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

Year Number of Results
2008 2
2009 1
2013 1
2015 1
2016 3
2017 6
2018 7
2019 9
2020 9
2021 4
2022 7
2023 7
2024 2

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54 results

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Page 1
Clinical and molecular description of the first Italian cohort of 33 subjects with hypophosphatasia.
Cinque L, Pugliese F, Salcuni AS, Trombetta D, Battista C, Biagini T, Augello B, Nardella G, Conti F, Corbetta S, Fischetto R, Foiadelli T, Gaudio A, Giannini C, Grosso E, Guabello G, Massuras S, Palermo A, Politano L, Pigliaru F, Ruggeri RM, Scarano E, Vicchio P, Cannavò S, Celli M, Petrizzelli F, Mastroianno M, Castori M, Scillitani A, Guarnieri V. Cinque L, et al. Among authors: biagini t. Front Endocrinol (Lausanne). 2023 Aug 1;14:1205977. doi: 10.3389/fendo.2023.1205977. eCollection 2023. Front Endocrinol (Lausanne). 2023. PMID: 37600704 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: biagini t. 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.
Molecular dynamics recipes for genome research.
Biagini T, Chillemi G, Mazzoccoli G, Grottesi A, Fusilli C, Capocefalo D, Castellana S, Vescovi AL, Mazza T. Biagini T, et al. Brief Bioinform. 2018 Sep 28;19(5):853-862. doi: 10.1093/bib/bbx006. Brief Bioinform. 2018. PMID: 28334084
RhythmicDB: A Database of Predicted Multi-Frequency Rhythmic Transcripts.
Castellana S, Biagini T, Petrizzelli F, Cabibbo A, Mazzoccoli G, Mazza T. Castellana S, et al. Among authors: biagini t. Front Genet. 2022 Jun 14;13:882044. doi: 10.3389/fgene.2022.882044. eCollection 2022. Front Genet. 2022. PMID: 35774515 Free PMC article.
microRNA-mRNA network model in patients with achalasia.
Palmieri O, Mazza T, Bassotti G, Merla A, Tolone S, Biagini T, Cuttitta A, Bossa F, Martino G, Latiano T, Corritore G, Gioffreda D, Palumbo O, Carella M, Panza A, Andriulli A, Latiano A. Palmieri O, et al. Among authors: biagini t. Neurogastroenterol Motil. 2020 Mar;32(3):e13764. doi: 10.1111/nmo.13764. Epub 2019 Nov 26. Neurogastroenterol Motil. 2020. PMID: 31773868
Further case of enlarged spinal nerve roots in KRAS-related Noonan syndrome.
Leoni C, Viscogliosi G, Onesimo R, Verdolotti T, Biagini T, Mazza T, De Luca A, Perri L, Trevisan V, Flex E, Tartaglia M, Zampino G. Leoni C, et al. Among authors: biagini t. Clin Genet. 2023 Jul;104(1):136-138. doi: 10.1111/cge.14308. Epub 2023 Feb 21. Clin Genet. 2023. PMID: 36757675
Dystonia as Presenting Feature of Compound Heterozygous PMPCA Gene Variants.
De Santis T, Serpieri V, Biagini T, Lanotte M, Criffò C, Mazza T, Valente EM, Albanese A. De Santis T, et al. Among authors: biagini t. Mov Disord Clin Pract. 2023 Apr 27;10(6):1020-1023. doi: 10.1002/mdc3.13749. eCollection 2023 Jun. Mov Disord Clin Pract. 2023. PMID: 37332652 No abstract available.
54 results