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Journal Abstract Search

212 related items for PubMed ID: 8244340

  • 41.
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  • 42. [Glycolytic enzyme defects and neurodegeneration].
    Hollán S, Vécsei L, Karg E, Németh I, Horanyi M, Inselt-Kovács M, Farkas T.
    C R Seances Soc Biol Fil; 1998; 192(5):929-45. PubMed ID: 9871806
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  • 43. [Congenital hemolytic anemia due to triosephosphate isomerase deficiency].
    Freycon F, Lauras B, Bovier-Lapierre F, Goddon R.
    Pediatrie; 1975; 30(1):55-65. PubMed ID: 1129019
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  • 44. Triosephosphate isomerase activity-deficient mice show haemolytic anaemia in homozygous condition.
    Pretsch W.
    Genet Res (Camb); 2009 Feb; 91(1):1-4. PubMed ID: 19220926
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  • 47. Triosephosphate isomerase deficiency: haemolytic anaemia, myopathy with altered mitochondria and mental retardation due to a new variant with accelerated enzyme catabolism and diminished specific activity.
    Eber SW, Pekrun A, Bardosi A, Gahr M, Krietsch WK, Krüger J, Matthei R, Schröter W.
    Eur J Pediatr; 1991 Sep; 150(11):761-6. PubMed ID: 1959537
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  • 48. Quantification of Dihydroxyacetone Phosphate (DHAP) in Human Red Blood Cells by HPLC-TripleTOF 5600™ Mass Spectrometer.
    Deng S, Scott D, Myers D, Garg U.
    Methods Mol Biol; 2016 Sep; 1378():81-6. PubMed ID: 26602120
    [Abstract] [Full Text] [Related]

  • 49. Myopathy with altered mitochondria due to a triosephosphate isomerase (TPI) deficiency.
    Bardosi A, Eber SW, Hendrys M, Pekrun A.
    Acta Neuropathol; 1990 Sep; 79(4):387-94. PubMed ID: 2339591
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  • 50. 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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  • 53. Itavastatin and resveratrol increase triosephosphate isomerase protein in a newly identified variant of TPI deficiency.
    VanDemark AP, Hrizo SL, Eicher SL, Kowalski J, Myers TD, Pfeifer MR, Riley KN, Koeberl DD, Palladino MJ.
    Dis Model Mech; 2022 May 01; 15(5):. PubMed ID: 35315486
    [Abstract] [Full Text] [Related]

  • 54. 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 01; 9(3):195-202. PubMed ID: 113220
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  • 57. Degradation of functional triose phosphate isomerase protein underlies sugarkill pathology.
    Seigle JL, Celotto AM, Palladino MJ.
    Genetics; 2008 Jun 01; 179(2):855-62. PubMed ID: 18458110
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  • 58.
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  • 59. Origin of human triosephosphate isomerase isozymes: further evidence for the single structural locus hypothesis with Japanese variants.
    Asakawa J, Iida S.
    Hum Genet; 1985 Jun 01; 71(1):22-6. PubMed ID: 3861565
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  • 60.
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