137 related articles for article (PubMed ID: 6232925)
1. Red cell enzyme deficiencies as non-disease.
Beutler E
Biomed Biochim Acta; 1983; 42(11-12):S234-41. PubMed ID: 6232925
[TBL] [Abstract][Full Text] [Related]
2. Erythrocyte enzyme deficiencies assessed with a miniature centrifugal analyzer.
Fielek S; Mohrenweiser HW
Clin Chem; 1979 Mar; 25(3):384-8. PubMed ID: 162438
[TBL] [Abstract][Full Text] [Related]
3. Red cell enzymopathies in the newborn. II. Inherited deficiencies of red cell enzymes.
Travis SF
Ann Clin Lab Sci; 1982; 12(3):163-77. PubMed ID: 6284015
[No Abstract] [Full Text] [Related]
4. On the screening for inborn errors of galactose metabolism.
Vaca G; Sànchez-Corona J; Olivares N; Medina C; Ibarra B; Cantú JM
Ann Genet; 1983; 26(3):191-2. PubMed ID: 6606384
[TBL] [Abstract][Full Text] [Related]
5. [Erythrocyte enzymes and drugs].
Löhr GW; Arnold H; Blume KG
Haematol Blood Transfus; 1978; 21():215-24. PubMed ID: 367895
[No Abstract] [Full Text] [Related]
6. [Tests for galactose metabolism].
Ohya N
Nihon Rinsho; 1997 Mar; 55 Suppl 1():244-7. PubMed ID: 9097598
[No Abstract] [Full Text] [Related]
7. Molecular basis of disorders of human galactose metabolism: past, present, and future.
Novelli G; Reichardt JK
Mol Genet Metab; 2000; 71(1-2):62-5. PubMed ID: 11001796
[TBL] [Abstract][Full Text] [Related]
8. [Galactosemia].
Ohtake A; Amemiya S
Nihon Rinsho; 2006 Sep; Suppl 3():215-9. PubMed ID: 17022534
[No Abstract] [Full Text] [Related]
9. Structure and function of enzymes of the Leloir pathway for galactose metabolism.
Holden HM; Rayment I; Thoden JB
J Biol Chem; 2003 Nov; 278(45):43885-8. PubMed ID: 12923184
[No Abstract] [Full Text] [Related]
10. Hereditary disorders of erythrocyte enzymes in non-glycolytic metabolic pathways.
Paglia DE; Valentine WN
Haematologia (Budap); 1982 Dec; 15(4):381-8. PubMed ID: 7186478
[TBL] [Abstract][Full Text] [Related]
11. [Double heterozygosity (transferase-/epimerase-defect) and galactosemia cataract].
Heyne K; Shin YS; Schwinger E
Monatsschr Kinderheilkd; 1988 Dec; 136(12):828-30. PubMed ID: 2853298
[TBL] [Abstract][Full Text] [Related]
12. Cord blood red-cell enzymes and reduced glutathione in Indian neonates, normal and with pathologic jaundice.
Pati HP; Singh M; Paul VK; Gupta RK; Saraya AK
J Trop Med Hyg; 1990 Aug; 93(4):290-4. PubMed ID: 2391727
[TBL] [Abstract][Full Text] [Related]
13. [Hypergalactosemia in newborns as uncovered by the Austrian screening program in 12 years (author's transl)].
Thalhammer O; Scheibenreiter S; Knoll E; Wehle E
Klin Padiatr; 1980 Nov; 192(6):613-9. PubMed ID: 6452554
[TBL] [Abstract][Full Text] [Related]
14. Galactose and cataract.
Stambolian D
Surv Ophthalmol; 1988; 32(5):333-49. PubMed ID: 3043741
[TBL] [Abstract][Full Text] [Related]
15. Problems in the diagnosis of transferase and galactokinase deficient galactosemia.
Pesce MA; Bodourian SH
Ann Clin Lab Sci; 1980; 10(1):26-32. PubMed ID: 7362195
[TBL] [Abstract][Full Text] [Related]
16. [Hemolytic anemias caused by erythrocyte enzyme disorders].
Maldonado Martín A; Mederer Hengstl S; Gil Extremera B
An Med Interna; 1989 May; 6(5):266-73. PubMed ID: 2491542
[TBL] [Abstract][Full Text] [Related]
17. Transfusion requirements of patients with enzyme deficient red blood cells.
Roeckel IE
Ann Clin Lab Sci; 1977; 7(6):511-4. PubMed ID: 145206
[TBL] [Abstract][Full Text] [Related]
18. Galactosemia caused by generalized uridine diphosphate galactose-4-epimerase deficiency.
Garibaldi L; Superti-Furga A; Borrone C
J Pediatr; 1986 Dec; 109(6):1074-5. PubMed ID: 3783336
[No Abstract] [Full Text] [Related]
19. [Enzyme deficiencies of blood cells in bone marrow insufficiency (author's transl].
Waller HD; Benöhr HC
Klin Wochenschr; 1978 May; 56(10):483-91. PubMed ID: 148542
[TBL] [Abstract][Full Text] [Related]
20. [Clinical significance and interpretation of red cell enzyme analyses].
Kanno H; Fujii H
Rinsho Byori; 2001 Nov; Suppl 116():139-47. PubMed ID: 11797375
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]