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PUBMED FOR HANDHELDS

Journal Abstract Search


159 related items for PubMed ID: 1129019

  • 21. 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
    [Abstract] [Full Text] [Related]

  • 22. Hemolytic anemia and progressive neurologic impairment: think about triosephosphate isomerase deficiency.
    Aissa K, Kamoun F, Sfaihi L, Ghedira ES, Aloulou H, Kamoun T, Pissard S, Hachicha M.
    Fetal Pediatr Pathol; 2014 Aug 19; 33(4):234-8. PubMed ID: 24840153
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  • 23. Prenatal diagnosis of triose phosphate isomerase deficiency.
    Bellingham AJ, Lestas AN.
    Lancet; 1990 Jan 27; 335(8683):230. PubMed ID: 1967698
    [No Abstract] [Full Text] [Related]

  • 24. [Congenital hemolytic anemia associated with phosphoglycerate kinase deficiency in erythrocytes, polynuclear cells and lymphocytes].
    Cartier P, Habibi B, Leroux JP, Marchand JC.
    Nouv Rev Fr Hematol; 1971 Jan 27; 11(4):565-78. PubMed ID: 4257431
    [No Abstract] [Full Text] [Related]

  • 25. Occurrence of defective hexosephosphate isomerization in human erythrocytes and leukocytes.
    Paglia DE, Holland P, Baughan MA, Valentine WN.
    N Engl J Med; 1969 Jan 09; 280(2):66-71. PubMed ID: 5782480
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  • 29. Myopathy with altered mitochondria due to a triosephosphate isomerase (TPI) deficiency.
    Bardosi A, Eber SW, Hendrys M, Pekrun A.
    Acta Neuropathol; 1990 Jan 09; 79(4):387-94. PubMed ID: 2339591
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  • 31. Congenital non-spherocytic haemolytic anaemias.
    Zanella A, Colombo MB, Rossi F, Merati G, Sirchia G.
    Haematologica; 1989 Jan 09; 74(4):387-96. PubMed ID: 2551797
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  • 32. [Erythrocyte enzyme defects and their clinical significance (author's transl)].
    Schröter W.
    Monatsschr Kinderheilkd; 1981 Aug 09; 129(8):432-43. PubMed ID: 6116182
    [No Abstract] [Full Text] [Related]

  • 33. Diminished blood levels of reduced glutathione and alpha-tocopherol in two triosephosphate isomerase-deficient brothers.
    Karg E, Németh I, Horányi M, Pintér S, Vécsei L, Hollán S.
    Blood Cells Mol Dis; 2000 Feb 09; 26(1):91-100. PubMed ID: 10772880
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  • 34. 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 Feb 09; 67(3):336-9. PubMed ID: 6381286
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  • 37. [Deficiency of red cell glucose-6-phosphate-dehydrogenase due to a slow variant in a French family. Relationship with the Gd (-) Seattle variant (author's transl)].
    Kahn A, Boivin P, Lagneau J, Cruveiller J.
    Nouv Rev Fr Hematol; 1973 Feb 09; 13(2):163-71. PubMed ID: 4270706
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  • 38. [Glucosephosphate dehydrogenase deficiency in erythrocytes and leukocytes of patients with congenital nonspherocytic hemolytic anemia and favism].
    Jabłońska-Skwiecińska E, Staniszewska K.
    Pol Tyg Lek; 1988 Feb 15; 43(7):207-9. PubMed ID: 3405890
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  • 39. [Red cell enzyme deficiencies - clinical manifestation and pathophysiology (author's transl)].
    Gahr M.
    Monatsschr Kinderheilkd; 1981 Aug 15; 129(8):444-53. PubMed ID: 6116183
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  • 40. Hereditary triosephosphate isomerase (TPI) deficiency: two severely affected brothers one with and one without neurological symptoms.
    Hollán S, Fujii H, Hirono A, Hirono K, Karro H, Miwa S, Harsányi V, Gyódi E, Inselt-Kovács M.
    Hum Genet; 1993 Nov 15; 92(5):486-90. PubMed ID: 8244340
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