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R Galanello

Showing results (41-50 of 138) with videos related to

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Progress in Clinical and Biological Research|January 1, 1989
Interaction between deletion delta-thalassemia and beta zero-thalassemia (codon 39 nonsense mutation) in a Sardinian familyR Galanello, A Podda, M A Melis, et al.
Acta Haematologica|January 1, 1984
Hemoglobin inclusions in heterozygous alpha-thalassemia according to their alpha-globin genotypeR Galanello, E Paglietti, M A Melis, et al.
Hemoglobin|November 1, 1994
Hb A2-Sant' Antioco [alpha 2 delta (2)93(F9)Cys-->Gly]: a new delta chain variant identified by sequencing of amplified DNAR Galanello, D Gasperini, L Perseu, et al.
Hemoglobin|March 11, 1998
Hb Sassari [alpha 126(H9)Asp-->His] results from a GAC-->CAC mutation in the alpha 1-globin geneE Paglietti, S Barella, S Satta, et al.
Haematologica|July 1, 1990
Preliminary experience with the differential pH technique for glucose-6-phosphate dehydrogenase (G6PD) measurement in whole blood: application to an area with high prevalence of thalassaemia and G6PD deficiencyA Mosca, M Paderi, A Sanna, et al.
Seminars in Hematology|January 1, 1996
Clinical experience of management of thalassemia: the Sardinian experienceA Cao, R Galanello, M C Rosatelli, et al.
Hemoglobin|January 1, 1992
Normal delta-globin gene sequences in Sardinian nondeletional delta beta-thalassemiaG Loudianos, P Moi, J Lavinha, et al.
Human Mutation|January 1, 1994
A novel delta O-thalassemia mutation: TGG-->TAG (TRP-->STOP) at codon 37D Gasperini, L Perseu, P Cossu, et al.
Journal of Medical Genetics|December 1, 1983
Phenotype-genotype correlation in haemoglobin H disease in childhoodR Galanello, M Pirastu, M A Melis, et al.
British Journal of Haematology|February 26, 2000
Safety profile of the oral iron chelator deferiprone: a multicentre studyA R Cohen, R Galanello, A Piga, et al.
Pageof 14

Showing results (41-50 of 138) with videos related to

Sort By:
Pageof 14
Progress in Clinical and Biological Research|January 1, 1989
Interaction between deletion delta-thalassemia and beta zero-thalassemia (codon 39 nonsense mutation) in a Sardinian familyR Galanello, A Podda, M A Melis, et al.
Acta Haematologica|January 1, 1984
Hemoglobin inclusions in heterozygous alpha-thalassemia according to their alpha-globin genotypeR Galanello, E Paglietti, M A Melis, et al.
Hemoglobin|November 1, 1994
Hb A2-Sant' Antioco [alpha 2 delta (2)93(F9)Cys-->Gly]: a new delta chain variant identified by sequencing of amplified DNAR Galanello, D Gasperini, L Perseu, et al.
Hemoglobin|March 11, 1998
Hb Sassari [alpha 126(H9)Asp-->His] results from a GAC-->CAC mutation in the alpha 1-globin geneE Paglietti, S Barella, S Satta, et al.
Haematologica|July 1, 1990
Preliminary experience with the differential pH technique for glucose-6-phosphate dehydrogenase (G6PD) measurement in whole blood: application to an area with high prevalence of thalassaemia and G6PD deficiencyA Mosca, M Paderi, A Sanna, et al.
Seminars in Hematology|January 1, 1996
Clinical experience of management of thalassemia: the Sardinian experienceA Cao, R Galanello, M C Rosatelli, et al.
Hemoglobin|January 1, 1992
Normal delta-globin gene sequences in Sardinian nondeletional delta beta-thalassemiaG Loudianos, P Moi, J Lavinha, et al.
Human Mutation|January 1, 1994
A novel delta O-thalassemia mutation: TGG-->TAG (TRP-->STOP) at codon 37D Gasperini, L Perseu, P Cossu, et al.
Journal of Medical Genetics|December 1, 1983
Phenotype-genotype correlation in haemoglobin H disease in childhoodR Galanello, M Pirastu, M A Melis, et al.
British Journal of Haematology|February 26, 2000
Safety profile of the oral iron chelator deferiprone: a multicentre studyA R Cohen, R Galanello, A Piga, et al.
Pageof 14