Devid Damiani
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Explore the profile of Devid Damiani including associated specialties, affiliations and a list of published articles.
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Articles
14
Citations
285
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Recent Articles
1.
De Riso G, Naef V, Damiani D, Doccini S, Santorelli F, Galatolo D
Cerebellum
. 2025 Jan;
24(2):36.
PMID: 39853590
Autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS) is a rare inherited condition described worldwide and characterized by a wide spectrum of heterogeneity in terms of genotype and phenotype. How sacsin...
2.
Naef V, Damiani D, Licitra R, Marchese M, Della Vecchia S, Baggiani M, et al.
Neurobiol Dis
. 2025 Jan;
205:106793.
PMID: 39778749
Biallelic mutations in the SACS gene, encoding sacsin, cause early-onset autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS), a neurodegenerative disease also characterized by unique and poorly understood retinal abnormalities. While...
3.
Della Vecchia S, Imbrici P, Liantonio A, Naef V, Damiani D, Licitra R, et al.
Biomed Pharmacother
. 2025 Jan;
183:117800.
PMID: 39753095
Lafora disease (LD) is an ultra-rare and still incurable neurodegenerative condition. Although several therapeutic strategies are being explored, including gene therapy, there are currently no treatments that can alleviate the...
4.
Baggiani M, Damiani D, Privitera F, Della Vecchia S, Tessa A, Santorelli F
Int J Mol Sci
. 2024 Oct;
25(19).
PMID: 39408944
Hereditary spastic paraplegias are rare genetic disorders characterized by corticospinal tract impairment. Spastic paraplegia 83 (SPG83) is associated with biallelic mutations in the gene, leading to varied severities from neonatal...
5.
Baggiani M, Santorelli F, Mero S, Privitera F, Damiani D, Tessa A
Stem Cell Res
. 2024 Jun;
79:103472.
PMID: 38889632
Hereditary spastic paraplegias (HSPs) a group of rare, clinically, and genetically heterogeneous disorders characterized by progressive degeneration of the corticospinal tract. Among these HSPs, SPG31 is due to autosomal dominant...
6.
Damiani D, Baggiani M, Della Vecchia S, Naef V, Santorelli F
Int J Mol Sci
. 2024 Mar;
25(5).
PMID: 38473862
Hereditary spastic paraplegias (HSPs) comprise a family of degenerative diseases mostly hitting descending axons of corticospinal neurons. Depending on the gene and mutation involved, the disease could present as a...
7.
Mangoni D, Simi A, Lau P, Armaos A, Ansaloni F, Codino A, et al.
Nat Commun
. 2023 Aug;
14(1):4974.
PMID: 37591988
Long Interspersed Nuclear Elements-1s (L1s) are transposable elements that constitute most of the genome's transcriptional output yet have still largely unknown functions. Here we show that L1s are required for...
8.
Licitra R, Naef V, Marchese M, Damiani D, Ogi A, Doccini S, et al.
Int J Mol Sci
. 2023 Mar;
24(6).
PMID: 36982531
Milk oligosaccharides are a complex class of carbohydrates that act as bioactive factors in numerous defensive and physiological functions, including brain development. Early nutrition can modulate nervous system development and...
9.
Turco E, Giovenale A, Rotundo G, Mazzoni M, Zanfardino P, Frezza K, et al.
Stem Cell Res
. 2022 Oct;
65:102946.
PMID: 36272304
Charcot-Marie-Tooth type 4B3 (CMT4B3) is a rare subtype of hereditary neuropathy associated with variants in the MTMR5/SBF1 gene. Herein, we report the generation and characterization of a hiPSC line from...
10.
Espinoza S, Bon C, Valentini P, Pierattini B, Matey A, Damiani D, et al.
Essays Biochem
. 2021 Oct;
65(4):775-789.
PMID: 34623427
RNA molecules have emerged as a new class of promising therapeutics to expand the range of druggable targets in the genome. In addition to 'canonical' protein-coding mRNAs, the emerging richness...