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Journal Abstract Search
192 related items for PubMed ID: 13066515
1. Further studies on hemoglobin C. II. The hematologic effects of hemoglobin C alone and in combination with sickle cell hemoglobin. KAPLAN E, ZUELZER WW, NEEL JV. Blood; 1953 Aug; 8(8):735-46. PubMed ID: 13066515 [No Abstract] [Full Text] [Related]
2. Further studies on hemoglobin C. I. A description of three additional families segregating for hemoglobin C and sickle cell hemoglobin. NEEL JV, KAPLAN E, ZUELZER WW. Blood; 1953 Aug; 8(8):724-34. PubMed ID: 13066514 [No Abstract] [Full Text] [Related]
3. Studies on abnormal hemoglobins. VI. Electrophoretic demonstration of type S (sickle cell) hemoglobin in erythrocytes incapable of showing the sickle cell phenomenon. SINGER K, FISHER B. Blood; 1953 Mar; 8(3):270-5. PubMed ID: 13032196 [No Abstract] [Full Text] [Related]
4. Studies on abnormal hemoglobins. III. The interrelationship of type S (sickle cell) hemoglobin and type F (alkali resistant) hemoglobin in sickle cell anemia. SINGER K, CHERNOFF AI. Blood; 1952 Jan; 7(1):47-52. PubMed ID: 14886409 [No Abstract] [Full Text] [Related]
5. Observations on the inheritance of sickle-cell hemoglobin and hemoglobin C. RANNEY HM. J Clin Invest; 1954 Dec; 33(12):1634-41. PubMed ID: 13211820 [No Abstract] [Full Text] [Related]
6. INTRAERYTHROCYTIC HEMOGLOBIN CRYSTALS IN SICKLE CELL-HEMOGLOBIN C DISEASE. DIGGS LW, BELL A. Blood; 1965 Feb; 25():218-23. PubMed ID: 14267697 [No Abstract] [Full Text] [Related]
7. Studies on abnormal hemoglobins. V. The distribution of type S, sickle cell, hemoglobin and type F, alkali resistant, hemoglobin within the red cell population in sickle cell anemia. SINGER K, FISHER B. Blood; 1952 Dec; 7(12):1216-26. PubMed ID: 12997538 [No Abstract] [Full Text] [Related]
8. Hematologic observations on patients with sickle cell anemia sustained at normal hemoglobin levels by multiple transfusions. CHAPLIN H, KEITEL HG, PETERSON RE. Blood; 1956 Sep; 11(9):834-45. PubMed ID: 13355893 [No Abstract] [Full Text] [Related]
9. Studies on the destruction of red blood cells. VIII. Molecular orientation in sickle cell hemoglobin solutions. HARRIS JW. Proc Soc Exp Biol Med; 1950 Oct; 75(1):197-201. PubMed ID: 14797780 [No Abstract] [Full Text] [Related]
10. Clinical manifestations of inherited abnormal hemoglobins. I. The interaction of hemoglobin-S with hemoglobin-D. STURGEON P, ITANO HA, BERGREN WR. Blood; 1955 May; 10(5):389-404. PubMed ID: 14363320 [No Abstract] [Full Text] [Related]
11. The role of surgery in sickle cell disease. Flye MW, Silver D. Surg Gynecol Obstet; 1973 Jul; 137(1):115-26. PubMed ID: 4576837 [No Abstract] [Full Text] [Related]
12. Studies on abnormal hemoglobins. XIII. Hemoglobin S-thalassemia disease and hemoglobin C-thalassemia disease in siblings. SINGER K, JOSEPHSON AM, SINGER L, HELLER P, ZIMMERMAN HJ. Blood; 1957 Jul; 12(7):593-602. PubMed ID: 13436515 [No Abstract] [Full Text] [Related]
20. CORRELATION OF S HEMOGLOBIN WITH GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCY AND ITS SIGNIFICANCE. LEWIS RA, HATHORN M. Blood; 1965 Aug 15; 26():176-80. PubMed ID: 14332479 [No Abstract] [Full Text] [Related] Page: [Next] [New Search]