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3. Combination of congenital nonspherocytic haemolytic anaemia and impairment of granulocyte function in severe glucosephosphate isomerase deficiency. A new variant enzyme designated GPI Calden. Neubauer BA; Eber SW; Lakomek M; Gahr M; Schröter W Acta Haematol; 1990; 83(4):206-10. PubMed ID: 2115718 [TBL] [Abstract][Full Text] [Related]
5. A case of congenital nonspherocytic hemolytic anemia associated with glucosephosphate isomerase (GPI) deficiency-GPI 'Kinki'. Takegawa S; Fujii H; Miwa S; Ohba Y; Yamauchi H; Miyata H Nihon Ketsueki Gakkai Zasshi; 1983 Feb; 46(1):11-7. PubMed ID: 6858560 [No Abstract] [Full Text] [Related]
6. Glucosephosphate-isomerase type Kaiserslautern. A new variant causing congenital nonspherocytic hemolytic anemia. Arnold H; Hasslinger K; Witt I Blut; 1983 May; 46(5):271-7. PubMed ID: 6839028 [TBL] [Abstract][Full Text] [Related]
7. 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]
8. Clinical symptoms and biochemical properties of three new glucosephosphate isomerase variants. Eber SW; Gahr M; Lakomek M; Prindull G; Schröter W Blut; 1986 Jul; 53(1):21-8. PubMed ID: 3719111 [TBL] [Abstract][Full Text] [Related]
9. Glucose phosphate isomerase (GPI) "Morcone": a new variant from Italy. Alfinito F; Ferraro F; Rocco S; De Vendittis E; Piccirillo G; Sementa A; Colombo MB; Zanella A; Rotoli B Eur J Haematol; 1994 May; 52(5):263-6. PubMed ID: 8020625 [TBL] [Abstract][Full Text] [Related]
11. Hereditary deficiency of glucosephosphate isomerase as a cause of nonspherocytic hemolytic anemia. Löhr GW; Arnold H; Blume KG; Engelhardt R; Beutler E Blut; 1973 Jun; 26(6):393-8. PubMed ID: 4715119 [No Abstract] [Full Text] [Related]
12. 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]
13. Generalised glucosephosphate isomerase (GPI) deficiency causing haemolytic anaemia, neuromuscular symptoms and impairment of granulocytic function: a new syndrome due to a new stable GPI variant with diminished specific activity (GPI Homburg). Schröter W; Eber SW; Bardosi A; Gahr M; Gabriel M; Sitzmann FC Eur J Pediatr; 1985 Nov; 144(4):301-5. PubMed ID: 4076245 [TBL] [Abstract][Full Text] [Related]
14. Haemolytic anaemia associated with glucosephosphate isomerase (GPI) deficiency in a Black South African child. Cayanis E; Penfold GK; Freiman I; MacDougall LG Br J Haematol; 1977 Nov; 37(3):363-71. PubMed ID: 603768 [TBL] [Abstract][Full Text] [Related]
15. Glucose Phosphate Isomerase Deficiency: High Prevalence of p.Arg347His Mutation in Indian Population Associated with Severe Hereditary Non-Spherocytic Hemolytic Anemia Coupled with Neurological Dysfunction. Kedar PS; Dongerdiye R; Chilwirwar P; Gupta V; Chiddarwar A; Devendra R; Warang P; Prasada H; Sampagar A; Bhat S; Chandrakala S; Madkaikar M Indian J Pediatr; 2019 Aug; 86(8):692-699. PubMed ID: 31030358 [TBL] [Abstract][Full Text] [Related]
16. Combined glucose phosphate isomerase and glucose-6-phosphate dehydrogenase deficiency of erythrocytes. Steiman I; Kaufman S; Zaidman JL; Leiba H Isr J Med Sci; 1978 Nov; 14(11):1186-90. PubMed ID: 750548 [TBL] [Abstract][Full Text] [Related]
17. 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]
18. Augsburg-type glucosephosphate isomerase deficiency. A new variant causing congenital nonspherocytic hemolytic anemia in a German family. Arnold H; Löhr GW; Hasslinger K; Podgajny T Blut; 1980 Feb; 40(2):107-15. PubMed ID: 7353078 [TBL] [Abstract][Full Text] [Related]
19. Hereditary nonspherocytic hemolytic anemia caused by glucose-6-phosphate isomerase (GPI) deficiency in a Chinese patient: a case report. Zu Y; Wang H; Lin W; Zou C BMC Pediatr; 2022 Aug; 22(1):461. PubMed ID: 35915427 [TBL] [Abstract][Full Text] [Related]
20. [Clinical trial of mannose treatment of hemolytic anemia caused by congenital deficiency of erythrocyte glucosephosphate isomerase]. Jabłońska-Skwiecińska E; Giro E; Rokicka-Milewska R Acta Haematol Pol; 1992; 23(2):123-8. PubMed ID: 1488862 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]