• 24 Citations
  • 2 h-Index
20172019
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Fingerprint Dive into the research topics where giulio calcagni is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

  • 8 Similar Profiles
Congenital Heart Defects Medicine & Life Sciences
Mutation Medicine & Life Sciences
Hypertrophic Cardiomyopathy Medicine & Life Sciences
DiGeorge Syndrome Medicine & Life Sciences
Noonan Syndrome Medicine & Life Sciences
Heart Diseases Medicine & Life Sciences
Missense Mutation Medicine & Life Sciences
LEOPARD Syndrome Medicine & Life Sciences

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Research Output 2017 2019

  • 24 Citations
  • 2 h-Index
  • 9 Article
  • 4 Review article

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

Digilio, M. C., Pugnaloni, F., De Luca, A., Calcagni, G., Baban, A., Dentici, M. L., Versacci, P., Dallapiccola, B., Tartaglia, M. & Marino, B., 2019, In : Clinical Genetics. 95, 2, p. 268-276 9 p.

Research output: Contribution to journalArticle

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

Mastromoro, G., Calcagni, G., Versacci, P., Putotto, C., Chinali, M., Lambiase, C., Unolt, M., Pelliccione, E., Anaclerio, S., Caprio, C., Cioffi, S., Bilio, M., Baban, A., Drago, F., Digilio, M. C., Marino, B. & Baldini, A., Apr 1 2019, In : PLoS One. 14, 4, p. e0211170

Research output: Contribution to journalArticle

DiGeorge Syndrome
pulmonary artery
Pulmonary Artery
Defects
mice
LEOPARD Syndrome
Hypertrophic Cardiomyopathy
Noonan Syndrome
Pediatrics
Mutation

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

Pinna, V., Daniele, P., Calcagni, G., Mariniello, L., Criscione, R., Giardina, C., Lepri, F. R., Hozhabri, H., Alberico, A., Cavone, S., Morella, A. T., Mandile, R., Annunziata, F., Di Giosaffatte, N., D'Asdia, M. C., Versacci, P., Capolino, R., Strisciuglio, P., Giustini, S., Melis, D. & 4 others, Digilio, M. C., Tartaglia, M., Marino, B. & De Luca, A., Sep 4 2019, In : Genes. 10, 9

Research output: Contribution to journalArticle

Open Access
Neurofibromatosis 1
Pulmonary Valve Stenosis
Heart Diseases
Mutation
Odds Ratio
Noonan Syndrome
Congenital Heart Defects
Cardiomyopathies
Mutation
Cytidine Monophosphate