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Pediatric Endocrinology Reviews : PER|April 2, 2009
A critical review of non invasive procedures for the evaluation of body iron burden in thalassemia major patientsAurelio Maggio, Marcello Capra, Alessia Pepe, et al.European Journal of Haematology|October 12, 2013
Quantification of HBG mRNA in primary erythroid cultures: prediction of the response to hydroxyurea in sickle cell and beta-thalassemiaAlice Pecoraro, Paolo Rigano, Antonio Troia, et al.Hemoglobin|June 4, 2016
Coinheritance of a Rare Nucleotide Substitution on the β-Globin Gene and Other Known Mutations in the Globin Clusters: Management in Genetic CounselingMargherita Vinciguerra, Cristina Passarello, Filippo Leto, et al.Hemoglobin|November 25, 2017
HBB: c.316-125A>G and HBB: c.316-42delC: Phenotypic Evaluations of Two Rare Changes in the Second Intron of the HBB GeneMargherita Vinciguerra, Monica Cannata, Filippo Cassarà, et al.Journal of Clinical Pathology|August 11, 2017
Phenotypic evaluations of <i>HBB</i>:c.93-23T>C, a nucleotide substitution in the IVS I nt 108 of β-globin geneMargherita Vinciguerra, Filippo Cassarà, Monica Cannata, et al.Clinical Biochemistry|January 12, 2005
Analytical evaluation of the Tosoh HLC-723 G7 automated HPLC analyzer for hemoglobin A2 and F determinationRenata Paleari, Monica Cannata, Filippo Leto, et al.European Journal of Haematology|August 24, 2007
Typing of the immunological system in human embryos by coelocentesisMaria Concetta Renda, George Makrydimas, Kipros H Nicolaides, et al.Bioelectrochemistry (Amsterdam, Netherlands)|May 20, 2008
New analytical tools and epidemiological data for the identification of HbA2 borderline subjects in the screening for beta-thalassemiaAndrea Mosca, Renata Paleari, Renzo Galanello, et al.International Journal of Molecular Sciences|March 3, 2018
Chronic Administration of Hydroxyurea (HU) Benefits Caucasian Patients with Sickle-Beta ThalassemiaRosario Di Maggio, Matthew M Hsieh, Xiongce Zhao, et al.Haematologica|July 8, 2008
Significance of borderline hemoglobin A2 values in an Italian population with a high prevalence of beta-thalassemiaAntonino Giambona, Cristina Passarello, Margherita Vinciguerra, et al.Pageof 13