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

Year Number of Results
1982 1
2000 1
2005 1
2006 1
2007 3
2008 2
2009 2
2010 4
2011 4
2012 6
2013 2
2014 1
2015 2
2016 2
2017 2
2018 10
2019 12
2020 13
2021 11
2022 9
2023 1
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76 results
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Page 1
The Nrf2 induction prevents ferroptosis in Friedreich's Ataxia.
La Rosa P, Petrillo S, Turchi R, Berardinelli F, Schirinzi T, Vasco G, Lettieri-Barbato D, Fiorenza MT, Bertini ES, Aquilano K, Piemonte F. La Rosa P, et al. Among authors: vasco g. Redox Biol. 2021 Jan;38:101791. doi: 10.1016/j.redox.2020.101791. Epub 2020 Nov 5. Redox Biol. 2021. PMID: 33197769 Free PMC article.
Heterozygous KIF1A variants underlie a wide spectrum of neurodevelopmental and neurodegenerative disorders.
Nicita F, Ginevrino M, Travaglini L, D'Arrigo S, Zorzi G, Borgatti R, Terrone G, Catteruccia M, Vasco G, Brankovic V, Siliquini S, Romano S, Veredice C, Pedemonte M, Armando M, Lettori D, Stregapede F, Bosco L, Sferra A, Tessarollo V, Romaniello R, Ristori G, Bertini E, Valente EM, Zanni G. Nicita F, et al. Among authors: vasco g. J Med Genet. 2021 Jul;58(7):475-483. doi: 10.1136/jmedgenet-2020-107007. Epub 2020 Jul 31. J Med Genet. 2021. PMID: 32737135
Antioxidant Response in Human X-Linked Adrenoleukodystrophy Fibroblasts.
Petrillo S, D'Amico J, Nicita F, Torda C, Vasco G, Bertini ES, Cappa M, Piemonte F. Petrillo S, et al. Among authors: vasco g. Antioxidants (Basel). 2022 Oct 28;11(11):2125. doi: 10.3390/antiox11112125. Antioxidants (Basel). 2022. PMID: 36358497 Free PMC article.
A clinical diagnostic algorithm for early onset cerebellar ataxia.
Brandsma R, Verschuuren-Bemelmans CC, Amrom D, Barisic N, Baxter P, Bertini E, Blumkin L, Brankovic-Sreckovic V, Brouwer OF, Bürk K, Catsman-Berrevoets CE, Craiu D, de Coo IFM, Gburek J, Kennedy C, de Koning TJ, Kremer HPH, Kumar R, Macaya A, Micalizzi A, Mirabelli-Badenier M, Nemeth A, Nuovo S, Poll-The B, Lerman-Sagie T, Steinlin M, Synofzik M, Tijssen MAJ, Vasco G, Willemsen MAAP, Zanni G, Valente EM, Boltshauser E, Sival DA. Brandsma R, et al. Among authors: vasco g. Eur J Paediatr Neurol. 2019 Sep;23(5):692-706. doi: 10.1016/j.ejpn.2019.08.004. Epub 2019 Aug 10. Eur J Paediatr Neurol. 2019. PMID: 31481303 Review.
Movement disorders in ADAR1 disease: Insights from a comprehensive cohort.
Di Lazzaro G, Graziola F, Sancesario A, Insalaco A, Moneta GM, Castelli E, Bertini E, Travaglini L, Stregapede F, Capuano A, Vasco G, Schirinzi T. Di Lazzaro G, et al. Among authors: vasco g. Parkinsonism Relat Disord. 2020 Oct;79:100-104. doi: 10.1016/j.parkreldis.2020.08.039. Epub 2020 Aug 30. Parkinsonism Relat Disord. 2020. PMID: 32911246 Review.
Serum uric acid in Friedreich Ataxia.
Schirinzi T, Vasco G, Zanni G, Petrillo S, Piemonte F, Castelli E, Bertini ES. Schirinzi T, et al. Among authors: vasco g. Clin Biochem. 2018 Apr;54:139-141. doi: 10.1016/j.clinbiochem.2018.01.022. Epub 2018 Feb 2. Clin Biochem. 2018. PMID: 29409831
Human COQ4 deficiency: delineating the clinical, metabolic and neuroimaging phenotypes.
Laugwitz L, Seibt A, Herebian D, Peralta S, Kienzle I, Buchert R, Falb R, Gauck D, Müller A, Grimmel M, Beck-Woedel S, Kern J, Daliri K, Katibeh P, Danhauser K, Leiz S, Alesi V, Baertling F, Vasco G, Steinfeld R, Wagner M, Caglayan AO, Gumus H, Burmeister M, Mayatepek E, Martinelli D, Tamhankar PM, Tamhankar V, Joset P, Steindl K, Rauch A, Bonnen PE, Froukh T, Groeschel S, Krägeloh-Mann I, Haack TB, Distelmaier F. Laugwitz L, et al. Among authors: vasco g. J Med Genet. 2022 Sep;59(9):878-887. doi: 10.1136/jmedgenet-2021-107729. Epub 2021 Oct 16. J Med Genet. 2022. PMID: 34656997 Free PMC article.
[Influence of the male genomic imprinting on the reproduction].
Vasco GC, Gil Villa AM, Piedrahita Ochoa C, Cardona Maya W, Cadavid Jaramillo A. Vasco GC, et al. Actas Urol Esp. 2008 Nov-Dec;32(10):1004-12. doi: 10.1016/s0210-4806(08)73979-2. Actas Urol Esp. 2008. PMID: 19143292 Review. Spanish.
76 results