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Journal Abstract Search
151 related items for PubMed ID: 2917200
1. G6PD Avenches and G6PD Moosburg: biochemical and erythrocyte membrane characterization. Pekrun A, Eber SW, Schröter W. Blut; 1989 Jan; 58(1):11-4. PubMed ID: 2917200 [Abstract] [Full Text] [Related]
2. Haemolytic anaemia due to glucose-6-phosphate dehydrogenase (G6PD) deficiency: demonstration of two new biochemical variants, G6PD Hamm and G6PD Tarsus. Gahr M, Bornhalm D, Schröter W. Br J Haematol; 1976 Jul; 33(3):363-70. PubMed ID: 1276080 [Abstract] [Full Text] [Related]
3. Incidence and characteristics of glucose-6-phosphate dehydrogenase variants in Japan. Nakatsuji T, Miwa S. Hum Genet; 1979 Oct 02; 51(3):297-305. PubMed ID: 511159 [Abstract] [Full Text] [Related]
5. G6PD Varadero. A new variant of glucose-6-phosphate dehydrogenase associated with congenital nonspherocytic hemolytic anemia. Estrada M, García M, Gutiérrez A, Quintero I, González R. Vox Sang; 1982 Oct 02; 43(2):102-4. PubMed ID: 7123903 [Abstract] [Full Text] [Related]
6. Three glucose 6-phosphate dehydrogenase variants found in Japan. Miwa SH, Nakashima K, Ono J, Fujii H, Suzuki E. Hum Genet; 1977 May 10; 36(3):327-34. PubMed ID: 15940 [Abstract] [Full Text] [Related]
7. G6PD San Jose: a new variant characterized by NADPH inhibition studies. Castro GA, Snyder LM. Humangenetik; 1974 Mar 28; 21(4):361-3. PubMed ID: 4151903 [No Abstract] [Full Text] [Related]
11. Glucose-6-phosphate dehydrogenase (G6PD) Iserlohn and G6PD Regensburg: two new severe enzyme defects in German families. Eber SW, Gahr M, Schröter W. Blut; 1985 Aug 28; 51(2):109-15. PubMed ID: 3849316 [Abstract] [Full Text] [Related]
12. Chronic nonspherocytic hemolytic anemia (CNSHA) and glucose 6 phosphate dehydrogenase (G6PD) deficiency in a patient with familial amyloidotic polyneuropathy (FAP). Molecular study of a new variant (G6PD Clinic) with markedly acidic pH optimum. Vives-Corrons JL, Pujades MA, Petit J, Colomer D, Corbella M, Aguilar i Bascompte JL, Merino A. Hum Genet; 1989 Jan 28; 81(2):161-4. PubMed ID: 2912886 [Abstract] [Full Text] [Related]
13. Characterization of glucose-6-phosphate dehydrogenase variants. II. G6PD Kephalonia, G6PD Attica, and G6PD "Seattle-like" found in Greece. Rattazzi MC, Lenzerini L, Meera Khan P, Luzzatto L. Am J Hum Genet; 1969 Mar 28; 21(2):154-67. PubMed ID: 5770172 [No Abstract] [Full Text] [Related]
15. Three new electrophoretically normal glucose-6-phosphate dehydrogenase variants associated with congenital nonspherocytic hemolytic anemia found in Japan: G6PD Ogikubo, Yokohama, and Akita. Miwa S, Fujii H, Nakashima K, Miura Y, Yamada K, Hagiwara T, Fukuda M. Hum Genet; 1978 Nov 24; 45(1):11-7. PubMed ID: 730178 [Abstract] [Full Text] [Related]
16. Three new G6PD variants, G6PD Adana, G6PD Samandağ, and G6PD Balcali in Cukurova, Turkey. Aksoy K, Yüregir GT, Dikmen N, Unlükurt I. Hum Genet; 1987 Jun 24; 76(2):199-201. PubMed ID: 3610149 [Abstract] [Full Text] [Related]
17. Genetic heterogeneity at the glucose-6-phosphate dehydrogenase locus in southern Italy: a study on a population from the Matera district. Calabrò V, Giacobbe A, Vallone D, Montanaro V, Cascone A, Filosa S, Battistuzzi G. Hum Genet; 1990 Nov 24; 86(1):49-53. PubMed ID: 2253938 [Abstract] [Full Text] [Related]
18. G6PD kuanyama: a new variant of human erythrocyte glucose-6-phosphate dehydrogenase showing slower than normal electrophoretic mobility. Balinsky D, Rootman AJ, Nurse GT, Cayanis E, Lane A, Jenkins T, Bersohn I. S Afr J Med Sci; 1974 Nov 24; 39(1):5-13. PubMed ID: 4153368 [No Abstract] [Full Text] [Related]