Results 61 to 70 of about 459 (116)
Mitapivat improves ineffective erythropoiesis and iron overload in adult patients with pyruvate kinase deficiency. [PDF]
van Beers EJ +11 more
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Enzymatic anomaly of erythrocytes in congenital nonspherocytic hemolytic anemia. 2.
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Erythrocyte Pyruvate Kinase Deficiency Resulting in Congenital Nonspherocytic Hemolytic Anemia
New England Journal of Medicine, 1963HEREDITARY spherocytosis with its associated congenital hemolytic anemia is generally easily recognized and satisfactorily treated with splenectomy. A rarer group of congenital hemolytic anemias, however, is sometimes confused with hereditary spherocytosis because of the occasional presence of small numbers of spherocytes in association with varying ...
Oski Frank A, L K Diamond, F A Oski
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Hemochromatosis and Congenital Nonspherocytic Hemolytic Anemia in Siblings
JAMA - Journal of the American Medical Association, 1963The unusual occurrence of both congenital nonspherocytic hemolytic anemia and hemochromatosis in a brother and sister is reported. The strikingly similar clinicopathologic abnormalities, including extraordinarily severe cardiac lesions in these relatively young siblings, is discussed.
Charles P Emerson, C P Emerson
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Congenital Nonspherocytic Hemolytic Anemias
Postgraduate Medicine, 1967A specific diagnosis must be established in congenital nonspherocytic hemolytic anemia, for guidance in therapy and family counseling. Diagnostic methods have recently progressed rapidly and include determination of deficiencies in the activity of certain enzymes. Further definitions of enzymatic deficiencies are anticipated.
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Journal of Pediatrics, 1959
Summary The clinical course, hematologic data, and red cell glutathione and glucose-6-phosphate dehydrogenase studies are reported for 6 patients who had a congenital nonspherocytic hemolytic anemia. On the basis of these findings the patients could be divided into three groups. Group 1 consists of three Caucasian boys belonging to two families. The
W H Zinkham
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Summary The clinical course, hematologic data, and red cell glutathione and glucose-6-phosphate dehydrogenase studies are reported for 6 patients who had a congenital nonspherocytic hemolytic anemia. On the basis of these findings the patients could be divided into three groups. Group 1 consists of three Caucasian boys belonging to two families. The
W H Zinkham
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ENZYME DEFICIENCY IN ERYTHROCYTES IN CONGENITAL NONSPHEROCYTIC HEMOLYTIC ANEMIA
Pediatrics, 1959Two cases of congenital nonspherocytic hemolytic anemia are reported. The patients were brothers and both showed severe metabolic defects in the erythrocytes, consisting of a low content of reduced glutathione, markedly abnormal reduced glutathione stability test, and a very low activity of glucose-6-phosphate dehydrogenase.
Diamond Louis K
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Screening Tests for the Congenital Nonspherocytic Hemolytic Anemias
Laboratory Medicine, 1971Virgil F Fairbanks, Fairbanks Virgil F
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