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Journal Abstract Search

192 related items for PubMed ID: 1745252

  • 1. [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
    [Abstract] [Full Text] [Related]

  • 2. [Comments on the contribution, Therapy of hyperammonemia in carbamylphosphate synthetase deficiency with peritoneal dialysis and venovenous hemofiltration, by B. Lettgen et al].
    Brockstedt M.
    Monatsschr Kinderheilkd; 1992 Jul; 140(7):431. PubMed ID: 1308100
    [No Abstract] [Full Text] [Related]

  • 3. 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]

  • 4. [Lethal neonatal deficiency of carbamyl phosphate synthetase (author's transl)].
    Plöchl E, Bachmann C, Stöllinger O, Colombo JP, Rassem T, Czihak G.
    Padiatr Padol; 1982 May; 17(2):371-82. PubMed ID: 7099689
    [Abstract] [Full Text] [Related]

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

  • 6. High-volume continuous venovenous hemofiltration as an effective therapy for acute management of inborn errors of metabolism in young children.
    Lai YC, Huang HP, Tsai IJ, Tsau YK.
    Blood Purif; 2007 May; 25(4):303-8. PubMed ID: 17643056
    [Abstract] [Full Text] [Related]

  • 7. Continuous venovenous haemofiltration in the acute treatment of inborn errors of metabolism.
    Falk MC, Knight JF, Roy LP, Wilcken B, Schell DN, O'Connell AJ, Gillis J.
    Pediatr Nephrol; 1994 Jun; 8(3):330-3. PubMed ID: 7917860
    [Abstract] [Full Text] [Related]

  • 8. [Carbamyl phosphate synthase deficiency: clinical symptoms, diagnosis and dietary-medicamentous treatment in the neonatal period and infancy].
    Hochreutener H, Issakainen J, Bachmann C, Baerlocher K.
    Helv Paediatr Acta; 1989 Jun; 43(5-6):493-505. PubMed ID: 2745145
    [Abstract] [Full Text] [Related]

  • 9. [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
    [Abstract] [Full Text] [Related]

  • 10. Prospective versus clinical diagnosis and therapy of acute neonatal hyperammonaemia in two sisters with carbamyl phosphate synthetase deficiency.
    Tuchman M, Mauer SM, Holzknecht RA, Summar ML, Vnencak-Jones CL.
    J Inherit Metab Dis; 1992 Feb; 15(2):269-77. PubMed ID: 1356172
    [Abstract] [Full Text] [Related]

  • 11. 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; 25(4):1257-65. PubMed ID: 19934086
    [Abstract] [Full Text] [Related]

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

  • 13. Ammonia detoxification by continuous venovenous haemofiltration in an infant with urea cycle defect.
    Chan WK, But WM, Law CW.
    Hong Kong Med J; 2002 Jun; 8(3):207-10. PubMed ID: 12055368
    [Abstract] [Full Text] [Related]

  • 14. [Hyperammonemia: partial carbamyl phosphate synthetase deficiency].
    Szentpéteri J, Kovács J, Földes G.
    Orv Hetil; 1982 Aug 01; 123(31):1923-6. PubMed ID: 7133689
    [No Abstract] [Full Text] [Related]

  • 15. A case of carbamylphosphate synthetase-I deficiency associated with secondary carnitine deficiency--L-carnitine treatment of CPS-I deficiency.
    Mori T, Tsuchiyama A, Nagai K, Nagao M, Oyanagi K, Tsugawa S.
    Eur J Pediatr; 1990 Jan 01; 149(4):272-4. PubMed ID: 2303075
    [Abstract] [Full Text] [Related]

  • 16. 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]

  • 17. [Pulmonary hemorrhages in newborn infants with inborn errors of the 1st 2 phases of the urea cycle].
    Plöchl E, Bachmann C.
    Monatsschr Kinderheilkd; 1983 Oct 01; 131(10):714-5. PubMed ID: 6646142
    [Abstract] [Full Text] [Related]

  • 18. [Hyperammonemia].
    Arashima S.
    Nihon Rinsho; 1978 May 01; Suppl():1352-3. PubMed ID: 691351
    [No Abstract] [Full Text] [Related]

  • 19. [Carbamyl phosphate synthetase I deficiency].
    Hoshide R.
    Ryoikibetsu Shokogun Shirizu; 1998 May 01; (18 Pt 1):167-9. PubMed ID: 9590018
    [No Abstract] [Full Text] [Related]

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