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Seminars in Hematology|September 30, 2009
Mutations in the gene encoding DMT1: clinical presentation and treatmentAchille Iolascon, Luigia De FalcoHaematologica|February 3, 2009
Molecular basis of inherited microcytic anemia due to defects in iron acquisition or heme synthesisAchille Iolascon, Luigia De Falco, Carole BeaumontSeminars in Hematology|September 26, 2015
How I Diagnose Non-thalassemic Microcytic AnemiasMariasole Bruno, Luigia De Falco, Achille IolasconHaematologica|January 19, 2007
Seven novel mutations of the UGT1A1 gene in patients with unconjugated hyperbilirubinemiaMaria D'Apolito, Agnese Marrone, Veronica Servedio, et al.Neuroscience Research|September 24, 2013
Trasferrin receptor 2 gene regulation by microRNA 221 in SH-SY5Y cells treated with MPP⁺ as Parkinson's disease cellular modelRoberta Asci, Fara Vallefuoco, Immacolata Andolfo, et al.American Journal of Medical Genetics. Part A|March 22, 2017
Novel compound heterozygous mutations in BCS1L gene causing Bjornstad syndrome in two siblingsMariateresa Falco, Annamaria Franzè, Sandra Iossa, et al.The Turkish Journal of Pediatrics|January 3, 2014
Is the acronym IRIDA acceptable for slow responders to iron in the presence of TMPRSS6 mutations?Ebru Yilmaz-Keskin, Ertan Sal, Luigia de Falco, et al.Cells|July 12, 2024
Trisomy 21 with Maternally Inherited Balanced Translocation (15q;22q) in a Female Fetus: A Rare Case of Probable Interchromosomal EffectAlessandro De Falco, Antonella Gambale, Michele Pinelli, et al.Haematologica|April 23, 2010
Regulation of divalent metal transporter 1 (DMT1) non-IRE isoform by the microRNA Let-7d in erythroid cellsImmacolata Andolfo, Luigia De Falco, Roberta Asci, et al.Blood|May 9, 2007
The human counterpart of zebrafish shiraz shows sideroblastic-like microcytic anemia and iron overloadClara Camaschella, Alessandro Campanella, Luigia De Falco, et al.Pageof 27