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

Year Number of Results
2003 1
2004 1
2005 2
2006 2
2007 2
2008 2
2010 1
2011 1
2012 2
2013 4
2014 1
2015 2
2017 4
2018 1
2019 2
2020 2
2021 3
2022 5
2023 7
2024 1

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41 results

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Page 1
FOXG1 variants can be associated with milder phenotypes than congenital Rett syndrome with unassisted walking and language development.
Mazel B, Delanne J, Garde A, Racine C, Bruel AL, Duffourd Y, Lopergolo D, Santorelli FM, Marchi V, Pinto AM, Mencarelli MA, Canitano R, Valentino F, Papa FT, Fallerini C, Mari F, Renieri A, Munnich A, Niclass T, Le Guyader G, Thauvin-Robinet C, Philippe C, Faivre L. Mazel B, et al. Among authors: canitano r. Am J Med Genet B Neuropsychiatr Genet. 2024 Mar 8:e32970. doi: 10.1002/ajmg.b.32970. Online ahead of print. Am J Med Genet B Neuropsychiatr Genet. 2024. PMID: 38459409
Natural Course of IQSEC2-Related Encephalopathy: An Italian National Structured Survey.
Leoncini S, Boasiako L, Lopergolo D, Altamura M, Fazzi C, Canitano R, Grosso S, Meloni I, Baldassarri M, Croci S, Renieri A, Mastrangelo M, De Felice C. Leoncini S, et al. Among authors: canitano r. Children (Basel). 2023 Aug 24;10(9):1442. doi: 10.3390/children10091442. Children (Basel). 2023. PMID: 37761403 Free PMC article.
Autism care pathway in Europe.
Mendez MA, Oakley B, Canitano R, San José-Cáceres A, Tinelli M, Knapp M, Cusack J, Parellada M, Violland P, Derk Plas JR, Canal-Bedia R, Bejarano-Martin A, Murphy DGM, Quoidbach V, Arango C. Mendez MA, et al. Among authors: canitano r. Eur Psychiatry. 2023 Sep 11;66(1):e81. doi: 10.1192/j.eurpsy.2023.2435. Eur Psychiatry. 2023. PMID: 37694810 Free PMC article.
Autism with co-occurring epilepsy care pathway in Europe.
Mendez MA, Canitano R, Oakley B, San José-Cáceres A, Tinelli M, Knapp M, Cusack J, Parellada M, Violland P, Derk Plas JR, Murphy DGM, Quoidbach V, Arango C. Mendez MA, et al. Among authors: canitano r. Eur Psychiatry. 2023 Jul 20;66(1):e61. doi: 10.1192/j.eurpsy.2023.2426. Eur Psychiatry. 2023. PMID: 37470323 Free PMC article.
Natural history of KBG syndrome in a large European cohort.
Loberti L, Bruno LP, Granata S, Doddato G, Resciniti S, Fava F, Carullo M, Rahikkala E, Jouret G, Menke LA, Lederer D, Vrielynck P, Ryba L, Brunetti-Pierri N, Lasa-Aranzasti A, Cueto-González AM, Trujillano L, Valenzuela I, Tizzano EF, Spinelli AM, Bruno I, Currò A, Stanzial F, Benedicenti F, Lopergolo D, Santorelli FM, Aristidou C, Tanteles GA, Maystadt I, Tkemaladze T, Reimand T, Lokke H, Õunap K, Haanpää MK, Holubová A, Zoubková V, Schwarz M, Žordania R, Muru K, Roht L, Tihveräinen A, Teek R, Thomson U, Atallah I, Superti-Furga A, Buoni S, Canitano R, Scandurra V, Rossetti A, Grosso S, Battini R, Baldassarri M, Mencarelli MA, Rizzo CL, Bruttini M, Mari F, Ariani F, Renieri A, Pinto AM. Loberti L, et al. Among authors: canitano r. Hum Mol Genet. 2022 Dec 16;31(24):4131-4142. doi: 10.1093/hmg/ddac167. Hum Mol Genet. 2022. PMID: 35861666 Free PMC article.
41 results