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Severe iron overload with a novel aminolevulinate synthase mutation and hepatitis C infection. A case report.

Severe iron overload with a novel aminolevulinate synthase mutation and hepatitis C infection. A case report.

http://www.wikidata.org/entity/Q37227785

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Role of heme in cardiovascular physiology and disease.Increased Heme Levels in the Heart Lead to Exacerbated Ischemic Injury.Delta-aminolevulinate synthase 2 polymorphism is associated with maximal oxygen uptake after Living-high exercise-high training-low in a male Chinese population.Sideroblastic anemia: functional study of two novel missense mutations in ALAS2 Iron metabolism in transplantation.

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Severe iron overload with a novel aminolevulinate synthase mutation and hepatitis C infection. A case report.

http://www.wikidata.org/entity/Q37227785

description

article científic

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article scientifique

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articolo scientifico

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artigo científico

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bilimsel makale

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scientific article published on 26 September 2008

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vedecký článok

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vetenskaplig artikel

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videnskabelig artikel

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vědecký článek

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name

Severe iron overload with a no ...... is C infection. A case report.

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Severe iron overload with a no ...... is C infection. A case report.

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Severe iron overload with a no ...... is C infection. A case report.

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Severe iron overload with a no ...... is C infection. A case report.

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Severe iron overload with a no ...... is C infection. A case report.

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Severe iron overload with a no ...... is C infection. A case report.

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J.BCMD.2008.08.001

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Blood Cells, Molecules and Diseases

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Severe iron overload with a no ...... is C infection. A case report.

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Ernest Beutler

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John J McCarthy

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Lawrence Rice

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Pauline Lee

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P2860

Human erythroid 5-aminolevulinate synthase: promoter analysis and identification of an iron-responsive element in the mRNA

Mutant antimicrobial peptide hepcidin is associated with severe juvenile hemochromatosis

Disruption of ferroportin 1 regulation causes dynamic alterations in iron homeostasis and erythropoiesis in polycythaemia mice

A study of genes that may modulate the expression of hereditary hemochromatosis: transferrin receptor-1, ferroportin, ceruloplasmin, ferritin light and heavy chains, iron regulatory proteins (IRP)-1 and -2, and hepcidin

X-linked sideroblastic anemia associated with a novel ALAS2 mutation and unfortunate skewed X-chromosome inactivation patterns

Spectrum of hemojuvelin gene mutations in 1q-linked juvenile hemochromatosis.

A mutation, in the iron-responsive element of H ferritin mRNA, causing autosomal dominant iron overload.

Absent phenotypic expression of X-linked sideroblastic anemia in one of 2 brothers with a novel ALAS2 mutation.

A promoter mutation in the erythroid-specific 5-aminolevulinate synthase (ALAS2) gene causes X-linked sideroblastic anemia.

Iron, the HFE gene, and hepatitis C.

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scholarly article

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10.1016/J.BCMD.2008.08.001

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