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 *

108 related articles for article (PubMed ID: 20870434)

  • 21. Coexistence of congenital red cell pyruvate kinase and band 3 deficiency.
    Branca R; Costa E; Rocha S; Coelho H; Quintanilha A; Cabeda JM; Santos-Silva A; Barbot J
    Clin Lab Haematol; 2004 Aug; 26(4):297-300. PubMed ID: 15279669
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Glucose-6-phosphate dehydrogenase and red cell pyruvate kinase deficiency in neonatal jaundice cases in egypt.
    Abdel Fattah M; Abdel Ghany E; Adel A; Mosallam D; Kamal S
    Pediatr Hematol Oncol; 2010 May; 27(4):262-71. PubMed ID: 20426517
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Red cell pyruvate kinase deficiency: 17 new mutations of the PK-LR gene.
    Fermo E; Bianchi P; Chiarelli LR; Cotton F; Vercellati C; Writzl K; Baker K; Hann I; Rodwell R; Valentini G; Zanella A
    Br J Haematol; 2005 Jun; 129(6):839-46. PubMed ID: 15953013
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Partial pyruvate kinase deficiency aggravates the phenotypic expression of band 3 deficiency in a family with hereditary spherocytosis.
    van Zwieten R; van Oirschot BA; Veldthuis M; Dobbe JG; Streekstra GJ; van Solinge WW; Schutgens RE; van Wijk R
    Am J Hematol; 2015 Mar; 90(3):E35-9. PubMed ID: 25388786
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Co-existence of hereditary spherocytosis and a new red cell pyruvate kinase variant: PK mallorca.
    Zarza R; Moscardó M; Alvarez R; García J; Morey M; Pujades A; Vives-Corrons JL
    Haematologica; 2000 Mar; 85(3):227-32. PubMed ID: 10702808
    [TBL] [Abstract][Full Text] [Related]  

  • 26. [Molecular genetic diagnostics and screening of hereditary hemochromatosis].
    Zlocha J; Kovács L; Pozgayová S; Kupcová V; Durínová S
    Vnitr Lek; 2006 Jun; 52(6):602-8. PubMed ID: 16871764
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Red cell pyruvate kinase deficiency: from genetics to clinical manifestations.
    Zanella A; Bianchi P
    Baillieres Best Pract Res Clin Haematol; 2000 Mar; 13(1):57-81. PubMed ID: 10916678
    [TBL] [Abstract][Full Text] [Related]  

  • 28. A family case of pyruvate kinase variant, PK 'Nichinan'.
    Uno H; Sawano F; Fujii H; Miwa S; Tsuda K
    Jpn J Med; 1990; 29(2):168-73. PubMed ID: 2232365
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Erythrocyte pyruvate kinase deficiency in the Ohio Amish: origin and characterization of the mutant enzyme.
    Muir WA; Beutler E; Wasson C
    Am J Hum Genet; 1984 May; 36(3):634-9. PubMed ID: 6731438
    [TBL] [Abstract][Full Text] [Related]  

  • 30. A novel and a previously described compound heterozygous PKLR gene mutations causing pyruvate kinase deficiency in a Chinese child.
    Li H; Gu P; Yao RE; Wang J; Fu Q; Wang J
    Fetal Pediatr Pathol; 2014 Jun; 33(3):182-90. PubMed ID: 24601847
    [TBL] [Abstract][Full Text] [Related]  

  • 31. [Red cell enzyme anomalies and hemolytic anemia].
    Miwa S
    Rinsho Byori; 1986 Apr; 34(4):378-82. PubMed ID: 3018329
    [No Abstract]   [Full Text] [Related]  

  • 32. [Congenital hemolytic anemia caused by pyruvate kinase variants (PK 'Kasumi')].
    Katoh O; Fujimura K; Kuramoto A; Fujii H; Miwa S; Ohya T; Kajiyama G
    Rinsho Ketsueki; 1988 Mar; 29(3):369-74. PubMed ID: 3294473
    [No Abstract]   [Full Text] [Related]  

  • 33. Ten cases of pyruvate kinase (PK) deficiency found in Japan: enzymatic characterization of the patients' PK.
    Morisaki T; Tani K; Takahashi K; Tsutsumi H; Horiuchi N; Ogura H; Kanno H; Fujimura K; Nakayama S; Watanabe C
    Nihon Ketsueki Gakkai Zasshi; 1988 Sep; 51(6):1080-5. PubMed ID: 3201900
    [No Abstract]   [Full Text] [Related]  

  • 34. Coexistence of alpha-thalassemia and a new pyruvate kinase variant: PK Fukien.
    Beutler E; Forman L
    Acta Haematol; 1983; 69(1):3-8. PubMed ID: 6297220
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Fifteen novel mutations in PKLR associated with pyruvate kinase (PK) deficiency: structural implications of amino acid substitutions in PK.
    van Wijk R; Huizinga EG; van Wesel AC; van Oirschot BA; Hadders MA; van Solinge WW
    Hum Mutat; 2009 Mar; 30(3):446-53. PubMed ID: 19085939
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Erythrocytic pyruvate kinase mutations causing hemolytic anemia, osteosclerosis, and secondary hemochromatosis in dogs.
    Gultekin GI; Raj K; Foureman P; Lehman S; Manhart K; Abdulmalik O; Giger U
    J Vet Intern Med; 2012; 26(4):935-44. PubMed ID: 22805166
    [TBL] [Abstract][Full Text] [Related]  

  • 37. [Pyruvate kinase (PK) isozyme switching and genetic heterogeneity of PK deficiency].
    Kanno H
    Nihon Rinsho; 1995 May; 53(5):1213-20. PubMed ID: 7602781
    [TBL] [Abstract][Full Text] [Related]  

  • 38. [Biochemistry and enzymatic diagnosis of red blood cell pyruvate kinase deficiency].
    Kanno H
    Nihon Rinsho; 2004 Dec; 62 Suppl 12():830-4. PubMed ID: 15658462
    [No Abstract]   [Full Text] [Related]  

  • 39. Pyruvate kinase deficiency: the genotype-phenotype association.
    Zanella A; Fermo E; Bianchi P; Chiarelli LR; Valentini G
    Blood Rev; 2007 Jul; 21(4):217-31. PubMed ID: 17360088
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Novel type of red blood cell pyruvate kinase hyperactivity predicts a remote regulatory locus involved in PKLR gene expression.
    Am J Hematol; ; . PubMed ID: 24375447
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.