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M D Cappellini

Showing results (141-150 of 179) with videos related to

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Blood|November 9, 2000
Hereditary hemochromatosis in a patient with congenital dyserythropoietic anemiaS Fargion, L Valenti, A L Fracanzani, et al.
Alcoholism, Clinical and Experimental Research|November 7, 2001
Non-transferrin-bound iron in alcohol abusersT M De Feo, S Fargion, L Duca, et al.
Journal of Viral Hepatitis|April 23, 2014
Ribavirin suppresses erythroid differentiation and proliferation in chronic hepatitis C patientsL Ronzoni, A Aghemo, M G Rumi, 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.
Blood|December 1, 1980
Organization of alpha-globin genes in Hb Hasharon (alpha 47 asp replaced by his) carriersB Giglioni, P Comi, R Taramelli, et al.
American Journal of Nephrology|January 1, 1992
Uremic inhibitors of erythropoiesis: a study during treatment with recombinant human erythropoietinC Brunati, M D Cappellini, T De Feo, et al.
Human Genetics|March 26, 2009
Novel human pathological mutations. Gene symbol: PPOX. Disease: porphyria, variegateSabrina Ausenda, V Moriondo, S Marchini, et al.
Haematologica|April 29, 1998
The effect of dietary magnesium supplementation on the cellular abnormalities of erythrocytes in patients with beta thalassemia intermediaL De Franceschi, M D Cappellini, G Graziadei, et al.
Pageof 18

Showing results (141-150 of 179) with videos related to

Sort By:
Pageof 18
Blood|November 9, 2000
Hereditary hemochromatosis in a patient with congenital dyserythropoietic anemiaS Fargion, L Valenti, A L Fracanzani, et al.
Alcoholism, Clinical and Experimental Research|November 7, 2001
Non-transferrin-bound iron in alcohol abusersT M De Feo, S Fargion, L Duca, et al.
Journal of Viral Hepatitis|April 23, 2014
Ribavirin suppresses erythroid differentiation and proliferation in chronic hepatitis C patientsL Ronzoni, A Aghemo, M G Rumi, 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.
Blood|December 1, 1980
Organization of alpha-globin genes in Hb Hasharon (alpha 47 asp replaced by his) carriersB Giglioni, P Comi, R Taramelli, et al.
American Journal of Nephrology|January 1, 1992
Uremic inhibitors of erythropoiesis: a study during treatment with recombinant human erythropoietinC Brunati, M D Cappellini, T De Feo, et al.
Human Genetics|March 26, 2009
Novel human pathological mutations. Gene symbol: PPOX. Disease: porphyria, variegateSabrina Ausenda, V Moriondo, S Marchini, et al.
Haematologica|April 29, 1998
The effect of dietary magnesium supplementation on the cellular abnormalities of erythrocytes in patients with beta thalassemia intermediaL De Franceschi, M D Cappellini, G Graziadei, et al.
Pageof 18