Salta al contenuto principale
Ricerc@Sapienza
Toggle navigation
Home
Login
Home
Persone
paolo.versacci@uniroma1.it
Paolo Versacci
Ricercatore
Struttura:
DIPARTIMENTO MATERNO INFANTILE E SCIENZE UROLOGICHE
E-mail:
paolo.versacci@uniroma1.it
Pagina istituzionale corsi di laurea
Curriculum Sapienza
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
« prima
< precedente
1
2
3
4
seguente ›
ultima »
© Università degli Studi di Roma "La Sapienza" - Piazzale Aldo Moro 5, 00185 Roma