Authors:
Biondi, ML
Marasini, B
Leviti, S
Turri, O
Bernini, M
Seminati, R
Porreca, W
Guagnellini, E
Citation: Ml. Biondi et al., Genotyping method for point mutation detection in the endothelial nitric oxide synthase exon 7 using fluorescent probes. Clinical validation in systemic sclerosis patients, CLIN CH L M, 39(3), 2001, pp. 281-282
Authors:
Ghilardi, G
Biondi, ML
Mangoni, J
Leviti, S
DeMonti, M
Guagnellini, E
Scorza, R
Citation: G. Ghilardi et al., Matrix metalloproteinase-1 promoter polymorphism 1G/2G is correlated with colorectal cancer invasiveness, CLIN CANC R, 7(8), 2001, pp. 2344-2346
Authors:
Marasini, B
Casari, S
Bestetti, A
Maioli, C
Cugno, M
Zeni, S
Turri, O
Guagnelli, E
Biondi, ML
Citation: B. Marasini et al., Homocysteine concentration in primary and systemic sclerosis associated Raynaud's phenomenon, J RHEUMATOL, 27(11), 2000, pp. 2621-2623
Authors:
Rottoli, A
Gianni, ML
Verduci, E
Biondi, ML
Fiori, L
Giovannini, M
Riva, E
Citation: A. Rottoli et al., Should genetic analysis in newborn screening and a heterozygote test for hyperphenylalaninaemia be recommended? An Italian study, J MED SCREE, 6(4), 1999, pp. 193-194
Authors:
Biondi, ML
Turri, O
Dilillo, D
Stival, G
Guagnellini, E
Citation: Ml. Biondi et al., Contribution of the TATA-box genotype (Gilbert syndrome) to serum bilirubin concentrations in the Italian population., CLIN CHEM, 45(6), 1999, pp. 897-898