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Journal Abstract Search

169 related items for PubMed ID: 18338235

  • 21. Partial N-acetylglutamate synthetase deficiency in a 13-year-old girl: diagnosis and response to treatment with N-carbamylglutamate.
    Plecko B, Erwa W, Wermuth B.
    Eur J Pediatr; 1998 Dec; 157(12):996-8. PubMed ID: 9877039
    [Abstract] [Full Text] [Related]

  • 22. Hyperammonaemia as a cause of psychosis in an adolescent.
    Bélanger-Quintana A, Martínez-Pardo M, García MJ, Wermuth B, Torres J, Pallarés E, Ugarte M.
    Eur J Pediatr; 2003 Nov; 162(11):773-5. PubMed ID: 12942317
    [Abstract] [Full Text] [Related]

  • 23. Long-term N-carbamylglutamate treatment of hyperammonemia in patients with classic organic acidemias.
    Kiykim E, Oguz O, Duman C, Zubarioglu T, Cansever MS, Zeybek ACA.
    Mol Genet Metab Rep; 2021 Mar; 26():100715. PubMed ID: 33552909
    [Abstract] [Full Text] [Related]

  • 24. [N-carbamyl glutamate treatment in hyperammoniemia decompensated propionic acidaemia].
    Fernández de Miguel S, Gimeno Díaz de Atauri A, Torres Peral R, Fernández Carrión F, Serrano Ayestarán O.
    An Pediatr (Barc); 2009 Dec; 71(6):579-80. PubMed ID: 19850540
    [No Abstract] [Full Text] [Related]

  • 25. Ammonia clearance with haemofiltration in adults with liver disease.
    Slack AJ, Auzinger G, Willars C, Dew T, Musto R, Corsilli D, Sherwood R, Wendon JA, Bernal W.
    Liver Int; 2014 Jan; 34(1):42-8. PubMed ID: 23786538
    [Abstract] [Full Text] [Related]

  • 26. Therapeutic effect of N-carbamylglutamate in CPS1 deficiency.
    Sugiyama Y, Shimura M, Ogawa-Tominaga M, Ebihara T, Kinouchi Y, Isozaki K, Matsuhashi T, Tajika M, Fushimi T, Ichimoto K, Matsunaga A, Ishida T, Mizutani K, Tsuruoka T, Murayama K.
    Mol Genet Metab Rep; 2020 Sep; 24():100622. PubMed ID: 32670798
    [Abstract] [Full Text] [Related]

  • 27. Overnight glucose infusion suppresses renal ammoniagenesis and reduces hyperammonaemia induced by a simulated bleed in cirrhotic patients.
    Mpabanzi L, Deutz N, Hayes PC, Dejong CH, Olde Damink SW, Jalan R.
    Aliment Pharmacol Ther; 2012 Apr; 35(8):921-8. PubMed ID: 22360430
    [Abstract] [Full Text] [Related]

  • 28. The efficacy of Carbamylglutamate impacts the nutritional management of patients with N-Acetylglutamate synthase deficiency.
    Singh RH, Bourdages MH, Kurtz A, MacLoed E, Norman C, Ratko S, van Calcar SC, Kenneson A.
    Orphanet J Rare Dis; 2024 Apr 18; 19(1):168. PubMed ID: 38637895
    [Abstract] [Full Text] [Related]

  • 29. Insulin-resistant hyperglycaemia complicating neonatal onset of methylmalonic and propionic acidaemias.
    Filippi L, Gozzini E, Cavicchi C, Morrone A, Fiorini P, Donzelli G, Malvagia S, la Marca G.
    J Inherit Metab Dis; 2009 Dec 18; 32 Suppl 1():S179-86. PubMed ID: 19588269
    [Abstract] [Full Text] [Related]

  • 30. Severe renal failure and hyperammonemia in a newborn with propionic acidemia: effects of treatment on the clinical course.
    Kasapkara CS, Akar M, Yürük Yıldırım ZN, Tüzün H, Kanar B, Ozbek MN.
    Ren Fail; 2014 Apr 18; 36(3):451-2. PubMed ID: 24329397
    [Abstract] [Full Text] [Related]

  • 31. A trial with N-carbamylglutamate may not detect all patients with NAGS deficiency and neonatal onset.
    Nordenström A, Halldin M, Hallberg B, Alm J.
    J Inherit Metab Dis; 2007 Jun 18; 30(3):400. PubMed ID: 17510757
    [Abstract] [Full Text] [Related]

  • 32. The first use of N-carbamylglutamate in a patient with decompensated maple syrup urine disease.
    Kalkan Ucar S, Coker M, Habif S, Saz EU, Karapinar B, Ucar H, Kitis O, Duran M.
    Metab Brain Dis; 2009 Sep 18; 24(3):409-14. PubMed ID: 19688253
    [Abstract] [Full Text] [Related]

  • 33. Presentation and management of N-acetylglutamate synthase deficiency: a review of the literature.
    Kenneson A, Singh RH.
    Orphanet J Rare Dis; 2020 Oct 09; 15(1):279. PubMed ID: 33036647
    [Abstract] [Full Text] [Related]

  • 34. N-acetylglutamate synthetase deficiency: diagnosis, management and follow-up of a rare disorder of ammonia detoxication.
    Schubiger G, Bachmann C, Barben P, Colombo JP, Tönz O, Schüpbach D.
    Eur J Pediatr; 1991 Mar 09; 150(5):353-6. PubMed ID: 2044610
    [Abstract] [Full Text] [Related]

  • 35. Hyperammonaemia in Neonates and Young Children: Potential Metabolic Causes, Diagnostic Approaches and Clinical Consequences.
    Giva S, Finnegan J, Ihidero P, Maguire G, Power B, Knerr I, Monavari A.
    Ir Med J; 2019 Jan 15; 112(1):858. PubMed ID: 30719899
    [Abstract] [Full Text] [Related]

  • 36. Urea cycle disorders.
    Leonard JV, Morris AA.
    Semin Neonatol; 2002 Feb 15; 7(1):27-35. PubMed ID: 12069536
    [Abstract] [Full Text] [Related]

  • 37. The relationship of plasma glutamine to ammonium and of glycine to acid-base balance in propionic acidaemia.
    Al-Hassnan ZN, Boyadjiev SA, Praphanphoj V, Hamosh A, Braverman NE, Thomas GH, Geraghty MT.
    J Inherit Metab Dis; 2003 Feb 15; 26(1):89-91. PubMed ID: 12872849
    [Abstract] [Full Text] [Related]

  • 38. Continuous hemofiltration in the control of neonatal hyperammonemia: a 10-year experience.
    Westrope C, Morris K, Burford D, Morrison G.
    Pediatr Nephrol; 2010 Sep 15; 25(9):1725-30. PubMed ID: 20495829
    [Abstract] [Full Text] [Related]

  • 39. Treatment of a neonate with propionic acidaemia and severe hyperammonaemia by peritoneal dialysis.
    Robert MF, Schultz DJ, Wolf B, Cochran WD, Schwartz AL.
    Arch Dis Child; 1979 Dec 15; 54(12):962-5. PubMed ID: 533302
    [Abstract] [Full Text] [Related]

  • 40.
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    [No Abstract] [Full Text] [Related]

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