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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1993 1
2002 3
2003 2
2004 5
2005 4
2006 1
2007 4
2008 4
2009 5
2010 6
2011 7
2012 5
2013 2
2014 3
2015 7
2016 3
2017 3
2018 7
2019 1
2020 6
2021 8
2022 7
2023 5
2024 2

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87 results

Results by year

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Page 1
Hereditary Hyperferritinemia.
Piperno A, Pelucchi S, Mariani R. Piperno A, et al. Int J Mol Sci. 2023 Jan 29;24(3):2560. doi: 10.3390/ijms24032560. Int J Mol Sci. 2023. PMID: 36768886 Free PMC article. Review.
Commentary.
Piperno A. Piperno A. Clin Chem. 2020 Feb 1;66(2):281. doi: 10.1093/clinchem/hvz009. Clin Chem. 2020. PMID: 32040588 No abstract available.
Juvenile Hemochromatosis.
Piperno A, Bertola F, Bentivegna A. Piperno A, et al. 2005 Feb 17 [updated 2020 Jan 9]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. 2005 Feb 17 [updated 2020 Jan 9]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. PMID: 20301349 Free Books & Documents. Review.
Inherited iron overload disorders.
Piperno A, Pelucchi S, Mariani R. Piperno A, et al. Transl Gastroenterol Hepatol. 2020 Apr 5;5:25. doi: 10.21037/tgh.2019.11.15. eCollection 2020. Transl Gastroenterol Hepatol. 2020. PMID: 32258529 Free PMC article. Review.
Myelodysplastic Syndromes and Iron Chelation Therapy.
Angelucci E, Urru SA, Pilo F, Piperno A. Angelucci E, et al. Among authors: piperno a. Mediterr J Hematol Infect Dis. 2017 Mar 1;9(1):e2017021. doi: 10.4084/MJHID.2017.021. eCollection 2017. Mediterr J Hematol Infect Dis. 2017. PMID: 28293409 Free PMC article. Review.
Molecular diagnosis of hemochromatosis.
Piperno A. Piperno A. Expert Opin Med Diagn. 2013 Mar;7(2):161-77. doi: 10.1517/17530059.2013.763794. Epub 2013 Jan 23. Expert Opin Med Diagn. 2013. PMID: 23530886 Review.
Long-term outcome of a cohort of Italian patients affected with alpha-Mannosidosis.
Bertolini A, Rigoldi M, Cianflone A, Mariani R, Piperno A, Canonico F, Cefalo G, Carubbi F, Simonati A, Urban ML, Beccari T, Parini R. Bertolini A, et al. Among authors: piperno a. Clin Dysmorphol. 2024 Jan 1;33(1):1-8. doi: 10.1097/MCD.0000000000000474. Epub 2023 Nov 23. Clin Dysmorphol. 2024. PMID: 37791705 Free PMC article.
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: piperno a. Int J Mol Sci. 2021 Jan 27;22(3):1245. doi: 10.3390/ijms22031245. Int J Mol Sci. 2021. PMID: 33513852 Free PMC article.
Ferroportin disease: A novel SLC40A1 mutation.
Ravasi G, Pelucchi S, Russo A, Mariani R, Piperno A. Ravasi G, et al. Among authors: piperno a. 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.
87 results