P Pavone
Overview
Explore the profile of P Pavone including associated specialties, affiliations and a list of published articles.
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Articles
255
Citations
782
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Recent Articles
1.
Leonardi R, Pellino G, Floridia E, Lo Bianco M, Ruggieri M, Cho S, et al.
Glob Med Genet
. 2025 Feb;
12(1):100033.
PMID: 39925448
Background: Polydactyly and syndactyly, which are commonly encountered congenital limb deformities, rarely occur together and are linked with significant genetic mutations. This report sheds light on a unique co-presentation involving...
2.
Di Nora A, Consentino M, Messina G, Timpanaro T, Smilari P, Pavone P
Glob Med Genet
. 2023 Nov;
10(4):335-338.
PMID: 38025195
Netherton syndrome is a rare, multisystem, autosomal recessive genodermatosis characterized by a triad of manifestations: congenital ichthyosis, immune dysregulation, and scalp anomalies. We report the case of a 1-month-old male...
3.
Di Nora A, Pellino G, Di Mari A, Scarlata F, Greco F, Pavone P
Glob Med Genet
. 2023 Nov;
10(4):345-347.
PMID: 38025191
In the clinical practice, it is not common for pediatricians to visit children with overgrowth phenotype. When it happens, it is important to focus on the age of manifestations and...
4.
Di Nora A, Costanza G, Pizzo F, Di Mari A, Sapuppo A, Basile A, et al.
Acta Neurol Belg
. 2022 Sep;
123(3):903-909.
PMID: 36068432
Objective: To investigate the clinical characteristics, the neuroimaging features and associated anomalies observed in children affected by Dandy-Walker malformations (DWM) and variants (DWV) in a single tertiary hospital in Catania...
5.
Pavone P, Gulizia C, DAmico S, Grassi P, La Rosa G, Leotta R, et al.
Eur Rev Med Pharmacol Sci
. 2022 Jul;
26(13):4863-4871.
PMID: 35856378
Objective: Human brucellosis is a zoonosis with an extremely wide spectrum of clinical manifestations. Focal splenic involvement is very uncommon, particularly in the pediatric age group, during the illness' acute...
6.
Comella M, Collotta A, Pavone V, Ciccia L, Bellinvia A, Cerruto C, et al.
Case Rep Pediatr
. 2022 Apr;
2022:3793226.
PMID: 35449525
Charcot- Marie- Tooth (CMT) disease includes a group of clinically and genetically heterogeneous neuropathic disorders with an estimated frequency of 1 on 2.500 individuals. CMTs are differently classified according to...
7.
Di Nora A, Costanza G, Pizzo F, Oliva C, Di Mari A, Greco F, et al.
Acta Neurol Belg
. 2021 Sep;
122(1):153-162.
PMID: 34471972
Objective: To investigate the clinical characteristics and neuroimaging features of childhood presenting with gray matter heterotopia observed in a single tertiary Pediatric Department in Catania and compare the data with...
8.
Ceccarelli M, Pavone P, Venanzi Rullo E, Nunnari G
Eur Rev Med Pharmacol Sci
. 2021 Apr;
25(6):2473-2474.
PMID: 33829431
No abstract available.
9.
Pirisi M, Rigamonti C, DAlfonso S, Nebuloni M, Fanni D, Gerosa C, et al.
Eur Rev Med Pharmacol Sci
. 2021 Mar;
25(4):2146-2151.
PMID: 33660834
Objective: COVID-19, the newly emerging infectious disease, has been associated with acute liver injury, often related to progression to severe pneumonia. The association between moderate-severe liver injury and more severe...
10.
Faa G, Piras M, Mancuso L, Coni P, Pichiri G, Orru G, et al.
Eur Rev Med Pharmacol Sci
. 2021 Jan;
25(1):431-437.
PMID: 33506933
Objective: Thymosin beta 4 (TB4) is the most abundant member of the beta-thymosin family in humans. The main physiological role of TB4 is the regulation of actin polymerization. TB4 is...