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R Galanello

Showing results (81-90 of 138) with videos related to

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Pathologica|October 13, 2000
[Histological picture of liver disease in thalassemia intermedia]M G Mancosu, R Galanello, R Ambu, et al.
Haematologica|September 1, 1992
Hemoglobin Sabine [beta 91 (F7) Leu-->Pro]: occurrence in a Sardinian individual with hemolytic anemia and inclusion bodiesD Gasperini, R Galanello, M A Melis, et al.
Journal of Medical Genetics|June 1, 1982
Delta beta (F)-thalassaemia in SardiniaA Cao, M A Melis, R Galanello, et al.
Clinical Genetics|March 1, 1988
Pitfalls in genetic counselling for beta-thalassemia: an individual with 4 different thalassemia mutationsR Galanello, M E Paglietti, M Addis, et al.
Clinical Chemistry|January 23, 1999
Posttranslational deamidation of proteins: the case of hemoglobin J Sardegna [alpha50(CD8)His-->Asn-->Asp]R Paleari, E Paglietti, A Mosca, et al.
Blood|August 1, 1988
Delineation of the molecular basis of delta- and normal HbA2 beta-thalassemiaP Moi, E Paglietti, A Sanna, et al.
Acta Haematologica|January 1, 1980
Hematological characteristics of sardinian alpha-thalassemia carriers detected in a population studyM A Melis, C Rosatelli, A M Falchi, et al.
Blood|August 1, 1983
Delta +-thalassemia in SardiniaM Pirastu, R Galanello, M A Melis, et al.
Nouvelle Revue Francaise D'Hematologie|January 1, 1981
Globin chain synthesis analysis in obligate beta 0-thalassemia heterozygotes with isolated increase of hemoglobin A2 levelsR Galanello, M A Melis, M Furbetta, et al.
British Journal of Haematology|September 1, 1999
Soluble transferrin receptor as a potential determinant of iron loading in congenital anaemias due to ineffective erythropoiesisM Cazzola, Y Beguin, G Bergamaschi, et al.
Pageof 14

Showing results (81-90 of 138) with videos related to

Sort By:
Pageof 14
Pathologica|October 13, 2000
[Histological picture of liver disease in thalassemia intermedia]M G Mancosu, R Galanello, R Ambu, et al.
Haematologica|September 1, 1992
Hemoglobin Sabine [beta 91 (F7) Leu-->Pro]: occurrence in a Sardinian individual with hemolytic anemia and inclusion bodiesD Gasperini, R Galanello, M A Melis, et al.
Journal of Medical Genetics|June 1, 1982
Delta beta (F)-thalassaemia in SardiniaA Cao, M A Melis, R Galanello, et al.
Clinical Genetics|March 1, 1988
Pitfalls in genetic counselling for beta-thalassemia: an individual with 4 different thalassemia mutationsR Galanello, M E Paglietti, M Addis, et al.
Clinical Chemistry|January 23, 1999
Posttranslational deamidation of proteins: the case of hemoglobin J Sardegna [alpha50(CD8)His-->Asn-->Asp]R Paleari, E Paglietti, A Mosca, et al.
Blood|August 1, 1988
Delineation of the molecular basis of delta- and normal HbA2 beta-thalassemiaP Moi, E Paglietti, A Sanna, et al.
Acta Haematologica|January 1, 1980
Hematological characteristics of sardinian alpha-thalassemia carriers detected in a population studyM A Melis, C Rosatelli, A M Falchi, et al.
Blood|August 1, 1983
Delta +-thalassemia in SardiniaM Pirastu, R Galanello, M A Melis, et al.
Nouvelle Revue Francaise D'Hematologie|January 1, 1981
Globin chain synthesis analysis in obligate beta 0-thalassemia heterozygotes with isolated increase of hemoglobin A2 levelsR Galanello, M A Melis, M Furbetta, et al.
British Journal of Haematology|September 1, 1999
Soluble transferrin receptor as a potential determinant of iron loading in congenital anaemias due to ineffective erythropoiesisM Cazzola, Y Beguin, G Bergamaschi, et al.
Pageof 14