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Fatty acid supplementation in a case of maternal phenylketonuria.
Giovannini M, Biasucci G, Agostoni C, Bellù R, Riva E. Giovannini M, et al. Among authors: biasucci g. J Inherit Metab Dis. 1994;17(5):630-1. doi: 10.1007/BF00711606. J Inherit Metab Dis. 1994. PMID: 7837774 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.
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.
Maternal Carriage in Late-Onset Group B Streptococcus Disease, Italy.
Berardi A, Spada C, Creti R, Auriti C, Gambini L, Rizzo V, Capretti M, Laforgia N, Papa I, Tarocco A, Lanzoni A, Biasucci G, Piccinini G, Nardella G, Latorre G, Merazzi D, Travan L, Reggiani MLB, Baroni L, Ciccia M, Lucaccioni L, Iughetti L, Lugli L. Berardi A, et al. Among authors: biasucci g. Emerg Infect Dis. 2021;27(9):2279-2287. doi: 10.3201/eid2709.210049. Emerg Infect Dis. 2021. PMID: 34423765 Free PMC article.
141 results