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

Year Number of Results
1978 1
1980 2
1985 1
1986 2
1987 2
1988 6
1989 2
1990 3
1991 4
1992 2
1993 5
1994 7
1995 7
1996 8
1997 5
1998 9
1999 7
2000 7
2001 9
2002 7
2003 8
2004 13
2005 18
2006 15
2007 19
2008 18
2009 8
2010 12
2011 15
2012 21
2013 13
2014 24
2015 20
2016 13
2017 21
2018 16
2019 8
2020 12
2021 10
2022 5
2023 3
2024 1
2025 1

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342 results

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Page 1
NGS in Hereditary Ataxia: When Rare Becomes Frequent.
Galatolo D, De Michele G, Silvestri G, Leuzzi V, Casali C, Musumeci O, Antenora A, Astrea G, Barghigiani M, Battini R, Battisti C, Caputi C, Cioffi E, De Michele G, Dotti MT, Fico T, Fiorillo C, Galosi S, Lieto M, Malandrini A, Melone MAB, Mignarri A, Natale G, Pegoraro E, Petrucci A, Ricca I, Riso V, Rossi S, Rubegni A, Scarlatti A, Tinelli F, Trovato R, Tedeschi G, Tessa A, Filla A, Santorelli FM. Galatolo D, et al. Among authors: dotti mt. Int J Mol Sci. 2021 Aug 6;22(16):8490. doi: 10.3390/ijms22168490. Int J Mol Sci. 2021. PMID: 34445196 Free PMC article.
Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE): Position paper on diagnosis, prognosis, and treatment by the MNGIE International Network.
Hirano M, Carelli V, De Giorgio R, Pironi L, Accarino A, Cenacchi G, D'Alessandro R, Filosto M, Martí R, Nonino F, Pinna AD, Baldin E, Bax BE, Bolletta A, Bolletta R, Boschetti E, Cescon M, D'Angelo R, Dotti MT, Giordano C, Gramegna LL, Levene M, Lodi R, Mandel H, Morelli MC, Musumeci O, Pugliese A, Scarpelli M, Siniscalchi A, Spinazzola A, Tal G, Torres-Torronteras J, Vignatelli L, Zaidman I, Zoller H, Rinaldi R, Zeviani M. Hirano M, et al. Among authors: dotti mt. J Inherit Metab Dis. 2021 Mar;44(2):376-387. doi: 10.1002/jimd.12300. Epub 2020 Sep 8. J Inherit Metab Dis. 2021. PMID: 32898308 Free PMC article. Review.
Pregnancy in CADASIL.
Donnini I, Rinnoci V, Nannucci S, Valenti R, Pescini F, Mariani G, Bianchi S, Dotti MT, Federico A, Inzitari D, Pantoni L. Donnini I, et al. Among authors: dotti mt. Acta Neurol Scand. 2017 Dec;136(6):668-671. doi: 10.1111/ane.12784. Epub 2017 Jun 12. Acta Neurol Scand. 2017. PMID: 28608406
Cerebrotendinous xanthomatosis.
Federico A, Dotti MT. Federico A, et al. Among authors: dotti mt. Neurology. 2001 Nov 13;57(9):1743. doi: 10.1212/wnl.57.9.1743. Neurology. 2001. PMID: 11706139 No abstract available.
Congenital myopathies: clinical phenotypes and new diagnostic tools.
Cassandrini D, Trovato R, Rubegni A, Lenzi S, Fiorillo C, Baldacci J, Minetti C, Astrea G, Bruno C, Santorelli FM; Italian Network on Congenital Myopathies. Cassandrini D, et al. Ital J Pediatr. 2017 Nov 15;43(1):101. doi: 10.1186/s13052-017-0419-z. Ital J Pediatr. 2017. PMID: 29141652 Free PMC article. Review.
Hereditary cerebral small vessel diseases: a review.
Federico A, Di Donato I, Bianchi S, Di Palma C, Taglia I, Dotti MT. Federico A, et al. Among authors: dotti mt. J Neurol Sci. 2012 Nov 15;322(1-2):25-30. doi: 10.1016/j.jns.2012.07.041. Epub 2012 Aug 4. J Neurol Sci. 2012. PMID: 22868088 Review.
Hippocampal atrophy and white matter lesions characteristics can predict evolution to dementia in patients with vascular mild cognitive impairment.
Manco C, Cortese R, Leoncini M, Plantone D, Gentile G, Luchetti L, Zhang J, Di Donato I, Salvadori E, Poggesi A, Cosottini M, Mascalchi M, Federico A, Dotti MT, Battaglini M, Inzitari D, Pantoni L, De Stefano N; VMCI-Tuscany Study Group. Manco C, et al. Among authors: dotti mt. J Neurol Sci. 2024 Sep 15;464:123163. doi: 10.1016/j.jns.2024.123163. Epub 2024 Aug 6. J Neurol Sci. 2024. PMID: 39128160 Free article.
342 results