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.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

325 related items for PubMed ID: 15880727

  • 21.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 22.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 23.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 24. 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]

  • 25.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 26.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 27. Simple method for detection of mutations causing hereditary fructose intolerance.
    Kullberg-Lindh C, Hannoun C, Lindh M.
    J Inherit Metab Dis; 2002 Nov; 25(7):571-5. PubMed ID: 12638940
    [Abstract] [Full Text] [Related]

  • 28. Molecular and clinical findings of Turkish patients with hereditary fructose intolerance.
    Gunduz M, Ünal-Uzun Ö, Koç N, Ceylaner S, Özaydın E, Kasapkara ÇS.
    J Pediatr Endocrinol Metab; 2021 Aug 26; 34(8):1017-1022. PubMed ID: 34162028
    [Abstract] [Full Text] [Related]

  • 29. Identification of a novel mutation in the ALDOB gene in hereditary fructose intolerance.
    Beyzaei Z, Ezgu F, Imanieh MH, Haghighat M, Dehghani SM, Honar N, Geramizadeh B.
    J Pediatr Endocrinol Metab; 2023 Mar 28; 36(3):331-334. PubMed ID: 36659819
    [Abstract] [Full Text] [Related]

  • 30.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 31.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 32. [Hereditary fructose intolerance].
    Lopes AI, Almeida AG, Costa AE, Costa A, Leite M.
    Acta Med Port; 1998 Dec 28; 11(12):1121-5. PubMed ID: 10192989
    [Abstract] [Full Text] [Related]

  • 33.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 34. 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 28; 72(1):201-13. PubMed ID: 6348085
    [Abstract] [Full Text] [Related]

  • 35. 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 28; 33(9):786-8. PubMed ID: 8880583
    [Abstract] [Full Text] [Related]

  • 36. Clinical and genetic analysis for a Chinese family with hereditary fructose intolerance.
    Chi ZN, Hong J, Yang J, Zhang HJ, Dai M, Cui B, Zhang Y, Gu WQ, Zhang YF, Liu QR, Wang WQ, Li XY, Ning G.
    Endocrine; 2007 Aug 28; 32(1):122-6. PubMed ID: 17955389
    [Abstract] [Full Text] [Related]

  • 37. Aldolase B mutations in Turkish families from central Anatolia.
    Karabulut HG, Halsall D, Sayin BD, Tonyukuk V, Cox TM, Bökesoy I.
    Genet Couns; 2006 Aug 28; 17(4):457-60. PubMed ID: 17375533
    [No Abstract] [Full Text] [Related]

  • 38.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 39.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 40. Alteration of substrate specificity by a naturally-occurring aldolase B mutation (Ala337-->Val) in fructose intolerance.
    Rellos P, Ali M, Vidailhet M, Sygusch J, Cox TM.
    Biochem J; 1999 May 15; 340 ( Pt 1)(Pt 1):321-7. PubMed ID: 10229688
    [Abstract] [Full Text] [Related]

    Page: [Previous] [Next] [New Search]
    of 17.