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Results by year

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

Year Number of Results
1948 1
1950 1
1952 5
1953 5
1954 1
1956 3
1957 5
1958 4
1959 1
1961 1
1962 2
1963 8
1964 6
1965 4
1966 3
1967 6
1968 5
1969 5
1970 8
1971 3
1972 1
1973 2
1977 1
1978 1
1979 2
1980 4
1981 4
1982 6
1983 2
1984 3
1985 6
1986 4
1987 2
1988 2
1989 7
1990 7
1991 4
1992 9
1993 8
1994 6
1995 6
1996 11
1997 3
1998 6
1999 3
2000 4
2001 2
2002 4
2003 4
2004 5
2005 5
2006 3
2007 8
2008 10
2009 13
2010 6
2011 9
2012 6
2013 6
2014 8
2015 8
2016 5
2017 5
2018 6
2019 2
2020 16
2021 27
2022 14
2023 16
2024 4

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Article type

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359 results

Results by year

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Page 1
Hereditary Hyperferritinemia.
Piperno A, Pelucchi S, Mariani R. Piperno A, et al. Among authors: mariani r. 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.
Inherited iron overload disorders.
Piperno A, Pelucchi S, Mariani R. Piperno A, et al. Among authors: mariani r. 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.
Dominant ARF3 variants disrupt Golgi integrity and cause a neurodevelopmental disorder recapitulated in zebrafish.
Fasano G, Muto V, Radio FC, Venditti M, Mosaddeghzadeh N, Coppola S, Paradisi G, Zara E, Bazgir F, Ziegler A, Chillemi G, Bertuccini L, Tinari A, Vetro A, Pantaleoni F, Pizzi S, Conti LA, Petrini S, Bruselles A, Prandi IG, Mancini C, Chandramouli B, Barth M, Bris C, Milani D, Selicorni A, Macchiaiolo M, Gonfiantini MV, Bartuli A, Mariani R, Curry CJ, Guerrini R, Slavotinek A, Iascone M, Dallapiccola B, Ahmadian MR, Lauri A, Tartaglia M. Fasano G, et al. Among authors: mariani r. Nat Commun. 2022 Nov 11;13(1):6841. doi: 10.1038/s41467-022-34354-x. Nat Commun. 2022. PMID: 36369169 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: mariani r. 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: mariani r. 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.
New trends in neuronal migration disorders.
Verrotti A, Spalice A, Ursitti F, Papetti L, Mariani R, Castronovo A, Mastrangelo M, Iannetti P. Verrotti A, et al. Among authors: mariani r. Eur J Paediatr Neurol. 2010 Jan;14(1):1-12. doi: 10.1016/j.ejpn.2009.01.005. Epub 2009 Mar 4. Eur J Paediatr Neurol. 2010. PMID: 19264520 Review.
Eponym : Rasmussen syndrome.
Mastrangelo M, Mariani R, Menichella A. Mastrangelo M, et al. Among authors: mariani r. Eur J Pediatr. 2010 Aug;169(8):919-24. doi: 10.1007/s00431-010-1148-0. Epub 2010 Feb 23. Eur J Pediatr. 2010. PMID: 20177700 Review.
359 results