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Tracking the Initial Diffusion of SARS-CoV-2 Omicron Variant in Italy by RT-PCR and Comparison with Alpha and Delta Variants Spreading.
Diagnostics (Basel). 2022 Feb 11;12(2):467. doi: 10.3390/diagnostics12020467.
Diagnostics (Basel). 2022.
PMID: 35204558
Free PMC article.
Age and Sex Modulate SARS-CoV-2 Viral Load Kinetics: A Longitudinal Analysis of 1735 Subjects.
Caputo V, Termine A, Fabrizio C, Calvino G, Luzzi L, Fusco C, Ingrascì A, Peconi C, D'Alessio R, Mihali S, Trastulli G, Megalizzi D, Cascella R, Rossini A, Salvia A, Strafella C, Giardina E.
Caputo V, et al. Among authors: trastulli g.
J Pers Med. 2021 Sep 2;11(9):882. doi: 10.3390/jpm11090882.
J Pers Med. 2021.
PMID: 34575659
Free PMC article.
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Analysis of Genetic Variants Associated with COVID-19 Outcome Highlights Different Distributions among Populations.
Fabrizio C, Termine A, Caputo V, Megalizzi D, Calvino G, Trastulli G, Ingrascì A, Ferrante S, Peconi C, Rossini A, Salvia A, Caltagirone C, Strafella C, Giardina E, Cascella R.
Fabrizio C, et al. Among authors: trastulli g.
J Pers Med. 2022 Nov 5;12(11):1851. doi: 10.3390/jpm12111851.
J Pers Med. 2022.
PMID: 36579599
Free PMC article.
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Epigenetic profiling of the D4Z4 locus: Optimization of the protocol for studying DNA methylation at single CpG site level.
Megalizzi D, Trastulli G, Caputo V, Colantoni L, Caltagirone C, Strafella C, Cascella R, Giardina E.
Megalizzi D, et al. Among authors: trastulli g.
Electrophoresis. 2023 Oct;44(19-20):1588-1594. doi: 10.1002/elps.202300058. Epub 2023 Aug 11.
Electrophoresis. 2023.
PMID: 37565369
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Innovations in Medicine: Exploring ChatGPT's Impact on Rare Disorder Management.
Zampatti S, Peconi C, Megalizzi D, Calvino G, Trastulli G, Cascella R, Strafella C, Caltagirone C, Giardina E.
Zampatti S, et al. Among authors: trastulli g.
Genes (Basel). 2024 Mar 28;15(4):421. doi: 10.3390/genes15040421.
Genes (Basel). 2024.
PMID: 38674356
Free PMC article.
Review.
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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: trastulli g.
Clin Genet. 2024 Mar;105(3):335-339. doi: 10.1111/cge.14466. Epub 2023 Dec 2.
Clin Genet. 2024.
PMID: 38041579
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Whole exome sequencing highlights rare variants in CTCF, DNMT1, DNMT3A, EZH2 and SUV39H1 as associated with FSHD.
Strafella C, Caputo V, Bortolani S, Torchia E, Megalizzi D, Trastulli G, Monforte M, Colantoni L, Caltagirone C, Ricci E, Tasca G, Cascella R, Giardina E.
Strafella C, et al. Among authors: trastulli g.
Front Genet. 2023 Aug 22;14:1235589. doi: 10.3389/fgene.2023.1235589. eCollection 2023.
Front Genet. 2023.
PMID: 37674478
Free PMC article.
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