List of works - Paolo Versacci

Association of OPG-RANKL ratio with left ventricular hypertrophy and geometric remodeling in male overweight/obese youths

scientific article published on 21 August 2018

Atrioventricular canal defect and genetic syndromes: The unifying role of sonic hedgehog

scientific article published on 23 May 2018

Cardiac defects, morbidity and mortality in patients affected by RASopathies. CARNET study results.

scientific article published on 21 July 2017

Cardiovascular disease in Down syndrome

scientific article published on 01 October 2018

Clinical Presentation and Natural History of Hypertrophic Cardiomyopathy in RASopathies

scientific article published in April 2018

Clinical and functional characterization of a novel RASopathy-causing SHOC2 mutation associated with prenatal-onset hypertrophic cardiomyopathy

scientific article published on 06 May 2019

Congenital heart disease and genetic syndromes: new insights into molecular mechanisms.

scientific article published on 26 July 2017

Congenital heart diseases and cardiovascular abnormalities in 22q11.2 deletion syndrome: From well-established knowledge to new frontiers.

scientific article published on 16 April 2018

Congenital superior caval vein aneurysm in a newborn with cystic lymphangioma: a rare case report

scientific article published on 01 August 2018

Data on cardiac defects, morbidity and mortality in patients affected by RASopathies. CARNET study results.

scientific article published on 2 December 2017

Difficult diagnosis of atypical kawasaki disease in an infant younger than six months: a case report.

scientific article

Echocardiographic long-term follow-up of adult survivors of pediatric cancer treated with Dexrazoxane-Anthracyclines association

scientific article published on 05 August 2019

Genetics of atrioventricular canal defects

scientific article published on 13 May 2020

Genotype-phenotype correlation study in 364 osteogenesis imperfecta Italian patients

scientific article published on 18 March 2019

Heterozygous missense mutations in NFATC1 are associated with atrioventricular septal defect

scientific article published on 30 July 2018

Isolated persistence of the fifth aortic arch in an infant presenting with congestive heart failure

scientific article published on 22 November 2019

Left pulmonary artery in 22q11.2 deletion syndrome. Echocardiographic evaluation in patients without cardiac defects and role of Tbx1 in mice

scientific article published on 01 April 2019

Lifestyle and awareness of cholesterol blood levels among 29159 community school children in Italy

scientific article published on 22 May 2019

Long-term renal function in unilateral non-syndromic renal tumor survivors treated according to International Society of Pediatric Oncology protocols

scientific article published on 20 April 2015

Neonatal Marfan Syndrome by Inherited Mutation

scientific article published on 17 June 2020

Neuroinflammatory Markers in the Serum of Prepubertal Children with Down Syndrome

scientific article published on 23 March 2020

Prevalence, Type, and Molecular Spectrum of NF1 Mutations in Patients with Neurofibromatosis Type 1 and Congenital Heart Disease

scientific article published on 04 September 2019

Respiratory complications in patients with heterotaxy syndrome ⬇️

scientific article published on 01 March 2012

Right-Dominant Unbalanced Atrioventricular Canal and Genetic Syndromes ⬇️

scientific article published on November 15, 2011

Surgical Results in Patients With Cardiac Defects and Del 22q11.2 Syndrome ⬇️

scientific article published on January 15, 2011

Surgical outcomes for patients with Turner syndrome

scientific article published on 07 May 2014

Transposition of great arteries: new insights into the pathogenesis