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S Fargion

Showing results (41-50 of 106) with videos related to

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Human Mutation|March 29, 2000
A novel polymorphism (219G>A) in the transferrin receptor geneM Meregalli, N Corbetta, A Pellagatti, et al.
Digestive and Liver Disease : Official Journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver|June 12, 2004
Searching for coeliac disease in patients with non-alcoholic fatty liver diseaseM T Bardella, L Valenti, C Pagliari, et al.
Hepatology (Baltimore, Md.)|April 27, 1999
Inherited HFE-unrelated hemochromatosis in Italian familiesC Camaschella, S Fargion, M Sampietro, et al.
Gastroenterology|April 1, 1989
Immunohistochemical evidence for a lack of ferritin in duodenal absorptive epithelial cells in idiopathic hemochromatosisA L Francanzani, S Fargion, R Romano, et al.
Journal of Clinical Pathology|October 1, 1980
Chronic liver disease in transfusion-dependent thalassaemia: hepatitis B virus marker studiesS De Virgiliis, G Fiorelli, S Fargion, 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.
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.
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.
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.
Pageof 11

Showing results (41-50 of 106) with videos related to

Sort By:
Pageof 11
Human Mutation|March 29, 2000
A novel polymorphism (219G>A) in the transferrin receptor geneM Meregalli, N Corbetta, A Pellagatti, et al.
Digestive and Liver Disease : Official Journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver|June 12, 2004
Searching for coeliac disease in patients with non-alcoholic fatty liver diseaseM T Bardella, L Valenti, C Pagliari, et al.
Hepatology (Baltimore, Md.)|April 27, 1999
Inherited HFE-unrelated hemochromatosis in Italian familiesC Camaschella, S Fargion, M Sampietro, et al.
Gastroenterology|April 1, 1989
Immunohistochemical evidence for a lack of ferritin in duodenal absorptive epithelial cells in idiopathic hemochromatosisA L Francanzani, S Fargion, R Romano, et al.
Journal of Clinical Pathology|October 1, 1980
Chronic liver disease in transfusion-dependent thalassaemia: hepatitis B virus marker studiesS De Virgiliis, G Fiorelli, S Fargion, 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.
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.
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.
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.
Pageof 11