Search Results - "Haghshenass, M."

β‐Globin gene cluster haplotypes in sickle cell patients from southwest Iran by Rahimi, Z., Karimi, M., Haghshenass, M., Merat, A.

“…Sickle cell anemia in Iran is accompanied by a high level of HbF and mild clinical presentation. Here we report haplotypes of the β gene cluster found in 81…”
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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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Mild sickle-cell anaemia in Iran associated with high levels of fetal haemoglobin by Haghshenass, M, Ismail-Beigi, F, Clegg, J B, Weatherall, D J

“…Sixteen subjects, with sickle-cell anaemia, all Iranians (ages 3 to 56 years), with very mild symptomatology are reported. Some of the subjects had been…”
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Cloning of syngeneic hematopoietic cells in the spleens of mice and rats pretreated with cytotoxic drugs by Santos, G W, Haghshenass, M

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Primary upper small-intestinal lymphoma and alpha-chain disease. Report of 10 cases emphasizing pathological aspects by Haghighi, P, Kharazmi, A, Gerami, C, Haghshenass, M, Abadi, P, Omidi, H, Mostafavi, N

“…Ten cases of primary upper small-intestinal lymphoma associated with alpha-chain protein in serum were discovered in a prospective study of the sera of…”
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Serum folate levels during anticonvulsant therapy with diphenylhydantoin by Haghshenass, M, Rao, D B

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Immunoperoxidase study in alpha-chain disease by Haghighi, P, Tabei, Z, Kharazmi, A, Gerami, S, Abadi, P, Haghshenass, M

“…Peroxidase-antiperoxidase technique was applied to search for the presence of alpha-chain protein in cells of the infiltrate from six cases of alpha-chain…”
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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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Combined zinc and iron compared with iron supplementation of diets of 6- to 12-year old village schoolchildren in southern Iran by Mahloudji, M, Reinhold, JG, Haghshenass, M, Ronaghy, HA, Fox, MR, Halsted, JA

“…The effects of supplementation of the diets of 6- to 12-year-old children in a village near Shiraz in Iran with zinc plus iron or iron alone, together with the…”
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Alpha heavy-chain disease in southern Iran by Haghshenass, M, Haghighi, P, Abadi, P, Kharazmi, A, Gerami, C, Nasr, K

“…A prospective study of 32 patients with primary upper small intestinal lymphoma in our region revealed 10 cases of alpha heavy-chain disease. Patients were…”
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Intracellular pH of the human lymphocyte by Zieve, P D, Haghshenass, M, Krevans, J R

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β-Globin Gene Cluster Haplotypes in Iranian Patients with β-Thalassemia by Z Rahimi, A Merat, M Akhzari, M Haghshenass, Nagel Ronald L, Gerard Nathalie, Krish-namoorthy Rajagopal

“…Introduction: β-globin gene cluster haplotypes are useful in diagnosis of particular molecular defects in β-thalassemia, prenatal diagnosis of β-thalassemia,…”
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β-Globin Gene Cluster Haplotypes in Iranian Patients with β-Thalassemia by Rahimi Z., Merat A., Akhzari M., Haghshenass M., Ronald L. Nagel, Nathalie Gerard, Rajagopal Krish-namoorthy

“…Introduction: β-globin gene cluster haplotypes are useful in diagnosis of particular molecular defects in β-thalassemia, prenatal diagnosis of…”
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Acute leukemia in adults by Dabestani, A, Toosi, A, Haghshenass, M, Beigi, F I

“…Prospective data on 40 new cases of adult onset (greater than 15 years of age) acute leukemia is presented. Acute lymphoblastic leukemia (ALL) accounted for…”
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Current concepts immunoproliferative small intestinal disease. A "Third-World lesion" by Khojasteh, A, Haghshenass, M, Haghighi, P

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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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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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