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Journal Abstract Search

174 related items for PubMed ID: 1524867

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  • 3. Null alleles of the aldolase B gene in patients with hereditary fructose intolerance.
    Ali M, Tunçman G, Cross NC, Vidailhet M, Bökesoy I, Gitzelmann R, Cox TM.
    J Med Genet; 1994 Jun; 31(6):499-503. PubMed ID: 8071980
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  • 6. 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
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  • 8. 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
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  • 10. A partially active mutant aldolase B from a patient with hereditary fructose intolerance.
    Brooks CC, Tolan DR.
    FASEB J; 1994 Jan; 8(1):107-13. PubMed ID: 8299883
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  • 11. 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
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  • 12. 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
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  • 15. 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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  • 16. Partial aldolase B gene deletions in hereditary fructose intolerance.
    Cross NC, Cox TM.
    Am J Hum Genet; 1990 Jul 17; 47(1):101-6. PubMed ID: 2349937
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  • 17. Hereditary fructose intolerance.
    Ali M, Rellos P, Cox TM.
    J Med Genet; 1998 May 17; 35(5):353-65. PubMed ID: 9610797
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  • 18. Simple method for detection of mutations causing hereditary fructose intolerance.
    Kullberg-Lindh C, Hannoun C, Lindh M.
    J Inherit Metab Dis; 2002 Nov 17; 25(7):571-5. PubMed ID: 12638940
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  • 19. Case report: heterogeneity of aldolase B in hereditary fructose intolerance.
    Kaiser UB, Hegele RA.
    Am J Med Sci; 1991 Dec 17; 302(6):364-8. PubMed ID: 1772121
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  • 20. Semi-automated, reverse-hybridization detection of multiple mutations causing hereditary fructose intolerance.
    Kriegshäuser G, Halsall D, Rauscher B, Oberkanins C.
    Mol Cell Probes; 2007 Jun 17; 21(3):226-8. PubMed ID: 17292585
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