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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.Italian Journal of Gastroenterology and Hepatology|March 26, 1998
High prevalence of hepatitis C virus type 1b in Italian patients with Porphyria cutanea tardaM Sampietro, A L Fracanzani, N Corbetta, 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.Blood|March 1, 1988
Characteristics and expression of binding sites specific for ferritin H-chain on human cell linesS Fargion, P Arosio, A L Fracanzani, et al.Journal of Hepatology|November 1, 1992
Liver damage in Italian patients with hereditary hemochromatosis is highly influenced by hepatitis B and C virus infectionA Piperno, S Fargion, R D'Alba, et al.Journal of Endocrinological Investigation|June 1, 1992
Preclinical hypogonadism in genetic hemochromatosis in the early stage of the disease: evidence of hypothalamic dysfunctionA Piperno, M R Rivolta, R D'Alba, et al.Proceedings of the National Academy of Sciences of the United States of America|March 28, 1995
Functional estrogen receptors in a human preosteoclastic cell lineG Fiorelli, F Gori, M Petilli, 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.International Journal of Immunopathology and Pharmacology|February 9, 2005
Alcohol dehydrogenase: an autoantibody target in patients with alcoholic liver diseaseY Ma, M Meregalli, S Hodges, et al.Pageof 17