Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

M D Cappellini

Showing results (111-120 of 179) with videos related to

Pageof 18
Sort By:
Blood|May 1, 1996
Multiple G6PD mutations are associated with a clinical and biochemical phenotype similar to that of G6PD MediterraneanM 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 intermediaM 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 erythroblastsM 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 genotypesC 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 populationJ 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 deficiencyM Sampietro, L Lupica, L Perrero, et al.
British Journal of Haematology|July 1, 1986
Alpha thalassaemia in an Italian populationC Velati, M Sampietro, M Biassoni, et al.
Advances in Experimental Medicine and Biology|January 1, 1991
Behaviour of glucose-6-phosphate dehydrogenase during erythroid maturationM 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 cirrhosisGemino 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 phenotypeM D Cappellini, M Sampietro, D Toniolo, et al.
Pageof 18

Showing results (111-120 of 179) with videos related to

Sort By:
Pageof 18
Blood|May 1, 1996
Multiple G6PD mutations are associated with a clinical and biochemical phenotype similar to that of G6PD MediterraneanM 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 intermediaM 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 erythroblastsM 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 genotypesC 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 populationJ 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 deficiencyM Sampietro, L Lupica, L Perrero, et al.
British Journal of Haematology|July 1, 1986
Alpha thalassaemia in an Italian populationC Velati, M Sampietro, M Biassoni, et al.
Advances in Experimental Medicine and Biology|January 1, 1991
Behaviour of glucose-6-phosphate dehydrogenase during erythroid maturationM 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 cirrhosisGemino 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 phenotypeM D Cappellini, M Sampietro, D Toniolo, et al.
Pageof 18