Zobrazeno 1 - 10
of 692
pro vyhledávání: '"Castaldo, I"'
Autor:
De Joanna, G., De Rosa, A., Salvatore, E., Castaldo, I., De Luca, N., Izzo, R., Manzo, V., Filla, A., De Michele, G.
Publikováno v:
In Journal of the Neurological Sciences 15 December 2008 275(1-2):60-63
Autor:
Bhat, Asif Ahmad1 (AUTHOR), Moglad, Ehssan2 (AUTHOR), Afzal, Muhammad3 (AUTHOR), Thapa, Riya1 (AUTHOR), Almalki, Waleed Hassan4 (AUTHOR), Kazmi, Imran5 (AUTHOR), Alzarea, Sami I.6 (AUTHOR), Ali, Haider7,8 (AUTHOR), Pant, Kumud9 (AUTHOR), Singh, Thakur Gurjeet10 (AUTHOR) gurjeet.singh@chitkara.edu.in, Dureja, Harish11 (AUTHOR), Singh, Sachin Kumar12,13 (AUTHOR), Dua, Kamal13,14 (AUTHOR), Gupta, Gaurav15,16 (AUTHOR) gauravpharma25@gmail.com, Subramaniyan, Vetriselvan17,18 (AUTHOR) subramaniyan.vetriselvan@monash.edu
Publikováno v:
CNS Neuroscience & Therapeutics. Oct2024, Vol. 30 Issue 10, p1-28. 28p.
Autor:
Varrone A, Barone P, Sansone V, Pellecchia MT, Castaldo I, Coppola G, Brunetti A, Salvatore M, Pappatà S, SALVATORE, ELENA, DE MICHELE, GIUSEPPE, FILLA, ALESSANDRO
Degeneration of substantia nigra has been described in spinocerebellar ataxia type 2 (SCA2). In this study, dopamine transporter (DAT) density with [123 I]FP-CIT SPECT was studied in six SCA2 patients with no parkinsonian signs, six Parkinson's disea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::1cdc83ce8718846c277cc1c52e4cfff0
http://hdl.handle.net/11588/204018
http://hdl.handle.net/11588/204018
Autor:
MALTECCA F, FILLA, ALESSANDRO, CASTALDO I, COPPOLA G, CARELLA M, BRUNI A, COCOZZA, SERGIO, CASARI G, SERVADIO A, DE MICHELE, GIUSEPPE, FRAGASSI, NINA ANTONETTA
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3730::dc55608235232f647da5d4f7a852e14a
http://hdl.handle.net/11588/172128
http://hdl.handle.net/11588/172128
Publikováno v:
Antioxidants & redox signalling (2013).
info:cnr-pdr/source/autori:Castaldo I, Vergara P, Pinelli M, Filla A, De Michele G, Cocozza S, Monticelli A./titolo:Can Telomere Shortening in Human Peripheral Blood Leukocytes Serve as a Disease Biomarker of Friedreich's Ataxia?/doi:/rivista:Antioxidants & redox signalling/anno:2013/pagina_da:/pagina_a:/intervallo_pagine:/volume
info:cnr-pdr/source/autori:Castaldo I, Vergara P, Pinelli M, Filla A, De Michele G, Cocozza S, Monticelli A./titolo:Can Telomere Shortening in Human Peripheral Blood Leukocytes Serve as a Disease Biomarker of Friedreich's Ataxia?/doi:/rivista:Antioxidants & redox signalling/anno:2013/pagina_da:/pagina_a:/intervallo_pagine:/volume
Enhanced oxidative stress and inflammation contribute to telomere erosion. Friedreich's ataxia is a neurodegenerative disorder caused by a reduction in frataxin expression that results in mitochondrial dysfunction and oxidative damage. Furthermore, f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=cnr_________::d014fe593f4adcd3bb7f74a4398c028e
https://publications.cnr.it/doc/207327
https://publications.cnr.it/doc/207327
Autor:
Wu, Lin1 (AUTHOR), Huang, Fei2 (AUTHOR), Yang, Lu1 (AUTHOR), Yang, Liu1 (AUTHOR), Sun, Zichen1 (AUTHOR), Zhang, Jinghua1 (AUTHOR), Xia, Siyu2 (AUTHOR), Zhao, Hongting1 (AUTHOR), Ding, Yibing1 (AUTHOR), Bian, Dezhi2 (AUTHOR) bianrz2008@163.com, Li, Kuanyu1 (AUTHOR) likuanyu@nju.edu.cn
Publikováno v:
Scientific Reports. 8/27/2024, Vol. 14 Issue 1, p1-14. 14p.
