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pro vyhledávání: '"ROETTO A"'
Akademický článek
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Publikováno v:
Italian Journal of Pediatrics, Vol 37, Iss 1, p 20 (2011)
Abstract Hereditary hyperferritinemia cataract syndrome (HHCS) is a rare condition caused by mutations in the gene coding for the light chain of ferritin; it does not lead to iron overload, but it is associated with the risk of developing a bilateral
Externí odkaz:
https://doaj.org/article/1bf280c2d9224bf1b74a3cd913e79142
Publikováno v:
Scientific Reports, Vol 12, Iss 1, Pp 1-11 (2022)
Abstract During physiological aging, iron accumulates in the brain with a preferential distribution in regions that are more vulnerable to age-dependent neurodegeneration such as the cerebral cortex and hippocampus. In the brain of aged wild-type mic
Externí odkaz:
https://doaj.org/article/a14ccda48eab47e8a23bfe588ee973a3
Autor:
Marie Angèle Cucci, Margherita Grattarola, Chiara Monge, Antonella Roetto, Giuseppina Barrera, Emilia Caputo, Chiara Dianzani, Stefania Pizzimenti
Publikováno v:
Antioxidants, Vol 12, Iss 6, p 1313 (2023)
The use of specific inhibitors towards mutant BRAF (BRAFi) and MEK (MEKi) in BRAF-mutated patients has significantly improved progression-free and overall survival of metastatic melanoma patients. Nevertheless, half of the patients still develop resi
Externí odkaz:
https://doaj.org/article/535882587ff54a7b88dfd08d881d032c
Autor:
Ciamporcero, Eric, Daga, Martina, Pizzimenti, Stefania, Roetto, Antonella, Dianzani, Chiara, Compagnone, Alessandra, Palmieri, Antonietta, Ullio, Chiara, Cangemi, Luigi, Pili, Roberto, Barrera, Giuseppina
Publikováno v:
In Free Radical Biology and Medicine 1 February 2018 115:447-457
Autor:
Ylenia Barbanera, Francesco Arcioni, Hovirag Lancioni, Roberta La Starza, Irene Cardinali, Caterina Matteucci, Valeria Nofrini, Antonella Roetto, Antonio Piga, Paola Grammatico, Maurizio Caniglia, Cristina Mecucci, Paolo Gorello
Publikováno v:
PLoS ONE, Vol 15, Iss 10, p e0240632 (2020)
The hemoglobin disorders are the most common single gene disorders in the world. Previous studies have suggested that they are deeply geographically structured and a variety of genetic determinants influences different clinical phenotypes between pat
Externí odkaz:
https://doaj.org/article/7153e7955694454b9f074c5c3b33e9ac
Akademický článek
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Publikováno v:
Antioxidants, Vol 10, Iss 12, p 1864 (2021)
Iron accumulation is a key mediator of several cytotoxic mechanisms leading to the impairment of redox homeostasis and cellular death. Iron overload is often associated with haematological diseases which require regular blood transfusion/phlebotomy,
Externí odkaz:
https://doaj.org/article/2d1ddbe91257491ca12ff7878bf7e2fb
Autor:
Pizzimenti, Marie Angèle Cucci, Margherita Grattarola, Chiara Monge, Antonella Roetto, Giuseppina Barrera, Emilia Caputo, Chiara Dianzani, Stefania
Publikováno v:
Antioxidants; Volume 12; Issue 6; Pages: 1313
The use of specific inhibitors towards mutant BRAF (BRAFi) and MEK (MEKi) in BRAF-mutated patients has significantly improved progression-free and overall survival of metastatic melanoma patients. Nevertheless, half of the patients still develop resi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=multidiscipl::7cd0b8574704830c84ca04f77e5842d0
Autor:
Johnston, John J., Windberg, Lamar A., Furcolow, Carol A., Engeman, Richard M., Roetto, Marianna
Publikováno v:
The Journal of Wildlife Management, 1998 Jan 01. 62(1), 410-421.
Externí odkaz:
https://www.jstor.org/stable/3802307