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Page 1
Mutation analysis in hyperphenylalaninemia patients from South Italy.
Trunzo R, Santacroce R, D'Andrea G, Longo V, De Girolamo G, Dimatteo C, Leccese A, Lillo V, Papadia F, Margaglione M. Trunzo R, et al. Among authors: lillo v. Clin Biochem. 2013 Dec;46(18):1896-8. doi: 10.1016/j.clinbiochem.2013.06.009. Epub 2013 Jun 18. Clin Biochem. 2013. PMID: 23792259
Phenylalanine hydroxylase deficiency in south Italy: Genotype-phenotype correlations, identification of a novel mutant PAH allele and prediction of BH4 responsiveness.
Trunzo R, Santacroce R, D'Andrea G, Longo V, De Girolamo G, Dimatteo C, Leccese A, Bafunno V, Lillo V, Papadia F, Margaglione M. Trunzo R, et al. Among authors: lillo v. Clin Chim Acta. 2015 Oct 23;450:51-5. doi: 10.1016/j.cca.2015.07.014. Epub 2015 Jul 23. Clin Chim Acta. 2015. PMID: 26210745
Pseudodiastrophic dysplasia type Burgio in a newborn.
Fischetto R, Causio F, Corso G, Lillo V, Natale B, Papadia F. Fischetto R, et al. Among authors: lillo v. Am J Med Genet. 1997 Aug 8;71(2):222-5. doi: 10.1002/(sici)1096-8628(19970808)71:2<222::aid-ajmg20>3.0.co;2-f. Am J Med Genet. 1997. PMID: 9217227
Homochiral Metal-Organic Frameworks for Enantioselective Separations in Liquid Chromatography.
Corella-Ochoa MN, Tapia JB, Rubin HN, Lillo V, González-Cobos J, Núñez-Rico JL, Balestra SRG, Almora-Barrios N, Lledós M, Güell-Bara A, Cabezas-Giménez J, Escudero-Adán EC, Vidal-Ferran A, Calero S, Reynolds M, Martí-Gastaldo C, Galán-Mascarós JR. Corella-Ochoa MN, et al. Among authors: lillo v. J Am Chem Soc. 2019 Sep 11;141(36):14306-14316. doi: 10.1021/jacs.9b06500. Epub 2019 Sep 3. J Am Chem Soc. 2019. PMID: 31426632
24 results