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Journal Abstract Search

105 related items for PubMed ID: 7235517

  • 1. [Severe neonatal type of citrullinemia. Difficulties to expose heterozygotic state. Advantage of prenatal diagnosis (author's transl)].
    Plasse M, Serre JC, Joannard A, Favier A, Grandgeorges D, Frappat P, Bost M.
    Ann Pediatr (Paris); 1980 Oct; 27(8):491-6. PubMed ID: 7235517
    [No Abstract] [Full Text] [Related]

  • 2. [Severe metabolic diseases in neonates. Diagnosis and treatment (author's transl)].
    Koepp P, Grüttner R.
    Klin Padiatr; 1975 Jan; 187(1):14-9. PubMed ID: 1168276
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  • 3. Severe neonatal citrullinaemia.
    Danks DM, Tippett P, Zentner G.
    Arch Dis Child; 1974 Jul; 49(7):579-81. PubMed ID: 4854268
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  • 6. Citrullinemia, report of a case, with studies on antenatal diagnosis.
    Roerdink FH, Gouw WL, Okken A, van der Blij JF, Luit-de Haan G, Hommes FA, Huisjes HJ.
    Pediatr Res; 1973 Nov; 7(11):863-9. PubMed ID: 4749002
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  • 11. A case of transient neonatal citrullinemia.
    Ohtake A, Takayanagi M, Ogura N, Nakajima H.
    Eur J Pediatr; 1983 Oct; 141(1):60-1. PubMed ID: 6641770
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  • 13. Carrier detection of urea cycle disorders.
    Ng WG, Oizumi J, Koch R, Shaw KN, McLaren J, Donnel GN, Carter M.
    Pediatrics; 1981 Sep; 68(3):448-52. PubMed ID: 7279481
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  • 14. Transient hyperammonemias in infants with and without organic acidemia.
    Nyhan WL, Rubio V, Jordá A, Grisolia S, Gutierez F, Canosa C.
    Adv Exp Med Biol; 1982 Sep; 153():331-8. PubMed ID: 7164908
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  • 18. [Early detection of hereditary metabolic disturbances (author's transl)].
    Pfändler U.
    Schweiz Rundsch Med Prax; 1975 Feb 18; 64(7):192-6. PubMed ID: 1167694
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  • 20. Citrullinemia: elevated serum citrulline levels in healthy siblings.
    Wick H, Brechbühler T, Girard J.
    Experientia; 1970 Aug 15; 26(8):823-4. PubMed ID: 5451998
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