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Journal Abstract Search
143 related items for PubMed ID: 6239628
1. [Hereditary erythroenzymopathies. I. Biochemical and genetic aspects]. Vaca G, Velázquez AL, Cantú JM. Bol Oficina Sanit Panam; 1984 Sep; 97(3):225-39. PubMed ID: 6239628 [No Abstract] [Full Text] [Related]
8. [Erythroenzymopathies: present status and prospects]. Miwa S. Rinsho Ketsueki; 1986 Jul; 27(7):1119-22. PubMed ID: 3537367 [No Abstract] [Full Text] [Related]
9. G6PD deficiency and chronic hemolysis: four new mutants--relationships between clinical syndrome and enzyme kinetics. Rattazzi MC, Corash LM, van Zanen GE, Jaffé ER, Piomelli S. Blood; 1971 Aug; 38(2):205-18. PubMed ID: 4397482 [No Abstract] [Full Text] [Related]
10. Heterozygous erythrocyte glutathione peroxidase deficiency associated with neonatal hyperbilirubinemia found in a Japanese family. Miwa S, Nakashima K, Ariyoshi K, Uemura M, Murashima N. Nihon Ketsueki Gakkai Zasshi; 1974 Jun; 37(3):266-70. PubMed ID: 4479916 [No Abstract] [Full Text] [Related]