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Journal Abstract Search
133 related items for PubMed ID: 5724497
1. [Favism in a German family]. Johannsen LP, Witt I, Künzer W. Dtsch Med Wochenschr; 1968 Dec 20; 93(51):2463-70 passim. PubMed ID: 5724497 [No Abstract] [Full Text] [Related]
2. Family investigations of erythrocyte glucose-6-phosphate dehydrogenase in favism. Rozynkowa D, Gebala A, Zagórski Z. Pol Med J; 1970 Dec 20; 9(5):1093-9. PubMed ID: 5510280 [No Abstract] [Full Text] [Related]
3. Favism in GdMediterranean heterozygous females. Sanna G, De Virgiliis S, Palmas C, Argiolu F, Frau F, Cao A. Pediatr Res; 1979 Jul 20; 13(7):812-6. PubMed ID: 481952 [No Abstract] [Full Text] [Related]
4. [Favism - a familial enzymatic defect of the red blood cells in a 7-year-old girl]. Pohorecka J, Jabłońska-Skwiecińska E, Powiertowska-Ryszka G. Pediatr Pol; 1982 Jul 20; 57(9):731-4. PubMed ID: 7170153 [No Abstract] [Full Text] [Related]
5. [Enzyme-deficient hemolytic anemia due to glucose-6-phosphate dehydrogenase deficiency in a child of German descent]. Sitzmann FC, Kornhuber B, Stephan U, Truckenbrodt H. Z Kinderheilkd; 1965 Jul 09; 93(2):189-96. PubMed ID: 5320727 [No Abstract] [Full Text] [Related]
6. Enzymic studies in surgical jaundice. Kochhar KS, Parkash V, Sachdev KS, Singh G. J Indian Med Assoc; 1973 Mar 01; 60(5):153-61. PubMed ID: 4723075 [No Abstract] [Full Text] [Related]
7. [Biochemistry of 5 families with G-6pdh deficiency]. Donas MA, Hernández Pascual A. Rev Clin Esp; 1975 Aug 31; 138(4):335-43. PubMed ID: 1178983 [No Abstract] [Full Text] [Related]
8. Serum levels of 5'-nucleotidase, bilirubin, alkaline phosphatase and transaminase in liver diseases--a comparative study. Singh YN, Hameed F, Khan R, Husain Z. Indian J Pathol Microbiol; 1987 Jan 31; 30(1):55-67. PubMed ID: 2824355 [No Abstract] [Full Text] [Related]
9. Serum glutamic oxalacetic transaminase, glutamic pyruvic transaminase, gamma-glutamyl transpeptidase and glutamic dehydrogenase levels in favism. Meloni T, Pilo G, Gallisai D, Dore A. Acta Haematol; 1979 Jan 31; 62(2):71-3. PubMed ID: 43648 [Abstract] [Full Text] [Related]
10. Favism in a Portuguese family due to a deficient glucose-phosphate dehydrogenase variant (Canton) or (cpanton-like) type. Kahn A, Marie J, Desbois JC, Boivin P. Acta Haematol; 1976 Jan 31; 56(1):58-64. PubMed ID: 822676 [Abstract] [Full Text] [Related]
11. G6PD Aures: a new mutation (48 Ile-->Thr) causing mild G6PD deficiency is associated with favism. Nafa K, Reghis A, Osmani N, Baghli L, Benabadji M, Kaplan JC, Vulliamy TJ, Luzzatto L. Hum Mol Genet; 1993 Jan 31; 2(1):81-2. PubMed ID: 8490627 [No Abstract] [Full Text] [Related]
12. Hepatitis B antigen-positive hepatitis in an Israeli family. Alkan WJ, Swartz TA, Mundel G, Eshchar J, Hirshfeld T, Versano D. Isr J Med Sci; 1973 Jan 31; 9(11):1542-6. PubMed ID: 4204971 [No Abstract] [Full Text] [Related]
13. [Favism in Polish families]. Jabłońska-Skwiecińska E, Pogłód R, Skrobowska A. Pol Tyg Lek; 1973 Jan 31; 45(38-39):778-81. PubMed ID: 2095545 [Abstract] [Full Text] [Related]
14. Hematologic findings in certain small cetaceans. Ridgway SH, Simpson JG, Patton GS, Gilmartin. J Am Vet Med Assoc; 1970 Sep 01; 157(5):566-75. PubMed ID: 4195008 [No Abstract] [Full Text] [Related]
15. [Biochemical indices of the blood serum in various liver diseases]. Tokarskaia ZB, Chernova GV, Dorozhko VA. Ter Arkh; 1974 Sep 01; 46(4):53-8. PubMed ID: 4139774 [No Abstract] [Full Text] [Related]
16. [Progressive dementia associated with vision and gait disorders (Kuf's syndrome?)]. Perris C, Strandqvist B. Psychiatr Neurol Med Psychol (Leipz); 1969 Oct 01; 21(10):380-4. PubMed ID: 5363773 [No Abstract] [Full Text] [Related]
17. [Significance of liver function tests in cholelithiasis]. Anazawa Y, Watabe O, Okamoto H. Shujutsu; 1969 Aug 01; 23(8):1044-53. PubMed ID: 5358422 [No Abstract] [Full Text] [Related]
18. Several mutations including two novel mutations of the glucose-6-phosphate dehydrogenase gene in Polish G6PD deficient subjects with chronic nonspherocytic hemolytic anemia, acute hemolytic anemia, and favism. Jablonska-Skwiecinska E, Lewandowska I, Plochocka D, Topczewski J, Zimowski JG, Klopocka J, Burzynska B. Hum Mutat; 1999 Aug 01; 14(6):477-84. PubMed ID: 10571945 [Abstract] [Full Text] [Related]