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Year | Number of Results |
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2020 | 1 |
2021 | 1 |
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2023 | 3 |
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Page 1
Inherited Disorders of Coenzyme A Biosynthesis: Models, Mechanisms, and Treatments.
Int J Mol Sci. 2023 Mar 21;24(6):5951. doi: 10.3390/ijms24065951.
Int J Mol Sci. 2023.
PMID: 36983025
Free PMC article.
Review.
Identification of Autophagy as a Functional Target Suitable for the Pharmacological Treatment of Mitochondrial Membrane Protein-Associated Neurodegeneration (MPAN) In Vitro.
Zanuttigh E, Derderian K, Güra MA, Geerlof A, Di Meo I, Cavestro C, Hempfling S, Ortiz-Collazos S, Mauthe M, Kmieć T, Cammarota E, Panzeri MC, Klopstock T, Sattler M, Winkelmann J, Messias AC, Iuso A.
Zanuttigh E, et al. Among authors: cavestro c.
Pharmaceutics. 2023 Jan 12;15(1):267. doi: 10.3390/pharmaceutics15010267.
Pharmaceutics. 2023.
PMID: 36678896
Free PMC article.
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PPAR Gamma Agonist Leriglitazone Recovers Alterations Due to Pank2-Deficiency in hiPS-Derived Astrocytes.
Santambrogio P, Cozzi A, Di Meo I, Cavestro C, Vergara C, Rodríguez-Pascau L, Martinell M, Pizcueta P, Tiranti V, Levi S.
Santambrogio P, et al. Among authors: cavestro c.
Pharmaceutics. 2023 Jan 6;15(1):202. doi: 10.3390/pharmaceutics15010202.
Pharmaceutics. 2023.
PMID: 36678831
Free PMC article.
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Massive iron accumulation in PKAN-derived neurons and astrocytes: light on the human pathological phenotype.
Santambrogio P, Ripamonti M, Cozzi A, Raimondi M, Cavestro C, Di Meo I, Rubio A, Taverna S, Tiranti V, Levi S.
Santambrogio P, et al. Among authors: cavestro c.
Cell Death Dis. 2022 Feb 25;13(2):185. doi: 10.1038/s41419-022-04626-x.
Cell Death Dis. 2022.
PMID: 35217637
Free PMC article.
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Novel deep intronic mutation in PLA2G6 causing early-onset Parkinson's disease with brain iron accumulation through pseudo-exon activation.
Cavestro C, Panteghini C, Reale C, Nasca A, Fenu S, Salsano E, Chiapparini L, Garavaglia B, Pareyson D, Di Meo I, Tiranti V.
Cavestro C, et al.
Neurogenetics. 2021 Oct;22(4):347-351. doi: 10.1007/s10048-021-00667-0. Epub 2021 Aug 13.
Neurogenetics. 2021.
PMID: 34387792
Free PMC article.
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Neuronal Ablation of CoA Synthase Causes Motor Deficits, Iron Dyshomeostasis, and Mitochondrial Dysfunctions in a CoPAN Mouse Model.
Di Meo I, Cavestro C, Pedretti S, Fu T, Ligorio S, Manocchio A, Lavermicocca L, Santambrogio P, Ripamonti M, Levi S, Ayciriex S, Mitro N, Tiranti V.
Di Meo I, et al. Among authors: cavestro c.
Int J Mol Sci. 2020 Dec 19;21(24):9707. doi: 10.3390/ijms21249707.
Int J Mol Sci. 2020.
PMID: 33352696
Free PMC article.
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