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 *

145 related articles for article (PubMed ID: 6851228)

  • 21. Postpartum coma and death due to carbamoyl-phosphate synthetase I deficiency.
    Wong LJ; Craigen WJ; O'Brien WE
    Ann Intern Med; 1994 Feb; 120(3):216-7. PubMed ID: 8273985
    [No Abstract]   [Full Text] [Related]  

  • 22. Ornithine aminotransferase deficiency: diagnostic difficulties in neonatal presentation.
    Cleary MA; Dorland L; de Koning TJ; Poll-The BT; Duran M; Mandell R; Shih VE; Berger R; Olpin SE; Besley GT
    J Inherit Metab Dis; 2005; 28(5):673-9. PubMed ID: 16151897
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Valproate-induced hyperammonemia.
    Batshaw ML; Brusilow SW
    Ann Neurol; 1982 Mar; 11(3):319-21. PubMed ID: 6807193
    [TBL] [Abstract][Full Text] [Related]  

  • 24. [Hyperammonemia].
    Arashima S
    Nihon Rinsho; 1978 May; Suppl():1352-3. PubMed ID: 691351
    [No Abstract]   [Full Text] [Related]  

  • 25. The activity of carbamoyl-phosphate synthetase I and ornithine carbamoyltransferase (OCT) in the intestine and screening for OCT deficiency in the rectal mucosa.
    Matsushima A; Orii T
    J Inherit Metab Dis; 1981; 4(2):83-4. PubMed ID: 6790859
    [No Abstract]   [Full Text] [Related]  

  • 26. [Prenatal diagnosis of carbamyl phosphate synthetase deficiency by fetal liver biopsy].
    Murotsuki J; Uehara S; Okamura K; Yajima A; Kikuchi M; Oura T; Miyabayashi S
    Nihon Sanka Fujinka Gakkai Zasshi; 1991 Dec; 43(12):1613-6. PubMed ID: 1744457
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Dysautonomia in an infant with secondary hyperammonemia due to propionyl coenzyme A carboxylase deficiency.
    Harris DJ; Yang BI; Wolf B; Snodgrass PJ
    Pediatrics; 1980 Jan; 65(1):107-10. PubMed ID: 7355003
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Carbamylphosphate synthetase-I deficiency in a newborn: survival after early diagnosis and therapy.
    Raghavan K; Chabra S; Mondkar J; Aiyar R; Ambani LM; Fernandez A
    Indian Pediatr; 1991 May; 28(5):551-4. PubMed ID: 1752685
    [No Abstract]   [Full Text] [Related]  

  • 29. Carbamyl phosphate synthetase and ornithine transcarbamylase activities in enzyme-deficient human liver measured by radiochromatography and correlated with outcome.
    Tuchman M; Tsai MY; Holzknecht RA; Brusilow SW
    Pediatr Res; 1989 Jul; 26(1):77-82. PubMed ID: 2771513
    [TBL] [Abstract][Full Text] [Related]  

  • 30. [Therapy of hyperammonemia in carbamyl phosphate synthase deficiency with peritoneal dialysis and venovenous hemofiltration].
    Lettgen B; Bonzel KE; Colombo JP; Fuchs B; Kordass U; Wendel K; Rascher W
    Monatsschr Kinderheilkd; 1991 Sep; 139(9):612-7. PubMed ID: 1745252
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Immunochemical analysis of carbamyl phosphate synthetase I and ornithine transcarbamylase deficient livers: elevated N-acetylglutamate level in a liver lacking carbamyl phosphate synthetase protein.
    Zhang W; Holzknecht RA; Butkowski RJ; Tuchman M
    Clin Invest Med; 1990 Aug; 13(4):183-8. PubMed ID: 2208834
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Survival after early treatment for carbamyl phosphate synthetase (CPS) I deficiency associated with increase of intramitochondrial CPS I.
    Zimmer KP; Naim HY; Koch HG; Colombo JP; Rossi R; Schmid KW; Deufel T; Ullrich K; Harms E
    Lancet; 1995 Dec; 346(8989):1530-1. PubMed ID: 7491050
    [TBL] [Abstract][Full Text] [Related]  

  • 33. [Urea cycle disorders].
    Tazawa Y
    Ryoikibetsu Shokogun Shirizu; 1995; (8):367-9. PubMed ID: 8581654
    [No Abstract]   [Full Text] [Related]  

  • 34. [Remarks on a clinical case of partial carbamyl phosphate synthetase deficiency].
    Gomirato G; Giaretto G; Bonomi A; Rossi E; Rovere A; Radeschi G; Crosato M
    Minerva Pediatr; 1989 Feb; 41(2):105-8. PubMed ID: 2739630
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Fetal liver biopsy for prenatal diagnosis of carbamoyl phosphate synthetase deficiency.
    Murotsuki J; Uehara S; Okamura K; Yajima A; Oura T; Miyabayashi S
    Am J Perinatol; 1994 Mar; 11(2):160-2. PubMed ID: 8198660
    [TBL] [Abstract][Full Text] [Related]  

  • 36. [Hyperammonemia: partial carbamyl phosphate synthetase deficiency].
    Szentpéteri J; Kovács J; Földes G
    Orv Hetil; 1982 Aug; 123(31):1923-6. PubMed ID: 7133689
    [No Abstract]   [Full Text] [Related]  

  • 37. Immunological evidence for a carbamylphosphate synthetase lesion resulting in the formation of enzyme with altered sub-unit size.
    Hoogenraad NJ; Weston HJ; Mackenzie N
    J Inherit Metab Dis; 1986; 9(4):367-73. PubMed ID: 3104674
    [TBL] [Abstract][Full Text] [Related]  

  • 38. [Neonatal hyperammonemia].
    Jaeken J; Devlieger H; Evens M; Casaer P; Eggermont E
    Tijdschr Kindergeneeskd; 1983 Jun; 51(3):101-4. PubMed ID: 6636106
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Detection of urea cycle enzymopathies in childhood.
    Trauner DA; Self TW
    Arch Neurol; 1984 Jul; 41(7):758-60. PubMed ID: 6743067
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Qualitative abnormality of liver argininosuccinate synthetase in a patient with citrullinemia.
    Matsuda Y; Tsuji A; Katunuma N
    Adv Exp Med Biol; 1982; 153():77-82. PubMed ID: 7164924
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.