Alessia Casamassa
Overview
Explore the profile of Alessia Casamassa including associated specialties, affiliations and a list of published articles.
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13
Citations
57
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0
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Recent Articles
1.
Sollazzo R, Li Puma D, Aceto G, Paciello F, Colussi C, Vita M, et al.
Alzheimers Res Ther
. 2024 Dec;
16(1):267.
PMID: 39702316
Background: Alzheimer's Disease (AD) is a neurodegenerative disorder characterized by the accumulation of pathological proteins and synaptic dysfunction. This study aims to investigate the molecular and functional differences between human...
2.
Pietrafesa D, Casamassa A, Benassi B, Santoro M, Marano M, Consales C, et al.
Int J Mol Sci
. 2024 Nov;
25(21).
PMID: 39518995
Heterozygous mutations or genetic variants in the gene, which encodes for the β-glucocerebrosidase (GCase), a lysosomal hydrolase enzyme, may increase the risk of Parkinson's disease (PD) onset. The heterozygous E326K...
3.
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...
4.
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....
5.
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.].
6.
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...
7.
Casamassa A, Zanetti A, Ferrari D, Lombardi I, Galluzzi G, DAvanzo F, et al.
Stem Cell Res
. 2022 Jun;
63:102846.
PMID: 35759972
Mucopolysaccharidosis type II (Hunter Syndrome) is a rare X-linked inherited lysosomal storage disorder presenting a wide genetic heterogeneity. It is due to pathogenic variants in the IDS gene, causing the...
8.
Stampanoni Bassi M, Nuzzo T, Gilio L, Miroballo M, Casamassa A, Buttari F, et al.
J Neurochem
. 2021 Sep;
159(5):857-866.
PMID: 34547109
Excessive extracellular concentrations of L-glutamate (L-Glu) can be neurotoxic and contribute to neurodegenerative processes in multiple sclerosis (MS). The association between cerebrospinal fluid (CSF) L-Glu levels, clinical features, and inflammatory...
9.
Nuzzo T, Mancini A, Miroballo M, Casamassa A, Di Maio A, Donati G, et al.
Amino Acids
. 2021 Feb;
53(3):435-449.
PMID: 33616735
Altered glutamatergic neurotransmission is thought to play a crucial role in the progression of Alzheimer's disease (AD). Accordingly, the identification of peculiar biochemical patterns reflecting AD-related synaptopathy in blood and...
10.
Battista T, Pascarella G, Staid D, Colotti G, Rosati J, Fiorillo A, et al.
Int J Mol Sci
. 2021 Feb;
22(3).
PMID: 33525510
Huntington disease (HD) is a devastating and presently untreatable neurodegenerative disease characterized by progressively disabling motor and mental manifestations. The sigma-1 receptor (σ1R) is a protein expressed in the central...