2021. PMID: 34828384 Free PMC article.

10

Hepcidin expression in iron overload diseases is variably modulated by circulating factors.

Ravasi G, Pelucchi S, Trombini P, Mariani R, Tomosugi N, Modignani GL, Pozzi M, Nemeth E, Ganz T, Hayashi H, Barisani D, Piperno A. Ravasi G, et al. PLoS One. 2012;7(5):e36425. doi: 10.1371/journal.pone.0036425. Epub 2012 May 7. PLoS One. 2012. PMID: 22586470 Free PMC article.

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