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Trasferrin receptor 2 gene regulation by microRNA 221 in SH-SY5Y cells treated with MPP⁺ as Parkinson's disease cellular model.
Neurosci Res. 2013 Nov;77(3):121-7. doi: 10.1016/j.neures.2013.09.003. Epub 2013 Sep 17.
Neurosci Res. 2013.
PMID: 24055409
Multiple clinical forms of dehydrated hereditary stomatocytosis arise from mutations in PIEZO1.
Andolfo I, Alper SL, De Franceschi L, Auriemma C, Russo R, De Falco L, Vallefuoco F, Esposito MR, Vandorpe DH, Shmukler BE, Narayan R, Montanaro D, D'Armiento M, Vetro A, Limongelli I, Zuffardi O, Glader BE, Schrier SL, Brugnara C, Stewart GW, Delaunay J, Iolascon A.
Andolfo I, et al. Among authors: vallefuoco f.
Blood. 2013 May 9;121(19):3925-35, S1-12. doi: 10.1182/blood-2013-02-482489. Epub 2013 Mar 11.
Blood. 2013.
PMID: 23479567
Free article.
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Hypomorphic mutations of SEC23B gene account for mild phenotypes of congenital dyserythropoietic anemia type II.
Russo R, Langella C, Esposito MR, Gambale A, Vitiello F, Vallefuoco F, Ek T, Yang E, Iolascon A.
Russo R, et al. Among authors: vallefuoco f.
Blood Cells Mol Dis. 2013 Jun;51(1):17-21. doi: 10.1016/j.bcmd.2013.02.003. Epub 2013 Mar 1.
Blood Cells Mol Dis. 2013.
PMID: 23453696
Free PMC article.
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Transient erythroblastopenia of childhood after COVID-19 infection: a case report.
Rivetti G, Abbate FG, Longobardi M, Marrapodi MM, Lanzaro F, Di Martino M, Vallefuoco F, D'Angelo V, Casale M, Tartaglione I, Perrotta S, Roberti D.
Rivetti G, et al. Among authors: vallefuoco f.
Ital J Pediatr. 2024 Jul 29;50(1):131. doi: 10.1186/s13052-024-01700-2.
Ital J Pediatr. 2024.
PMID: 39075575
Free PMC article.
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