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Blood
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November 9, 2000
Hereditary hemochromatosis in a patient with congenital dyserythropoietic anemia
S Fargion, L Valenti, A L Fracanzani, et al.
Alcoholism, Clinical and Experimental Research
|
November 7, 2001
Non-transferrin-bound iron in alcohol abusers
T 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 patients
L 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 mutations
F 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 overload
S 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 cells
D 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) carriers
B 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 erythropoietin
C Brunati, M D Cappellini, T De Feo, et al.
Human Genetics
|
March 26, 2009
Novel human pathological mutations. Gene symbol: PPOX. Disease: porphyria, variegate
Sabrina 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 intermedia
L De Franceschi, M D Cappellini, G Graziadei, et al.
Page
of 18
Search research articles
Search
Showing results (141-150 of 179) with videos related to
Sort By:
Page
of 18
Blood
|
November 9, 2000
Hereditary hemochromatosis in a patient with congenital dyserythropoietic anemia
S Fargion, L Valenti, A L Fracanzani, et al.
Alcoholism, Clinical and Experimental Research
|
November 7, 2001
Non-transferrin-bound iron in alcohol abusers
T 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 patients
L 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 mutations
F 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 overload
S 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 cells
D 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) carriers
B 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 erythropoietin
C Brunati, M D Cappellini, T De Feo, et al.
Human Genetics
|
March 26, 2009
Novel human pathological mutations. Gene symbol: PPOX. Disease: porphyria, variegate
Sabrina 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 intermedia
L De Franceschi, M D Cappellini, G Graziadei, et al.
Page
of 18