Paolo Versacci

Pubblicazioni

Titolo Pubblicato in Anno
Commentary: sVEGFR1 Is Enriched in Hepatic Vein Blood—Evidence for a Provisional Hepatic Factor Candidate? FRONTIERS IN PEDIATRICS 2021
When to test fetuses for RASopathies? Proposition from a systematic analysis of 352 multicenter cases and a postnatal cohort GENETICS IN MEDICINE 2021
Incidental SOS1 variant identified by non-invasive prenatal screening: Prenatal diagnosis and family clinical reassessment EUROPEAN JOURNAL OF OBSTETRICS, GYNECOLOGY, AND REPRODUCTIVE BIOLOGY 2021
Impaction of Regurgitation Jet on Anterior Mitral Leaflet Causes Diastolic Dysfunction in Patients With Bicuspid Aortic Valve and Mild Insufficiency: A Cardiovascular Magnetic Resonance Study THE INTERNATIONAL JOURNAL OF CARDIOVASCULAR IMAGING 2021
Neuroinflammatory markers in the serum of prepubertal children with down syndrome JOURNAL OF IMMUNOLOGY RESEARCH 2020
Neonatal Marfan Syndrome by Inherited Mutation INDIAN JOURNAL OF PEDIATRICS 2020
Isolated persistence of the fifth aortic arch in an infant presenting with congestive heart failure ANNALS OF PEDIATRIC CARDIOLOGY 2020
KBG syndrome: common and uncommon clinical features based on 31 new patients AMERICAN JOURNAL OF MEDICAL GENETICS. PART A 2020
Genetics of atrioventricular canal defects THE ITALIAN JOURNAL OF PEDIATRICS 2020
Atypical cardiac defects in patients with RASopathies: Updated data on CARNET study BIRTH DEFECTS RESEARCH 2020
Nerve growth factor, stress and diseases CURRENT MEDICINAL CHEMISTRY 2020
Common atrium/atrioventricular canal defect and postaxial polydactyly: a mild clinical subtype of Ellis-van Creveld syndrome caused by hypomorphic mutations in the EVC gene HUMAN MUTATION 2020
Echocardiography-Guided Management of Preterms With Patent Ductus Arteriosus Influences the Outcome: A Cohort Study FRONTIERS IN PEDIATRICS 2020
Common atrium/atrioventricular canal defect and postaxial polydactyly: A mild clinical subtype of Ellis-van Creveld syndrome caused by hypomorphic mutations in the EVC gene HUMAN MUTATION 2020
Uniparental disomy of chromosome 16: a case report with a new cardiac malformation Abstracts from the 53rd European Society of Human Genetics (ESHG) Conference: e-Posters EUROPEAN JOURNAL OF HUMAN GENETICS 2020
Atrioventricular canal defect and genetic syndromes: the unifying role of sonic hedgehog CLINICAL GENETICS 2019
Left pulmonary artery in 22q11.2 deletion syndrome. Echocardiographic evaluation in patients without cardiac defects and role of Tbx1 in mice. PLOS ONE 2019
Genotype-phenotype correlation study in 364 osteogenesis imperfecta Italian patients EUROPEAN JOURNAL OF HUMAN GENETICS 2019
Clinical and functional characterization of a novel RASopathy-causing SHOC2 mutation associated with prenatal-onset hypertrophic cardiomyopathy HUMAN MUTATION 2019
Echocardiographic long-term follow-up of adult survivors of pediatric cancer treated with dexrazoxane-anthracyclines association INTERNATIONAL JOURNAL OF CARDIOLOGY 2019

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