Search Results - "Haghshenass, Mansour"

Plasma lipids in Iranians with sickle cell disease: Hypocholesterolemia in sickle cell anemia and increase of HDL-cholesterol in sickle cell trait by Rahimi, Zohreh, Merat, Ahmad, Haghshenass, Mansour, Madani, Hamid, Rezaei, Mansour, Nagel, Ronald L.

“…The metabolism of lipids may be altered in sickle cell anemia and β-thalassemia patients. Plasma lipids in 24 patients with sickle cell anemia (SS), 15…”
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Brief Report: Cloning of Syngeneic Hematopoietic Cells in the Spleens of Mice and Rats Pretreated with Cytotoxic Drugs by Santos, George W., Haghshenass, Mansour

“…Abstract A method is described for the quantitative cloning of syngeneic hematopoietic cells in the spleens of mice or rats pretreated with a combination of…”
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Zinc deficiency in man. The Shiraz experiment by Halsted, J A, Ronaghy, H A, Abadi, P, Haghshenass, M, Amirhakemi, G H, Barakat, R M, Reinhold, J G

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Iron-deficiency anemia in an Iranian population associated with high intakes of iron12 by Haghshenass, Mansour, Mahloudji, Mohsen, Reinhold, John G., Mohammadi, N.

“…In five villages typical of those in southern Iran, 30% of the children, 24% of females, and 7% of the males over 16 had hemoglobin concentrations of 12 g/100…”
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Iron-deficiency anemia in an Iranian population associated with high intakes of iron by Haghshenass, M, Mahloudij, M, Reinhold, J G, Mohammadi, N

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The dependence of the hemoglobin (beta plus gamma)/alpha chain synthetic ratio on the degree of anemia in beta-thalassemia (38561) by Ismail-Beigi, F, Haghshenass, M

“…The peripheral blood hemoglobin (beta plus gamma)/alpha chain synthetic ratio in three homozygous beta-thalassemic subjects was shown to increase towards unity…”
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Vacuolization of the neutrophil. An aid in the diagnosis of septicemia by Zieve, P D, Haghshenass, M, Blanks, M, Krevans, J R

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