162 related articles for article (PubMed ID: 6305188)
1. Red cell adenylate kinase deficiency associated with hereditary nonspherocytic hemolytic anemia: clinical and biochemical studies.
Miwa S; Fujii H; Tani K; Takahashi K; Takizawa T; Igarashi T
Am J Hematol; 1983 Jun; 14(4):325-33. PubMed ID: 6305188
[TBL] [Abstract][Full Text] [Related]
2. Erythrocyte adenylate kinase deficiency: characterization of recombinant mutant forms and relationship with nonspherocytic hemolytic anemia.
Abrusci P; Chiarelli LR; Galizzi A; Fermo E; Bianchi P; Zanella A; Valentini G
Exp Hematol; 2007 Aug; 35(8):1182-9. PubMed ID: 17662886
[TBL] [Abstract][Full Text] [Related]
3. Hereditary erythrocyte adenylate kinase deficiency: a defect of multiple phosphotransferases?
Lachant NA; Zerez CR; Barredo J; Lee DW; Savely SM; Tanaka KR
Blood; 1991 Jun; 77(12):2774-84. PubMed ID: 1646049
[TBL] [Abstract][Full Text] [Related]
4. Metabolic compensation for profound erythrocyte adenylate kinase deficiency. A hereditary enzyme defect without hemolytic anemia.
Beutler E; Carson D; Dannawi H; Forman L; Kuhl W; West C; Westwood B
J Clin Invest; 1983 Aug; 72(2):648-55. PubMed ID: 6308059
[TBL] [Abstract][Full Text] [Related]
5. Two cases of red cell aldolase deficiency associated with hereditary hemolytic anemia in a Japanese family.
Miwa S; Fujii H; Tani K; Takahashi K; Takegawa S; Fujinami N; Sakurai M; Kubo M; Tanimoto Y; Kato T; Matsumoto N
Am J Hematol; 1981 Dec; 11(4):425-37. PubMed ID: 7331996
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. [Hemolytic anemia due to abnormalities in erythrocyte nucleotide metabolism].
Masuda M; Mizoguchi H
Nihon Rinsho; 1996 Sep; 54(9):2473-7. PubMed ID: 8890581
[TBL] [Abstract][Full Text] [Related]
8. Hereditary nonspherocytic hemolytic anemia due to a new hexokinase variant with reduced stability.
Magnani M; Stocchi V; Cucchiarini L; Novelli G; Lodi S; Isa L; Fornaini G
Blood; 1985 Sep; 66(3):690-7. PubMed ID: 4027385
[TBL] [Abstract][Full Text] [Related]
9. Red cell adenylate kinase deficiency in India: identification of two novel missense mutations (c.71A>G and c.413G>A).
Dongerdiye R; Kamat P; Jain P; Warang P; Devendra R; Wasekar N; Sharma R; Mhaskar K; Madkaikar MR; Manglani MV; Kedar PS
J Clin Pathol; 2019 Jun; 72(6):393-398. PubMed ID: 30918013
[TBL] [Abstract][Full Text] [Related]
10. Hereditary nonspherocytic hemolytic anemia and hexokinase deficiency.
Beutler E; Dyment PG; Matsumoto F
Blood; 1978 May; 51(5):935-40. PubMed ID: 638252
[TBL] [Abstract][Full Text] [Related]
11. Elevated pyruvate kinase activity in patients with hemolytic anemia due to red cell pyruvate kinase "deficiency".
Beutler E; Forman L; Rios-Larrain E
Am J Med; 1987 Nov; 83(5):899-904. PubMed ID: 3674096
[TBL] [Abstract][Full Text] [Related]
12. Hereditary hemolytic anemia with increased red cell adenosine deaminase (45- to 70-fold) and decreased adenosine triphosphate.
Valentine WN; Paglia DE; Tartaglia AP; Gilsanz F
Science; 1977 Feb; 195(4280):783-5. PubMed ID: 836588
[TBL] [Abstract][Full Text] [Related]
13. Studies on human erythrocyte nucleotide metabolism. II. Nonspherocytic hemolytic anemia, high red cell ATP, and ribosephosphate pyrophosphokinase (RPK, E.C.2.7.6.1) deficiency.
Valentine WN; Anderson HM; Paglia DE; Jaffé ER; Konrad PN; Harris SR
Blood; 1972 May; 39(5):674-84. PubMed ID: 5022715
[No Abstract] [Full Text] [Related]
14. Introduction to discussion of regulation of erythrocyte glycolysis.
Valentine WN
Exp Eye Res; 1971 May; 11(3):273-9. PubMed ID: 4941673
[No Abstract] [Full Text] [Related]
15. Red cell adenylate kinase deficiency: molecular study of 3 new mutations (118G>A, 190G>A, and GAC deletion) associated with hereditary nonspherocytic hemolytic anemia.
Corrons JL; Garcia E; Tusell JJ; Varughese KI; West C; Beutler E
Blood; 2003 Jul; 102(1):353-6. PubMed ID: 12649162
[TBL] [Abstract][Full Text] [Related]
16. HEREDITARY NON-SPHEROCYTIC HAEMOLYTIC ANAEMIA. A STUDY OF RED-CELL CARBOHYDRATE METABOLISM IN TWELVE CASES OF PYRUVATE-KINASE DEFICIENCY.
GRIMES AJ; MEISLER A; DACIE JV
Br J Haematol; 1964 Jul; 10():403-11. PubMed ID: 14179493
[No Abstract] [Full Text] [Related]
17. G-6-PD Guadalajara. A new mutant associated with chronic nonspherocytic hemolytic anemia.
Vaca G; Ibarra B; Romero F; Olivares N; Cantú JM; Beutler E
Hum Genet; 1982; 61(2):175-6. PubMed ID: 7129446
[TBL] [Abstract][Full Text] [Related]
18. Generalized hexokinase deficiency in the blood cells of a patient with nonspherocytic hemolytic anemia.
Rijksen G; Akkerman JW; van den Wall Bake AW; Hofstede DP; Staal GE
Blood; 1983 Jan; 61(1):12-8. PubMed ID: 6848140
[TBL] [Abstract][Full Text] [Related]
19. Adenosine deaminase (ADA) overproduction associated with congenital hemolytic anemia: case report and molecular analysis.
Kanno H; Tani K; Fujii H; Iguchi-Ariga SM; Ariga H; Kozaki T; Miwa S
Jpn J Exp Med; 1988 Feb; 58(1):1-8. PubMed ID: 3164080
[TBL] [Abstract][Full Text] [Related]
20. Hereditary hemolytic anemia with human erythrocyte pyrimidine 5'-nucleotidase deficiency.
Valentine WN; Fink K; Paglia DE; Harris SR; Adams WS
J Clin Invest; 1974 Oct; 54(4):866-79. PubMed ID: 4372252
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
