Bruno Marino Taussig De Bodonia

Pubblicazioni

Titolo Pubblicato in Anno
Atrioventricular canal defect as partial expression of heterotaxia in patients with Bardet-Biedl syndrome JOURNAL OF PEDIATRICS 2019
Some Isolated Cardiac Malformations Can Be Related to Laterality Defects JOURNAL OF CARDIOVASCULAR DEVELOPMENT AND DISEASE 2018
Congenital heart diseases and cardiovascular abnormalities in 22q11.2 deletion syndrome: From well-established knowledge to new frontiers AMERICAN JOURNAL OF MEDICAL GENETICS. PART A 2018
Cardiovascular disease in Down syndrome CURRENT OPINION IN PEDIATRICS 2018
Clinical presentation and natural history of hypertrophic cardiomyopathy in RASopathies HEART FAILURE CLINICS 2018
Late arrhytmias after repair of atrioventricular septal defect: Down's Syndrome is not the culprit INTERNATIONAL JOURNAL OF CARDIOLOGY 2018
Biallelic mutations in DYNC2LI1 are a rare cause of Ellis-van Creveld syndrome CLINICAL GENETICS 2018
Primary lymphedema and other lymphatic anomalies are associated with 22q11.2 deletion syndrome EUROPEAN JOURNAL OF MEDICAL GENETICS 2018
Long-term survival and phenotypic spectrum in heterotaxy syndrome: a 25-year follow-up experience INTERNATIONAL JOURNAL OF CARDIOLOGY 2018
Data on cardiac defects, morbidity and mortality in patients affected by RASopathies. CARNET study results DATA IN BRIEF 2018
Impact of genetic studies on comprehension and treatment of congenital heart disease PROGRESS IN PEDIATRIC CARDIOLOGY 2018
Heterozygous missense mutations in NFATC1 are associated with atrioventricular septal defect HUMAN MUTATION 2018
Surgery for Complex forms of Atrioventricular Septal Defect: Early Survival and Probability of Cure JOURNAL OF RARE DISORDERS. DIAGNOSIS & THERAPY 2018
Partial atrioventricular septal defect in infancy: Don't we need to know more? HEART 2018
Cardiac defects, morbidity and mortality in patients affected by RASopathies. CARNET study results INTERNATIONAL JOURNAL OF CARDIOLOGY 2017
Congenital heart disease and genetic syndromes: new insights into molecular mechanisms EXPERT REVIEW OF MOLECULAR DIAGNOSTICS 2017
Congenital heart defects in molecularly proven Kabuki syndrome patients AMERICAN JOURNAL OF MEDICAL GENETICS. PART A 2017
Genome-wide association study to find modifiers for tetralogy of fallot in the 22q11.2 deletion syndrome identifies variants in the GPR98 locus on 5q14.3 CIRCULATION, CARDIOVASCULAR GENETICS 2017
What Is New in Genetics of Congenital Heart Defects? FRONTIERS IN PEDIATRICS 2016
Direct cerebral perfusion and cooling in experimental cardiac arrest CRITICAL CARE AND RESUSCITATION 2016

Progetti di Ricerca

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