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

Year Number of Results
1997 1
2001 1
2010 2
2011 5
2012 4
2013 2
2015 2
2017 1
2019 4
2020 4
2021 15
2022 9
2023 8
2024 8

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60 results

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Page 1
Genotype-phenotype correlates in Joubert syndrome: A review.
Gana S, Serpieri V, Valente EM. Gana S, et al. Am J Med Genet C Semin Med Genet. 2022 Mar;190(1):72-88. doi: 10.1002/ajmg.c.31963. Epub 2022 Mar 3. Am J Med Genet C Semin Med Genet. 2022. PMID: 35238134 Free PMC article. Review.
Routine sterile glove and instrument change at the time of abdominal wound closure to prevent surgical site infection (ChEETAh): a pragmatic, cluster-randomised trial in seven low-income and middle-income countries.
NIHR Global Research Health Unit on Global Surgery. NIHR Global Research Health Unit on Global Surgery. Lancet. 2022 Nov 19;400(10365):1767-1776. doi: 10.1016/S0140-6736(22)01884-0. Epub 2022 Oct 31. Lancet. 2022. PMID: 36328045 Free article. Clinical Trial.
Movement Disorders in Genetic Pediatric Ataxias.
Gana S, Valente EM. Gana S, et al. Mov Disord Clin Pract. 2020 Apr 6;7(4):383-393. doi: 10.1002/mdc3.12937. eCollection 2020 May. Mov Disord Clin Pract. 2020. PMID: 32373654 Free PMC article. Review.
RFC1 expansions are a common cause of idiopathic sensory neuropathy.
Currò R, Salvalaggio A, Tozza S, Gemelli C, Dominik N, Galassi Deforie V, Magrinelli F, Castellani F, Vegezzi E, Businaro P, Callegari I, Pichiecchio A, Cosentino G, Alfonsi E, Marchioni E, Colnaghi S, Gana S, Valente EM, Tassorelli C, Efthymiou S, Facchini S, Carr A, Laura M, Rossor AM, Manji H, Lunn MP, Pegoraro E, Santoro L, Grandis M, Bellone E, Beauchamp NJ, Hadjivassiliou M, Kaski D, Bronstein AM, Houlden H, Reilly MM, Mandich P, Schenone A, Manganelli F, Briani C, Cortese A. Currò R, et al. Among authors: gana s. Brain. 2021 Jun 22;144(5):1542-1550. doi: 10.1093/brain/awab072. Brain. 2021. PMID: 33969391 Free PMC article.
Recurrent, founder and hypomorphic variants contribute to the genetic landscape of Joubert syndrome.
Serpieri V, Mortarini G, Loucks H, Biagini T, Micalizzi A, Palmieri I, Dempsey JC, D'Abrusco F, Mazzotta C, Battini R, Bertini ES, Boltshauser E, Borgatti R, Brockmann K, D'Arrigo S, Nardocci N, Fischetto R, Agolini E, Novelli A, Romano A, Romaniello R, Stanzial F, Signorini S, Strisciuglio P, Gana S, Mazza T, Doherty D, Valente EM. Serpieri V, et al. Among authors: gana s. J Med Genet. 2023 Sep;60(9):885-893. doi: 10.1136/jmg-2022-108725. Epub 2023 Feb 14. J Med Genet. 2023. PMID: 36788019 Free PMC article.
Appendiceal Schistosomiasis Presenting as an Appendiceal Mass.
Nwabuoku SE, Mukoro GD, Daniyan M, Dauda MM, Khalid L, Aliyu HO, Shittu SM, Gana SG, Suraj A, Idokoko E, Okeke C, Iji L, Audu JA. Nwabuoku SE, et al. Among authors: gana sg. J West Afr Coll Surg. 2022 Jan-Mar;12(1):100-103. doi: 10.4103/jwas.jwas_82_22. Epub 2022 Aug 23. J West Afr Coll Surg. 2022. PMID: 36203918 Free PMC article.
CDKL5 deficiency disorder in males: Five new variants and review of the literature.
Siri B, Varesio C, Freri E, Darra F, Gana S, Mei D, Porta F, Fontana E, Galati G, Solazzi R, Niceta M, Veggiotti P, Alfei E. Siri B, et al. Among authors: gana s. Eur J Paediatr Neurol. 2021 Jul;33:9-20. doi: 10.1016/j.ejpn.2021.04.007. Epub 2021 Apr 30. Eur J Paediatr Neurol. 2021. PMID: 33989939 Review.
60 results