These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

200 related articles for article (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
    [No Abstract]   [Full Text] [Related]  

  • 2. [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; 118(36):1276-80. PubMed ID: 8375297
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Pyrimidine-5'-nucleotidase anomaly].
    Miwa S
    Tanpakushitsu Kakusan Koso; 1988 Apr; 33(5):625-8. PubMed ID: 2855950
    [No Abstract]   [Full Text] [Related]  

  • 4. Congenital non-spherocytic haemolytic anaemias.
    Zanella A; Colombo MB; Rossi F; Merati G; Sirchia G
    Haematologica; 1989; 74(4):387-96. PubMed ID: 2551797
    [TBL] [Abstract][Full Text] [Related]  

  • 5. New missense homozygous mutation (Q270Ter) in the pyrimidine 5' nucleotidase type I-related gene in two Indian families with hereditary non-spherocytic hemolytic anemia.
    Warang P; Kedar P; Kar R; Ghosh K; Colah R
    Ann Hematol; 2013 May; 92(5):715-7. PubMed ID: 23139015
    [No Abstract]   [Full Text] [Related]  

  • 6. [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; 93(10):380-2. PubMed ID: 2558262
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Chronic non-spherocytic haemolytic anaemia due to congenital pyrimidine 5' nucleotidase deficiency: 25 years later.
    Vives i Corrons JL
    Baillieres Best Pract Res Clin Haematol; 2000 Mar; 13(1):103-18. PubMed ID: 10916681
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Pyrimidine-5'-nucleotidase deficiency--congenital hemolytic anemia with basophilic stippling of erythrocytes].
    Seip M
    Tidsskr Nor Laegeforen; 1999 Aug; 119(20):2996-8. PubMed ID: 10504847
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [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]  

  • 11. 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; 24(4):229-33. PubMed ID: 1844231
    [No Abstract]   [Full Text] [Related]  

  • 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; 184(2):175-80. PubMed ID: 2557985
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 50(5):359-401. PubMed ID: 4954293
    [No Abstract]   [Full Text] [Related]  

  • 14. 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; 73(5):587-90. PubMed ID: 26489818
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Diagnosis of pyrimidine 5'-nucleotidase deficiency suspected from a blood film.
    Al-Jafar HA; Layton DM; Robertson L; Escuredo E; Bain BJ
    Am J Hematol; 2013 Dec; 88(12):1089. PubMed ID: 23897698
    [No Abstract]   [Full Text] [Related]  

  • 16. 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; 91(9):1244-7. PubMed ID: 16956825
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Recommended screening test for pyrimidine 5'-nucleotidase deficiency. International Committee for Standardization in Haematology.
    Clin Lab Haematol; 1989; 11(1):55-6. PubMed ID: 2539936
    [No Abstract]   [Full Text] [Related]  

  • 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; 91(2):266-7. PubMed ID: 16461318
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Pyrimidine-5'-nucleotidase deficiency].
    Sumi S; Wada Y
    Ryoikibetsu Shokogun Shirizu; 1998; (18 Pt 1):487-9. PubMed ID: 9590109
    [No Abstract]   [Full Text] [Related]  

  • 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; 53(4):246-52. PubMed ID: 25153905
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.