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S Fargion

Showing results (71-80 of 106) with videos related to

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Hepatology (Baltimore, Md.)|April 1, 1992
Survival and prognostic factors in 212 Italian patients with genetic hemochromatosisS Fargion, C Mandelli, A Piperno, et al.
Human Molecular Genetics|May 1, 1993
Linkage analysis of 6p21 polymorphic markers and the hereditary hemochromatosis: localization of the gene centromeric to HLA-FP Gasparini, L Borgato, A Piperno, et al.
Clinical and Experimental Immunology|October 27, 2001
Autoantibodies to human cytosol: a marker of sporadic porphyria cutanea tardaY Ma, A L Fracanzani, M Sampietro, et al.
Human Mutation|May 2, 2000
Molecular analysis of the hydroxymethylbilane synthase (HMBS) gene in Italian patients with acute intermittent porphyria: report of four novel mutationsF Martinez di Montemuros, E Di Pierro, S Fargion, et al.
Journal of Hepatology|May 1, 1996
Genetic hemochromatosis in Italian patients with porphyria cutanea tarda: possible explanation for iron overloadS Fargion, A L Fracanzani, R Romano, et al.
Journal of Inorganic Biochemistry|August 15, 1992
Functional roles of the ferritin receptors of human liver, hepatoma, lymphoid and erythroid cellsD Moss, S Fargion, A L Fracanzani, et al.
Annales De Genetique|January 1, 1997
A recombination event close to HFE gene in hereditary hemochromatosisA Roetto, L Sbaiz, S Bosio, et al.
British Journal of Haematology|October 29, 2000
Relationship between TNF-alpha and iron metabolism in differentiating human monocytic THP-1 cellsA Scaccabarozzi, P Arosio, G Weiss, et al.
Haematologica|April 11, 2000
Immunohistochemistry of HFE in the duodenum of C282Y homozygotes with antisera for recombinant HFE proteinL Zuccon, B Corsi, S Levi, et al.
Hepatology (Baltimore, Md.)|October 1, 1995
Portal hypertension and iron depletion in patients with genetic hemochromatosisA L Fracanzani, S Fargion, R Romano, et al.
Pageof 11

Showing results (71-80 of 106) with videos related to

Sort By:
Pageof 11
Hepatology (Baltimore, Md.)|April 1, 1992
Survival and prognostic factors in 212 Italian patients with genetic hemochromatosisS Fargion, C Mandelli, A Piperno, et al.
Human Molecular Genetics|May 1, 1993
Linkage analysis of 6p21 polymorphic markers and the hereditary hemochromatosis: localization of the gene centromeric to HLA-FP Gasparini, L Borgato, A Piperno, et al.
Clinical and Experimental Immunology|October 27, 2001
Autoantibodies to human cytosol: a marker of sporadic porphyria cutanea tardaY Ma, A L Fracanzani, M Sampietro, et al.
Human Mutation|May 2, 2000
Molecular analysis of the hydroxymethylbilane synthase (HMBS) gene in Italian patients with acute intermittent porphyria: report of four novel mutationsF Martinez di Montemuros, E Di Pierro, S Fargion, et al.
Journal of Hepatology|May 1, 1996
Genetic hemochromatosis in Italian patients with porphyria cutanea tarda: possible explanation for iron overloadS Fargion, A L Fracanzani, R Romano, et al.
Journal of Inorganic Biochemistry|August 15, 1992
Functional roles of the ferritin receptors of human liver, hepatoma, lymphoid and erythroid cellsD Moss, S Fargion, A L Fracanzani, et al.
Annales De Genetique|January 1, 1997
A recombination event close to HFE gene in hereditary hemochromatosisA Roetto, L Sbaiz, S Bosio, et al.
British Journal of Haematology|October 29, 2000
Relationship between TNF-alpha and iron metabolism in differentiating human monocytic THP-1 cellsA Scaccabarozzi, P Arosio, G Weiss, et al.
Haematologica|April 11, 2000
Immunohistochemistry of HFE in the duodenum of C282Y homozygotes with antisera for recombinant HFE proteinL Zuccon, B Corsi, S Levi, et al.
Hepatology (Baltimore, Md.)|October 1, 1995
Portal hypertension and iron depletion in patients with genetic hemochromatosisA L Fracanzani, S Fargion, R Romano, et al.
Pageof 11