Paolo Versacci
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Explore the profile of Paolo Versacci including associated specialties, affiliations and a list of published articles.
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Articles
81
Citations
652
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Recent Articles
1.
Cuzzocrea G, Fontana A, Mascanzoni M, Manca F, Pecora R, Trani L, et al.
Clin Neuropsychiatry
. 2024 Nov;
21(5):358-375.
PMID: 39540075
Objective: Syncope is defined as a spontaneous and transient loss of consciousness and postural tone due to brief and reversible cerebral hypoperfusion. This review aimed to summarize the research findings...
2.
Celli L, Garrelfs M, Sakkers R, Elting M, Celli M, Bokenkamp A, et al.
Calcif Tissue Int
. 2024 Nov;
115(6):960-975.
PMID: 39535563
Osteogenesis Imperfecta (OI), known as "brittle bone disease," presents a rare genetic disorder characterized by bone fragility, often accompanied by skeletal deformities and extraskeletal complications. OI is primarily associated with...
3.
Putotto C, Versacci P, Marino B
Pediatr Cardiol
. 2024 Sep;
46(2):508-509.
PMID: 39242439
A significant percentage of patients with heterotaxy show disharmony between abdominal, bronchopulmonary and atrial situs. This finding is interesting in light of the variable effects of ciliary and laterality genes...
4.
Accinni T, Buzzanca A, Frascarelli M, Carlone L, Ghezzi F, Kotzalidis G, et al.
Schizophr Bull Open
. 2024 Aug;
3(1):sgab049.
PMID: 39144801
Background: 22q11.2 Deletion Syndrome (22q11DS) represents one of the most important genetic risk factors for schizophrenia (SCZ) and a reliable biological model to study endophenotypic characters of SCZ. The aim...
5.
Putotto C, Pugnaloni F, Unolt M, Calcagni G, Versacci P, Marino B
Genome Med
. 2024 Aug;
16(1):100.
PMID: 39138574
To date, the role of NODAL in normal and abnormal L-R asymmetry has been well established. In a recent paper, mutations of this gene have been reported in heterotaxy but...
6.
Calcagni G, Ferrigno F, Franceschini A, Dentici M, Capolino R, Sinibaldi L, et al.
Diagnostics (Basel)
. 2024 Mar;
14(6).
PMID: 38535015
Sotos syndrome is an autosomal dominant condition characterized by overgrowth with advanced bone age, macrodolicocephaly, motor developmental delays and learning difficulties, and characteristic facial features caused by heterozygous pathogenetic variants...
7.
Verdonk S, Storoni S, Micha D, van den Aardweg J, Versacci P, Celli L, et al.
Calcif Tissue Int
. 2024 Jan;
114(3):210-221.
PMID: 38243143
Osteogenesis imperfecta (OI) is a rare genetic disorder caused by abnormal collagen type I production. While OI is primarily characterized by bone fragility and deformities, patients also have extraskeletal manifestations,...
8.
Pugnaloni F, Felici A, Corno A, Marino B, Versacci P, Putotto C
Transl Pediatr
. 2023 Oct;
12(9):1753-1764.
PMID: 37814719
Background And Objective: Congenital heart defects (CHD) represent the most frequent human birth defects, occurring in almost 1% of all live newborns. Understanding the effects of gender in the prevalence...
9.
Pugnaloni F, Onesimo R, Blandino R, Putotto C, Versacci P, Delogu A, et al.
Genes (Basel)
. 2023 Jan;
14(1).
PMID: 36672887
Chromosome 9p deletion syndrome is a rare autosomal dominant disorder presenting with a broad spectrum of clinical features, including congenital heart defects (CHDs). To date, studies focused on a deep...
10.
Putotto C, Pulvirenti F, Pugnaloni F, Isufi I, Unolt M, Anaclerio S, et al.
Genes (Basel)
. 2022 Dec;
13(12).
PMID: 36553601
Background: Aortic root dilation (ARD) has been described in 22q11.2DS, even without congenital heart disease (CHD). However, the clinical implications and longitudinal course are unclear. In this study, we evaluated...