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Journal Abstract Search

141 related items for PubMed ID: 7318170

  • 1. Improved method for the antenatal diagnosis of citrullinemia.
    Cathelineau L, Pham Dinh D, Boué J, Saudubray JM, Farriaux JP, Kamoun P.
    Clin Chim Acta; 1981 Oct 08; 116(1):111-5. PubMed ID: 7318170
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  • 3. Prenatal diagnosis of citrullinemia: elevated levels of citrulline in the amniotic fluid in the three affected pregnancies.
    Kleijer WJ, Blom W, Huijmans JG, Mooyman MC, Berger R, Niermeijer MF.
    Prenat Diagn; 1984 Oct 08; 4(2):113-8. PubMed ID: 6739433
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  • 4. Variation in argininosuccinate synthetase activity in amniotic fluid cell cultures: implications for prenatal diagnosis of citrullinemia.
    Jacoby LB, Shih VE, Struckmeyer C, Niermeijer MF, Boué J.
    Clin Chim Acta; 1981 Oct 08; 116(1):1-7. PubMed ID: 7318168
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  • 6. Exclusion of citrullinaemia in the first trimester of pregnancy by direct assay of argininosuccinate synthetase in chorionic villi.
    Christensen E, Brandt NJ, Philip J, Bang J.
    Prenat Diagn; 1985 Oct 08; 5(4):299-301. PubMed ID: 4048069
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  • 11. 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 08; 7(11):863-9. PubMed ID: 4749002
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  • 13. Citrullinemia, argininosuccinate synthetase deficiency. Repository identification No. GM-1044.
    Spector E, Kennaway N, Punnett H, Greene AE, Coriell LL.
    Cytogenet Cell Genet; 1977 Nov 08; 19(1):51-52. PubMed ID: 891263
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  • 14. Detection of kinetically abnormal argininosuccinate synthase in neonatal citrullinemia by conversion of citrulline to arginine in intact fibroblasts.
    Ben-Yoseph Y, Mitchell DA.
    Clin Chim Acta; 1989 Aug 15; 183(2):125-33. PubMed ID: 2791302
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  • 16. Improving the prenatal diagnosis of citrullinemia using citrulline/ornithine+arginine ratio in amniotic fluid.
    Chadefaux-Vekemans B, Rabier D, Chabli A, Blanc A, Aupetit J, Bardet J, Kamoun P.
    Prenat Diagn; 2002 Jun 15; 22(6):456-8. PubMed ID: 12116302
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  • 19. [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 15; 27(8):491-6. PubMed ID: 7235517
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