Lista de obras - Giulio Calcagni - Dominio Público Uruguay

An unusual case of left aberrant innominate artery with right aortic arch: evaluation with high-resolution CT.

artículo científico publicado en 2007

Arterial aneurysms and tuberous sclerosis: a classic but little known association

artículo científico publicado en 2008

Atresia of the coronary sinus ostium: surgical implications

artículo científico publicado en 2006

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

artículo científico publicado en 2018

Atypical cardiac defects in patients with RASopathies: Updated data on CARNET study

scientific article published on 01 June 2020

CT demonstration of "chicken trachea" resulting from complete cartilaginous rings of the trachea in ring-sling complex.

artículo científico publicado en 2008

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

artículo científico publicado en 2017

Cardiac tamponade and bilateral pleural effusion in a very low birth weight infant.

artículo científico publicado en 2009

Clinical Presentation and Natural History of Hypertrophic Cardiomyopathy in RASopathies.

artículo científico publicado en 2018

Concordant familial segregation of atrial septal defect and Axenfeld-Rieger anomaly in father and son.

artículo científico publicado en 2006

Congenital heart defects in Noonan syndrome and RIT1 mutation

artículo científico publicado en 2016

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

artículo científico publicado en 2017

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

artículo científico publicado en 2018

Coronary artery ectasia in Noonan syndrome: Report of an individual with SOS1 mutation and literature review.

artículo científico publicado en 2015

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

artículo científico publicado en 2017

Familial recurrence of congenital heart disease: an overview and review of the literature.

artículo científico publicado en 2006

Heterozygous missense mutations in NFATC1 are associated with atrioventricular septal defect

artículo científico publicado en 2018

Influence of heart rate on left ventricular isovolumic relaxation time: a Doppler study in healthy newborns

scientific article published on 01 April 2004

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

artículo científico publicado en 2019

Long-term survival and phenotypic spectrum in heterotaxy syndrome: A 25-year follow-up experience

artículo científico publicado en 2018

Multifaceted approach to plastic bronchitis

artículo científico publicado en 2015

Paroxysmal atrioventricular block after heart transplantation in children: an early sign of rejection?

artículo científico publicado en 2016

Pediatric coronary artery bypass after arterial switch operation: noninvasive evaluation with ECG-gated 64-slice CT in routine practice

scientific article published on 01 October 2007

Pediatric patients with RASopathy-associated hypertrophic cardiomyopathy: the multifaceted consequences of PTPN11 mutations

scientific article published on 05 July 2019

Percutaneous treatment of aorto-pulmonary window in a one year old child

scientific article published on 14 September 2007

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

artículo científico publicado en 2019

Right superior vena cava draining into the left atrium

artículo científico publicado en 2008

SOS1 mutations in Noonan syndrome: Cardiomyopathies and not only congenital heart defects! Report of six patients including two novel variants and literature review

artículo científico publicado en 2019

Some Isolated Cardiac Malformations Can Be Related to Laterality Defects.

artículo científico publicado en 2018

Three-dimensional CT scanning: a new diagnostic modality in congenital heart disease.

artículo científico publicado en 2006

Unusual systemic venous return with absence of superior caval veins

artículo científico publicado en 2007

Lista de obras de Giulio Calcagni

An unusual case of left aberrant innominate artery with right aortic arch: evaluation with high-resolution CT.

Arterial aneurysms and tuberous sclerosis: a classic but little known association

Atresia of the coronary sinus ostium: surgical implications

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

Atypical cardiac defects in patients with RASopathies: Updated data on CARNET study

CT demonstration of "chicken trachea" resulting from complete cartilaginous rings of the trachea in ring-sling complex.

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

Cardiac tamponade and bilateral pleural effusion in a very low birth weight infant.

Clinical Presentation and Natural History of Hypertrophic Cardiomyopathy in RASopathies.

Concordant familial segregation of atrial septal defect and Axenfeld-Rieger anomaly in father and son.

Congenital heart defects in Noonan syndrome and RIT1 mutation

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

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

Coronary artery ectasia in Noonan syndrome: Report of an individual with SOS1 mutation and literature review.

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

Familial recurrence of congenital heart disease: an overview and review of the literature.

Heterozygous missense mutations in NFATC1 are associated with atrioventricular septal defect

Influence of heart rate on left ventricular isovolumic relaxation time: a Doppler study in healthy newborns

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

Long-term survival and phenotypic spectrum in heterotaxy syndrome: A 25-year follow-up experience

Multifaceted approach to plastic bronchitis

Paroxysmal atrioventricular block after heart transplantation in children: an early sign of rejection?

Pediatric coronary artery bypass after arterial switch operation: noninvasive evaluation with ECG-gated 64-slice CT in routine practice

Pediatric patients with RASopathy-associated hypertrophic cardiomyopathy: the multifaceted consequences of PTPN11 mutations

Percutaneous treatment of aorto-pulmonary window in a one year old child

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

Right superior vena cava draining into the left atrium

SOS1 mutations in Noonan syndrome: Cardiomyopathies and not only congenital heart defects! Report of six patients including two novel variants and literature review

Some Isolated Cardiac Malformations Can Be Related to Laterality Defects.

Three-dimensional CT scanning: a new diagnostic modality in congenital heart disease.

Unusual systemic venous return with absence of superior caval veins