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The New England Journal of Medicine
|
December 19, 1985
Stimulation of F-cell production in patients with sickle-cell anemia treated with cytarabine or hydroxyurea
R Veith, R Galanello, T Papayannopoulou, et al.
Progress in Clinical and Biological Research
|
January 1, 1985
Pharmacologic stimulation of Hb F in patients with sickle cell anemia
R Galanello, R Veith, T Papayannopoulou, et al.
Annals of the New York Academy of Sciences
|
January 1, 1985
Hb F production in stressed erythropoiesis: observations and kinetic models
G Stamatoyannopoulos, R Veith, R Galanello, et al.
British Journal of Haematology
|
May 15, 2008
Glutathione S-transferase gene polymorphism and cardiac iron overload in thalassaemia major
R Origa, S Satta, G Matta, et al.
Acta Haematologica
|
January 1, 1977
Quantitation of Hb a2 with DE-52 microchromatography in whole blood as screening test for beta-thalassemia heterozygotes
R Galanello, M A Melis, P Muroni, et al.
JAMA
|
October 23, 1997
Molecular diagnosis and carrier screening for beta thalassemia
A Cao, L Saba, R Galanello, et al.
The Journal of Pediatrics
|
July 1, 1981
Prospective study of red blood cell indices, hemoglobin A2, and hemoglobin F in infants heterozygous for Beta-thalassemia
R Galanello, M A Melis, R Ruggeri, et al.
Indian Journal of Pediatrics
|
November 1, 1989
Prenatal diagnosis of inherited hemoglobinopathies
A Cao, C Rosatelli, R Galanello, et al.
Hemoglobin
|
January 1, 1984
Hemoglobin constitution of double heterozygotes for alpha or beta-thalassemia and Hb J Sardegna
L Maccioni, R Galanello, M A Melis, et al.
Science (New York, N.Y.)
|
March 2, 1984
Multiple mutations produce delta beta 0 thalassemia in Sardinia
M Pirastu, Y W Kan, R Galanello, et al.
Page
of 14
Search research articles
Search
Showing results (21-30 of 138) with videos related to
Sort By:
Page
of 14
The New England Journal of Medicine
|
December 19, 1985
Stimulation of F-cell production in patients with sickle-cell anemia treated with cytarabine or hydroxyurea
R Veith, R Galanello, T Papayannopoulou, et al.
Progress in Clinical and Biological Research
|
January 1, 1985
Pharmacologic stimulation of Hb F in patients with sickle cell anemia
R Galanello, R Veith, T Papayannopoulou, et al.
Annals of the New York Academy of Sciences
|
January 1, 1985
Hb F production in stressed erythropoiesis: observations and kinetic models
G Stamatoyannopoulos, R Veith, R Galanello, et al.
British Journal of Haematology
|
May 15, 2008
Glutathione S-transferase gene polymorphism and cardiac iron overload in thalassaemia major
R Origa, S Satta, G Matta, et al.
Acta Haematologica
|
January 1, 1977
Quantitation of Hb a2 with DE-52 microchromatography in whole blood as screening test for beta-thalassemia heterozygotes
R Galanello, M A Melis, P Muroni, et al.
JAMA
|
October 23, 1997
Molecular diagnosis and carrier screening for beta thalassemia
A Cao, L Saba, R Galanello, et al.
The Journal of Pediatrics
|
July 1, 1981
Prospective study of red blood cell indices, hemoglobin A2, and hemoglobin F in infants heterozygous for Beta-thalassemia
R Galanello, M A Melis, R Ruggeri, et al.
Indian Journal of Pediatrics
|
November 1, 1989
Prenatal diagnosis of inherited hemoglobinopathies
A Cao, C Rosatelli, R Galanello, et al.
Hemoglobin
|
January 1, 1984
Hemoglobin constitution of double heterozygotes for alpha or beta-thalassemia and Hb J Sardegna
L Maccioni, R Galanello, M A Melis, et al.
Science (New York, N.Y.)
|
March 2, 1984
Multiple mutations produce delta beta 0 thalassemia in Sardinia
M Pirastu, Y W Kan, R Galanello, et al.
Page
of 14