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Blood
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May 1, 1996
Multiple G6PD mutations are associated with a clinical and biochemical phenotype similar to that of G6PD Mediterranean
M D Cappellini, F Martinez di Montemuros, G De Bellis, et al.
British Journal of Haematology
|
March 23, 1999
Metabolic indicators of oxidative stress correlate with haemichrome attachment to membrane, band 3 aggregation and erythrophagocytosis in beta-thalassaemia intermedia
M D Cappellini, D Tavazzi, L Duca, et al.
European Journal of Clinical Investigation
|
March 1, 1993
Alternative splicing of human G6PD messenger RNA in K562 cells but not in cultured erythroblasts
M D Cappellini, D Tavazzi, F Martinez di Montemuros, et al.
Haematologica
|
September 1, 1996
Serum erythropoietin and circulating transferrin receptor in thalassemia intermedia patients with heterogeneous genotypes
C Camaschella, S Gonella, R Calabrese, et al.
British Journal of Haematology
|
March 1, 1986
Feasibility of prenatal diagnosis of beta thalassaemia by DNA polymorphisms in an Italian population
J S Wainscoat, S Work, M Sampietro, et al.
British Journal of Haematology
|
December 31, 1997
The expression of uridine diphosphate glucuronosyltransferase gene is a major determinant of bilirubin level in heterozygous beta-thalassaemia and in glucose-6-phosphate dehydrogenase deficiency
M Sampietro, L Lupica, L Perrero, et al.
British Journal of Haematology
|
July 1, 1986
Alpha thalassaemia in an Italian population
C Velati, M Sampietro, M Biassoni, et al.
Advances in Experimental Medicine and Biology
|
January 1, 1991
Behaviour of glucose-6-phosphate dehydrogenase during erythroid maturation
M D Cappellini, S Villa, A Gaviraghi, et al.
European Journal of Clinical Investigation
|
March 12, 2002
Red blood cell antioxidant and iron status in alcoholic and nonalcoholic cirrhosis
Gemino Fiorelli, T M De Feo, L Duca, et al.
Human Genetics
|
February 1, 1994
G6PD Ferrara I has the same two mutations as G6PD A(-) but a distinct biochemical phenotype
M D Cappellini, M Sampietro, D Toniolo, et al.
Page
of 18
Search research articles
Search
Showing results (111-120 of 179) with videos related to
Sort By:
Page
of 18
Blood
|
May 1, 1996
Multiple G6PD mutations are associated with a clinical and biochemical phenotype similar to that of G6PD Mediterranean
M D Cappellini, F Martinez di Montemuros, G De Bellis, et al.
British Journal of Haematology
|
March 23, 1999
Metabolic indicators of oxidative stress correlate with haemichrome attachment to membrane, band 3 aggregation and erythrophagocytosis in beta-thalassaemia intermedia
M D Cappellini, D Tavazzi, L Duca, et al.
European Journal of Clinical Investigation
|
March 1, 1993
Alternative splicing of human G6PD messenger RNA in K562 cells but not in cultured erythroblasts
M D Cappellini, D Tavazzi, F Martinez di Montemuros, et al.
Haematologica
|
September 1, 1996
Serum erythropoietin and circulating transferrin receptor in thalassemia intermedia patients with heterogeneous genotypes
C Camaschella, S Gonella, R Calabrese, et al.
British Journal of Haematology
|
March 1, 1986
Feasibility of prenatal diagnosis of beta thalassaemia by DNA polymorphisms in an Italian population
J S Wainscoat, S Work, M Sampietro, et al.
British Journal of Haematology
|
December 31, 1997
The expression of uridine diphosphate glucuronosyltransferase gene is a major determinant of bilirubin level in heterozygous beta-thalassaemia and in glucose-6-phosphate dehydrogenase deficiency
M Sampietro, L Lupica, L Perrero, et al.
British Journal of Haematology
|
July 1, 1986
Alpha thalassaemia in an Italian population
C Velati, M Sampietro, M Biassoni, et al.
Advances in Experimental Medicine and Biology
|
January 1, 1991
Behaviour of glucose-6-phosphate dehydrogenase during erythroid maturation
M D Cappellini, S Villa, A Gaviraghi, et al.
European Journal of Clinical Investigation
|
March 12, 2002
Red blood cell antioxidant and iron status in alcoholic and nonalcoholic cirrhosis
Gemino Fiorelli, T M De Feo, L Duca, et al.
Human Genetics
|
February 1, 1994
G6PD Ferrara I has the same two mutations as G6PD A(-) but a distinct biochemical phenotype
M D Cappellini, M Sampietro, D Toniolo, et al.
Page
of 18