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Genetic Testing and Molecular Biomarkers|September 1, 2009
Detection of new deletions in a group of Italian patients with Hemophilia A by multiplex ligation-dependent probe amplificationRosa Santacroce, Vittoria Longo, Valeria Bafunno, et al.
Clinical Immunology (Orlando, Fla.)|March 7, 2015
Characterization of patients with angioedema without wheals: the importance of F12 gene screeningDavide Firinu, Valeria Bafunno, Gennaro Vecchione, et al.
The American Journal of Cardiology|June 15, 2007
A novel mutation in human ether-a-go-go-related gene, alanine to proline at position 490, found in a large family with autosomal dominant long QT syndromePier Luigi Pellegrino, Valeria Bafunno, Riccardo Ieva, et al.
Thrombosis Research|April 19, 2011
Sex modulation of the occurrence of jak2 v617f mutation in patients with splanchnic venous thrombosisDonatella Colaizzo, Giovanni Luca Tiscia, Valeria Bafunno, et al.
Thrombosis Research|September 23, 2014
A novel congenital dysprothrombinemia leading to defective prothrombin maturationValeria Bafunno, Loredana Bury, Giovanni Luca Tiscia, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|July 27, 2015
Phenylalanine hydroxylase deficiency in south Italy: Genotype-phenotype correlations, identification of a novel mutant PAH allele and prediction of BH4 responsivenessRoberta Trunzo, Rosa Santacroce, Giovanna D'Andrea, et al.
Forensic Science International|August 30, 2011
Fatal pulmonary thromboembolism. A retrospective autopsy study: searching for genetic thrombophilias (Factor V Leiden (G1691A) and FII (G20210A) gene variants) and dating the thrombusVittorio Fineschi, Valeria Bafunno, Stefania Bello, et al.
The Journal of Allergy and Clinical Immunology|June 12, 2017
Mutation of the angiopoietin-1 gene (ANGPT1) associates with a new type of hereditary angioedemaValeria Bafunno, Davide Firinu, Maria D'Apolito, et al.
Thrombosis and Haemostasis|January 26, 2012
Obstetric complications and pregnancy-related venous thromboembolism: the effect of low-molecular-weight heparin on their prevention in carriers of factor V Leiden or prothrombin G20210A mutationDaniela Tormene, Elvira Grandone, Valerio De Stefano, et al.
Allergy|December 21, 2019
Impaired control of the contact system in hereditary angioedema with normal C1-inhibitorMaria Bova, Chiara Suffritti, Valeria Bafunno, et al.
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