158 related articles for article (PubMed ID: 1969579)
21. [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]
22. Identification of a novel mutation (Leu256-->Pro) in the human aldolase B gene associated with hereditary fructose intolerance.
Ali M; Sebastio G; Cox TM
Hum Mol Genet; 1994 Apr; 3(4):684. PubMed ID: 8069328
[No Abstract] [Full Text] [Related]
23. Hereditary fructose intolerance.
Cross NC; Cox TM
Int J Biochem; 1990; 22(7):685-9. PubMed ID: 2205519
[No Abstract] [Full Text] [Related]
24. Mutation analysis in Turkish patients with hereditary fructose intolerance.
Dursun A; Kalkanoğlu HS; Coşkun T; Tokatli A; Bittner R; Koçak N; Yüce A; Ozalp I; Boehme HJ
J Inherit Metab Dis; 2001 Oct; 24(5):523-6. PubMed ID: 11757579
[TBL] [Abstract][Full Text] [Related]
25. Diverse mutations in the aldolase B gene that underlie the prevalence of hereditary fructose intolerance.
Ali M; Cox TM
Am J Hum Genet; 1995 Apr; 56(4):1002-5. PubMed ID: 7717389
[No Abstract] [Full Text] [Related]
26. Congenital hereditary fructose intolerance and pregnancy.
Marks F; Ordorica S; Hoskins I; Young BK
Am J Obstet Gynecol; 1989 Feb; 160(2):362-3. PubMed ID: 2916618
[TBL] [Abstract][Full Text] [Related]
27. Clinical course of hereditary fructose intolerance in 56 patients.
Endres W; Sierck T; Shin YS
Acta Paediatr Jpn; 1988 Aug; 30(4):452-6. PubMed ID: 3150235
[No Abstract] [Full Text] [Related]
28. Molecular analysis of the aldolase B gene in patients with hereditary fructose intolerance from Spain.
Sánchez-Gutiérrez JC; Benlloch T; Leal MA; Samper B; García-Ripoll I; Felíu JE
J Med Genet; 2002 Sep; 39(9):e56. PubMed ID: 12205126
[No Abstract] [Full Text] [Related]
29. The molecular basis of hereditary fructose intolerance in Italian children.
Santamaria R; Scarano MI; Esposito G; Chiandetti L; Izzo P; Salvatore F
Eur J Clin Chem Clin Biochem; 1993 Oct; 31(10):675-8. PubMed ID: 8292669
[TBL] [Abstract][Full Text] [Related]
30. DNA diagnosis of fatal fructose intolerance from archival tissue.
Ali M; Rosien U; Cox TM
Q J Med; 1993 Jan; 86(1):25-30. PubMed ID: 8438046
[TBL] [Abstract][Full Text] [Related]
31. 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]
32. [Hereditary fructose intolerance].
Mochizuki H
Nihon Rinsho; 2006 Sep; Suppl 3():220-3. PubMed ID: 17022535
[No Abstract] [Full Text] [Related]
33. [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]
34. 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]
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. 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]
37. Aldolase B mutations and prevalence of hereditary fructose intolerance in a Polish population.
Gruchota J; Pronicka E; Korniszewski L; Stolarski B; Pollak A; Rogaszewska M; Płoski R
Mol Genet Metab; 2006 Apr; 87(4):376-8. PubMed ID: 16406649
[TBL] [Abstract][Full Text] [Related]
38. Molecular basis of hereditary fructose intolerance in Italy: identification of two novel mutations in the aldolase B gene.
Santamaria R; Tamasi S; Del Piano G; Sebastio G; Andria G; Borrone C; Faldella G; Izzo P; Salvatore F
J Med Genet; 1996 Sep; 33(9):786-8. PubMed ID: 8880583
[TBL] [Abstract][Full Text] [Related]
39. Isoelectrofocusing of aldolase B from normal human livers and from livers with hereditary fructose intolerance.
Schapira F; Gregori C; Hatzfeld A
Clin Chim Acta; 1977 Jul; 78(1):1-8. PubMed ID: 884843
[TBL] [Abstract][Full Text] [Related]
40. Neonatal screening for hereditary fructose intolerance: frequency of the most common mutant aldolase B allele (A149P) in the British population.
James CL; Rellos P; Ali M; Heeley AF; Cox TM
J Med Genet; 1996 Oct; 33(10):837-41. PubMed ID: 8933337
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]