316 results on '"Versacci, Paolo"'
Search Results
2. Laterality, heterotaxy, and isolated congenital heart defects: The genetic basis of the segmental nature of the heart
3. Is Osteogenesis Imperfecta Associated with Cardiovascular Abnormalities? A Systematic Review of the Literature
4. COVID-19 Severity, Cardiological Outcome, and Immunogenicity of mRNA Vaccine on Adult Patients With 22q11.2 DS
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
7. 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
8. Contributors
9. Congenital heart disease and cardiovascular abnormalities associated with 22q11.2 deletion syndrome
10. When to test fetuses for RASopathies? Proposition from a systematic analysis of 352 multicenter cases and a postnatal cohort
11. Impact of genetic studies on comprehension and treatment of congenital heart disease
12. Congenital Heart Defects in Patients with Molecularly Confirmed Sotos Syndrome.
13. Gender differences in congenital heart defects: a narrative review
14. Clinical Presentation and Natural History of Hypertrophic Cardiomyopathy in RASopathies
15. Genotype–phenotype correlation study in 364 osteogenesis imperfecta Italian patients
16. The Embryology of the Interatrial Septum
17. Cardiac defects, morbidity and mortality in patients affected by RASopathies. CARNET study results
18. Genetics of atrioventricular canal defects
19. Neonatal Marfan Syndrome by Inherited Mutation
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
23. “Neurodevelopmental outcome of a child with UPD(16)mat: A case report”
24. Cardiovascular disease in Down syndrome
25. 22q11.2 Deletion Syndrome: Impact of Genetics in the Treatment of Conotruncal Heart Defects
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
27. Hybrid Single-Stage Repair of Kommerell’s Diverticulum in a Right Aortic Arch in a Patient With 22q11.2 Deletion Syndrome
28. Cardiopulmonary Response to Exercise and Cardiac Assessment in Patients With Turner Syndrome
29. Congenital heart defects in molecularly confirmed KBG syndrome patients
30. Reply to: Comment on Long-Term Renal Function in Unilateral Non-Syndromic Renal Tumor Survivors Treated According to International Society of Pediatric Oncology Protocols
31. Social Cognition Impairments in 22q11.2DS Individuals With and Without Psychosis: A Comparison Study With a Large Population of Patients With Schizophrenia
32. Commentary: sVEGFR1 Is Enriched in Hepatic Vein Blood—Evidence for a Provisional Hepatic Factor Candidate?
33. Long-term Renal Function in Unilateral Non-Syndromic Renal Tumor Survivors Treated According to International Society of Pediatric Oncology Protocols
34. Incidental SOS1 variant identified by non-invasive prenatal screening: Prenatal diagnosis and family clinical reassessment
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
37. 77 - Congenital Cardiac Disease in the Setting of Genetic Syndromes
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
42. Prevalence and Clinical Significance of Cardiovascular Abnormalities in Patients With the LEOPARD Syndrome
43. Atrioventricular canal defect is the classic congenital heart disease in Bardet–Biedl syndrome
44. Anatomical substrate for biventricular repair in patients with left isomerism
45. Echocardiography-Guided Management of Preterms With Patent Ductus Arteriosus Influences the Outcome: A Cohort Study
46. Abnormalities of Situs
47. Congenital heart defects in molecularly confirmed KBG syndrome patients.
48. Influence of physical activity on cardiorespiratory fitness in children after renal transplantation
49. Respiratory complications in patients with heterotaxy syndrome
50. Ebstein anomaly: Genetic heterogeneity and association with microdeletions 1p36 and 8p23.1
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