Luigi Michele Pavone
Overview
Explore the profile of Luigi Michele Pavone including associated specialties, affiliations and a list of published articles.
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Articles
58
Citations
845
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Recent Articles
1.
Scarcella M, Fecarotta S, Alagia M, Barretta F, Uomo F, De Pasquale V, et al.
Mol Genet Metab
. 2025 Jan;
144(2):109008.
PMID: 39788860
Background: Newborn screening (NBS) is a simple, non-invasive test that allows for the early identification of genetic diseases within the first days of a newborn's life. The aim of NBS...
2.
Ruiz-Blazquez P, Fernandez-Fernandez M, Pistorio V, Martinez-Sanchez C, Costanzo M, Iruzubieta P, et al.
Mol Metab
. 2024 Jul;
87:101989.
PMID: 39019115
Background And Objectives: Fibrosis contributes to 45% of deaths in industrialized nations and is characterized by an abnormal accumulation of extracellular matrix (ECM). There are no specific anti-fibrotic treatments for...
3.
Costanzo M, Cevenini A, Kollipara L, Caterino M, Bianco S, Pirozzi F, et al.
Cell Biosci
. 2024 May;
14(1):63.
PMID: 38760822
Background: Methylmalonic acidemia (MMA) is a rare inborn error of propionate metabolism caused by deficiency of the mitochondrial methylmalonyl-CoA mutase (MUT) enzyme. As matter of fact, MMA patients manifest impairment...
4.
Scarcella M, Scerra G, Ciampa M, Caterino M, Costanzo M, Rinaldi L, et al.
iScience
. 2024 Feb;
27(3):108959.
PMID: 38361619
Mucopolysaccharidoses (MPSs) are lysosomal disorders with neurological involvement for which no cure exists. Here, we show that recombinant NK1 fragment of hepatocyte growth factor rescues substrate accumulation and lysosomal defects...
5.
Giuliano P, La Rosa G, Capozzi S, Cassano E, Damiano S, Habetswallner F, et al.
Int J Mol Sci
. 2024 Feb;
25(3).
PMID: 38338973
Multiple sclerosis (MS) is an autoimmune chronic disease characterized by inflammation and demyelination of the central nervous system (CNS). Despite numerous studies conducted, valid biomarkers enabling a definitive diagnosis of...
6.
De Pasquale V, Esposito A, Scerra G, Scarcella M, Ciampa M, Luongo A, et al.
J Med Chem
. 2023 Jan;
66(3):1790-1808.
PMID: 36696678
Sanfilippo syndrome comprises a group of four genetic diseases due to the lack or decreased activity of enzymes involved in heparan sulfate (HS) catabolism. HS accumulation in lysosomes and other...
7.
Scerra G, De Pasquale V, Scarcella M, Caporaso M, Pavone L, DAgostino M
Open Biol
. 2022 Oct;
12(10):220155.
PMID: 36285443
Lysosomal storage diseases (LSDs) comprise a group of inherited monogenic disorders characterized by lysosomal dysfunctions due to undegraded substrate accumulation. They are caused by a deficiency in specific lysosomal hydrolases...
8.
Scarcella M, dAngelo D, Ciampa M, Tafuri S, Avallone L, Pavone L, et al.
Int J Mol Sci
. 2022 Aug;
23(16).
PMID: 36012353
Cathepsins encompass a family of lysosomal proteases that mediate protein degradation and turnover. Although mainly localized in the endolysosomal compartment, cathepsins are also found in the cytoplasm, nucleus, and extracellular...
9.
De Pasquale V, Scarcella M, Pavone L
Biomedicines
. 2022 Apr;
10(4).
PMID: 35453672
Lysosomal storage diseases (LSDs) are a group of metabolic diseases caused by inborn mutations of lysosomal enzymes, which lead to lysosome substrate accumulation in various cell types [...].
10.
Wegrzyn G, Pierzynowska K, Pavone L
Front Mol Biosci
. 2022 Mar;
9:874267.
PMID: 35295844
No abstract available.