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

Year Number of Results
2002 1
2003 2
2004 2
2006 4
2007 4
2008 9
2009 6
2010 9
2011 11
2012 13
2013 13
2014 18
2015 18
2016 25
2017 26
2018 25
2019 17
2020 20
2021 25
2022 19
2023 21
2024 5

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240 results

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Page 1
Genetic variants affecting NQO1 protein levels impact the efficacy of idebenone treatment in Leber hereditary optic neuropathy.
Aleo SJ, Del Dotto V, Romagnoli M, Fiorini C, Capirossi G, Peron C, Maresca A, Caporali L, Capristo M, Tropeano CV, Zanna C, Ross-Cisneros FN, Sadun AA, Pignataro MG, Giordano C, Fasano C, Cavaliere A, Porcelli AM, Tioli G, Musiani F, Catania A, Lamperti C, Marzoli SB, De Negri A, Cascavilla ML, Battista M, Barboni P, Carbonelli M, Amore G, La Morgia C, Smirnov D, Vasilescu C, Farzeen A, Blickhaeuser B, Prokisch H, Priglinger C, Livonius B, Catarino CB, Klopstock T, Tiranti V, Carelli V, Ghelli AM. Aleo SJ, et al. Among authors: giordano c. Cell Rep Med. 2024 Feb 20;5(2):101383. doi: 10.1016/j.xcrm.2023.101383. Epub 2024 Jan 24. Cell Rep Med. 2024. PMID: 38272025 Free PMC article.
Adrenal Cushing's syndrome in children.
Guarnotta V, Emanuele F, Salzillo R, Giordano C. Guarnotta V, et al. Among authors: giordano c. Front Endocrinol (Lausanne). 2023 Dec 12;14:1329082. doi: 10.3389/fendo.2023.1329082. eCollection 2023. Front Endocrinol (Lausanne). 2023. PMID: 38192416 Free PMC article. Review.
Clinical and histological features of patients with primary Sjögren's syndrome and autoimmune thyroiditis: a national multicentre cross-sectional study.
Colafrancesco S, Celia AI, Baldini C, Quartuccio L, Bartoloni E, Carubbi F, Orlandi M, Barbati C, Pignataro MG, Cerbelli B, Giordano C, Ferro F, Gattamelata A, Giardina F, Izzo R, Longhino S, De Vita S, Gerli R, Giacomelli R, Conti F, Priori R. Colafrancesco S, et al. Among authors: giordano c. Clin Exp Rheumatol. 2023 Dec;41(12):2389-2396. doi: 10.55563/clinexprheumatol/eh36vs. Epub 2023 Dec 23. Clin Exp Rheumatol. 2023. PMID: 38149510 Free article.
The application of a multidisciplinary approach in the diagnosis of Castleman disease and Castleman-like lymphadenopathies: A 20-year retrospective analysis of clinical and pathological features.
Pelliccia S, Rogges E, Cardoni A, Lopez G, Conte E, Faccini AL, De Vito R, Girardi K, Bianchi A, Annibali O, Fratoni S, Remotti D, De Angelis G, Giordano C, Palumbo G, Scarpino S, Del Porto F, Bianchi MP, Di Gregorio F, Tafuri A, Di Napoli A. Pelliccia S, et al. Among authors: giordano c. Br J Haematol. 2024 Feb;204(2):534-547. doi: 10.1111/bjh.19171. Epub 2023 Nov 12. Br J Haematol. 2024. PMID: 37953489
The role of genetic testing in suspected fulminant myocarditis: A case report.
Mistrulli R, Micolonghi C, Follesa F, Fabiani M, Pagannone E, D'Amati G, Giordano C, Caroselli S, Savio C, Germani A, Pizzuti A, Visco V, Petrucci S, Rubattu S, Piane M, Autore C. Mistrulli R, et al. Among authors: giordano c. Mol Genet Metab Rep. 2023 Aug 22;37:101000. doi: 10.1016/j.ymgmr.2023.101000. eCollection 2023 Dec. Mol Genet Metab Rep. 2023. PMID: 37662494 Free PMC article.
240 results