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Journal Abstract Search

152 related items for PubMed ID: 1356172

  • 21.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 22. 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 09; 346(8989):1530-1. PubMed ID: 7491050
    [Abstract] [Full Text] [Related]

  • 23. [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 09; 43(12):1613-6. PubMed ID: 1744457
    [Abstract] [Full Text] [Related]

  • 24. Prospective prevention of neonatal hyperammonaemia in argininosuccinic acidura by arginine therapy.
    Donn SM, Thoene JG.
    J Inherit Metab Dis; 1985 Dec 09; 8(1):18-20. PubMed ID: 3921755
    [Abstract] [Full Text] [Related]

  • 25. [Carbamyl phosphate synthetase I deficiency].
    Ohtake A, Mori M.
    Tanpakushitsu Kakusan Koso; 1988 Apr 09; 33(5):497-9. PubMed ID: 3270854
    [No Abstract] [Full Text] [Related]

  • 26. Sodium benzoate and arginine: alternative pathway therapy in inborn errors of urea synthesis.
    Batshaw ML.
    Prog Clin Biol Res; 1983 Apr 09; 127():69-83. PubMed ID: 6889404
    [No Abstract] [Full Text] [Related]

  • 27. Identification of benzoylcarnitine in the urine of a patient of hyperammonemia.
    Sakuma T, Asai K, Ichiki T, Sugiyama N, Kidouchi K, Wada Y.
    Tohoku J Exp Med; 1989 Oct 09; 159(2):147-51. PubMed ID: 2609332
    [Abstract] [Full Text] [Related]

  • 28. A lethal neonatal variant of carbamoyl-phosphate synthetase deficiency in combination with an intermediate activity of L-ornithine: 2-oxoglutarate amino-transferase.
    van der Heiden C, Beemer FA, van Dijk HA, Desplanque J, Gerards LJ.
    Clin Genet; 1983 May 09; 23(5):363-8. PubMed ID: 6851228
    [Abstract] [Full Text] [Related]

  • 29. Severe neonatal deficiency of carbamylphosphate synthetase.
    Lambotte C, Adam A, Van Der Hofstadt J, Dodinval-Versie J, Gielen J.
    Acta Paediatr Belg; 1977 May 09; 30(3):151-5. PubMed ID: 204150
    [No Abstract] [Full Text] [Related]

  • 30. [Cerebral edema with hyperammonemia in valpromide poisoning. Manifestation in an adult, of a partial deficit in type I carbamylphosphate synthetase].
    Bourrier P, Varache N, Alquier P, Rabier D, Kamoun P, Lorre G, Alhayek G.
    Presse Med; 1988 Nov 05; 17(39):2063-6. PubMed ID: 2974563
    [Abstract] [Full Text] [Related]

  • 31. [Neonatal hyperammonemia].
    Jaeken J, Devlieger H, Evens M, Casaer P, Eggermont E.
    Tijdschr Kindergeneeskd; 1983 Jun 05; 51(3):101-4. PubMed ID: 6636106
    [Abstract] [Full Text] [Related]

  • 32. Treatment of inborn errors of urea synthesis: activation of alternative pathways of waste nitrogen synthesis and excretion.
    Batshaw ML, Brusilow S, Waber L, Blom W, Brubakk AM, Burton BK, Cann HM, Kerr D, Mamunes P, Matalon R, Myerberg D, Schafer IA.
    N Engl J Med; 1982 Jun 10; 306(23):1387-92. PubMed ID: 7078580
    [Abstract] [Full Text] [Related]

  • 33. Postpartum coma and death due to carbamoyl-phosphate synthetase I deficiency.
    Wong LJ, Craigen WJ, O'Brien WE.
    Ann Intern Med; 1994 Feb 01; 120(3):216-7. PubMed ID: 8273985
    [No Abstract] [Full Text] [Related]

  • 34. Treatment of urea cycle disorders.
    Batshaw ML, Monahan PS.
    Enzyme; 1987 Feb 01; 38(1-4):242-50. PubMed ID: 3326732
    [Abstract] [Full Text] [Related]

  • 35. Continuous venovenous haemodialysis (CVVHD) and continuous peritoneal dialysis (CPD) in the acute management of 21 children with inborn errors of metabolism.
    Arbeiter AK, Kranz B, Wingen AM, Bonzel KE, Dohna-Schwake C, Hanssler L, Neudorf U, Hoyer PF, Büscher R.
    Nephrol Dial Transplant; 2010 Apr 01; 25(4):1257-65. PubMed ID: 19934086
    [Abstract] [Full Text] [Related]

  • 36. A carbamylphosphate synthetase deficiency with no detectable immunoreactive enzyme and no translatable mRNA.
    Graf L, McIntyre P, Hoogenraad N, Brown G, Haan EA.
    J Inherit Metab Dis; 1984 Apr 01; 7(3):104-6. PubMed ID: 6438391
    [Abstract] [Full Text] [Related]

  • 37. 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 01; 11(2):160-2. PubMed ID: 8198660
    [Abstract] [Full Text] [Related]

  • 38. Inborn errors of the urea cycle.
    Walter JH, Leonard JV.
    Br J Hosp Med; 1987 Sep 01; 38(3):176-83. PubMed ID: 3315071
    [Abstract] [Full Text] [Related]

  • 39. Carbamyl phosphate synthetase deficiency and postpartum hyperammonemia.
    Kotani Y, Shiota M, Umemoto M, Tsuritani M, Hoshiai H.
    Am J Obstet Gynecol; 2010 Jul 01; 203(1):e10-1. PubMed ID: 20471629
    [Abstract] [Full Text] [Related]

  • 40. Efficacy of peritoneal dialysis in neonates presenting with hyperammonaemia due to urea cycle defects and organic acidaemia.
    Celik M, Akdeniz O, Ozgun N.
    Nephrology (Carlton); 2019 Mar 01; 24(3):330-335. PubMed ID: 29356227
    [Abstract] [Full Text] [Related]

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