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Volumn 40, Issue 2, 1998, Pages 185-193

Citrullinemia: Clinical experience with 23 cases

Author keywords

Asymptomatic; Citrullinemia; Late onset; Neonatal; Subacute

Indexed keywords

ARGININE; ARGININOSUCCINATE SYNTHASE; BENZOIC ACID; BENZOIC ACID DERIVATIVE; CITRULLINE; FOOD PRESERVATIVE;

EID: 0032037687     PISSN: 00414301     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (11)

References (18)
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    • Inherited and acquired syndromes of hyperammonemia and encephalopathy in children
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  • 4
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    • Urea cycle disorders: Diagnosis, pathophysiology and therapy
    • Brusilow SW, Maestri NE. Urea cycle disorders: diagnosis, pathophysiology and therapy. Adv Pediatr 1996; 43: 127-170.
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    • Brusilow, S.W.1    Maestri, N.E.2
  • 8
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    • Clinical aspects of disorder of the urea cycle
    • Synderman SE. Clinical aspects of disorder of the urea cycle. Pediatrics 1981; 68: 284-289, 295-297.
    • (1981) Pediatrics , vol.68 , pp. 284-289
    • Synderman, S.E.1
  • 9
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    • Citrullinemia: Phenotypic variations
    • Whelan DT, Brusso T, Spate M. Citrullinemia: phenotypic variations. Pediatrics 1976; 57: 935.
    • (1976) Pediatrics , vol.57 , pp. 935
    • Whelan, D.T.1    Brusso, T.2    Spate, M.3
  • 12
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    • Long-term survival of patients with argininosuccinate synthetase deficiency
    • Maestri NE, Clissold DB, Brusilow SW. Long-term survival of patients with argininosuccinate synthetase deficiency. J Pediatr 1995; 127: 929-935.
    • (1995) J Pediatr , vol.127 , pp. 929-935
    • Maestri, N.E.1    Clissold, D.B.2    Brusilow, S.W.3
  • 14
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    • Urea cycle disorders and other hereditary hyperammonemic syndromes
    • Stanbury JB, Wyngaarden JB, Fredericson DS, Goldstein JL, Brown MS (eds). New York: McGraw-Hill
    • Walser W. Urea cycle disorders and other hereditary hyperammonemic syndromes. In: Stanbury JB, Wyngaarden JB, Fredericson DS, Goldstein JL, Brown MS (eds). The Metabolic Basis of Inherited Disease. New York: McGraw-Hill; 1983: 402-438.
    • (1983) The Metabolic Basis of Inherited Disease , pp. 402-438
    • Walser, W.1
  • 15
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    • Citrullinemia. Elevated serum citrulline levels in healthy siblings
    • Wick HT, Brechbühler T, Girard J. Citrullinemia. Elevated serum citrulline levels in healthy siblings. Experientia 1970; 26: 823.
    • (1970) Experientia , vol.26 , pp. 823
    • Wick, H.T.1    Brechbühler, T.2    Girard, J.3
  • 16
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    • Fifteen years' experience with 212 hyperammonaemic cases at a metabolic unit
    • Tokatli A, Coşkun T, Özalp İ. Fifteen years' experience with 212 hyperammonaemic cases at a metabolic unit. J Inher Metab Dis 1991; 14: 698-706.
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    • Tokatli, A.1    Coşkun, T.2    Özalp, I.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.