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Hereditary fructose intolerance: functional study of two novel ALDOB natural variants and characterization of a partial gene deletion.
Hum Mutat. 2010 Dec;31(12):1294-303. doi: 10.1002/humu.21359. Epub 2010 Nov 16.
Hum Mutat. 2010.
PMID: 20848650
Six novel alleles identified in Italian hereditary fructose intolerance patients enlarge the mutation spectrum of the aldolase B gene.
Esposito G, Santamaria R, Vitagliano L, Ieno L, Viola A, Fiori L, Parenti G, Zancan L, Zagari A, Salvatore F.
Esposito G, et al. Among authors: ieno l.
Hum Mutat. 2004 Dec;24(6):534. doi: 10.1002/humu.9290.
Hum Mutat. 2004.
PMID: 15532022
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Transglutaminase 1 deficiency and corneocyte collapse: an indication for targeted molecular screening in autosomal recessive congenital ichthyosis.
Esposito G, Tadini G, Paparo F, Viola A, Ieno L, Pennacchia W, Messina F, Giordano L, Piccirillo A, Auricchio L.
Esposito G, et al. Among authors: ieno l.
Br J Dermatol. 2007 Oct;157(4):808-10. doi: 10.1111/j.1365-2133.2007.08070.x. Epub 2007 Jul 16.
Br J Dermatol. 2007.
PMID: 17635512
No abstract available.
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Six novel mutations in the proopiomelanocortin and melanocortin receptor 4 genes in severely obese adults living in southern Italy.
Buono P, Pasanisi F, Nardelli C, Ieno L, Capone S, Liguori R, Finelli C, Oriani G, Contaldo F, Sacchetti L.
Buono P, et al. Among authors: ieno l.
Clin Chem. 2005 Aug;51(8):1358-64. doi: 10.1373/clinchem.2005.047886. Epub 2005 Jun 10.
Clin Chem. 2005.
PMID: 15951321
Free article.
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The unpredictable clinical course of an abdominal cyst diagnosed in the prenatal period: A case report.
Sica C, Orlandi G, Schiattarella A, Sica G, Toscano P, Lettieri A, Gabrielli O, Manzo L, Mazzarelli LL, Di Meglio L, Di Meglio L, Gulino FA, Incognito GG, Tuscano A, Ieno L, Palumbo M, Guida M, Di Meglio A.
Sica C, et al. Among authors: ieno l.
Case Rep Womens Health. 2023 Nov 28;40:e00568. doi: 10.1016/j.crwh.2023.e00568. eCollection 2023 Dec.
Case Rep Womens Health. 2023.
PMID: 38094079
Free PMC article.
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