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Journal Abstract Search

400 related items for PubMed ID: 9610797

  • 1. Hereditary fructose intolerance.
    Ali M, Rellos P, Cox TM.
    J Med Genet; 1998 May; 35(5):353-65. PubMed ID: 9610797
    [Abstract] [Full Text] [Related]

  • 2. Association of the widespread A149P hereditary fructose intolerance mutation with newly identified sequence polymorphisms in the aldolase B gene.
    Brooks CC, Tolan DR.
    Am J Hum Genet; 1993 Apr; 52(4):835-40. PubMed ID: 8096362
    [Abstract] [Full Text] [Related]

  • 3. 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
    [Abstract] [Full Text] [Related]

  • 4. The biochemical basis of hereditary fructose intolerance.
    Bouteldja N, Timson DJ.
    J Inherit Metab Dis; 2010 Apr; 33(2):105-12. PubMed ID: 20162364
    [Abstract] [Full Text] [Related]

  • 5. Aldolase B mutations in Italian families affected by hereditary fructose intolerance.
    Sebastio G, de Franchis R, Strisciuglio P, Andria G, Dionisi Vici C, Sabetta G, Gatti R, Cross NC, Cox TM.
    J Med Genet; 1991 Apr; 28(4):241-3. PubMed ID: 1856829
    [Abstract] [Full Text] [Related]

  • 6. Structure of the thermolabile mutant aldolase B, A149P: molecular basis of hereditary fructose intolerance.
    Malay AD, Allen KN, Tolan DR.
    J Mol Biol; 2005 Mar 18; 347(1):135-44. PubMed ID: 15733923
    [Abstract] [Full Text] [Related]

  • 7. Hereditary fructose intolerance.
    Wong D.
    Mol Genet Metab; 2005 Jul 18; 85(3):165-7. PubMed ID: 16086449
    [No Abstract] [Full Text] [Related]

  • 8. Catalytic deficiency of human aldolase B in hereditary fructose intolerance caused by a common missense mutation.
    Cross NC, Tolan DR, Cox TM.
    Cell; 1988 Jun 17; 53(6):881-5. PubMed ID: 3383242
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  • 12. [Congenital fructose intolerance. New molecular aspects].
    Larsen K, Adnanes O, Aarskog NK, Runde I, Ogreid D.
    Tidsskr Nor Laegeforen; 1994 Nov 20; 114(28):3312-4. PubMed ID: 7809888
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  • 13. Isolation and characterization of a mutant liver aldolase in adult hereditary fructose intolerance. Identification of the enzyme variant by radioassay in tissue biopsy specimens.
    Cox TM, O'Donnell MW, Camilleri M, Burghes AH.
    J Clin Invest; 1983 Jul 20; 72(1):201-13. PubMed ID: 6348085
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  • 15. Increased prevalence of mutant null alleles that cause hereditary fructose intolerance in the American population.
    Coffee EM, Yerkes L, Ewen EP, Zee T, Tolan DR.
    J Inherit Metab Dis; 2010 Feb 20; 33(1):33-42. PubMed ID: 20033295
    [Abstract] [Full Text] [Related]

  • 16. [Hereditary fructose intolerance].
    Mochizuki H.
    Nihon Rinsho; 2006 Sep 28; Suppl 3():220-3. PubMed ID: 17022535
    [No Abstract] [Full Text] [Related]

  • 17. Structural and functional analysis of aldolase B mutants related to hereditary fructose intolerance.
    Esposito G, Vitagliano L, Santamaria R, Viola A, Zagari A, Salvatore F.
    FEBS Lett; 2002 Nov 06; 531(2):152-6. PubMed ID: 12417303
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  • 20. Case report: heterogeneity of aldolase B in hereditary fructose intolerance.
    Kaiser UB, Hegele RA.
    Am J Med Sci; 1991 Dec 06; 302(6):364-8. PubMed ID: 1772121
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