169 related articles for article (PubMed ID: 8417789)
1. Glucose-6-phosphate isomerase deficiency associated with nonspherocytic hemolytic anemia in the mouse: an animal model for the human disease.
Merkle S; Pretsch W
Blood; 1993 Jan; 81(1):206-13. PubMed ID: 8417789
[TBL] [Abstract][Full Text] [Related]
2. Erythrocyte pyruvate kinase- and glucose phosphate isomerase deficiency: perturbation of glycolysis by structural defects and functional alterations of defective enzymes and its relation to the clinical severity of chronic hemolytic anemia.
Lakomek M; Winkler H
Biophys Chem; 1997 Jun; 66(2-3):269-84. PubMed ID: 9362562
[TBL] [Abstract][Full Text] [Related]
3. Hemolytic anemias due to erythrocyte enzyme deficiencies.
Jacobasch G; Rapoport SM
Mol Aspects Med; 1996 Apr; 17(2):143-70. PubMed ID: 8813716
[TBL] [Abstract][Full Text] [Related]
4. Hereditary nonspherocytic hemolytic anemia caused by glucose-6-phosphate isomerase (GPI) deficiency in a Chinese patient: a case report.
Zu Y; Wang H; Lin W; Zou C
BMC Pediatr; 2022 Aug; 22(1):461. PubMed ID: 35915427
[TBL] [Abstract][Full Text] [Related]
5. A mutation affecting the lactate dehydrogenase locus Ldh-1 in the mouse. II. Mechanism of the LDH-A deficiency associated with hemolytic anemia.
Pretsch W; Merkle S; Favor J; Werner T
Genetics; 1993 Sep; 135(1):161-70. PubMed ID: 8224816
[TBL] [Abstract][Full Text] [Related]
6. Glucose phosphate isomerase enzyme-activity mutants in Mus musculus: genetical and biochemical characterization.
Pretsch W; Merkle S
Biochem Genet; 1990 Feb; 28(1-2):97-110. PubMed ID: 2344351
[TBL] [Abstract][Full Text] [Related]
7. Hereditary nonspherocytic hemolytic anemia caused by red cell glucose-6-phosphate isomerase (GPI) deficiency in two Portuguese patients: Clinical features and molecular study.
Manco L; Bento C; Victor BL; Pereira J; Relvas L; Brito RM; Seabra C; Maia TM; Ribeiro ML
Blood Cells Mol Dis; 2016 Sep; 60():18-23. PubMed ID: 27519939
[TBL] [Abstract][Full Text] [Related]
8. Glucosephosphate-isomerase (GPI) deficiency: GPI elyria.
Beutler E; Sigalove WH; Muir WA; Matsumoto F; West C
Ann Intern Med; 1974 Jun; 80(6):730-2. PubMed ID: 4832160
[No Abstract] [Full Text] [Related]
9. Glucose-6-phosphate isomerase deficiency.
Kugler W; Lakomek M
Baillieres Best Pract Res Clin Haematol; 2000 Mar; 13(1):89-101. PubMed ID: 10916680
[TBL] [Abstract][Full Text] [Related]
10. Hereditary deficiency of glucosephosphate isomerase as a cause of nonspherocytic hemolytic anemia.
Löhr GW; Arnold H; Blume KG; Engelhardt R; Beutler E
Blut; 1973 Jun; 26(6):393-8. PubMed ID: 4715119
[No Abstract] [Full Text] [Related]
11. Red cell glucose phosphate isomerase (GPI): a molecular study of three novel mutations associated with hereditary nonspherocytic hemolytic anemia.
Repiso A; Oliva B; Vives-Corrons JL; Beutler E; Carreras J; Climent F
Hum Mutat; 2006 Nov; 27(11):1159. PubMed ID: 17041899
[TBL] [Abstract][Full Text] [Related]
12. Combined glucose phosphate isomerase and glucose-6-phosphate dehydrogenase deficiency of erythrocytes.
Steiman I; Kaufman S; Zaidman JL; Leiba H
Isr J Med Sci; 1978 Nov; 14(11):1186-90. PubMed ID: 750548
[TBL] [Abstract][Full Text] [Related]
13. [Clinical trial of mannose treatment of hemolytic anemia caused by congenital deficiency of erythrocyte glucosephosphate isomerase].
Jabłońska-Skwiecińska E; Giro E; Rokicka-Milewska R
Acta Haematol Pol; 1992; 23(2):123-8. PubMed ID: 1488862
[TBL] [Abstract][Full Text] [Related]
14. Glucose phosphate isomerase deficiency with congenital nonspherocytic hemolytic anemia: a new variant (type Nordhorn). I. Clinical and genetic studies.
Schröter W; Koch HH; Wonneberger B; Kalinowsky W; Arnold A; Blume KG; Hüther W
Pediatr Res; 1974 Jan; 8(1):18-25. PubMed ID: 4809302
[No Abstract] [Full Text] [Related]
15. A glucosephosphate isomerase (GPI) null mutation in Mus musculus: evidence that anaerobic glycolysis is the predominant energy delivering pathway in early post-implantation embryos.
Merkle S; Pretsch W
Comp Biochem Physiol B; 1992 Mar; 101(3):309-14. PubMed ID: 1582174
[TBL] [Abstract][Full Text] [Related]
16. Two novel mutations (p.(Ser160Pro) and p.(Arg472Cys)) causing glucose-6-phosphate isomerase deficiency are associated with erythroid dysplasia and inappropriately suppressed hepcidin.
Mojzikova R; Koralkova P; Holub D; Saxova Z; Pospisilova D; Prochazkova D; Dzubak P; Horvathova M; Divoky V
Blood Cells Mol Dis; 2018 Mar; 69():23-29. PubMed ID: 28803808
[TBL] [Abstract][Full Text] [Related]
17. [Hereditary non-spherocytic hemolytic anemia caused by glucosephosphate isomerase deficiency: 1. case observed in Switzerland].
Müller E; Marti HR; Bach J; Micheli JL; Gasser C
Schweiz Med Wochenschr; 1974 Sep; 104(39):1379-81. PubMed ID: 4419288
[No Abstract] [Full Text] [Related]
18. Hereditary non-spherocytic hemolytic anemia and severe glucose phosphate isomerase deficiency in an Indian patient homozygous for the L487F mutation in the human GPI gene.
Warang P; Kedar P; Ghosh K; Colah RB
Int J Hematol; 2012 Aug; 96(2):263-7. PubMed ID: 22782259
[TBL] [Abstract][Full Text] [Related]
19. Glucose phosphate isomerase deficiency: enzymatic and familial characterization of Arg346His mutation.
Repiso A; Oliva B; Vives Corrons JL; Carreras J; Climent F
Biochim Biophys Acta; 2005 Jun; 1740(3):467-71. PubMed ID: 15949716
[TBL] [Abstract][Full Text] [Related]
20. Glucose Phosphate Isomerase Deficiency: High Prevalence of p.Arg347His Mutation in Indian Population Associated with Severe Hereditary Non-Spherocytic Hemolytic Anemia Coupled with Neurological Dysfunction.
Kedar PS; Dongerdiye R; Chilwirwar P; Gupta V; Chiddarwar A; Devendra R; Warang P; Prasada H; Sampagar A; Bhat S; Chandrakala S; Madkaikar M
Indian J Pediatr; 2019 Aug; 86(8):692-699. PubMed ID: 31030358
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
