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Versacci, Paolo
121
results:
Search for persons
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Online (121)
Mediatypes
Articles (Online) (57)
Bookchapter (Online) (2)
OpenAccess-fulltext (62)
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?
1
Congenital Heart Defects in Patients with Molecularly Confi..:
Calcagni, Giulio
;
Ferrigno, Federica
;
Franceschini, Alessio
...
Diagnostics. 14 (2024) 6 - p. 594 , 2024
Link:
https://doi.org/10.3390/..
?
2
Is Osteogenesis Imperfecta Associated with Cardiovascular A..:
Verdonk, Sara J. E.
;
Storoni, Silvia
;
Micha, Dimitra
...
Calcified Tissue International. 114 (2024) 3 - p. 210-221 , 2024
Link:
https://doi.org/10.1007/..
?
3
Neurodevelopmental outcome of a child with UPD(16)mat: A ca..:
Novelli, Maria
;
Mammarella, Valeria
;
Calandriello, Francesca
...
Global Pediatrics. 9 (2024) - p. 100179 , 2024
Link:
https://doi.org/10.1016/..
?
4
Cardiac function in adolescents and young adults with 22q11..:
Putotto, Carolina
;
Unolt, Marta
;
Lambiase, Caterina
...
European Journal of Medical Genetics. 66 (2023) 1 - p. 104651 , 2023
Link:
https://doi.org/10.1016/..
?
5
COVID-19 Severity, Cardiological Outcome, and Immunogenicit..:
Pulvirenti, Federica
;
Mortari, Eva Piano
;
Putotto, Carolina
...
The Journal of Allergy and Clinical Immunology: In Practice. 11 (2023) 1 - p. 292-305.e2 , 2023
Link:
https://doi.org/10.1016/..
?
6
Insights into the Cardiac Phenotype in 9p Deletion Syndrome..:
Pugnaloni, Flaminia
;
Onesimo, Roberta
;
Blandino, Rita
...
Genes. 14 (2023) 1 - p. 146 , 2023
Link:
https://doi.org/10.3390/..
?
7
Clinical Risk Factors for Aortic Root Dilation in Patients ..:
Putotto, Carolina
;
Pulvirenti, Federica
;
Pugnaloni, Flaminia
...
Genes. 13 (2022) 12 - p. 2334 , 2022
Link:
https://doi.org/10.3390/..
?
8
Congenital heart disease and cardiovascular abnormalities a..:
, In:
The Chromosome 22q11.2 Deletion Syndrome
,
Unolt, Marta
;
Calcagni, Giulio
;
Putotto, Carolina
... - p. 78-100 , 2022
Link:
https://doi.org/10.1016/..
?
9
Crossed pulmonary arteries: An underestimated cardiovascula..:
Mastromoro, Gioia
;
Calcagni, Giulio
;
Vignaroli, Walter
...
American Journal of Medical Genetics Part A. 188 (2022) 8 - p. 2351-2359 , 2022
Link:
https://doi.org/10.1002/..
?
10
Contributors:
, In:
The Chromosome 22q11.2 Deletion Syndrome
,
Bassett, Anne S.
;
Van Batavia, Jason P.
;
Boot, Erik
... - p. xv-xvii , 2022
Link:
https://doi.org/10.1016/..
?
11
22q11.2 Deletion Syndrome: Impact of Genetics in the Treatm..:
Putotto, Carolina
;
Pugnaloni, Flaminia
;
Unolt, Marta
...
Children. 9 (2022) 6 - p. 772 , 2022
Link:
https://doi.org/10.3390/..
?
12
Hybrid Single-Stage Repair of Kommerell's Diverticulum in a..:
Chourda, Emmanouela
;
Putotto, Carolina
;
Versacci, Paolo
...
Vascular and Endovascular Surgery. 56 (2022) 6 - p. 595-601 , 2022
Link:
https://doi.org/10.1177/..
?
13
The heart in RASopathies:
Delogu, Angelica Bibiana
;
Limongelli, Giuseppe
;
Versacci, Paolo
...
American Journal of Medical Genetics Part C: Seminars in Medical Genetics. 190 (2022) 4 - p. 440-451 , 2022
Link:
https://doi.org/10.1002/..
?
14
Smith–Magenis syndrome: Report of morphological and new fun..:
Onesimo, Roberta
;
Versacci, Paolo
;
Delogu, Angelica Bibiana
...
American Journal of Medical Genetics Part A. 185 (2021) 7 - p. 2003-2011 , 2021
Link:
https://doi.org/10.1002/..
?
15
Commentary: sVEGFR1 Is Enriched in Hepatic Vein Blood—Evide..:
Putotto, Carolina
;
Marino, Bruno
;
Versacci, Paolo
Frontiers in Pediatrics. 9 (2021) - p. , 2021
Link:
https://doi.org/10.3389/..
1-15