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Volumn 19, Issue 1, 2004, Pages 39-42

Poor outcome for neonatal-type nonketotic hyperglycinemia treated with high-dose sodium benzoate and dextromethorphan

Author keywords

[No Author keywords available]

Indexed keywords

BENZOIC ACID; DEXTROMETHORPHAN; GLYCINE; KETAMINE;

EID: 1542603300     PISSN: 08830738     EISSN: None     Source Type: Journal    
DOI: 10.1177/08830738040190010702     Document Type: Article
Times cited : (39)

References (13)
  • 1
    • 0000086555 scopus 로고    scopus 로고
    • Nonketotic hyperglycinemia
    • Scriver CR, Beaudet AL, Sly WS, Valle D (eds): 8th ed. New York, McGraw-Hill
    • Hamosh A, Johnston MV: Nonketotic hyperglycinemia, in Scriver CR, Beaudet AL, Sly WS, Valle D (eds): The Metabolic and Molecular Bases of Inherited Disease, 8th ed. New York, McGraw-Hill, 2065-2078.
    • The Metabolic and Molecular Bases of Inherited Disease , pp. 2065-2078
    • Hamosh, A.1    Johnston, M.V.2
  • 2
    • 0023259537 scopus 로고
    • Non-ketotic hyperglycinaemia: Clinical and bio-chemical aspects
    • Tada K, Hayasaka K: Non-ketotic hyperglycinaemia: Clinical and bio-chemical aspects. Eur J Pediatr 1987;146:221-227.
    • (1987) Eur. J. Pediatr. , vol.146 , pp. 221-227
    • Tada, K.1    Hayasaka, K.2
  • 3
    • 0034788469 scopus 로고    scopus 로고
    • Nonketotic hyperglycinemia (glycine encephalopathy): Laboratory diagnosis
    • Applegarth DA, Toone JR: Nonketotic hyperglycinemia (glycine encephalopathy): Laboratory diagnosis. Mol Genet Metab 2001; 74:139-146.
    • (2001) Mol. Genet. Metab. , vol.74 , pp. 139-146
    • Applegarth, D.A.1    Toone, J.R.2
  • 4
    • 0031949102 scopus 로고    scopus 로고
    • Long-term use of high-dose benzoate and dextromethorphan for the treatment of nonketotic hyperglycinemia
    • Hamosh A, Maher JF, Bellus GA, et al: Long-term use of high-dose benzoate and dextromethorphan for the treatment of nonketotic hyperglycinemia. J Pediatr 1998;132:709-713.
    • (1998) J. Pediatr. , vol.132 , pp. 709-713
    • Hamosh, A.1    Maher, J.F.2    Bellus, G.A.3
  • 5
    • 0032939225 scopus 로고    scopus 로고
    • Neonatal type of nonketotic hyperglycinemia
    • Lu FL, Wang PJ, Hwu WL, et al: Neonatal type of nonketotic hyperglycinemia. Pediatr Neurol 1999;20:295-300.
    • (1999) Pediatr. Neurol. , vol.20 , pp. 295-300
    • Lu, F.L.1    Wang, P.J.2    Hwu, W.L.3
  • 6
    • 0034772648 scopus 로고    scopus 로고
    • Early epileptic encephalopathy with suppression burst electroencephalographic pattern - An analysis of eight Taiwanese patients
    • Chen PT, Young C, Lee WT, et al: Early epileptic encephalopathy with suppression burst electroencephalographic pattern - An analysis of eight Taiwanese patients. Brain Dev 2001;23:715-720.
    • (2001) Brain Dev. , vol.23 , pp. 715-720
    • Chen, P.T.1    Young, C.2    Lee, W.T.3
  • 7
    • 0026773083 scopus 로고
    • Dextromethorphan and high-dose benzoate therapy for nonketotic hyperglycinemia in an infant
    • Hamosh A, McDonald JW, Valle D, et al: Dextromethorphan and high-dose benzoate therapy for nonketotic hyperglycinemia in an infant. J Pediatr 1992;121:131-135.
