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Journal Abstract Search

115 related items for PubMed ID: 22078096

  • 1. A new simple approach for the determination of pyrimidine 5'-nucleotidase activity in human erythrocytes using an ELISA reader.
    Warang P, Kedar P, Ghosh K, Colah R.
    Int J Lab Hematol; 2012 Jun; 34(3):232-6. PubMed ID: 22078096
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  • 3. Hereditary pyrimidine 5'-nucleotidase deficiency: from genetics to clinical manifestations.
    Zanella A, Bianchi P, Fermo E, Valentini G.
    Br J Haematol; 2006 Apr; 133(2):113-23. PubMed ID: 16611302
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  • 4. Genetic basis of hemolytic anemia caused by pyrimidine 5' nucleotidase deficiency.
    Marinaki AM, Escuredo E, Duley JA, Simmonds HA, Amici A, Naponelli V, Magni G, Seip M, Ben-Bassat I, Harley EH, Thein SL, Rees DC.
    Blood; 2001 Jun 01; 97(11):3327-32. PubMed ID: 11369620
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  • 5. Molecular basis of pyrimidine 5'-nucleotidase deficiency caused by 3 newly identified missense mutations (c.187T>C, c.469G>C and c.740T>C) and a tabulation of known mutations.
    Chiarelli LR, Morera SM, Galizzi A, Fermo E, Zanella A, Valentini G.
    Blood Cells Mol Dis; 2008 Jun 01; 40(3):295-301. PubMed ID: 18499901
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  • 6. A New Homozygous Mutation (c.393-394del TA/c.393-394del TA) in the NT5C3 Gene Associated With Pyrimidine-5'-Nucleotidase Deficiency: A Case Report.
    Köker SA, Oymak Y, Bianchi P, Fermo E, Karapinar TH, Gözmen S, Ay Y, Vergin RC.
    J Pediatr Hematol Oncol; 2019 Nov 01; 41(8):e484-e486. PubMed ID: 30951028
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  • 8. Inhibition of hexose monophosphate shunt in young erythrocytes by pyrimidine nucleotides in hereditary pyrimidine 5' nucleotidase deficiency.
    David O, Ramenghi U, Camaschella C, Vota MG, Comino L, Pescarmona GP, Nicola P.
    Eur J Haematol; 1991 Jul 01; 47(1):48-54. PubMed ID: 1868914
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  • 10. 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 01; 91(9):1244-7. PubMed ID: 16956825
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  • 12. 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 Sep 01; 73(5):587-90. PubMed ID: 26489818
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  • 16. Pyrimidine 5'-nucleotidase acquired deficiency in beta-thalassemia: involvement of enzyme-SH groups in the inactivation process.
    David O, Vota MG, Piga A, Ramenghi U, Bosia A, Pescarmona GP.
    Acta Haematol; 1989 Sep 01; 82(2):69-74. PubMed ID: 2552730
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  • 17. [Microsequencing, analysis of molecular weight and amino acid composition for pyrimidine 5'-nucleotidase I of human erythrocytes].
    Pan ZL, Li JY, Min BH, Ying K, Zhou H, Xu XP, Shong XM, Han FL, Zhang WP, Zhang X.
    Zhongguo Shi Yan Xue Ye Xue Za Zhi; 2003 Feb 01; 11(1):61-5. PubMed ID: 12667292
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  • 18. [Assessment of erythrocyte pyrimidine 5'-nucleotidase test for screening of occupational lead poisoning].
    Lü L, Lin G, Wang Q.
    Zhonghua Yi Xue Za Zhi; 2000 Apr 01; 80(4):283-6. PubMed ID: 11798774
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  • 19. 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 Apr 01; 24(4):229-33. PubMed ID: 1844231
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