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Clinical Approach in the Management of Paediatric Patients with Familial Hypercholesterolemia: A National Survey Conducted by the LIPIGEN Paediatric Group.
Pederiva C, Gazzotti M, Arca M, Averna M, Banderali G, Biasucci G, Brambilla M, Buonuomo PS, Calabrò P, Cipollone F, Citroni N, D'Addato S, Del Ben M, Genovesi S, Guardamagna O, Iannuzzo G, Iughetti L, Mandraffino G, Maroni L, Mombelli G, Muntoni S, Nascimbeni F, Passaro A, Pellegatta F, Pirro M, Pisciotta L, Pujia R, Sarzani R, Scicali R, Suppressa P, Zambon S, Zenti MG, Calandra S, Catapano AL, Tarugi P, Galimberti F, Casula M, Capra ME. Pederiva C, et al. Among authors: biasucci g. Nutrients. 2023 Aug 5;15(15):3468. doi: 10.3390/nu15153468. Nutrients. 2023. PMID: 37571405 Free PMC article.
Refinement of the diagnostic approach for the identification of children and adolescents affected by familial hypercholesterolemia: Evidence from the LIPIGEN study.
Casula M, Gazzotti M, Capra ME, Olmastroni E, Galimberti F, Catapano AL, Pederiva C; LIPIGEN Group and the LIPIGEN Paediatric Group. Casula M, et al. Atherosclerosis. 2023 Nov;385:117231. doi: 10.1016/j.atherosclerosis.2023.117231. Epub 2023 Aug 12. Atherosclerosis. 2023. PMID: 37648636 Free article.
Escherichia coli Is Overtaking Group B Streptococcus in Early-Onset Neonatal Sepsis.
Miselli F, Cuoghi Costantini R, Creti R, Sforza F, Fanaro S, Ciccia M, Piccinini G, Rizzo V, Pasini L, Biasucci G, Pagano R, Capretti M, China M, Gambini L, Pulvirenti RM, Dondi A, Lanari M, Pedna M, Ambretti S, Lugli L, Bedetti L, Berardi A. Miselli F, et al. Among authors: biasucci g. Microorganisms. 2022 Sep 20;10(10):1878. doi: 10.3390/microorganisms10101878. Microorganisms. 2022. PMID: 36296155 Free PMC article.
Structure and mutation analysis of the glycogen storage disease type 1b gene.
Marcolongo P, Barone V, Priori G, Pirola B, Giglio S, Biasucci G, Zammarchi E, Parenti G, Burchell A, Benedetti A, Sorrentino V. Marcolongo P, et al. Among authors: biasucci g. FEBS Lett. 1998 Oct 2;436(2):247-50. doi: 10.1016/s0014-5793(98)01129-6. FEBS Lett. 1998. PMID: 9781688 Free article.
Genotype-phenotype correlation in dihydropteridine reductase deficiency.
de Sanctis L, Alliaudi C, Spada M, Farrugia R, Cerone R, Biasucci G, Meli C, Zammarchi E, Coskun T, Blau N, Ponzone A, Dianzani I. de Sanctis L, et al. Among authors: biasucci g. J Inherit Metab Dis. 2000 Jun;23(4):333-7. doi: 10.1023/a:1005662710891. J Inherit Metab Dis. 2000. PMID: 10896287 No abstract available.
Clinical relevance of short-chain acyl-CoA dehydrogenase (SCAD) deficiency: Exploring the role of new variants including the first SCAD-disease-causing allele carrying a synonymous mutation.
Tonin R, Caciotti A, Funghini S, Pasquini E, Mooney SD, Cai B, Proncopio E, Donati MA, Baronio F, Bettocchi I, Cassio A, Biasucci G, Bordugo A, la Marca G, Guerrini R, Morrone A. Tonin R, et al. Among authors: biasucci g. BBA Clin. 2016 Mar 10;5:114-9. doi: 10.1016/j.bbacli.2016.03.004. eCollection 2016 Jun. BBA Clin. 2016. PMID: 27051597 Free PMC article.
130 results