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Chromosome Transplantation: A Possible Approach to Treat Human X-linked Disorders.
Paulis M, Susani L, Castelli A, Suzuki T, Hara T, Straniero L, Duga S, Strina D, Mantero S, Caldana E, Sergi LS, Villa A, Vezzoni P. Paulis M, et al. Among authors: straniero l. Mol Ther Methods Clin Dev. 2020 Jan 21;17:369-377. doi: 10.1016/j.omtm.2020.01.003. eCollection 2020 Jun 12. Mol Ther Methods Clin Dev. 2020. PMID: 32099849 Free PMC article.
Neurofascin (NFASC) gene mutation causes autosomal recessive ataxia with demyelinating neuropathy.
Monfrini E, Straniero L, Bonato S, Monzio Compagnoni G, Bordoni A, Dilena R, Rinchetti P, Silipigni R, Ronchi D, Corti S, Comi GP, Bresolin N, Duga S, Di Fonzo A. Monfrini E, et al. Among authors: straniero l. Parkinsonism Relat Disord. 2019 Jun;63:66-72. doi: 10.1016/j.parkreldis.2019.02.045. Epub 2019 Mar 1. Parkinsonism Relat Disord. 2019. PMID: 30850329 Free article.
Late-onset leukoencephalopathy in a patient with recessive EARS2 mutations.
Monfrini E, Ronchi D, Franco G, Garbellini M, Straniero L, Scola E, Arienti F, Duga S, Comi GP, Bresolin N, Di Fonzo A. Monfrini E, et al. Among authors: straniero l. Neurol Genet. 2020 Jul 13;6(5):e488. doi: 10.1212/NXG.0000000000000488. eCollection 2020 Oct. Neurol Genet. 2020. PMID: 32802952 Free PMC article. No abstract available.
Massive Accumulation of Sphingomyelin Affects the Lysosomal and Mitochondria Compartments and Promotes Apoptosis in Niemann-Pick Disease Type A.
Carsana EV, Lunghi G, Prioni S, Mauri L, Loberto N, Prinetti A, Zucca FA, Bassi R, Sonnino S, Chiricozzi E, Duga S, Straniero L, Asselta R, Soldà G, Samarani M, Aureli M. Carsana EV, et al. Among authors: straniero l. J Mol Neurosci. 2022 Jul;72(7):1482-1499. doi: 10.1007/s12031-022-02036-4. Epub 2022 Jun 21. J Mol Neurosci. 2022. PMID: 35727525 Free PMC article.
36 results