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5. Cardiac function in adolescents and young adults with 22q11.2 deletion syndrome without congenital heart disease

6. Clinical Manifestations of 22q11.2 Deletion Syndrome

8. Contributors

10. When to test fetuses for RASopathies? Proposition from a systematic analysis of 352 multicenter cases and a postnatal cohort

12. Congenital Heart Defects in Patients with Molecularly Confirmed Sotos Syndrome.

16. The Embryology of the Interatrial Septum

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

20. Insights into the Cardiac Phenotype in 9p Deletion Syndrome: A Multicenter Italian Experience and Literature Review

21. Clinical Risk Factors for Aortic Root Dilation in Patients with 22q11.2 Deletion Syndrome: A Longitudinal Single-Center Study

22. The heart in RASopathies

26. Crossed pulmonary arteries: An underestimated cardiovascular variant with a strong association with genetic syndromes—A report of 74 cases with systematic review of the literature

29. Congenital heart defects in molecularly confirmed KBG syndrome patients

31. Social Cognition Impairments in 22q11.2DS Individuals With and Without Psychosis: A Comparison Study With a Large Population of Patients With Schizophrenia

35. 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

36. Cardiac Defects and Genetic Syndromes: Old Uncertainties and New Insights

38. 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

39. Nerve Growth Factor, Stress and Diseases

40. Smith–Magenis syndrome: Report of morphological and new functional cardiac findings with review of the literature

41. 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

45. Echocardiography-Guided Management of Preterms With Patent Ductus Arteriosus Influences the Outcome: A Cohort Study

47. Congenital heart defects in molecularly confirmed KBG syndrome patients.

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