These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

139 related articles for article (PubMed ID: 3919380)

  • 1. Prenatal diagnosis of pyruvate carboxylase deficiency.
    Robinson BH; Toone JR; Benedict RP; Dimmick JE; Oei J; Applegarth DA
    Prenat Diagn; 1985; 5(1):67-71. PubMed ID: 3919380
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Citrullinemia: prenatal diagnosis of an affected fetus.
    Fleisher LD; Harris CJ; Mitchell DA; Nadler HL
    Am J Hum Genet; 1983 Jan; 35(1):85-90. PubMed ID: 6823975
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 4(2):113-8. PubMed ID: 6739433
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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; 116(1):111-5. PubMed ID: 7318170
    [No Abstract]   [Full Text] [Related]  

  • 5. Citrullinaemia: the possibility of prenatal diagnosis.
    Christensen E; Brandt NJ; Philip J; Kennaway NG
    J Inherit Metab Dis; 1980; 3(3):73-5. PubMed ID: 6775139
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Citrulline in amniotic fluid and the prenatal diagnosis of citrullinemia.
    Kamoun P; Parvy P; Pham Dinh D; Boué J; Cathelineau L
    Prenat Diagn; 1983 Jan; 3(1):53-6. PubMed ID: 6844264
    [No Abstract]   [Full Text] [Related]  

  • 7. Use of amniotic fluid amino acids in prenatal testing for argininosuccinic aciduria and citrullinaemia.
    Mandell R; Packman S; Laframboise R; Golbus MS; Schmidt K; Workman L; Saudubray JM; Shih VE
    Prenat Diagn; 1996 May; 16(5):419-24. PubMed ID: 8843999
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Prenatal diagnosis of pyruvate carboxylase deficiency.
    Marsac C; Augereau C; Feldman G; Wolf B; Hansen TL; Berger R
    Clin Chim Acta; 1982 Feb; 119(1-2):121-7. PubMed ID: 6800673
    [No Abstract]   [Full Text] [Related]  

  • 9. 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; 116(1):1-7. PubMed ID: 7318168
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Prenatal diagnosis of citrullinaemia: review of a 10-year experience including recent use of DNA analysis.
    Northrup H; Beaudet AL; O'Brien WE
    Prenat Diagn; 1990 Dec; 10(12):771-9. PubMed ID: 2075179
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Improved standards for prenatal diagnosis of citrullinemia.
    Miller MJ; Soler-Alfonso CR; Grund JE; Fang P; Sun Q; Elsea SH; Sutton VR
    Mol Genet Metab; 2014 Jul; 112(3):205-9. PubMed ID: 24889030
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Prenatal exclusion of the HHH syndrome.
    Gray RG; Green A; Hall S; McKeown C
    Prenat Diagn; 1995 May; 15(5):474-6. PubMed ID: 7644438
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Prenatal diagnosis of bovine citrullinaemia.
    Healy P; Dennis J; Rawlinson R; Andersson L
    Res Vet Sci; 1993 Nov; 55(3):271-4. PubMed ID: 8284487
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Pyruvate carboxylase deficiencies: complementation studies between "French" and "American" phenotypes in cultured fibroblasts.
    Augereau C; Pham Dinh D; Moncion A; Marsac C; Saudubray JM; Robinson BH
    J Inherit Metab Dis; 1985; 8(2):59-62. PubMed ID: 3939532
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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; 5(4):299-301. PubMed ID: 4048069
    [TBL] [Abstract][Full Text] [Related]  

  • 16. The molecular basis for the two different clinical presentations of classical pyruvate carboxylase deficiency.
    Robinson BH; Oei J; Sherwood WG; Applegarth D; Wong L; Haworth J; Goodyer P; Casey R; Zaleski LA
    Am J Hum Genet; 1984 Mar; 36(2):283-94. PubMed ID: 6424438
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Late-onset holocarboxylase synthetase-deficiency: pre- and post-natal diagnosis and evaluation of effectiveness of antenatal biotin therapy.
    Suormala T; Fowler B; Jakobs C; Duran M; Lehnert W; Raab K; Wick H; Baumgartner ER
    Eur J Pediatr; 1998 Jul; 157(7):570-5. PubMed ID: 9686819
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Attempt at antenatal diagnosis of argininosuccinic aciduria].
    Dhondt JL; Farriaux JP; Pollitt RJ; Vamos E; Richard P; Blanckaert D; Delecour M; Monnier JC; Fontaine G
    Ann Genet; 1976 Mar; 19(1):23-7. PubMed ID: 1084118
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Pitfalls in the prenatal diagnosis of propionic acidemia.
    Buchanan PD; Kahler SG; Sweetman L; Nyhan WL
    Clin Genet; 1980 Sep; 18(3):177-83. PubMed ID: 6934053
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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; 183(2):125-33. PubMed ID: 2791302
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.