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8. EXTREME HEMOLYSIS AND RED-CELL DISTORTION IN ERYTHROCYTE PYRUVATE KINASE DEFICIENCY. I. MORPHOLOGY, ERYTHROKINETICS AND FAMILY ENZYME STUDIES. OSKI FA; NATHAN DG; SIDEL VW; DIAMOND LK N Engl J Med; 1964 May; 270():1023-30. PubMed ID: 14122798 [No Abstract] [Full Text] [Related]
9. [ON THE DIFFERENTIAL DIAGNOSIS OF HEREDITARY NON-SPHEROCYTIC HEMOLYTIC ANEMIAS]. WALLER HD Med Welt; 1963 Nov; 46():2338-45. PubMed ID: 14113207 [No Abstract] [Full Text] [Related]
10. [FURTHER ACQUISITIONS ON THE SUBJECT OF ENZYME-DEFICIENT HEMOLYTIC ANEMIAS]. LARIZZA P; BRUNETTI P Minerva Med; 1964 May; 55():SUPPL:1579-88. PubMed ID: 14162174 [No Abstract] [Full Text] [Related]
11. [Apropos of 3 new types of hemolytic anemia in children. Infantile pyknocytosis. Familial hemolytic anemia with erythrocytic inclusions and pigmenturia. Anemia caused by pyruvate-kinase deficiency]. GERMAIN D Pediatrie; 1962; 17():323-6. PubMed ID: 13897985 [No Abstract] [Full Text] [Related]
17. Case report. Hereditary elliptocytosis with glucose-6-phosphate dehyrogenase deficiency and haemolytic anaemia. RATNESAR VC Ghana Med J; 1963 Mar; 2():29-33. PubMed ID: 13973269 [No Abstract] [Full Text] [Related]
18. HEREDITARY HEMOLYTIC DISEASE SECONDARY TO GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCY: REPORT OF THREE CASES WITH SPECIAL EMPHASIS ON ATP METABOLISM. MOHLER DN; CROCKETT CL Blood; 1964 Apr; 23():427-44. PubMed ID: 14138235 [No Abstract] [Full Text] [Related]
19. [Apropos of 3 new types of hemolytic anemia in children. Infantile pyknocytosis. Familial hemolytic anemia with erythrocytic inclusions and pigmenturia. Anemia caused by a deficiency of pyruvate kinase]. GERMAIN D Rev Cubana Pediatr; 1962; 34():81-5. PubMed ID: 13960507 [No Abstract] [Full Text] [Related]
20. STUDIES IN CONGENITAL NON-SPHEROCYTIC HAEMOLYTIC ANAEMIAS WITH SPECIFIC ENZYME DEFECTS. BOWDLER AJ; PRANKERD TA Acta Haematol; 1964 Feb; 31():65-78. PubMed ID: 14131784 [No Abstract] [Full Text] [Related] [Next] [New Search]