Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Anna Choub"'
Publikováno v:
Neuropsychiatric Disease and Treatment, Vol 2010, Iss Issue 1, Pp 491-499 (2010)
Michelangelo Mancuso, Daniele Orsucci, Anna Choub, Gabriele SicilianoDepartment of Neuroscience, Neurological Clinic, University of Pisa, Pisa, ItalyAbstract: Friedreich ataxia (FRDA) is the most common autosomal recessive ataxia. Oxidative damage wi
Externí odkaz:
https://doaj.org/article/8c796c9f2a9c45cf9f70a36ecdc7b1a8
Publikováno v:
Pharmaceuticals, Vol 2, Iss 3, Pp 134-149 (2009)
Coenzyme Q10 (CoQ10, or ubiquinone) is a small electron carrier of the mitochondrial respiratory chain with antioxidant properties. CoQ10 supplementation has been widely used for mitochondrial disorders. The rationale for using CoQ10 is very powerful
Externí odkaz:
https://doaj.org/article/2a28ce9a5f7f41ee990facd7ae8b2479
Publikováno v:
Neuropsychiatric Disease and Treatment, Vol 2010, Iss Issue 1, Pp 491-499 (2010)
ResearcherID
Neuropsychiatric Disease and Treatment
ResearcherID
Neuropsychiatric Disease and Treatment
Michelangelo Mancuso, Daniele Orsucci, Anna Choub, Gabriele SicilianoDepartment of Neuroscience, Neurological Clinic, University of Pisa, Pisa, ItalyAbstract: Friedreich ataxia (FRDA) is the most common autosomal recessive ataxia. Oxidative damage wi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7dd4d146176388bac0c0eb8a2e162e29
http://www.dovepress.com/current-and-emerging-treatment-options-in-the-management-of-friedreich-a4953
http://www.dovepress.com/current-and-emerging-treatment-options-in-the-management-of-friedreich-a4953
Autor:
L. Murri, D Borghetti, E Di Coscio, Anna Choub, R Sposito, Gloria Tognoni, Enrica Bonanni, Nicola Salvati, M Fabbrini, Alfonso Iudice, Cristina Pagni, Michelangelo Maestri
Publikováno v:
Acta Neurologica Scandinavica. 122:389-397
Bonanni E, Tognoni G, Maestri M, Salvati N, Fabbrini M, Borghetti D, Di Coscio E, Choub A, Sposito R, Pagni C, Iudice A, Murri L. Sleep disturbances in elderly subjects: an epidemiological survey in an Italian district. Acta Neurol Scand: 2010: 122:
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e29d46aefd0186e31db0c84b3b29a2c5
https://doi.org/10.1111/j.1600-0404.2010.01324.x
https://doi.org/10.1111/j.1600-0404.2010.01324.x
Publikováno v:
Pharmaceuticals
Pharmaceuticals, Vol 2, Iss 3, Pp 134-149 (2009)
Pharmaceuticals, Vol 2, Iss 3, Pp 134-149 (2009)
Coenzyme Q10 (CoQ10, or ubiquinone) is a small electron carrier of the mitochondrial respiratory chain with antioxidant properties. CoQ10 supplementation has been widely used for mitochondrial disorders. The rationale for using CoQ10 is very powerful
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6fdac873fd3441638c2985b45232dce9
http://europepmc.org/articles/PMC3978538
http://europepmc.org/articles/PMC3978538
Autor:
Massimiliano Filosto, Alessandro Padovani, Laura Broglio, Anna Choub, Gabriele Siciliano, Marta Tentorio, Michelangelo Mancuso
Publikováno v:
Bioscience Reports. 27:31-37
Mitochondrial diseases are a group of disorders due to a mitochondrial respiratory chain deficiency. They may depend on mitochondrial genome (mtDNA-related disorders) as well as on a nuclear genome defect (nDNA-related disorders). mtDNA-related disor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3f4d66a98695ae6759be6a34c84abe17
https://doi.org/10.1007/s10540-007-9035-2
https://doi.org/10.1007/s10540-007-9035-2
Autor:
Anna Choub, Clara Lazzarini, Laura Broglio, Serena Buzio, Alessandro Padovani, Massimiliano Filosto, Maria Pia Pasolini, Maria Cotelli, Michelangelo Mancuso, Mauro Scarpelli, Marta Tentorio
Publikováno v:
Clinical Toxicology. 46:314-316
Disulfiram may cause a peripheral neuropathy that is considered dose- and duration-of-exposure-related. Axonal degeneration has been described as a pathological hallmark of disulfiram toxicity, but experiments have reported a primary toxic effect of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d722273413842f1dc19153ed1b37dfbe
https://doi.org/10.1080/15563650701636390
https://doi.org/10.1080/15563650701636390
Autor:
Anna Choub, Eleonora Pini, Michelangelo Mancuso, Daniele Orsucci, Gabriele Siciliano, Elena Caldarazzo Ienco
Mitochondrial disorders are caused by impairment of the respiratory chain. Psychiatric features often represent part of their clinical spectrum. However, the real incidence of psychiatric disorders in these diseases is unknown. The aim of this study
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2bc5972699cde7a9eb4b61386e4c77f8
http://hdl.handle.net/11568/159701
http://hdl.handle.net/11568/159701
CLOCK T3111C AND PER2 C111G SNPS DO NOT INFLUENCE CIRCADIAN RHYTMICITY IN HEALTHY ITALIAN POPULATION
Autor:
Daniele Orsucci, Michelangelo Mancuso, Enrica Bonanni, Gabriele Siciliano, Annalisa LoGerfo, Anna Rocchi, Michelangelo Maestri, Lucia Petrozzi, Fabio Coppedè, Anna Choub, Elisa DiCoscio, Luigi Murri
A possible relationship between human circadian rhythmicity and polymorphisms in clock genes have been documented. However, these data are controversial, and studies both corroborating and denying them have been reported. T3111C Clock polymorphism ha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::712a47b551e1bc6fce432575e9bfc1e9
http://hdl.handle.net/11568/141921
http://hdl.handle.net/11568/141921
Autor:
Anna Choub, Claudia Nesti, Gabriele Siciliano, Daniele Orsucci, Michelangelo Mancuso, Fabio Coppedè
Publikováno v:
ResearcherID
Mitochondrial diseases (MD) are disorders caused by impairment of the mitochondrial electron transport chain (ETC). Phenotypes are polymorphous and may range from pure myopathy to multisystemic disorders. The genetic defect can be located on mitochon
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9d8690900e8c69ea1a24f1124ca12117
http://hdl.handle.net/11568/131879
http://hdl.handle.net/11568/131879