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Journal Abstract Search

128 related items for PubMed ID: 5465716

  • 1. How to detect maple-syrup urine disease in newborn infants.
    Fogelson MH.
    Clin Pediatr (Phila); 1970 Sep; 9(9):538. PubMed ID: 5465716
    [No Abstract] [Full Text] [Related]

  • 2. Maple syrup urine disease: rapid prenatal diagnosis by enzyme assay.
    Wendel U, Rüdiger HW, Passarge E, Mikkelsen M.
    Humangenetik; 1973 Sep; 19(1):127-8. PubMed ID: 4725909
    [No Abstract] [Full Text] [Related]

  • 3. Diagnostic significance of amniotic fluid amino acids.
    O'Neill RT, Morrow G, Hammel D, Auerbach VH, Barness LA.
    Obstet Gynecol; 1971 Apr; 37(4):550-4. PubMed ID: 5547853
    [No Abstract] [Full Text] [Related]

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  • 5. Intermittent branched chain ketonuria (variant of maple syrup urine disease).
    Irwin WC, Martel SB, Goluboff N.
    Clin Biochem; 1971 Jun; 4(2):52-8. PubMed ID: 5128296
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  • 8. Biochemical studies on a variant of branched chain ketoaciduria in a 19-year-old female.
    Fischer MH, Gerritsen T.
    Pediatrics; 1971 Nov; 48(5):795-801. PubMed ID: 5125877
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  • 12. Heterozygote tests and genetic counseling in maple syrup urine disease: an application of Baye's theorem.
    Langenbeck U, Grimm T, Rüdiger HW, Passarge E.
    Humangenetik; 1975 Nov; 27(4):315-22. PubMed ID: 1150251
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  • 13. [Neonatal diagnosis of maple syrup urine disease and trial of exchange transfusion].
    Statter M, Ben-Zvi A, Russell A.
    Harefuah; 1976 Oct 01; 91(7):167-9. PubMed ID: 1002028
    [No Abstract] [Full Text] [Related]

  • 14. A rapid method for assay of branched-chain keto acid decarboxylation in cultured cells and its application to prenatal diagnosis of maple syrup urine disease.
    Fensom AH, Benson PF, Baker JE.
    Clin Chim Acta; 1978 Jul 01; 87(1):169-74. PubMed ID: 668138
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  • 15. A case of classical maple syrup urine disease "thiamine non-responsive".
    Wong PW, Justice P, Smith GF, Hsia DY.
    Clin Genet; 1972 Jul 01; 3(1):27-33. PubMed ID: 5066975
    [No Abstract] [Full Text] [Related]

  • 16. Recent developments in neonatal screening.
    Naylor EW.
    Semin Perinatol; 1985 Apr 01; 9(3):232-49. PubMed ID: 3832439
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  • 19. [Combined forms of metabolic errors detected in newborn infants].
    Tănase-Mogoş I, Ciortoloman H, Grigorescu G, Popescu M, Ankăr V.
    Physiologie; 1978 Apr 01; 15(4):239-43. PubMed ID: 106407
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