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Journal Abstract Search
187 related items for PubMed ID: 2558262
1. [Hemolytic anemia caused by pyrimidine 5'-nucleotidase (P5N) deficiency 15 years later. Apropos of 2 new cases of hereditary deficit and another one of lead poisoning]. de la Serna FJ, Gilsanz F, Ricard P, Urrutia A. Med Clin (Barc); 1989 Oct 07; 93(10):380-2. PubMed ID: 2558262 [Abstract] [Full Text] [Related]
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 07; 58(4):926-32. PubMed ID: 965496 [Abstract] [Full Text] [Related]
12. Effects of low-level lead exposure on pyrimidine 5'-nucleotidase and other erythrocyte enzymes. Possible role of pyrimidine 5'-nucleotidase in the pathogenesis of lead-induced anemia. Paglia DE, Valentine WN, Dahlgren JG. J Clin Invest; 1975 Nov 07; 56(5):1164-9. PubMed ID: 1184742 [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 07; 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 07; 43(2):184-5. PubMed ID: 16528122 [No Abstract] [Full Text] [Related]
17. Pyrimidine 5'-nucleotidase deficiency associated to a polymalformative syndrome. Altounian L, Perrin J, Fouyssac F, Fenneteau O, Da Costa L, Bahuau M, Leheup B, Jonveaux P, Lesesve JF. Ann Biol Clin (Paris); 2015 Feb 07; 73(5):587-90. PubMed ID: 26489818 [Abstract] [Full Text] [Related]
18. Report of the first case of pyrimidine 5' nucleotidase deficiency from Kuwait detected by a screening test. A case report. Ghosh K, Abdul Rahman HI, Torres EC, Abdul Wahab A, Hassanein AA. Haematologia (Budap); 1991 Feb 07; 24(4):229-33. PubMed ID: 1844231 [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 07; 91(9):1244-7. PubMed ID: 16956825 [Abstract] [Full Text] [Related] Page: [Next] [New Search]