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2. Lead poisoning: association with hemolytic anemia, basophilic stippling, erythrocyte pyrimidine 5'-nucleotidase deficiency, and intraerythrocytic accumulation of pyrimidines. Valentine WN, Paglia DE, Fink K, Madokoro G. J Clin Invest; 1976 Oct; 58(4):926-32. PubMed ID: 965496 [Abstract] [Full Text] [Related]
3. [Pyrimidine 5'-nucleotidase deficiency as the congenital cause of nonspherocytic hemolytic anemia]. Pekrun A, Lakomek M, Eng W, Schröter W. Dtsch Med Wochenschr; 1993 Sep 10; 118(36):1276-80. PubMed ID: 8375297 [Abstract] [Full Text] [Related]
4. [Hemolytic anemia due to abnormalities in erythrocyte nucleotide metabolism]. Masuda M, Mizoguchi H. Nihon Rinsho; 1996 Sep 10; 54(9):2473-7. PubMed ID: 8890581 [Abstract] [Full Text] [Related]
5. [Pyrimidine-5'-nucleotidase deficiency--congenital hemolytic anemia with basophilic stippling of erythrocytes]. Seip M. Tidsskr Nor Laegeforen; 1999 Aug 30; 119(20):2996-8. PubMed ID: 10504847 [Abstract] [Full Text] [Related]
6. A case of lead intoxication: clinical and biochemical studies. Miwa S, Ishida Y, Takegawa S, Urata G, Toyoda T. Am J Hematol; 1981 Aug 30; 11(1):99-105. PubMed ID: 6267939 [Abstract] [Full Text] [Related]
13. Molecular characterization of five Portuguese patients with pyrimidine 5'-nucleotidase deficient hemolytic anemia showing three new P5'N-I mutations. Manco L, Relvas L, Silva Pinto C, Pereira J, Almeida AB, Ribeiro ML. Haematologica; 2006 Feb 30; 91(2):266-7. PubMed ID: 16461318 [Abstract] [Full Text] [Related]
14. Hereditary pyrimidine 5'-nucleotidase deficiency: from genetics to clinical manifestations. Zanella A, Bianchi P, Fermo E, Valentini G. Br J Haematol; 2006 Apr 30; 133(2):113-23. PubMed ID: 16611302 [Abstract] [Full Text] [Related]
15. Evaluation of activity of erythrocyte pyrimidine 5'-nucleotidase (P5N) in lead exposed workers: with focus on the effect on hemoglobin. Kim Y, Yoo CI, Lee CR, Lee JH, Lee H, Kim SR, Chang SH, Lee WJ, Hwang CH, Lee YH. Ind Health; 2002 Jan 30; 40(1):23-7. PubMed ID: 11926511 [Abstract] [Full Text] [Related]
16. Congenital non spherocytic hemolytic anemia (CNSHA) due to pyrimidine 5' nucleotidase deficiency. Aparna KR, Elizabeth KE. Indian Pediatr; 2006 Feb 30; 43(2):184-5. PubMed ID: 16528122 [No Abstract] [Full Text] [Related]
20. Two new mutations of the P5'N-1 gene found in Italian patients with hereditary hemolytic anemia: the molecular basis of the red cell enzyme disorder. Chiarelli LR, Fermo E, Abrusci P, Bianchi P, Dellacasa CM, Galizzi A, Zanella A, Valentini G. Haematologica; 2006 Sep 30; 91(9):1244-7. PubMed ID: 16956825 [Abstract] [Full Text] [Related] Page: [Next] [New Search]