Angelo Luigi Vescovi
Overview
Explore the profile of Angelo Luigi Vescovi including associated specialties, affiliations and a list of published articles.
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Articles
57
Citations
716
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Recent Articles
1.
Giovenale A, Turco E, Mazzoni M, Ferrone I, Torres B, Bernardini L, et al.
Stem Cell Res
. 2024 Sep;
81():103544.
PMID: 39260069
Smith-Magenis syndrome (SMS) is a complex neurodevelopmental disorder with a birth incidence of 1:25,000. SMS is caused by haploinsufficiency of the retinoic acid-induced retinoic acid1 (RAI1) gene, determined by an...
2.
Casamassa A, Rotundo G, Ceresoni C, Turco E, Torrente I, Candido O, et al.
Stem Cell Res
. 2024 Jun;
78:103468.
PMID: 38852424
Hypomyelinating leukodystrophies (HLD) are a group of heterogeneous genetic disorders characterized by a deficit in myelin deposition during brain development. Specifically, 4H-Leukodystrophy is a recessive disease due to biallelic mutations...
3.
Bianco S, Parca L, Petrizzelli F, Biagini T, Giovannetti A, Liorni N, et al.
Nat Commun
. 2023 Aug;
14(1):5058.
PMID: 37598215
Mitochondrial dysfunction has pleiotropic effects and is frequently caused by mitochondrial DNA mutations. However, factors such as significant variability in clinical manifestations make interpreting the pathogenicity of variants in the...
4.
Bos E, Binda E, Verploegh I, Wembacher E, Hoefnagel D, Balvers R, et al.
Mol Cancer
. 2023 Aug;
22(1):129.
PMID: 37563568
Background: This Phase 1 study evaluates the intra- and peritumoral administration by convection enhanced delivery (CED) of human recombinant Bone Morphogenetic Protein 4 (hrBMP4) - an inhibitory regulator of cancer...
5.
Marano M, Rosati J, Magliozzi A, Casamassa A, Rappa A, Sergi G, et al.
Neurobiol Sleep Circadian Rhythms
. 2023 Apr;
14:100094.
PMID: 37025301
Circadian rhythm impairment may play a role in Parkinson's disease (PD) pathophysiology. Recent literature associated circadian rhythm features to the risk of developing Parkinson and to its progression through stages....
6.
Corrigendum: Deepening the understanding of CNVs on chromosome 15q11-13 by using hiPSCs: An overview
Giovenale A, Ruotolo G, Soriano A, Turco E, Rotundo G, Casamassa A, et al.
Front Cell Dev Biol
. 2023 Feb;
11:1141334.
PMID: 36819100
[This corrects the article DOI: 10.3389/fcell.2022.1107881.].
7.
Giovenale A, Ruotolo G, Soriano A, Turco E, Rotundo G, Casamassa A, et al.
Front Cell Dev Biol
. 2023 Jan;
10:1107881.
PMID: 36684422
The human α7 neuronal nicotinic acetylcholine receptor gene (CHRNA7) is widely expressed in the central and peripheral nervous systems. This receptor is implicated in both brain development and adult neurogenesis...
8.
Rotundo G, Turco E, Ruotolo G, Torrente I, Candido O, Lopez G, et al.
Stem Cell Res
. 2023 Jan;
67:103023.
PMID: 36638628
Familial Hypocalciuric Hypercalcemia (FHH1) is a rare autosomal dominant disease with low penetrance, caused by inactivating mutations of the calcium-sensing receptor (CaSR) gene, characterized by significant hypercalcemia, inappropriately normal serum...
9.
Turco E, Giovenale A, Sireno L, Mazzoni M, Cammareri A, Marchioretti C, et al.
Cell Death Dis
. 2022 Nov;
13(11):981.
PMID: 36411275
Smith-Magenis syndrome (SMS) is a neurodevelopmental disorder characterized by cognitive and behavioral symptoms, obesity, and sleep disturbance, and no therapy has been developed to alleviate its symptoms or delay disease...
10.
Profico D, Gelati M, Ferrari D, Sgaravizzi G, Ricciolini C, Projetti Pensi M, et al.
Int J Mol Sci
. 2022 Nov;
23(21).
PMID: 36362211
Translation of cell therapies into clinical practice requires the adoption of robust production protocols in order to optimize and standardize the manufacture and cryopreservation of cells, in compliance with good...