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Blood Cells, Molecules & Diseases|September 28, 2010
Red cell pyruvate kinase deficiency in Southern SardiniaL Perseu, N Giagu, S Satta, et al.Human Mutation|January 8, 2000
A new glucose 6 phosphate dehydrogenase variant G6PD Sinnai (34 G-->T). Mutations in brief no. 156. OnlineR Galanello, D Loi, C Sollaino, et al.Hemoglobin|January 1, 1978
Hemoglobin H disease in Sardinia: phenotypic and genetic observationsR Galanello, M A Melis, M Furbetta, et al.Blood|November 1, 1983
A family with segregating triplicated alpha globin loci and beta thalassemiaR Galanello, R Ruggeri, E Paglietti, et al.Journal of Clinical Pathology|October 1, 1980
Haematological characteristics of the beta 0 thalassaemia trait in Sardinian childrenR Galanello, S De Virgiliis, M Addis, et al.Journal of Medical Genetics|April 1, 1984
A genetic combination of silent beta-thalassaemia, high Hb A2 beta-thalassaemia, and single alpha globin gene deletion causing mild thalassaemia intermediaR Galanello, L Maccioni, M C Rosatelli, et al.Acta Haematologica|January 1, 1983
Serum ferritin levels in hemoglobin H diseaseR Galanello, M A Melis, E Paglietti, et al.Mutagenesis|September 10, 2003
Chromosomal aberration frequencies in patients with thalassaemia major undergoing therapy with deferiprone and deferoxamine in a comparative crossover studyR Marshall, F Tricta, R Galanello, et al.Blood Cells, Molecules & Diseases|July 3, 2013
Longitudinal analysis of heart and liver iron in thalassemia major patients according to chelation treatmentF Danjou, R Origa, F Anni, et al.Proceedings of the National Academy of Sciences of the United States of America|May 1, 1987
The same beta-globin gene mutation is present on nine different beta-thalassemia chromosomes in a Sardinian populationM Pirastu, R Galanello, M A Doherty, et al.Pageof 12