These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
Pubmed for Handhelds
PUBMED FOR HANDHELDS
Journal Abstract Search
205 related items for PubMed ID: 4268540
1. Red cell enzyme deficiencies as a cause of hemolytic disorders. Valentine WN. Annu Rev Med; 1972; 23():93-100. PubMed ID: 4268540 [No Abstract] [Full Text] [Related]
2. Disorders due to enzyme defects in the red blood cell. Beutler E. Adv Metab Disord; 1972; 60():131-60. PubMed ID: 4354659 [No Abstract] [Full Text] [Related]
3. Hereditary hemolytic anemia due to erythrocyte enzyme deficiency. Miwa S. Nihon Ketsueki Gakkai Zasshi; 1973 Oct; 36(5):573-61. PubMed ID: 4277504 [No Abstract] [Full Text] [Related]
4. Hereditary hemolytic disorders and enzymatic deficiencies of human erythrocytes. Jaffé ER. Blood; 1970 Jan; 35(1):116-34. PubMed ID: 4244328 [No Abstract] [Full Text] [Related]
10. [The hemolytic components of anemia in the cirrhotic]. Gasalla R, González Barón M, Fernández Chacón J. Sangre (Barc); 1973 Jan; 18(1):40-4. PubMed ID: 4708551 [No Abstract] [Full Text] [Related]
11. Deficiencies associated with Embden-Meyerhof pathway and other metabolic pathways. Valentine WN. Semin Hematol; 1971 Oct; 8(4):348-66. PubMed ID: 4256808 [No Abstract] [Full Text] [Related]
12. Red cell enzymopathies in the newborn. II. Inherited deficiencies of red cell enzymes. Travis SF. Ann Clin Lab Sci; 1982 Oct; 12(3):163-77. PubMed ID: 6284015 [No Abstract] [Full Text] [Related]
15. Screening methods for enzyme defects in erythrocytes. Madera-Orsini FM, Volini FI. Ann Clin Lab Sci (1971); 1972 Oct; 2(1):40-56. PubMed ID: 4263612 [No Abstract] [Full Text] [Related]
16. Hemolysis in dialyzed patients: tap water-induced red blood cell metabolic deficiency. Yawata Y, Kjellstrand C, Buselmeier T, Howe R, Jacob H. Trans Am Soc Artif Intern Organs; 1972 Oct; 18(0):301-4, 310. PubMed ID: 4679882 [No Abstract] [Full Text] [Related]
17. Clinical, metabolic and molecular consequences of genetic disorders of the pentose phosphate pathway. Carson PE. Proc R Soc Med; 1970 Feb; 63(2):175-6. PubMed ID: 4909475 [No Abstract] [Full Text] [Related]