Vittoria Longo

Familial X;Y translocation with distinct phenotypic consequences: Characterization using FISH and array CGH

Nenad Bukvić, Valeria Delli Carri, Maria Luisa Di Cosola et al. · American Journal of Medical Genetics Part A · 2010 · 88 citations

Life Sciences, Genetics, Molecular Genetics +17

Outcome of patients with splanchnic venous thrombosis presenting without overt MPN: A role for the JAK2 V617F mutation re-evaluation

Donatella Colaizzo, Lucio Amitrano, Maria Anna Guardascione et al. · Thrombosis Research · 2013 · 34 citations

Medicine, Genetics, Hematology +12

Screening of mutations of hemophilia A in 40 Italian patients: a novel G-to-A mutation in intron 10 of the F8 gene as a putative cause of mild hemophilia a in southern Italy

Rosa Santacroce, Rita Santoro, Francesco Sessa et al. · Blood Coagulation & Fibrinolysis · 2008 · 31 citations

Life Sciences, Genetics, Molecular Genetics +17

Phenylalanine hydroxylase deficiency in south Italy: Genotype–phenotype correlations, identification of a novel mutant PAH allele and prediction of BH4 responsiveness

Roberta Trunzo, Rosa Santacroce, Giovanna D’Andrea et al. · Clinica Chimica Acta · 2015 · 28 citations

Life Sciences, Genetics, Molecular Genetics +16

Mutation analysis in hyperphenylalaninemia patients from South Italy

Roberta Trunzo, Rosa Santacroce, Giovanna D’Andrea et al. · Clinical Biochemistry · 2013 · 15 citations

Life Sciences, Genetics, Molecular Genetics +14