G. Calcagni

发表

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

F. Drago, G. Grutter, F. Parisi, 2016, Pediatric transplantation.

Hypertrophic Cardiomyopathy in RASopathies: Diagnosis, Clinical Characteristics, Prognostic Implications, and Management.

M. Digilio, B. Gelb, M. Tartaglia, 2021, Heart failure clinics.

Clinical Presentation and Natural History of Hypertrophic Cardiomyopathy in RASopathies.

M. Digilio, B. Gelb, M. Tartaglia, 2018, Heart failure clinics.

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

M. Digilio, B. Dallapiccola, M. Tartaglia, 2020, Birth defects research.

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

M. Digilio, B. Dallapiccola, A. Novelli, 2019, American journal of medical genetics. Part A.

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

M. Digilio, B. Dallapiccola, M. Tartaglia, 2017, International journal of cardiology.

Acute Cardiovascular Manifestations in 286 Children with Multisystem Inflammatory Syndrome Associated with COVID-19 Infection in Europe.

D. De Wolf, I. Valverde, B. Manso, 2020, Circulation.

Cardiovascular Prevention Heart Failure Hemodynamics-Cardiovascular Interventions High Blood Pressure Ischemic Heart Disease Nuclear Cardiology Pediatric Cardiology Peripheral and Cerebral Vascular Diseases Sports Cardiology Transdisciplinary Cardiology and Mental Health in Cardiology Role of Yoga a

B. Marino, G. Calcagni, 2007 .

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

M. Digilio, B. Dallapiccola, B. Marino, 2006, European Journal of Pediatrics.

Right superior vena cava draining into the left atrium

D. Bonnet, D. Sidi, P. Vouhé, 2008, Pediatric Radiology.

Congenital heart defects in Noonan syndrome and RIT1 mutation

M. Digilio, M. Tartaglia, B. Marino, 2016, Genetics in Medicine.

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

M. Digilio, B. Leonardi, G. Pongiglione, 2016, American journal of medical genetics. Part A.

Cardiac Defects and Genetic Syndromes: Old Uncertainties and New Insights

M. Digilio, M. Tartaglia, B. Marino, 2021, Genes.

Differences in morbidity and mortality in Down syndrome are related to the type of congenital heart defect

M. Digilio, B. Dallapiccola, B. Marino, 2020, American journal of medical genetics. Part A.

Syndromic and Non-Syndromic Patients with Repaired Tetralogy of Fallot: Does It Affect the Long-Term Outcome?

M. Caputo, M. Digilio, B. Leonardi, 2022, Journal of clinical medicine.

M. L. Ciofi Degli Atti, F. Drago, S. Giannico, 2022, BMC Cardiovascular Disorders.

Some Isolated Cardiac Malformations Can Be Related to Laterality Defects

M. Digilio, B. Marino, Marta Unolt, 2018, Journal of cardiovascular development and disease.

Insights from Cardiopulmonary Exercise Testing in Pediatric Patients with Hypertrophic Cardiomyopathy

C. Autore, A. Maruotti, G. Limongelli, 2021, Biomolecules.

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

M. Digilio, B. Dallapiccola, B. Marino, 2018, International journal of cardiology.

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

M. Digilio, M. Tartaglia, B. Marino, 2019, Orphanet Journal of Rare Diseases.

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

M. Digilio, B. Marino, A. Secinaro, 2022, American journal of medical genetics. Part A.

22q11.2 Deletion Syndrome: Impact of Genetics in the Treatment of Conotruncal Heart Defects

M. Digilio, G. Limongelli, B. Marino, 2022, Children.

Coronary myocardial bridging in Noonan syndrome: definitive diagnosis with high-resolution CT.

F. Brunelle, D. Bonnet, D. Sidi, 2009, The British journal of radiology.

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

B. Marino, R. Lucchini, F. Ventriglia, 2004, Journal of the American Society of Echocardiography : official publication of the American Society of Echocardiography.

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

F. Brunelle, F. Gesualdo, D. Sidi, 2008, Pediatric Radiology.

The heart in RASopathies

B. Gelb, G. Limongelli, J. Kaski, 2022, American journal of medical genetics. Part C, Seminars in medical genetics.

Evolving Solutions in the Surgical Treatment of Isolated Pulmonary Valve Stenosis

M. Trezzi, F. Gatta, S. Albanese, 2021, Journal of Cardiology and Cardiovascular Research.

Outcome in Down syndrome fetuses with cardiac anomalies

B. Marino, P. Mastroiacovo, G. Calcagni, 2004, American journal of medical genetics. Part A.

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

A. Baldini, M. Digilio, B. Marino, 2019, bioRxiv.

Congenital heart defects in the recurrent 2q13 deletion syndrome.

B. Marino, B. Dallapiccola, I. Bottillo, 2021, European journal of medical genetics.

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

M. Digilio, C. Leoni, G. Zampino, 2023, Genes.

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

M. Digilio, B. Dallapiccola, R. Capolino, 2006, Clinical dysmorphology.

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

E. Zackai, M. Digilio, J. Gaynor, 2018, American journal of medical genetics. Part A.

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

A. Baldini, M. Digilio, M. Tartaglia, 2017, Expert review of molecular diagnostics.

Congenital heart defects in molecularly confirmed KBG syndrome patients

M. Digilio, B. Dallapiccola, R. Capolino, 2021, American journal of medical genetics. Part A.

Multifaceted approach to plastic bronchitis.

G. Grutter, G. Calcagni, D. Di Carlo, 2015, The Annals of thoracic surgery.

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

B. Marino, M. Digilio, B. Dallapiccola, 2019, Clinical genetics.

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

F. Brunelle, F. Gesualdo, P. Ou, 2007, Pediatric Radiology.

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

M. Digilio, C. Leoni, G. Zampino, 2021, American journal of medical genetics. Part A.

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

M. Digilio, M. Tartaglia, S. Giustini, 2019, Genes.

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

F. Brunelle, D. Bonnet, D. Sidi, 2008, Pediatric Radiology.

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

M. Piastra, G. Calcagni, D. D. De Paola, 2009, The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians.

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

Phalla Ou, Francis Brunelle, F. Brunelle, 2006, Heart.

Heterozygous missense mutations in NFATC1 are associated with atrioventricular septal defect

T. Mazza, M. Digilio, B. Dallapiccola, 2018, Human mutation.

SARS-CoV-2 and Pre-Tamponade Pericardial Effusion. Could Sotos Syndrome Be a Major Risk Factor?

M. Digilio, R. Capolino, M. Gagliardi, 2021, Genes.

Impact of genetic studies on comprehension and treatment of congenital heart disease

M. Digilio, B. Marino, Marta Unolt, 2018, Progress in Pediatric Cardiology.

Atrioventricular canal defect as partial expression of heterotaxia in patients with Bardet-Biedl syndrome.

M. Digilio, V. Guida, B. Marino, 2019, The Journal of pediatrics.

Percutaneous implantation of pulmonary valves for treatment of right ventricular outflow tract dysfunction: a single-centre experience

M. Gagliardi, G. Pongiglione, P. Guccione, 2009 .