BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

475 related articles for article (PubMed ID: 25388786)

  • 1. 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]  

  • 2. Dyserythropoiesis in a child with pyruvate kinase deficiency and coexistent unilateral multicystic dysplastic kidney.
    Haija MA; Qian YW; Muthukumar A
    Pediatr Blood Cancer; 2014 Aug; 61(8):1463-5. PubMed ID: 24481986
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Tanaka KR, Valentine WN, Miwa S. Pyruvate kinase (PK) deficiency hereditary nonspherocytic hemolytic anemia. Blood. 1962;19(3):267-295.
    Blood; 2016 May; 127(21):2505. PubMed ID: 27231390
    [No Abstract]   [Full Text] [Related]  

  • 5. Concomitant Hereditary Spherocytosis and Pyruvate Kinase Deficiency in a Spanish Family with Chronic Hemolytic Anemia: Contribution of Laser Ektacytometry to Clinical Diagnosis.
    Vives Corrons JL; Krishnevskaya E; Montllor L; Leguizamon V; Garcia Bernal M
    Cells; 2022 Mar; 11(7):. PubMed ID: 35406697
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Red blood cell PK deficiency: An update of PK-LR gene mutation database.
    Canu G; De Bonis M; Minucci A; Capoluongo E
    Blood Cells Mol Dis; 2016 Mar; 57():100-9. PubMed ID: 26832193
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Pyruvate kinase deficiency and severe congenital hemolytic anemia in a double heterozygous patient with paternal transmission of an early germ-line de novo mutation.
    Mañú-Pereira Mdel M; Gonzalez-Roca E; van Solinge WW; Llaudet-Planas E; Sevilla J; Montllor L; Mensa-Vilaro A; Ploos van Amstel HK; van Wijk R; Vives-Corrons J
    Am J Hematol; 2015 Dec; 90(12):E217-9. PubMed ID: 26315463
    [No Abstract]   [Full Text] [Related]  

  • 8. [Analysis of a pyruvate kinase deficiency consanguineous pedigree caused by Ile314Thr homozygous mutation].
    Qu Y; He H; Du J; Hou J; Fu W
    Zhonghua Xue Ye Xue Za Zhi; 2014 Jul; 35(7):601-4. PubMed ID: 25052601
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. A previously unknown mutation in the pyruvate kinase gene (PKLR) identified from a neonate with severe jaundice.
    Yaish HM; Nussenzveig RH; Agarwal AM; Siddiqui AH; Christensen RD
    Neonatology; 2014; 106(2):140-2. PubMed ID: 24969675
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Residual pyruvate kinase activity in PKLR-deficient erythroid precursors of a patient suffering from severe haemolytic anaemia.
    Klei TRL; Kheradmand Kia S; Veldthuis M; Beuger BM; Geissler J; Dehbozorgian J; Karimi M; van Bruggen R; van Zwieten R
    Eur J Haematol; 2017 Jun; 98(6):584-589. PubMed ID: 28295642
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Chronic haemolytic anaemia because of pyruvate kinase (PK) deficiency in a child heterozygous for haemoglobin S and no clinical features of sickle cell disease.
    Manco L; Vagace JM; Relvas L; Rebelo U; Bento C; Villegas A; Letícia Ribeiro M
    Eur J Haematol; 2010 Jan; 84(1):89-90. PubMed ID: 19758413
    [No Abstract]   [Full Text] [Related]  

  • 14. [Chronic non-spherocytic hemolytic anemia caused by pyruvate kinase deficiency in a Costa Rican family carrying hemoglobin C disease].
    Chaves M; Vives-Corrons JL; Sáenz GF; Pujades MA; Briceño J; Colomer D
    Sangre (Barc); 1990 Apr; 35(2):128-33. PubMed ID: 2363093
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A case of hereditary spherocytosis misdiagnosed as pyruvate kinase deficient hemolytic anemia.
    Vercellati C; Marcello AP; Fermo E; Barcellini W; Zanella A; Bianchi P
    Clin Lab; 2013; 59(3-4):421-4. PubMed ID: 23724634
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Hereditary spherocytosis is associated with decreased pyruvate kinase activity due to impaired structural integrity of the red blood cell membrane.
    Andres O; Loewecke F; Morbach H; Kraus S; Einsele H; Eber S; Speer CP
    Br J Haematol; 2019 Nov; 187(3):386-395. PubMed ID: 31273765
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Iron status in patients with pyruvate kinase deficiency: neonatal hyperferritinaemia associated with a novel frameshift deletion in the PKLR gene (p.Arg518fs), and low hepcidin to ferritin ratios.
    Mojzikova R; Koralkova P; Holub D; Zidova Z; Pospisilova D; Cermak J; Striezencova Laluhova Z; Indrak K; Sukova M; Partschova M; Kucerova J; Horvathova M; Divoky V
    Br J Haematol; 2014 May; 165(4):556-63. PubMed ID: 24533562
    [TBL] [Abstract][Full Text] [Related]  

  • 18. The mouse Char10 locus regulates severity of pyruvate kinase deficiency and susceptibility to malaria.
    Laroque A; Min-Oo G; Tam M; Ponka P; Stevenson MM; Gros P
    PLoS One; 2017; 12(5):e0177818. PubMed ID: 28542307
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Molecular basis of pyruvate kinase deficiency among Tunisians: description of new mutations affecting coding and noncoding regions in the PKLR gene.
    Jaouani M; Manco L; Kalai M; Chaouch L; Douzi K; Silva A; Macedo S; Darragi I; Boudriga I; Chaouachi D; Fitouri Z; Van Wijk R; Ribeiro ML; Abbes S
    Int J Lab Hematol; 2017 Apr; 39(2):223-231. PubMed ID: 28133914
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Hemolytic anemia associated with a novel heterozygote mutation 1183A in the PK-LR gene (PK- Jordan).
    Karadsheh NS; Gelbart T; Naffa RG
    Int J Lab Hematol; 2014 Aug; 36(4):e66-8. PubMed ID: 24330591
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 24.