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

Year Number of Results
1980 1
1981 1
1983 1
1984 2
1985 1
1986 1
1991 1
1992 3
1993 2
1994 1
1995 1
1998 1
2004 1
2008 5
2009 1
2012 2
2014 2
2015 5
2016 5
2017 6
2018 9
2019 2
2020 3
2021 2
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54 results
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Page 1
A Mild PUM1 Mutation Is Associated with Adult-Onset Ataxia, whereas Haploinsufficiency Causes Developmental Delay and Seizures.
Gennarino VA, Palmer EE, McDonell LM, Wang L, Adamski CJ, Koire A, See L, Chen CA, Schaaf CP, Rosenfeld JA, Panzer JA, Moog U, Hao S, Bye A, Kirk EP, Stankiewicz P, Breman AM, McBride A, Kandula T, Dubbs HA, Macintosh R, Cardamone M, Zhu Y, Ying K, Dias KR, Cho MT, Henderson LB, Baskin B, Morris P, Tao J, Cowley MJ, Dinger ME, Roscioli T, Caluseriu O, Suchowersky O, Sachdev RK, Lichtarge O, Tang J, Boycott KM, Holder JL Jr, Zoghbi HY. Gennarino VA, et al. Among authors: cardamone m. Cell. 2018 Feb 22;172(5):924-936.e11. doi: 10.1016/j.cell.2018.02.006. Cell. 2018. PMID: 29474920 Free PMC article.
Decoding the rosetta stone of mitonuclear communication.
English J, Son JM, Cardamone MD, Lee C, Perissi V. English J, et al. Among authors: cardamone md. Pharmacol Res. 2020 Nov;161:105161. doi: 10.1016/j.phrs.2020.105161. Epub 2020 Aug 23. Pharmacol Res. 2020. PMID: 32846213 Review.
Inherited myopathies and muscular dystrophies.
Cardamone M, Darras BT, Ryan MM. Cardamone M, et al. Semin Neurol. 2008 Apr;28(2):250-9. doi: 10.1055/s-2008-1062269. Semin Neurol. 2008. PMID: 18351526 Review.
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