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Highly reactive oxygen species: detection, formation, and possible functions.
Cell Mol Life Sci. 2011 Jun;68(12):2067-79. doi: 10.1007/s00018-011-0682-x. Epub 2011 May 2.
Cell Mol Life Sci. 2011.
PMID: 21533983
Review.
Mutations in KANSL1 cause the 17q21.31 microdeletion syndrome phenotype.
Zollino M, Orteschi D, Murdolo M, Lattante S, Battaglia D, Stefanini C, Mercuri E, Chiurazzi P, Neri G, Marangi G.
Zollino M, et al. Among authors: stefanini c.
Nat Genet. 2012 Apr 29;44(6):636-8. doi: 10.1038/ng.2257.
Nat Genet. 2012.
PMID: 22544367
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First-in-class thyrotropin-releasing hormone (TRH)-based compound binds to a pharmacologically distinct TRH receptor subtype in human brain and is effective in neurodegenerative models.
Kelly JA, Boyle NT, Cole N, Slator GR, Colivicchi MA, Stefanini C, Gobbo OL, Scalabrino GA, Ryan SM, Elamin M, Walsh C, Vajda A, Goggin MM, Campbell M, Mash DC, O'Mara SM, Brayden DJ, Callanan JJ, Tipton KF, Della Corte L, Hunter J, O'Boyle KM, Williams CH, Hardiman O.
Kelly JA, et al. Among authors: stefanini c.
Neuropharmacology. 2015 Feb;89:193-203. doi: 10.1016/j.neuropharm.2014.09.024. Epub 2014 Sep 30.
Neuropharmacology. 2015.
PMID: 25281210
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Migraine-like headache and status migrainosus as attacks of multiple sclerosis in a child.
Mariotti P, Nociti V, Cianfoni A, Stefanini C, De Rose P, Martinelli D, Dittoni S, Vollono C, Batocchi AP, Della Marca G.
Mariotti P, et al. Among authors: stefanini c.
Pediatrics. 2010 Aug;126(2):e459-64. doi: 10.1542/peds.2009-2098. Epub 2010 Jul 5.
Pediatrics. 2010.
PMID: 20603252
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