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Year | Number of Results |
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2020 | 1 |
2023 | 4 |
2024 | 1 |
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Page 1
Expanding the Spectrum of NUBPL-Related Leukodystrophy.
Neuropediatrics. 2023 Jun;54(3):161-166. doi: 10.1055/s-0043-1764214. Epub 2023 Mar 3.
Neuropediatrics. 2023.
PMID: 36868263
Review.
NGS-Based Genetic Analysis in a Cohort of Italian Patients with Suspected Inherited Myopathies and/or HyperCKemia.
Invernizzi F, Izzo R, Colangelo I, Legati A, Zanetti N, Garavaglia B, Lamantea E, Peverelli L, Ardissone A, Moroni I, Maggi L, Bonanno S, Fiori L, Velardo D, Magri F, Comi GP, Ronchi D, Ghezzi D, Lamperti C.
Invernizzi F, et al. Among authors: izzo r.
Genes (Basel). 2023 Jul 2;14(7):1393. doi: 10.3390/genes14071393.
Genes (Basel). 2023.
PMID: 37510298
Free PMC article.
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Fasting Drives Nrf2-Related Antioxidant Response in Skeletal Muscle.
Lettieri-Barbato D, Minopoli G, Caggiano R, Izzo R, Santillo M, Aquilano K, Faraonio R.
Lettieri-Barbato D, et al. Among authors: izzo r.
Int J Mol Sci. 2020 Oct 21;21(20):7780. doi: 10.3390/ijms21207780.
Int J Mol Sci. 2020.
PMID: 33096672
Free PMC article.
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Nanopore long-read next-generation sequencing for detection of mitochondrial DNA large-scale deletions.
Frascarelli C, Zanetti N, Nasca A, Izzo R, Lamperti C, Lamantea E, Legati A, Ghezzi D.
Frascarelli C, et al. Among authors: izzo r.
Front Genet. 2023 Jun 29;14:1089956. doi: 10.3389/fgene.2023.1089956. eCollection 2023.
Front Genet. 2023.
PMID: 37456669
Free PMC article.
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A Novel Pathogenic Variant in the SCA25-Related Gene Expanding the Etiology of Early-Onset and Progressive Cerebellar Ataxia in Childhood.
Ferrera G, Izzo R, Ghezzi D, Nanetti L, Lamantea E, Ardissone A.
Ferrera G, et al. Among authors: izzo r.
Neuropediatrics. 2024 Apr;55(2):135-139. doi: 10.1055/a-2205-2402. Epub 2023 Nov 7.
Neuropediatrics. 2024.
PMID: 37935417
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