590 related articles for article (PubMed ID: 8629088)
1. Red cell enzymopathies as a model of inborn errors of metabolism.
Miwa S; Kanno H; Hirono A; Fujii H
Southeast Asian J Trop Med Public Health; 1995; 26 Suppl 1():112-9. PubMed ID: 8629088
[TBL] [Abstract][Full Text] [Related]
2. Molecular basis of erythroenzymopathies associated with hereditary hemolytic anemia: tabulation of mutant enzymes.
Miwa S; Fujii H
Am J Hematol; 1996 Feb; 51(2):122-32. PubMed ID: 8579052
[TBL] [Abstract][Full Text] [Related]
3. [Pathophysiology and laboratory tests of hemolytic anemia: with special reference to erythroenzymopathies].
Fujii H; Miwa S
Rinsho Byori; 1989 Dec; 37(12):1331-43. PubMed ID: 2693773
[TBL] [Abstract][Full Text] [Related]
4. [Glucose-6-phosphate dehydrogenase].
Fujii H
Nihon Rinsho; 1995 May; 53(5):1221-5. PubMed ID: 7602782
[TBL] [Abstract][Full Text] [Related]
5. Pyruvate kinase deficiency in France: a 3-year study reveals 27 new mutations.
Pissard S; Max-Audit I; Skopinski L; Vasson A; Vivien P; Bimet C; Goossens M; Galacteros F; Wajcman H
Br J Haematol; 2006 Jun; 133(6):683-9. PubMed ID: 16704447
[TBL] [Abstract][Full Text] [Related]
6. Spectrum of novel mutations in the human PKLR gene in pyruvate kinase-deficient Indian patients with heterogeneous clinical phenotypes.
Kedar P; Hamada T; Warang P; Nadkarni A; Shimizu K; Fujji H; Ghosh K; Kanno H; Colah R
Clin Genet; 2009 Feb; 75(2):157-62. PubMed ID: 18759866
[TBL] [Abstract][Full Text] [Related]
7. Clinical and biochemical studies on mutant red cell enzymes mainly associated with hemolytic anemia.
Miwa S
Jinrui Idengaku Zasshi; 1980 Jun; 25(2):83-92. PubMed ID: 7431680
[No Abstract] [Full Text] [Related]
8. Molecular basis of red cell enzymopathies associated with hereditary nonspherocytic hemolytic anemia.
Miwa S
Haematologia (Budap); 1989; 22(4):215-31. PubMed ID: 2560452
[TBL] [Abstract][Full Text] [Related]
9. Molecular aspects of erythroenzymopathies associated with hereditary hemolytic anemia.
Miwa S; Fujii H
Am J Hematol; 1985 Jul; 19(3):293-305. PubMed ID: 2990202
[TBL] [Abstract][Full Text] [Related]
10. Fifteen novel mutations in PKLR associated with pyruvate kinase (PK) deficiency: structural implications of amino acid substitutions in PK.
van Wijk R; Huizinga EG; van Wesel AC; van Oirschot BA; Hadders MA; van Solinge WW
Hum Mutat; 2009 Mar; 30(3):446-53. PubMed ID: 19085939
[TBL] [Abstract][Full Text] [Related]
11. Chronic nonspherocytic hemolytic anemia due to glucose-6-phosphate dehydrogenase deficiency: report of two families with novel mutations causing G6PD Bangkok and G6PD Bangkok Noi.
Tanphaichitr VS; Hirono A; Pung-amritt P; Treesucon A; Wanachiwanawin W
Ann Hematol; 2011 Jul; 90(7):769-75. PubMed ID: 21302115
[TBL] [Abstract][Full Text] [Related]
12. [Molecular analysis of glucose-6-dehydrogenase deficiency in Spain].
Vives Corrons JL; Zarza R; Aymerich JM; Boixadera J; Carrera A; Colomer D; Corbella M; Castro M; Crespo JM; Del Arco A; Erkiaga S; Font L; González I; Juncá J; Lausin A; Manrubia E; Martín Núñez G; Murga MJ; Oliva E; Pérez de Mendiguren B; Pujades MA; Remacha A; Rovira A; Villegas A
Sangre (Barc); 1997 Oct; 42(5):391-8. PubMed ID: 9424740
[TBL] [Abstract][Full Text] [Related]
13. Variants of glucose-6-phosphate dehydrogenase are due to missense mutations spread throughout the coding region of the gene.
Vulliamy T; Beutler E; Luzzatto L
Hum Mutat; 1993; 2(3):159-67. PubMed ID: 8364584
[TBL] [Abstract][Full Text] [Related]
14. 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; 14(6):477-84. PubMed ID: 10571945
[TBL] [Abstract][Full Text] [Related]
15. Pyruvate kinase deficient hemolytic anemia in the Northern Irish population.
Percy MJ; van Wijk R; Haggan S; Savage GA; Boyd K; Dempsey S; Hamilton J; Kettle P; Kyle A; Shepherd CW; van Solinge WW; Lappin TR; McMullin MF
Blood Cells Mol Dis; 2007; 39(2):189-94. PubMed ID: 17574881
[TBL] [Abstract][Full Text] [Related]
16. First-trimester prenatal diagnosis of pyruvate kinase deficiency in an Indian family with the pyruvate kinase-Amish mutation.
Kedar PS; Nampoothiri S; Sreedhar S; Ghosh K; Shimizu K; Kanno H; Colah RB
Genet Mol Res; 2007 Jun; 6(2):470-5. PubMed ID: 17952871
[TBL] [Abstract][Full Text] [Related]
17. An inherited molecular lesion of erythrocyte pyruvate kinase. Identification of a kinetically aberrant isozyme associated with premature hemolysis.
Paglia DE; Valentine WN; Baughan MA; Miller DR; Reed CF; McIntyre OR
J Clin Invest; 1968 Aug; 47(8):1929-46. PubMed ID: 5666119
[TBL] [Abstract][Full Text] [Related]
18. [Molecular basis and pathophysiology of red cell enzymopathies].
Kanno H
Nihon Rinsho; 1996 Sep; 54(9):2382-9. PubMed ID: 8890566
[TBL] [Abstract][Full Text] [Related]
19. [Molecular study of red cell pyruvate kinase deficiency in 15 patients with chronic hemolytic anemia. Group of Erythropathology of Hematology and hemotherapy Association of Spain (HHAS)].
Zarza R; Pujades A; García J; Alvarez R; Carrera A; Estella J; Morey M; Remacha A; Pérez-Lungmus G; Nomdedeu B; Sánchez J; Gastearena J; Bureo E; Vives Corrons JL
Med Clin (Barc); 1999 May; 112(16):606-9. PubMed ID: 10374175
[TBL] [Abstract][Full Text] [Related]
20. Red cell pyruvate kinase deficiency: molecular and clinical aspects.
Zanella A; Fermo E; Bianchi P; Valentini G
Br J Haematol; 2005 Jul; 130(1):11-25. PubMed ID: 15982340
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
