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3. [From gene to disease; hereditary non-spherocytic hemolytic anemia caused by pyruvate kinase deficiency]. de Vooght KM; van Wijk R; Nieuwenhuis HK; Ploos van Amstel JK; Rijksen G; van Solinge WW Ned Tijdschr Geneeskd; 2002 Sep; 146(39):1828-31. PubMed ID: 12382367 [TBL] [Abstract][Full Text] [Related]
4. [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]
5. [Hereditary haemolytic anaemia due to pyruvate kinase deficiency. Prognosis of neonatal forms (author's transl)]. Boivin P; Ottenwaelter T Nouv Presse Med; 1982 Mar; 11(12):917-9. PubMed ID: 7063368 [TBL] [Abstract][Full Text] [Related]
6. The influence of magnesium ions on pyruvate kinase-deficient red blood cells. Wazewska-Czyzewska M; Gumińska M Folia Haematol Int Mag Klin Morphol Blutforsch; 1975; 102(5):576-83. PubMed ID: 54308 [TBL] [Abstract][Full Text] [Related]
7. Three cases of hemolytic anemia with erythrocyte pyruvate kinase deficiency in Alberta. Collier HB; Ashford DR; Bell RE Can Med Assoc J; 1966 Dec; 95(23):1188-92. PubMed ID: 5921478 [TBL] [Abstract][Full Text] [Related]
8. 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]
9. First-trimester prenatal diagnosis of pyruvate kinase deficiency in an Indian family with the pyruvate kinase-Amish mutation. Kedar PS; Nampoothiri S; Sreedhar S; Ghosh K; Shimizu K; Kanno H; Colah RB Genet Mol Res; 2007 Jun; 6(2):470-5. PubMed ID: 17952871 [TBL] [Abstract][Full Text] [Related]
17. [Deficiency of pyruvate kinase in erythrocytes: biochemical studies. Preliminary communication]. Stanulović M; Jerance D; Stojimirović E Bilt Hematol Transfuz; 1977; 5(3-4):95-6. PubMed ID: 615616 [TBL] [Abstract][Full Text] [Related]
18. Clinical heterogeneity of erythrocyte pyruvate kinase deficiency. Evidence of an impaired utilization of ATP in a clinically severe form. Schröter W Helv Paediatr Acta; 1972 Nov; 27(5):471-88. PubMed ID: 4640902 [No Abstract] [Full Text] [Related]
19. Inherited erythrocyte pyruvate kinase deficiency: Studies on 15 members of two related families. Dachà M; Canestrari F; Bossù M; Ferrini PL; Fornaini G Acta Haematol; 1977; 57(1):37-46. PubMed ID: 190844 [TBL] [Abstract][Full Text] [Related]
20. [Erythrocyte enzyme defects and their clinical significance (author's transl)]. Schröter W Monatsschr Kinderheilkd; 1981 Aug; 129(8):432-43. PubMed ID: 6116182 [No Abstract] [Full Text] [Related] [Next] [New Search]