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Hepatology (Baltimore, Md.)
|
April 1, 1992
Survival and prognostic factors in 212 Italian patients with genetic hemochromatosis
S 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-F
P Gasparini, L Borgato, A Piperno, et al.
Clinical and Experimental Immunology
|
October 27, 2001
Autoantibodies to human cytosol: a marker of sporadic porphyria cutanea tarda
Y 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 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.
Annales De Genetique
|
January 1, 1997
A recombination event close to HFE gene in hereditary hemochromatosis
A 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 cells
A 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 protein
L Zuccon, B Corsi, S Levi, et al.
Hepatology (Baltimore, Md.)
|
October 1, 1995
Portal hypertension and iron depletion in patients with genetic hemochromatosis
A L Fracanzani, S Fargion, R Romano, et al.
Page
of 11
Search research articles
Search
Showing results (71-80 of 106) with videos related to
Sort By:
Page
of 11
Hepatology (Baltimore, Md.)
|
April 1, 1992
Survival and prognostic factors in 212 Italian patients with genetic hemochromatosis
S 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-F
P Gasparini, L Borgato, A Piperno, et al.
Clinical and Experimental Immunology
|
October 27, 2001
Autoantibodies to human cytosol: a marker of sporadic porphyria cutanea tarda
Y 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 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.
Annales De Genetique
|
January 1, 1997
A recombination event close to HFE gene in hereditary hemochromatosis
A 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 cells
A 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 protein
L Zuccon, B Corsi, S Levi, et al.
Hepatology (Baltimore, Md.)
|
October 1, 1995
Portal hypertension and iron depletion in patients with genetic hemochromatosis
A L Fracanzani, S Fargion, R Romano, et al.
Page
of 11