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1. Glucose-phosphate isomerase deficiency due to a new variant (GP I Barcelona) and to a silent gene: biochemical, immunological and genetic studies. Kahn A; Vives JL; Bertrand O; Cottreau D; Marie J; Boivin P Clin Chim Acta; 1976 Jan; 66(2):145-55. PubMed ID: 1164 [TBL] [Abstract][Full Text] [Related]
2. Glucose phosphate isomerase deficiency with hereditary hemolytic anemia in a Spanish family: clinical and familial studies. Vives-Corrons JL; Rozman C; Kahn A; Carrera A; Triginer J Humangenetik; 1975 Oct; 29(4):291-7. PubMed ID: 240775 [TBL] [Abstract][Full Text] [Related]
3. A new variant of glucosephosphate isomerase deficiency. Van Biervliet JP; Vlug A; Bartstra H; Rotteveel JJ; de Vaan GA; Staal GE Humangenetik; 1975 Oct; 30(1):35-40. PubMed ID: 1339 [TBL] [Abstract][Full Text] [Related]
4. A new variant of glucosephosphate isomerase deficiency with mild haemolytic anemia (GPI-MYTHO). Galand C; Torres M; Boivin P; Bourgeaud JP Scand J Haematol; 1978 Jan; 20(1):77-84. PubMed ID: 625628 [TBL] [Abstract][Full Text] [Related]
5. A new variant of glucosephosphate isomerase deficiency (GPI-Utrecht). Van Biervliet JP; Van Milligen-Boersma L; Staal GE Clin Chim Acta; 1975 Dec; 65(2):157-65. PubMed ID: 241517 [TBL] [Abstract][Full Text] [Related]
6. Glucose phosphate isomerase deficiency with congenital nonspherocytic hemolytic anemia: a new variant (type Nordhorn). I. Clinical and genetic studies. Schröter W; Koch HH; Wonneberger B; Kalinowsky W; Arnold A; Blume KG; Hüther W Pediatr Res; 1974 Jan; 8(1):18-25. PubMed ID: 4809302 [No Abstract] [Full Text] [Related]
7. [Haemolytic anaemia due to congenital deffect in phosphohexoseisomerase. Report of a new variant (PHI-Barcelona) with stomatocytosis and increased osmotic fragility (author's transl)]. Vives-Corrons JL; Carrera A; Triginer J; Kahn A; Rozman C Sangre (Barc); 1975; 20(2):197-206. PubMed ID: 1145398 [No Abstract] [Full Text] [Related]
8. Human erythrocyte phosphoglycerate kinase deficiency: presence in a deficient patient of a stable variant with lowered catalytic activity. Kahn A; Cottreau D; Galand C; Boivin P Clin Chim Acta; 1976 May; 69(1):21-8. PubMed ID: 817852 [TBL] [Abstract][Full Text] [Related]
9. Genetic and molecular mechanisms of the congenital defects in glucose phosphate isomerase activity: studies of four families. Kahn A; Van Biervliet JP; Vives-Corrons JL; Cottreau D; Stall GE Pediatr Res; 1977 Nov; 11(11):1123-9. PubMed ID: 411100 [No Abstract] [Full Text] [Related]
10. Glucose phosphate isomerase deficiency with congenital nonspherocytic hemolytic anemia: a new variant (type Nordhorn). II. Purification and biochemical properties of the defective enzyme. Arnold H; Blume KG; Löhr GW; Schröter W; Koch HH; Wonneberger B Pediatr Res; 1974 Jan; 8(1):26-30. PubMed ID: 4809304 [No Abstract] [Full Text] [Related]
11. Stabilization and activation of a human glucose-6-phosphate dehydrogenase variant with enzyme deficiency by specific antibody. Kahn A; Boivin P; Leger J; Cottreau D; Hollard D Biochim Biophys Acta; 1974 Apr; 343(2):431-4. PubMed ID: 4209472 [No Abstract] [Full Text] [Related]
12. [Erythrocyte and leucocyte 3-phosphoglycerate kinase deficiency. Studies of properties of the enzyme, phagocytic activity of the polymorphonuclear leucoytes and a review of the literature]. Boivin P; Hakim J; Mandereau J; Galand C; Degos F; Schaison G Nouv Rev Fr Hematol; 1974; 14(4):495-508. PubMed ID: 4280558 [No Abstract] [Full Text] [Related]
13. A new variant of glucosephosphate isomerase deficiency: GPI-Kortrijk. Staal GE; Akkerman JW; Eggermont E; van Biervliet JP Clin Chim Acta; 1977 Jul; 78(1):121-7. PubMed ID: 18297 [TBL] [Abstract][Full Text] [Related]
14. Purification and properties of pyruvate kinase in normal and in pyruvate kinase deficient human red blood cells. Blume KG; Hoffbauer RW; Busch D; Arnold H; Löhr GW Biochim Biophys Acta; 1971 Feb; 227(2):364-72. PubMed ID: 5550823 [No Abstract] [Full Text] [Related]