THE RESPONSE OF ACUTE CHILDHOOD LEUKEMIA TO AN INITIAL AND A SECOND COURSE OF PREDNISONE.
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Acute Disease↗
Biomedical subjects
M E HAGGARD
Publications and source records attributed to M E HAGGARD.
AN INHOMOGENEOUS FOETAL HAEMOGLOBIN VARIANT (THE TEXAS TYPE).
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Biomedical Research↗
HEMOGLOBIN G-COUSHATTA: A NEW VARIANT IN AN AMERICAN INDIAN FAMILY.
A new hemoglobin variant, G(couhatta) (alpha2(A) beta2(iiiglu-->ala)), has been found in three generations of a family from the Alabama Coushatta Indian tribe in east Texas. The propositus suffers from an apparently unrelated, possibly genetic, agranulocytosis. According to the history and the blood grouping data there is considerable in breeding in the tribe and remarkably little admixture with other ethnic groups.
Agranulocytosis↗
CYCLOPHOSPHAMIDE (NSC-26271)-1 IN UNCOMMON MALIGNANT NEOPLASMS IN CHILDREN.
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Adolescent↗
THE COEXISTENCE OF SICKLE CELL DISEASE AND CONGENITAL HEART DISEASE: A REPORT OF THREE CASES, WITH REPAIR UNDER CARDIOPULMONARY BY-PASS IN TWO.
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Anemia↗
CYTOGENETIC STUDIES. DIAGNOSTIC TOOL IN CLINICAL MEDICINE.
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Child↗
BONE MARROW MORPHOLOGY STUDY.
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Bone Marrow↗
Studies of ACTH hydrocortisone, and 6-mercaptopurine in the treatment of children with acute leukemia.
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Acute Disease↗
The use of steroids as pharmacologic agents in diseases of children. I. Hematologic disorders.
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Child↗
The use of steroids as pharmacologic agents in diseases of children. 2. Hypersensitivity states.
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Adrenal Cortex Hormones↗
Hypoplastic anemia associated with chloramphenicol therapy.
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Anemia↗
Sickle cell anemia in the first 2 years of life.
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Anemia↗
Giant vascular tumors and thrombocytopenia.
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Blood Vessels↗
A family with hemoglobin G.
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Hemoglobins↗
A new haemoglobin variant in an American Negro.
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Black or African American↗
Staphylococcal pneumonia and empyema in infants in children.
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Child↗
Essential fatty acids in infant nutrition. III. Clinical manifestations of linoleic acid deficiency.
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Fatty Acids, Essential↗
Haemoglobin P (the Galveston type).
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Hemoglobins↗