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

Year Number of Results
1970 1
1972 1
1982 1
1984 1
1985 3
1986 1
1987 1
1989 1
1991 3
1994 2
1995 2
1996 5
1997 3
1998 9
1999 7
2000 5
2002 4
2003 1
2004 4
2005 3
2006 2
2008 2
2009 1
2010 4
2011 1
2012 3
2013 4
2014 5
2015 1
2016 6
2017 2
2018 3
2019 9
2020 6
2021 10
2022 6
2023 3
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117 results
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Page 1
Molecular logic of cellular diversification in the mouse cerebral cortex.
Di Bella DJ, Habibi E, Stickels RR, Scalia G, Brown J, Yadollahpour P, Yang SM, Abbate C, Biancalani T, Macosko EZ, Chen F, Regev A, Arlotta P. Di Bella DJ, et al. Nature. 2021 Jul;595(7868):554-559. doi: 10.1038/s41586-021-03670-5. Epub 2021 Jun 23. Nature. 2021. PMID: 34163074 Free PMC article.
Genetic dissection of the glutamatergic neuron system in cerebral cortex.
Matho KS, Huilgol D, Galbavy W, He M, Kim G, An X, Lu J, Wu P, Di Bella DJ, Shetty AS, Palaniswamy R, Hatfield J, Raudales R, Narasimhan A, Gamache E, Levine JM, Tucciarone J, Szelenyi E, Harris JA, Mitra PP, Osten P, Arlotta P, Huang ZJ. Matho KS, et al. Among authors: di bella dj. Nature. 2021 Oct;598(7879):182-187. doi: 10.1038/s41586-021-03955-9. Epub 2021 Oct 6. Nature. 2021. PMID: 34616069 Free PMC article.
Digenic inheritance of STUB1 variants and TBP polyglutamine expansions explains the incomplete penetrance of SCA17 and SCA48.
Magri S, Nanetti L, Gellera C, Sarto E, Rizzo E, Mongelli A, Ricci B, Fancellu R, Sambati L, Cortelli P, Brusco A, Bruzzone MG, Mariotti C, Di Bella D, Taroni F. Magri S, et al. Among authors: di bella d. Genet Med. 2022 Jan;24(1):29-40. doi: 10.1016/j.gim.2021.08.003. Epub 2021 Nov 30. Genet Med. 2022. PMID: 34906452 Free article.
RARS1-related hypomyelinating leukodystrophy: Expanding the spectrum.
Mendes MI, Green LMC, Bertini E, Tonduti D, Aiello C, Smith D, Salsano E, Beerepoot S, Hertecant J, von Spiczak S, Livingston JH, Emrick L, Fraser J, Russell L, Bernard G, Magri S, Di Bella D, Taroni F, Koenig MK, Moroni I, Cappuccio G, Brunetti-Pierri N, Rhee J, Mendelsohn BA, Helbig I, Helbig K, Muhle H, Ismayl O, Vanderver AL, Salomons GS, van der Knaap MS, Wolf NI. Mendes MI, et al. Among authors: di bella d. Ann Clin Transl Neurol. 2020 Jan;7(1):83-93. doi: 10.1002/acn3.50960. Epub 2019 Dec 8. Ann Clin Transl Neurol. 2020. PMID: 31814314 Free PMC article.
ER Stress and Unfolded Protein Response in Leukemia: Friend, Foe, or Both?
Féral K, Jaud M, Philippe C, Di Bella D, Pyronnet S, Rouault-Pierre K, Mazzolini L, Touriol C. Féral K, et al. Among authors: di bella d. Biomolecules. 2021 Jan 30;11(2):199. doi: 10.3390/biom11020199. Biomolecules. 2021. PMID: 33573353 Free PMC article. Review.
3-Methylglutaconic Aciduria Type I: A Rare Cause of Late-Onset Leukoencephalopathy.
Benzoni C, Magri S, Moscatelli M, Fenu S, Caccia C, Taroni F, Salsano E, Di Bella D. Benzoni C, et al. Among authors: di bella d. Neurol Genet. 2022 Sep 7;8(5):e200023. doi: 10.1212/NXG.0000000000200023. eCollection 2022 Oct. Neurol Genet. 2022. PMID: 36092981 Free PMC article. No abstract available.
Hypomyelinating leukodystrophies in adults: Clinical and genetic features.
Di Bella D, Magri S, Benzoni C, Farina L, Maccagnano C, Sarto E, Moscatelli M, Baratta S, Ciano C, Piacentini SHMJ, Draghi L, Mauro E, Pareyson D, Gellera C, Taroni F, Salsano E. Di Bella D, et al. Eur J Neurol. 2021 Mar;28(3):934-944. doi: 10.1111/ene.14646. Epub 2020 Dec 3. Eur J Neurol. 2021. PMID: 33190326
Familial Jarcho-Levin syndrome.
Romeo MG, Distefano G, Di Bella D, Mangiagli A, Caltabiano L, Roccaro S, Mollica F. Romeo MG, et al. Among authors: di bella d. Clin Genet. 1991 Apr;39(4):253-9. doi: 10.1111/j.1399-0004.1991.tb03023.x. Clin Genet. 1991. PMID: 2070546
117 results