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Haematologica
|
March 26, 1999
Co-inherited Gilbert's syndrome: a factor determining hyperbilirubinemia in homozygous beta-thalassemia
R Galanello, M D Cipollina, C Dessì, et al.
Blood
|
July 1, 1983
Phenotypic effect of heterozygous alpha and beta 0-thalassemia interaction
M A Melis, M Pirastu, R Galanello, et al.
Blood Cells, Molecules & Diseases
|
September 28, 2010
Red cell pyruvate kinase deficiency in Southern Sardinia
L 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. Online
R Galanello, D Loi, C Sollaino, et al.
Haematologica
|
March 26, 1999
C-->T mutation at -158 G gamma HPFH associated with 4 bp deletion (-225-222) in the promoter region of the A gamma gene in homozygous beta 0 39 nonsense thalassemia
F Ataulfo Gonzalez, P Ropero, J Sánchez, et al.
Hemoglobin
|
January 1, 1978
Hemoglobin H disease in Sardinia: phenotypic and genetic observations
R Galanello, M A Melis, M Furbetta, et al.
Blood
|
November 1, 1983
A family with segregating triplicated alpha globin loci and beta thalassemia
R Galanello, R Ruggeri, E Paglietti, et al.
Journal of Clinical Pathology
|
October 1, 1980
Haematological characteristics of the beta 0 thalassaemia trait in Sardinian children
R 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 intermedia
R Galanello, L Maccioni, M C Rosatelli, et al.
Acta Haematologica
|
January 1, 1983
Serum ferritin levels in hemoglobin H disease
R Galanello, M A Melis, E Paglietti, et al.
Page
of 14
Search research articles
Search
Showing results (51-60 of 138) with videos related to
Sort By:
Page
of 14
Haematologica
|
March 26, 1999
Co-inherited Gilbert's syndrome: a factor determining hyperbilirubinemia in homozygous beta-thalassemia
R Galanello, M D Cipollina, C Dessì, et al.
Blood
|
July 1, 1983
Phenotypic effect of heterozygous alpha and beta 0-thalassemia interaction
M A Melis, M Pirastu, R Galanello, et al.
Blood Cells, Molecules & Diseases
|
September 28, 2010
Red cell pyruvate kinase deficiency in Southern Sardinia
L 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. Online
R Galanello, D Loi, C Sollaino, et al.
Haematologica
|
March 26, 1999
C-->T mutation at -158 G gamma HPFH associated with 4 bp deletion (-225-222) in the promoter region of the A gamma gene in homozygous beta 0 39 nonsense thalassemia
F Ataulfo Gonzalez, P Ropero, J Sánchez, et al.
Hemoglobin
|
January 1, 1978
Hemoglobin H disease in Sardinia: phenotypic and genetic observations
R Galanello, M A Melis, M Furbetta, et al.
Blood
|
November 1, 1983
A family with segregating triplicated alpha globin loci and beta thalassemia
R Galanello, R Ruggeri, E Paglietti, et al.
Journal of Clinical Pathology
|
October 1, 1980
Haematological characteristics of the beta 0 thalassaemia trait in Sardinian children
R 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 intermedia
R Galanello, L Maccioni, M C Rosatelli, et al.
Acta Haematologica
|
January 1, 1983
Serum ferritin levels in hemoglobin H disease
R Galanello, M A Melis, E Paglietti, et al.
Page
of 14