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.
132 related articles for article (PubMed ID: 2372606)
21. [Hereditary intolerance to fructose in infants. Presentation of a clinical case]. Livolsi P Pediatr Med Chir; 1988; 10(6):649-52. PubMed ID: 3244544 [TBL] [Abstract][Full Text] [Related]
22. [Congenital fructose intolerance. New molecular aspects]. Larsen K; Adnanes O; Aarskog NK; Runde I; Ogreid D Tidsskr Nor Laegeforen; 1994 Nov; 114(28):3312-4. PubMed ID: 7809888 [TBL] [Abstract][Full Text] [Related]
23. Structural mutation of aldolase B in hereditary fructose intolerance: electrofocusing results. Schapira F; Hatzfeld A; Gregori C Monogr Hum Genet; 1978; 9():2-6. PubMed ID: 732841 [No Abstract] [Full Text] [Related]
24. Isolated fructose malabsorption. Wales JK; Primhak RA; Rattenbury J; Taylor CJ Arch Dis Child; 1990 Feb; 65(2):227-9. PubMed ID: 2317071 [TBL] [Abstract][Full Text] [Related]
25. Aldolase B mutations in Turkish families from central Anatolia. Karabulut HG; Halsall D; Sayin BD; Tonyukuk V; Cox TM; Bökesoy I Genet Couns; 2006; 17(4):457-60. PubMed ID: 17375533 [No Abstract] [Full Text] [Related]
30. [Study of hereditary fructose intolerance by methods of molecular biology]. Dreyfus JC; Schapira F; Besmond C; Gregori C; Kahn A Ann Med Interne (Paris); 1985; 136(6):456-8. PubMed ID: 3841265 [TBL] [Abstract][Full Text] [Related]
31. Screening for hereditary fructose intolerance mutations by reverse dot-blot. Lau J; Tolan DR Mol Cell Probes; 1999 Feb; 13(1):35-40. PubMed ID: 10024431 [TBL] [Abstract][Full Text] [Related]
32. Aldolase B A149P mutation and hereditary fructose intolerance are not associated with sudden infant death syndrome. Aarskog NK; Ogreid D Acta Paediatr; 1995 Aug; 84(8):947-8. PubMed ID: 7488826 [No Abstract] [Full Text] [Related]
33. Patients with hereditary fructose intolerance have normal erythrocyte aldolase activity. Gitzelmann R; Steinmann B; Tuchschmid P Clin Chim Acta; 1989 May; 181(2):163-6. PubMed ID: 2736779 [TBL] [Abstract][Full Text] [Related]
34. A newly identified aldolase B splicing mutation (G-->C, 5' intron 5) in hereditary fructose intolerance from New Zealand. Ali M; James CL; Cox TM Hum Mutat; 1996; 7(2):155-7. PubMed ID: 8829634 [No Abstract] [Full Text] [Related]
35. Allelic heterogeneity in adult hereditary fructose intolerance. Detection of structural mutations in the aldolase B molecule. Cox TM; O'Donnell MW; Camilleri M Mol Biol Med; 1983 Nov; 1(4):393-400. PubMed ID: 6680153 [TBL] [Abstract][Full Text] [Related]
36. Hereditary fructose intolerance. Ali M; Rellos P; Cox TM J Med Genet; 1998 May; 35(5):353-65. PubMed ID: 9610797 [TBL] [Abstract][Full Text] [Related]
38. Case report: heterogeneity of aldolase B in hereditary fructose intolerance. Kaiser UB; Hegele RA Am J Med Sci; 1991 Dec; 302(6):364-8. PubMed ID: 1772121 [TBL] [Abstract][Full Text] [Related]
39. Identification of a novel mutation (Leu 256-->Pro) in the human aldolase B gene associated with hereditary fructose intolerance. Ali M; Sebastio G; Cox TM Hum Mol Genet; 1994 Jan; 3(1):203-4. PubMed ID: 8162030 [No Abstract] [Full Text] [Related]
40. Pseudodominant transmission of fructose intolerance in an adult and three offspring: Heterozygote detection by intestinal biopsy. Cox TM; Camilleri M; O'Donnell MW; Chadwick VS N Engl J Med; 1982 Aug; 307(9):537-40. PubMed ID: 7099225 [No Abstract] [Full Text] [Related] [Previous] [Next] [New Search]