Paolo Versacci | Ricerc@Sapienza

Pubblicazioni

Titolo	Pubblicato in	Anno
Is Osteogenesis Imperfecta Associated with Cardiovascular Abnormalities? A Systematic Review of the Literature	CALCIFIED TISSUE INTERNATIONAL	2024
“Neurodevelopmental outcome of a child with UPD(16)mat: A case report”	GLOBAL PEDIATRICS	2024
Adapting to Adulthood: A Review of Transition Strategies for Osteogenesis Imperfecta	CALCIFIED TISSUE INTERNATIONAL	2024
Cardiac function in adolescents and young adults with 22q11.2 deletion syndrome without congenital heart disease	EUROPEAN JOURNAL OF MEDICAL GENETICS	2023
Congenital heart defects in the recurrent 2q13 deletion syndrome	EUROPEAN JOURNAL OF MEDICAL GENETICS	2022
Clinical Manifestations of 22q11.2 Deletion Syndrome	HEART FAILURE CLINICS	2022
Social Cognition Impairments in 22q11.2DS Individuals With and Without Psychosis: A Comparison Study With a Large Population of Patients With Schizophrenia	SCHIZOPHRENIA BULLETIN OPEN	2022
Hybrid Single-Stage Repair of Kommerell’s Diverticulum in a Right Aortic Arch in a Patient With 22q11.2 Deletion Syndrome	VASCULAR AND ENDOVASCULAR SURGERY	2022
COVID-19 Severity, Cardiological Outcome, and Immunogenicity of mRNA Vaccine on Adult Patients With 22q11.2 DS	JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY. IN PRACTICE	2022
The heart in RASsopathies	AMERICAN JOURNAL OF MEDICAL GENETICS. PART C, SEMINARS IN MEDICAL GENETICS	2022
22q11.2 Deletion Syndrome: Impact of Genetics in the Treatment of Conotruncal Heart Defects	CHILDREN	2022
Clinical Risk Factors for Aortic Root Dilation in Patients with 22q11.2 Deletion Syndrome: A Longitudinal Single-Center Study	GENES	2022
Crossed pulmonary arteries: An underestimated cardiovascular variant with a strong association with genetic syndromes{\textemdash}A report of 74 cases with systematic review of the literature	AMERICAN JOURNAL OF MEDICAL GENETICS. PART A	2022
Social cognition impairments in 22q11.2DS individuals with and without psychosis: a comparison study with a large population of patients with schizophrenia	SCHIZOPHRENIA BULLETIN OPEN	2022
Atrioventricular canal defect is the classic congenital heart disease in Bardet-Biedl syndrome	ANNALS OF HUMAN GENETICS	2021
Impaction of regurgitation jet on anterior mitral leaflet is associated with diastolic dysfunction in patients with bicuspid aortic valve and mild insufficiency: a cardiovascular magnetic resonance study	THE INTERNATIONAL JOURNAL OF CARDIOVASCULAR IMAGING	2021
Cardiac defects and genetic syndromes: old uncertainties and new insights	GENES	2021
Smith–Magenis syndrome: Report of morphological and new functional cardiac findings with review of the literature	AMERICAN JOURNAL OF MEDICAL GENETICS. PART A	2021
Anatomical substrate for biventricular repair in patients with left isomerism	ANNALS OF PEDIATRIC CARDIOLOGY	2021
Congenital heart defects in molecularly confirmed KBG syndrome patients	AMERICAN JOURNAL OF MEDICAL GENETICS. PART A	2021