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

Year Number of Results
1978 1
1996 1
2000 1
2001 2
2003 1
2004 1
2007 1
2008 2
2009 2
2010 2
2011 2
2012 2
2013 3
2015 1
2016 3
2017 4
2018 4
2019 3
2020 4
2021 5
2022 2
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43 results
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Page 1
The role of SUMOylation during development.
Talamillo A, Barroso-Gomila O, Giordano I, Ajuria L, Grillo M, Mayor U, Barrio R. Talamillo A, et al. Among authors: giordano i. Biochem Soc Trans. 2020 Apr 29;48(2):463-478. doi: 10.1042/BST20190390. Biochem Soc Trans. 2020. PMID: 32311032 Free PMC article. Review.
SALL1 Modulates CBX4 Stability, Nuclear Bodies, and Regulation of Target Genes.
Giordano I, Pirone L, Muratore V, Landaluze E, Pérez C, Lang V, Garde-Lapido E, Gonzalez-Lopez M, Barroso-Gomila O, Vertegaal ACO, Aransay AM, Rodriguez JA, Rodriguez MS, Sutherland JD, Barrio R. Giordano I, et al. Front Cell Dev Biol. 2021 Sep 21;9:715868. doi: 10.3389/fcell.2021.715868. eCollection 2021. Front Cell Dev Biol. 2021. PMID: 34621739 Free PMC article.
Onset features and time to diagnosis in Friedreich's Ataxia.
Indelicato E, Nachbauer W, Eigentler A, Amprosi M, Matteucci Gothe R, Giunti P, Mariotti C, Arpa J, Durr A, Klopstock T, Schöls L, Giordano I, Bürk K, Pandolfo M, Didszdun C, Schulz JB, Boesch S; EFACTS (European Friedreich’s Ataxia Consortium for Translational Studies). Indelicato E, et al. Among authors: giordano i. Orphanet J Rare Dis. 2020 Aug 3;15(1):198. doi: 10.1186/s13023-020-01475-9. Orphanet J Rare Dis. 2020. PMID: 32746884 Free PMC article.
Progression characteristics of the European Friedreich's Ataxia Consortium for Translational Studies (EFACTS): a 4-year cohort study.
Reetz K, Dogan I, Hilgers RD, Giunti P, Parkinson MH, Mariotti C, Nanetti L, Durr A, Ewenczyk C, Boesch S, Nachbauer W, Klopstock T, Stendel C, Rodríguez de Rivera Garrido FJ, Rummey C, Schöls L, Hayer SN, Klockgether T, Giordano I, Didszun C, Rai M, Pandolfo M, Schulz JB; EFACTS study group. Reetz K, et al. Among authors: giordano i. Lancet Neurol. 2021 May;20(5):362-372. doi: 10.1016/S1474-4422(21)00027-2. Epub 2021 Mar 23. Lancet Neurol. 2021. PMID: 33770527
Truncated SALL1 Impedes Primary Cilia Function in Townes-Brocks Syndrome.
Bozal-Basterra L, Martín-Ruíz I, Pirone L, Liang Y, Sigurðsson JO, Gonzalez-Santamarta M, Giordano I, Gabicagogeascoa E, de Luca A, Rodríguez JA, Wilkie AOM, Kohlhase J, Eastwood D, Yale C, Olsen JV, Rauchman M, Anderson KV, Sutherland JD, Barrio R. Bozal-Basterra L, et al. Among authors: giordano i. Am J Hum Genet. 2018 Feb 1;102(2):249-265. doi: 10.1016/j.ajhg.2017.12.017. Am J Hum Genet. 2018. PMID: 29395072 Free PMC article.
Safety and Efficacy of Acetyl-DL-Leucine in Certain Types of Cerebellar Ataxia: The ALCAT Randomized Clinical Crossover Trial.
Feil K, Adrion C, Boesch S, Doss S, Giordano I, Hengel H, Jacobi H, Klockgether T, Klopstock T, Nachbauer W, Schöls L, Steiner KM, Stendel C, Timmann D, Naumann I, Mansmann U, Strupp M; ALCAT Study Group. Feil K, et al. Among authors: giordano i. JAMA Netw Open. 2021 Dec 1;4(12):e2135841. doi: 10.1001/jamanetworkopen.2021.35841. JAMA Netw Open. 2021. PMID: 34905009 Free PMC article. Clinical Trial.
Prominent White Matter Involvement in Multiple System Atrophy of Cerebellar Type.
Faber J, Giordano I, Jiang X, Kindler C, Spottke A, Acosta-Cabronero J, Nestor PJ, Machts J, Düzel E, Vielhaber S, Speck O, Dudesek A, Kamm C, Scheef L, Klockgether T. Faber J, et al. Among authors: giordano i. Mov Disord. 2020 May;35(5):816-824. doi: 10.1002/mds.27987. Epub 2020 Jan 29. Mov Disord. 2020. PMID: 31994808
Clinical and genetic characteristics of sporadic adult-onset degenerative ataxia.
Giordano I, Harmuth F, Jacobi H, Paap B, Vielhaber S, Machts J, Schöls L, Synofzik M, Sturm M, Tallaksen C, Wedding IM, Boesch S, Eigentler A, van de Warrenburg B, van Gaalen J, Kamm C, Dudesek A, Kang JS, Timmann D, Silvestri G, Masciullo M, Klopstock T, Neuhofer C, Ganos C, Filla A, Bauer P, Tezenas du Montcel S, Klockgether T. Giordano I, et al. Neurology. 2017 Sep 5;89(10):1043-1049. doi: 10.1212/WNL.0000000000004311. Epub 2017 Aug 9. Neurology. 2017. PMID: 28794257 Clinical Trial.
43 results