    • (1992) J. Pediatr. , vol.121 , pp. 131-135
    • Hamosh, A.1    McDonald, J.W.2    Valle, D.3
  • 8
    • 0028007602 scopus 로고
    • Failure of early dextromethorphan and sodium benzoate therapy in an infant with nonketotic hyperglycinemia
    • Zammarchi E, Donati MA, Ciani F, et al: Failure of early dextromethorphan and sodium benzoate therapy in an infant with nonketotic hyperglycinemia. Neuropediatrics 1994;25:274-276.
    • (1994) Neuropediatrics , vol.25 , pp. 274-276
    • Zammarchi, E.1    Donati, M.A.2    Ciani, F.3
  • 9
    • 0025373350 scopus 로고
    • Prenatal diagnosis of nonketotic hyperglycinemia: Enzymatic analysis of the glycine cleavage system in chorionic villi
    • Hayasaka K, Tada K, Fueki N, Aikawa J: Prenatal diagnosis of nonketotic hyperglycinemia: Enzymatic analysis of the glycine cleavage system in chorionic villi. J Pediatr 1990;116:444-445.
    • (1990) J. Pediatr. , vol.116 , pp. 444-445
    • Hayasaka, K.1    Tada, K.2    Fueki, N.3    Aikawa, J.4
  • 10
    • 0032839145 scopus 로고    scopus 로고
    • Prenatal diagnosis of nonketotic hyperglycinemia: Enzymatic diagnosis in 28 families and DNA diagnosis detecting prevalent Finnish and Israeli-Arab mutations
    • Kure S, Rolland MO, Leisti J, et al: Prenatal diagnosis of nonketotic hyperglycinemia: Enzymatic diagnosis in 28 families and DNA diagnosis detecting prevalent Finnish and Israeli-Arab mutations. Prenat Diagn, 1999;19:717-720.
    • (1999) Prenat. Diagn. , vol.19 , pp. 717-720
    • Kure, S.1    Rolland, M.O.2    Leisti, J.3
  • 11
    • 0034097520 scopus 로고    scopus 로고
    • Non-concordance of CVS and liver glycine cleavage enzyme in three families with non-ketotic hyperglycinaemia (NKH) leading to false negative prenatal diagnoses
    • Applegarth DA, Toone JR, Rolland MO, et al: Non-concordance of CVS and liver glycine cleavage enzyme in three families with non-ketotic hyperglycinaemia (NKH) leading to false negative prenatal diagnoses. Prenat Diagn 2000;20:367 370.
    • (2000) Prenat. Diagn. , vol.20 , pp. 367-370
    • Applegarth, D.A.1    Toone, J.R.2    Rolland, M.O.3
  • 12
    • 0035715366 scopus 로고    scopus 로고
    • Recurrent mutations in P- and T-proteins of the glycine cleavage complex and a novel T-protein mutation (N1451): A strategy for the molecular investigation of patients with nonketotic hyperglycinemia (NKH)
    • Toone JR, Applegarth DA, Coulter-Mackie MB, James ER: Recurrent mutations in P- and T-proteins of the glycine cleavage complex and a novel T-protein mutation (N1451): A strategy for the molecular investigation of patients with nonketotic hyperglycinemia (NKH). Mol Genet Metab 2001;72:322-325.
    • (2001) Mol. Genet. Metab. , vol.72 , pp. 322-325
    • Toone, J.R.1    Applegarth, D.A.2    Coulter-Mackie, M.B.3    James, E.R.4
  • 13
    • 0034036029 scopus 로고    scopus 로고
    • Human glycine decarboxylase gene (GLDC) and its highly conserved processed pseudogene (psiGLDC): Their structure and expression, and the identification of a large deletion in a family with nonketotic hyperglycinemia
    • Takayanagi M, Kure S, