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Journal Abstract Search
239 related items for PubMed ID: 4700553
1. Galactokinase deficiency as a cause of cataracts. Beutler E, Matsumoto F, Kuhl W, Krill A, Levy N, Sparkes R, Degnan M. N Engl J Med; 1973 Jun 07; 288(23):1203-6. PubMed ID: 4700553 [No Abstract] [Full Text] [Related]
2. The lens, cataracts, and galactosemia. Cogan DG. N Engl J Med; 1973 Jun 07; 288(23):1239-40. PubMed ID: 4700558 [No Abstract] [Full Text] [Related]
3. Galactokinase deficiency in twins: clinical and biochemical studies. Olambiwonnu NO, McVie R, Ng WG, Frasier SD, Donnell GN. Pediatrics; 1974 Mar 07; 53(3):314-8. PubMed ID: 4360930 [No Abstract] [Full Text] [Related]
4. A patient with hereditary galactokinase deficiency. Dahlqvist A, Gamstorp I, Madsen H. Acta Paediatr Scand; 1970 Nov 07; 59(6):669-75. PubMed ID: 5482251 [No Abstract] [Full Text] [Related]
5. Galactokinase deficiency and cataracts. Levy NS, Krill AE, Beutler E. Am J Ophthalmol; 1972 Jul 07; 74(1):41-8. PubMed ID: 5036447 [No Abstract] [Full Text] [Related]
6. Cataracts related to enzymes of galactose metabolism. Schoon DV. Metab Pediatr Ophthalmol; 1981 Jul 07; 5(3-4):219-23. PubMed ID: 6273670 [No Abstract] [Full Text] [Related]
7. [Identification of inborn errors of galactose metabolism in patients with cataracts]. Vaca-Pacheco G, Medina C, García-Cruz D, Sánchez-Corona J, Chávez-Anaya E, Jaimes C, Hernández-Córdova A. Arch Invest Med (Mex); 1990 Jul 07; 21(2):127-32. PubMed ID: 2103700 [Abstract] [Full Text] [Related]
8. Heterozygous state of galactosemia with clinical signs of the disease? Ionăşescu V, Luca N. J Genet Hum; 1969 May 07; 17(1):53-64. PubMed ID: 5808540 [No Abstract] [Full Text] [Related]
10. [Galactokinase deficiency]. Colin J, Voyer M, Thomas D, Charlas J. Ann Pediatr (Paris); 1976 May 02; 23(5):371-7. PubMed ID: 16104211 [No Abstract] [Full Text] [Related]
11. Galactokinase deficiency in a newborn infant. Kerr MM, Logan RW, Cant JS, Hutchison JH. Arch Dis Child; 1971 Dec 02; 46(250):864-6. PubMed ID: 5129188 [No Abstract] [Full Text] [Related]
12. Association of presenile cataracts with heterozygosity for galactosaemic states and with riboflavin deficiency. Prchal JT, Conrad ME, Skalka HW. Lancet; 1978 Jan 07; 1(8054):12-3. PubMed ID: 74495 [Abstract] [Full Text] [Related]
13. Cataracts in patients heterozygous for galactokinase deficiency. Stambolian D, Scarpino-Myers V, Eagle RC, Hodes B, Harris H. Invest Ophthalmol Vis Sci; 1986 Mar 07; 27(3):429-33. PubMed ID: 3949470 [Abstract] [Full Text] [Related]
14. Galactokinase-deficiency cataracts in identical twins. Oberman AE, Wilson WA, Frasier SD, Donnell GN, Bergren WR. Am J Ophthalmol; 1972 Nov 07; 74(5):887-92. PubMed ID: 4644736 [No Abstract] [Full Text] [Related]
15. Some inferences from galactokinase deficiency. Sidbury JB. Pediatrics; 1974 Mar 07; 53(3):309-10. PubMed ID: 4360929 [No Abstract] [Full Text] [Related]
16. Maternal enzymes of galactose metabolism and the "inexplicable" infantile cataract. Harley JD, Mutton P, Irvine S, Gupta JD. Lancet; 1974 Aug 03; 2(7875):259-61. PubMed ID: 4136146 [No Abstract] [Full Text] [Related]
17. [Galactokinase deficiency, cause of hereditary cataract. Recent publications]. Lambotte C. Rev Med Liege; 1975 Jun 01; 30(11):378-82. PubMed ID: 178040 [No Abstract] [Full Text] [Related]
18. [Partial and transitory erythrocyte galactokinase deficiency in a newborn. Biochemical study]. Vigneron C, Marchal C, Deifts C, Vidailhet M, Pierson M, Neimann N. Arch Fr Pediatr; 1970 May 01; 27(5):523-31. PubMed ID: 5425825 [No Abstract] [Full Text] [Related]
19. Presenile cataract formation and decreased activity of galactosemic enzymes. Skalka HW, Prchal JT. Arch Ophthalmol; 1980 Feb 01; 98(2):269-73. PubMed ID: 7352874 [Abstract] [Full Text] [Related]
20. [The family of a patient with galactokinase-defect 2nd communication (author's transl)]. Kaloud H, Sitzmann FC, Paltauf F, Mayer R. Klin Padiatr; 1974 Jan 01; 186(1):33-6. PubMed ID: 4365835 [No Abstract] [Full Text] [Related] Page: [Next] [New Search]