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Volumn 21, Issue 2, 2007, Pages 215-218

Transient hyperammonemia due to urea cycle enzyme deficiency in Irish Wolfhounds

Author keywords

Amino acid; Citrulline; Congenital defect; Inborn error of metabolism

Indexed keywords

UREA;

EID: 34047160992     PISSN: 08916640     EISSN: None     Source Type: Journal    
DOI: 10.1892/0891-6640(2007)21[215:THDTUC]2.0.CO;2     Document Type: Article
Times cited : (22)

References (11)
  • 1
    • 0019985019 scopus 로고
    • Arterial and venous ammonia concentrations in the diagnosis of canine hepato-encephalopathy
    • Rothuizen J, van den Ingh TS. Arterial and venous ammonia concentrations in the diagnosis of canine hepato-encephalopathy. Res Vet Sci 1982;33:17-21.
    • (1982) Res Vet Sci , vol.33 , pp. 17-21
    • Rothuizen, J.1    van den Ingh, T.S.2
  • 2
    • 0028902062 scopus 로고
    • Hepatic encephalopathy: Clinical signs, pathogenesis, and treatment
    • Taboada J, Dimski DS. Hepatic encephalopathy: Clinical signs, pathogenesis, and treatment. Vet Clin North Am Small Anim Pract 1995;25:337-355.
    • (1995) Vet Clin North Am Small Anim Pract , vol.25 , pp. 337-355
    • Taboada, J.1    Dimski, D.S.2
  • 3
    • 1542288753 scopus 로고    scopus 로고
    • Ultrasonographic findings in dogs with hyperammonemia: 90 cases (2000-2002)
    • Szatmari V, Rothuizen J, van den Ingh TS, et al. Ultrasonographic findings in dogs with hyperammonemia: 90 cases (2000-2002). J Am Vet Med Assoc 2004;224:717-727.
    • (2004) J Am Vet Med Assoc , vol.224 , pp. 717-727
    • Szatmari, V.1    Rothuizen, J.2    van den Ingh, T.S.3
  • 4
    • 0032337559 scopus 로고    scopus 로고
    • Inborn errors of metabolism in infancy: A guide to diagnosis
    • Burton BK. Inborn errors of metabolism in infancy: A guide to diagnosis. Pediatrics 1998;102:E69.
    • (1998) Pediatrics , vol.102
    • Burton, B.K.1
  • 5
    • 0032493123 scopus 로고    scopus 로고
    • Hyperinsulinism and hyperammonemia in infants with regulatory mutations of the glutamate dehydrogenase gene
    • Stanley CA, Lieu YK, Hsu BY, et al. Hyperinsulinism and hyperammonemia in infants with regulatory mutations of the glutamate dehydrogenase gene. N Engl J Med 1998;338:1352-1357.
    • (1998) N Engl J Med , vol.338 , pp. 1352-1357
    • Stanley, C.A.1    Lieu, Y.K.2    Hsu, B.Y.3
  • 6
    • 0030567080 scopus 로고    scopus 로고
    • Transient metabolic hyperammonaemia in young Irish wolfhounds
    • Meyer HP, Rothuizen J, Tiemessen I, et al. Transient metabolic hyperammonaemia in young Irish wolfhounds. Vet Rec 1996;138:105-107.
    • (1996) Vet Rec , vol.138 , pp. 105-107
    • Meyer, H.P.1    Rothuizen, J.2    Tiemessen, I.3
  • 7
    • 0028364516 scopus 로고
    • Quantitation of portosystemic shunting in dogs by ultrasound-guided injection of 99MTc-macroaggregates into a splenic vein
    • Meyer HP, Rothuizen J, van den Brom WE, et al. Quantitation of portosystemic shunting in dogs by ultrasound-guided injection of 99MTc-macroaggregates into a splenic vein. Res Vet Sci 1994;57:58-62.
    • (1994) Res Vet Sci , vol.57 , pp. 58-62
    • Meyer, H.P.1    Rothuizen, J.2    van den Brom, W.E.3
  • 8
    • 0032253501 scopus 로고    scopus 로고
    • Prediction of inherited portosystemic shunts in Irish Wolfhounds on the basis of pedigree analysis
    • Ubbink GJ, van de Broek J, Meyer HP, et al. Prediction of inherited portosystemic shunts in Irish Wolfhounds on the basis of pedigree analysis. Am J Vet Res 1998;59:1553-1556.
    • (1998) Am J Vet Res , vol.59 , pp. 1553-1556
    • Ubbink, G.J.1    van de Broek, J.2    Meyer, H.P.3
  • 9
    • 32344449558 scopus 로고    scopus 로고
    • Diagnostic value of fasting plasma ammonia and bile acid concentrations in the identification of portosystemic shunting in dogs
    • Gerritzen-Bruning MJ, van den Ingh TS, Rothuizen J. Diagnostic value of fasting plasma ammonia and bile acid concentrations in the identification of portosystemic shunting in dogs. J Vet Intern Med 2006;20:13-19.
    • (2006) J Vet Intern Med , vol.20 , pp. 13-19
    • Gerritzen-Bruning, M.J.1    van den Ingh, T.S.2    Rothuizen, J.3
  • 10
    • 0036746765 scopus 로고    scopus 로고
    • Clinical, enzymatic, and molecular genetic characterization of a biochemical variant type of argininosuccinic aciduria: Prenatal and postnatal diagnosis in five unrelated families
    • Kleijer WJ, Garritsen VH, Linnebank M, et al. Clinical, enzymatic, and molecular genetic characterization of a biochemical variant type of argininosuccinic aciduria: Prenatal and postnatal diagnosis in five unrelated families. J Inherit Metab Dis 2002;25:399-410.
    • (2002) J Inherit Metab Dis , vol.25 , pp. 399-410
    • Kleijer, W.J.1    Garritsen, V.H.2    Linnebank, M.3
  • 11
    • 0032774859 scopus 로고    scopus 로고
    • Blood levels of ammonia and nitrogen scavenging amino acids in patients with inherited hyperammonemia
    • Tuchman M, Yudkoff M. Blood levels of ammonia and nitrogen scavenging amino acids in patients with inherited hyperammonemia. Mol Genet Metab 1999;66:10-15.
    • (1999) Mol Genet Metab , vol.66 , pp. 10-15
    • Tuchman, M.1    Yudkoff, M.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.