[CONGENITAL METHEMOGLOBINEMIAS].
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Humans↗
Biomedical subjects
K MURAWSKI
Publications and source records attributed to K MURAWSKI.
[THE PICTURE OF PROTEINS AND GLYCOPROTEINS IN MULTIPLE MYELOMA].
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Alpha-Globulins↗
Hereditary deficiency of NADPH-2-methaemoglobin reductase.
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Cytochrome-B(5) Reductase↗
[THE HEMOGLOBIN M-RADOM CLINICAL SYNDROME].
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Child↗
Binding of bilirubin to serum proteins.
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Bilirubin↗
[Electrophoretic se p aration of alpha A and beta B chains of human haemoglobin].
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Electrophoresis↗
[Metabolic disorders in hepatolenticular degeneration].
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Copper↗
[Metabolic disorders in hepatolenticular degeneration. I. Liver function tests].
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Hepatolenticular Degeneration↗
Haptoglobin types in Poland.
The frequency of the Hp(1) gene in Polish subjects is 0.36. This frequency is lower than that in Western European populations and higher than that in Asiatic populations. We suggest that the increase in frequency of this gene from East to West has a regular continuous character that may be attributed to a stillunclear genetic mechanism.
Genetic Therapy↗
[Serum haptoglobin content in normal subjects].
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Glycoproteins↗
[Ceruloplasmin in pre-placental, umbilical and infantile blood].
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Ceruloplasmin↗
[Studies on latent iron deficiency in blood donors].
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Anemia↗
Dysproteinemia induced in vitro by plasmin digestion of fibrinogen.
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Blood Protein Disorders↗
[Quantitative determination of aminoaciduria & other biochemical data in multiple sclerosis].
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Amino Acid Metabolism, Inborn Errors↗
[Studies on the application of globin solution as an anti-shock agent].
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Globins↗
[Poliglukan, partially hydrolyzed dextran solution with anti-shock action].
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Convulsive Therapy↗
[Comparative studies on dextran and other blood substitutes].
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Blood Substitutes↗
[Comparative studies on dextran and other plasma substitutes].
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Dextrans↗