Angelo Valetto
Overview
Explore the profile of Angelo Valetto including associated specialties, affiliations and a list of published articles.
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61
Citations
478
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Recent Articles
1.
Pifferi M, Boner A, Maj D, Michelucci A, Donzelli G, Doccioli C, et al.
Pediatr Pulmonol
. 2025 Feb;
60(2):e71015.
PMID: 39998908
No abstract available.
2.
Bertini V, Cambi F, Legitimo A, Costagliola G, Consolini R, Valetto A
Genes (Basel)
. 2025 Jan;
16(1).
PMID: 39858619
22q11.2 is a region prone to chromosomal rearrangements due to the presence of eight large blocks of low-copy repeats (LCR22s). The 3 Mb 22q11.2 "typical deletion", between LCR22-A and D,...
3.
Pifferi M, Boner A, Maj D, Michelucci A, Donzelli G, Cangiotti A, et al.
Thorax
. 2024 Aug;
79(11):1069-1076.
PMID: 39181709
Objective: Primary ciliary dyskinesia (PCD) severity has been related to genotype and levels of nasal nitric oxide (nNO). The most common TAS2R38 haplotypes (PAV/PAV, PAV/AVI, AVI/AVI) encoding the bitter taste...
4.
Pifferi M, Boner A, Cangiotti A, Cudazzo A, Maj D, Gracci S, et al.
Pediatr Pulmonol
. 2024 Jan;
59(4):891-898.
PMID: 38169302
Background: International guidelines disagree on how best to diagnose primary ciliary dyskinesia (PCD), not least because many tests rely on pattern recognition. We hypothesized that quantitative distribution of ciliary ultrastructural...
5.
Costagliola G, Legitimo A, Bertini V, Alberio A, Valetto A, Consolini R
J Clin Med
. 2023 Dec;
12(24).
PMID: 38137647
The clinical expression of 22q11.2 deletion syndrome (22q11.2 DS) is extremely variable, as patients can present with recurrent or severe infections, immune dysregulation, atopic diseases, or extra-immunological manifestations. The immunological...
6.
Simoncini M, Violi M, Valetto A, Bertini V, Cruz-Sanabria F, Massoni L, et al.
Front Psychiatry
. 2023 Dec;
14:1240663.
PMID: 38076678
Autism spectrum disorder (ASD) is characterized by multifactorial etiology and high heritability but can be challenging to be diagnosed, especially in cases presenting subthreshold symptoms with no cognitive or language...
7.
Bertini V, Baldinotti F, Parma P, Tyutyusheva N, Sepich M, Bertolucci G, et al.
Genes (Basel)
. 2023 Nov;
14(11).
PMID: 38003010
Disorders of sexual development (DSDs) encompass a group of congenital conditions associated with atypical development of internal and external genital structures. Among those with DSDs are 46,XX males, whose condition...
8.
Ramone T, Romei C, Ciampi R, Casalini R, Valetto A, Bertini V, et al.
Endocr Relat Cancer
. 2023 Jun;
30(9).
PMID: 37343157
Somatic copy number alterations (SCNA) involving either a whole chromosome or just one of the arms, or even smaller parts, have been described in about 88% of human tumors. This...
9.
Bertini V, Cambi F, Orsini A, Bonuccelli A, Fiorini A, Santangelo A, et al.
Genes (Basel)
. 2022 Dec;
13(12).
PMID: 36553517
The (nuclear factor I/A) gene encodes for a transcription factor belonging to the nuclear factor I family and has key roles in various embryonic differentiation pathways. In humans, is the...
10.
Grati F, Bestetti I, De Siero D, Malvestiti F, Villa N, Sala E, et al.
Prenat Diagn
. 2022 Nov;
42(13):1575-1586.
PMID: 36403097
Objectives: To establish the positive predictive values (PPV) of cfDNA testing based on data from a nationwide survey of independent clinical cytogenetics laboratories. Methods: Prenatal diagnostic test results obtained by...