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Page 1
Characterization of D4Z4 alleles and assessment of de novo cases in Facioscapulohumeral dystrophy (FSHD) in a cohort of Italian families.
Strafella C, Colantoni L, Megalizzi D, Trastulli G, Piorgo EP, Primiano G, Sancricca C, Ricci G, Siciliano G, Caltagirone C, Filosto M, Tasca G, Ricci E, Cascella R, Giardina E. Strafella C, et al. Among authors: colantoni l. Clin Genet. 2024 Mar;105(3):335-339. doi: 10.1111/cge.14466. Epub 2023 Dec 2. Clin Genet. 2024. PMID: 38041579
The variability of SMCHD1 gene in FSHD patients: evidence of new mutations.
Strafella C, Caputo V, Galota RM, Campoli G, Bax C, Colantoni L, Minozzi G, Orsini C, Politano L, Tasca G, Novelli G, Ricci E, Giardina E, Cascella R. Strafella C, et al. Among authors: colantoni l. Hum Mol Genet. 2019 Dec 1;28(23):3912-3920. doi: 10.1093/hmg/ddz239. Hum Mol Genet. 2019. PMID: 31600781 Free PMC article.
Comparative analysis of antigen and molecular tests for the detection of Sars-CoV-2 and related variants: A study on 4266 samples.
Caputo V, Bax C, Colantoni L, Peconi C, Termine A, Fabrizio C, Calvino G, Luzzi L, Panunzi GG, Fusco C, Strafella C, Cascella R, Battistini L, Caltagirone C, Salvia A, Sancesario G, Giardina E. Caputo V, et al. Among authors: colantoni l. Int J Infect Dis. 2021 Jul;108:187-189. doi: 10.1016/j.ijid.2021.04.048. Epub 2021 Apr 18. Int J Infect Dis. 2021. PMID: 33878460 Free PMC article.
14 results