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Journal Abstract Search

201 related items for PubMed ID: 16528122

  • 1. Congenital non spherocytic hemolytic anemia (CNSHA) due to pyrimidine 5' nucleotidase deficiency.
    Aparna KR, Elizabeth KE.
    Indian Pediatr; 2006 Feb; 43(2):184-5. PubMed ID: 16528122
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  • 4. Congenital non-spherocytic haemolytic anaemias.
    Zanella A, Colombo MB, Rossi F, Merati G, Sirchia G.
    Haematologica; 1989 Feb; 74(4):387-96. PubMed ID: 2551797
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  • 9. [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
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  • 10. [Hemolytic anemia due to abnormalities in erythrocyte nucleotide metabolism].
    Masuda M, Mizoguchi H.
    Nihon Rinsho; 1996 Sep 30; 54(9):2473-7. PubMed ID: 8890581
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  • 12. Pyrimidine 5'-nucleotidase deficiency: improved detection of carriers.
    de Korte D, Sijstermans JM, Seip M, van Doorn CC, van Gennip AH, Roos D.
    Clin Chim Acta; 1989 Sep 29; 184(2):175-80. PubMed ID: 2557985
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  • 13. [Congenital non spherocytic hemolytic anemia due to lack of glucose-6-phosphate dehydrogenase (G-6-PD)].
    Brunetti P, Nenci GG, Parma A, Berardi G, Migliorini E.
    Haematologica; 1965 Sep 29; 50(5):359-401. PubMed ID: 4954293
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  • 18. 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 29; 91(2):266-7. PubMed ID: 16461318
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  • 20. Pyrimidine-5'-nucleotidase Campinas, a new mutation (p.R56G) in the NT5C3 gene associated with pyrimidine-5'-nucleotidase type I deficiency and influence of Gilbert's Syndrome on clinical expression.
    Santos Ad, Dantas LE, Traina F, Albuquerque DM, Chaim EA, Saad ST.
    Blood Cells Mol Dis; 2014 Dec 29; 53(4):246-52. PubMed ID: 25153905
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