Autor:
Hoffman-Zacharska, Dorota1,2 (AUTHOR) anna.sulek@lazarski.pl, Sulek, Anna2,3 (AUTHOR)
Publikováno v:
International Journal of Molecular Sciences. Aug2024, Vol. 25 Issue 15, p8190. 11p.
Autor:
Castaldo I; Department of Molecular Medicine and Medical Biotechnology, University of Naples Federico II, Naples, Italy., De Rosa M; Department of Molecular Medicine and Medical Biotechnology, University of Naples Federico II, Naples, Italy., Romano A; Department of Biology, University of Naples Federico II, Naples, Italy., Zuchegna C; Department of Biology, University of Naples Federico II, Naples, Italy., Squitieri F; Huntington and Rare Diseases Unit, Scientific Institute for Research and Cure (IRCCS) Casa Sollievo della Sofferenza (Rome-Casa Sollievo della Sofferenza (CSS) Mendel), San Giovanni Rotondo, Italy., Mechelli R; Department of Human Science and Promotion of Quality of Life, San Raffaele Roma Open University, Rome, Italy., Peluso S; Department of Neurosciences, University of Naples Federico II, Naples, Italy., Borrelli C; Italian League for Research on Huntington and Related Diseases Foundation, Rome, Italy., Del Mondo A; Department of Biology, University of Naples Federico II, Naples, Italy., Salvatore E; Department of Neurosciences, University of Naples Federico II, Naples, Italy., Vescovi LA; Scientific Institute for Research and Cure (IRCCS) Casa Sollievo della Sofferenza, Institute for Stem Cell Biology, Regenerative Medicine, and Innovative Therapies, San Giovanni Rotondo, Italy., Migliore S; Huntington and Rare Diseases Unit, Scientific Institute for Research and Cure (IRCCS) Casa Sollievo della Sofferenza (Rome-Casa Sollievo della Sofferenza (CSS) Mendel), San Giovanni Rotondo, Italy., De Michele G; Department of Neurosciences, University of Naples Federico II, Naples, Italy., Ristori G; Center for Experimental Neurological Therapies, Department of Neurosciences, Mental Health, and Sensory Organs, Faculty of Medicine and Psychology, Sapienza University of Rome, Rome, Italy., Romano S; Center for Experimental Neurological Therapies, Department of Neurosciences, Mental Health, and Sensory Organs, Faculty of Medicine and Psychology, Sapienza University of Rome, Rome, Italy., Avvedimento EV; Department of Molecular Medicine and Medical Biotechnology, University of Naples Federico II, Naples, Italy., Porcellini A; Department of Biology, University of Naples Federico II, Naples, Italy.
Publikováno v:
Annals of neurology [Ann Neurol] 2019 Feb; Vol. 85 (2), pp. 296-301. Date of Electronic Publication: 2019 Jan 13.
Autor:
Pianese, L., Francesca Cavalcanti, Demichele, G., Filla, A., Campanella, G., Calabrese, O., Castaldo, I., Monticelli, A., Cocozza, S.
Publikováno v:
American journal of human genetics 60 (1997): 460–463.
info:cnr-pdr/source/autori:Pianese L, Cavalcanti F, DeMichele G, Filla A, Campanella G, Calabrese O, Castaldo I, MONTICELLI A, Cocozza S/titolo:The effect of parental gender on the GAA dynamic mutation in the FRDA gene/doi:/rivista:American journal of human genetics/anno:1997/pagina_da:460/pagina_a:463/intervallo_pagine:460–463/volume:60
ResearcherID
info:cnr-pdr/source/autori:Pianese L, Cavalcanti F, DeMichele G, Filla A, Campanella G, Calabrese O, Castaldo I, MONTICELLI A, Cocozza S/titolo:The effect of parental gender on the GAA dynamic mutation in the FRDA gene/doi:/rivista:American journal of human genetics/anno:1997/pagina_da:460/pagina_a:463/intervallo_pagine:460–463/volume:60
ResearcherID
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::2dd77886d1b8f3ef99561d4224b4781d
https://pubmed.ncbi.nlm.nih.gov/9012421
https://pubmed.ncbi.nlm.nih.gov/9012421