المؤلفون: Mirko Baglivo, Alessia Nasca, Eleonora Lamantea, Stefano Vinci, Manuela Spagnolo, Silvia Marchet, Holger Prokisch, Alessia Catania, Costanza Lamperti, Daniele Ghezzi

المساهمون: M. Baglivo, A. Nasca, E. Lamantea, S. Vinci, M. Spagnolo, S. Marchet, H. Prokisch, A. Catania, C. Lamperti, D. Ghezzi

مصطلحات موضوعية: Leber’s hereditary optic neuropathy, LHON, mtDNA, idebenone, fibroblast, biomarker, responsiveness, Settore MED/03 - Genetica Medica, Settore MED/26 - Neurologia

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/37628761; info:eu-repo/semantics/altIdentifier/wos/WOS:001056124700001; volume:24; issue:16; firstpage:1; lastpage:11; numberofpages:11; journal:INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES; https://hdl.handle.net/2434/993813Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85169127303

الإتاحة: https://doi.org/10.3390/ijms241612580Test
https://hdl.handle.net/2434/993813Test

المؤلفون: 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 G. P., Ronchi D., Ghezzi D., Lamperti C.

المساهمون: F. Invernizzi, R. Izzo, I. Colangelo, A. Legati, N. Zanetti, B. Garavaglia, E. Lamantea, L. Peverelli, A. Ardissone, I. Moroni, L. Maggi, S. Bonanno, L. Fiori, D. Velardo, F. Magri, G.P. Comi, D. Ronchi, D. Ghezzi, C. Lamperti

مصطلحات موضوعية: creatine kinase, hyperCKemia, myoglobinuria, Next Generation Sequencing (NGS), rhabdomyolysi, skeletal muscle damage, Settore MED/03 - Genetica Medica, Settore MED/26 - Neurologia

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/37510298; info:eu-repo/semantics/altIdentifier/wos/WOS:001036056200001; volume:14; issue:7; firstpage:1; lastpage:18; numberofpages:18; journal:GENES; https://hdl.handle.net/2434/993814Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85165879611

الإتاحة: https://doi.org/10.3390/genes14071393Test
https://hdl.handle.net/2434/993814Test

المؤلفون: Nasca A., Legati A., Meneri M., Ermert M. E., Frascarelli C., Zanetti N., Garbellini M., Comi G. P., Catania A., Lamperti C., Ronchi D., Ghezzi D.

المساهمون: A. Nasca, A. Legati, M. Meneri, M.E. Ermert, C. Frascarelli, N. Zanetti, M. Garbellini, G.P. Comi, A. Catania, C. Lamperti, D. Ronchi, D. Ghezzi

مصطلحات موضوعية: ENDOG, Endonuclease G, Mitochondrial DNA, Mitochondrial myopathy, Multiple mtDNA deletion, DNA, Mitochondrial, Endonuclease, Human, Mitochondria, Endodeoxyribonuclease, Mitochondrial Myopathie, Settore MED/26 - Neurologia

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/35326425; info:eu-repo/semantics/altIdentifier/wos/WOS:000775699200001; volume:11; issue:6; firstpage:1; lastpage:10; numberofpages:10; journal:CELLS; https://hdl.handle.net/2434/925382Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85126280294

الإتاحة: https://doi.org/10.3390/cells11060974Test
https://hdl.handle.net/2434/925382Test

المؤلفون: Claudia Ciaccio, Chiara Pantaleoni, Franco Taroni, Daniela Di Bella, Stefania Magri, Eleonora Lamantea, Daniele Ghezzi, Enza Maria Valente, Vincenzo Nigro, Stefano D'Arrigo

المساهمون: C. Ciaccio, C. Pantaleoni, F. Taroni, D. Di Bella, S. Magri, E. Lamantea, D. Ghezzi, E. Maria Valente, V. Nigro, S. D'Arrigo

مصطلحات موضوعية: pediatric ataxia, cerebellar atrophy, genetic ataxia, Settore MED/26 - Neurologia, Settore MED/03 - Genetica Medica

العلاقة: info:eu-repo/semantics/altIdentifier/wos/WOS:000627938300001; volume:11; issue:5; numberofpages:13; journal:APPLIED SCIENCES; http://hdl.handle.net/2434/826581Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85102687976

الإتاحة: https://doi.org/10.3390/app11052333Test
http://hdl.handle.net/2434/826581Test