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.
49. Biochemical characterization of three mutant isozymes of erythrocyte pyruvate kinase: PK-"Gainesville," PK-"San Juan," and PK-"Cape Canaveral". Paglia DE; Keitt AS; Valentine WN; Gordon S Am J Hematol; 1983 Jun; 14(4):335-44. PubMed ID: 6859032 [TBL] [Abstract][Full Text] [Related]
50. Molecular and clinical heterogeneity in pyruvate kinase deficiency in India. Warang P; Kedar P; Ghosh K; Colah R Blood Cells Mol Dis; 2013 Oct; 51(3):133-7. PubMed ID: 23770304 [TBL] [Abstract][Full Text] [Related]
51. Molecular characterisation of pyruvate kinase deficiency--concerns about the description of mutant PKLR alleles. van Wijk R; Rijksen G; van Solinge WW Br J Haematol; 2007 Jan; 136(1):167-9; author reply 169-70. PubMed ID: 17222205 [No Abstract] [Full Text] [Related]
52. Identification of a 6 base pair insertion in West Highland White Terriers with erythrocyte pyruvate kinase deficiency. Skelly BJ; Wallace M; Rajpurohit YR; Wang P; Giger U Am J Vet Res; 1999 Sep; 60(9):1169-72. PubMed ID: 10490091 [TBL] [Abstract][Full Text] [Related]
54. 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]
55. Point mutations in the L-type pyruvate kinase gene of two children with hemolytic anemia caused by pyruvate kinase deficiency. Neubauer B; Lakomek M; Winkler H; Parke M; Hofferbert S; Schröter W Blood; 1991 May; 77(9):1871-5. PubMed ID: 2018831 [TBL] [Abstract][Full Text] [Related]
56. Biphasic reaction kinetics in an anomalous isozyme of erythrocyte pyruvate kinase. Paglia DE; Konrad PN; Wolff JA; Valentine WN Clin Chim Acta; 1976 Dec; 73(3):395-405. PubMed ID: 1000857 [TBL] [Abstract][Full Text] [Related]
57. 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]
58. 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]
59. 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]
60. Hemolytic anemia due to pyruvate kinase deficiency: characterization of the enzymatic activity from eight patients. Black JA; Rittenberg MB; Bigley RH; Koler RD Am J Hum Genet; 1979 May; 31(3):300-10. PubMed ID: 463878 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]