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Journal Abstract Search

144 related items for PubMed ID: 7155666

  • 1. Elevated frequency of carriers for triosephosphate isomerase deficiency in newborn infants.
    Mohrenweiser HW, Fielek S.
    Pediatr Res; 1982 Nov; 16(11):960-3. PubMed ID: 7155666
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  • 2. Prevalence of partial deficiency of red cell triosephosphate isomerase in Germany--a study of 3000 people.
    Eber SW, Dünnwald M, Heinemann G, Hofstätter T, Weinmann HM, Belohradsky BH.
    Hum Genet; 1984 Nov; 67(3):336-9. PubMed ID: 6381286
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  • 3. Possibility of prenatal diagnosis of hereditary triose phosphate isomerase deficiency.
    Rosa R, Prehu MO, Calvin MC, Daffos F, Forestier F.
    Prenat Diagn; 1986 Nov; 6(3):231-4. PubMed ID: 3725742
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  • 4. The relationship of the -5, -8, and -24 variant alleles in African Americans to triosephosphate isomerase (TPI) enzyme activity and to TPI deficiency.
    Schneider A, Forman L, Westwood B, Yim C, Lin J, Singh S, Beutler E.
    Blood; 1998 Oct 15; 92(8):2959-62. PubMed ID: 9763583
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  • 5. Molecular analysis of a series of alleles in humans with reduced activity at the triosephosphate isomerase locus.
    Watanabe M, Zingg BC, Mohrenweiser HW.
    Am J Hum Genet; 1996 Feb 15; 58(2):308-16. PubMed ID: 8571957
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  • 6. Hereditary deficiency of triosephosphate isomerase in four unrelated families.
    Eber SW, Dünnwald M, Belohradsky BH, Bidlingmaier F, Schievelbein H, Weinmann HM, Krietsch KG.
    Eur J Clin Invest; 1979 Jun 15; 9(3):195-202. PubMed ID: 113220
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  • 7. Triosephosphate isomerase deficiency with hemolytic anemia and severe neuromuscular disease: familial and biochemical studies of a case found in Spain.
    Vives-Corrons JL, Rubinson-Skala H, Mateo M, Estella J, Feliu E, Dreyfus JC.
    Hum Genet; 1978 Jun 09; 42(2):171-80. PubMed ID: 669702
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  • 8. Triose phosphate isomerase deficiency: report of a family.
    Clark AC, Szobolotzky MA.
    Aust Paediatr J; 1986 May 09; 22(2):135-7. PubMed ID: 3729826
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  • 9. Hereditary triose phosphate isomerase deficiency: seven new homozygous cases.
    Rosa R, Prehu MO, Calvin MC, Badoual J, Alix D, Girod R.
    Hum Genet; 1985 May 09; 71(3):235-40. PubMed ID: 4065896
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  • 11. Triosephosphate isomerase deficiency: 2 new cases.
    Zanella A, Mariani M, Colombo MB, Borgna-Pignatti C, De Stefano P, Morgese G, Sirchia G.
    Scand J Haematol; 1985 May 09; 34(5):417-24. PubMed ID: 4012221
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  • 12. Prenatal diagnosis of a red-cell enzymopathy: triose phosphate isomerase deficiency.
    Bellingham AJ, Lestas AN, Williams LH, Nicolaides KH.
    Lancet; 1989 Aug 19; 2(8660):419-21. PubMed ID: 2569601
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  • 13. [Triosephosphate isomerase deficiency. Apropos of a new case].
    González Rodríguez MP, García Velázquez J, Reig del Moral C, Herrera Martín M, Hernández Martín H, Sánchez Martín S, Cuadrado Bello P.
    An Esp Pediatr; 1988 Sep 19; 29(3):251-3. PubMed ID: 2461674
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  • 14. Myopathy with altered mitochondria due to a triosephosphate isomerase (TPI) deficiency.
    Bardosi A, Eber SW, Hendrys M, Pekrun A.
    Acta Neuropathol; 1990 Sep 19; 79(4):387-94. PubMed ID: 2339591
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  • 15. [Triosephosphate isomerase deficiency. Familial survey and prenatal detection].
    Poinsot J, Alix D, Rosa R, Checoury A, Badoual J, Parent P, Castel Y.
    Arch Fr Pediatr; 1987 May 19; 44(5):365-8. PubMed ID: 3619568
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  • 16. Enhanced association of mutant triosephosphate isomerase to red cell membranes and to brain microtubules.
    Orosz F, Wágner G, Liliom K, Kovács J, Baróti K, Horányi M, Farkas T, Hollán S, Ovádi J.
    Proc Natl Acad Sci U S A; 2000 Feb 01; 97(3):1026-31. PubMed ID: 10655478
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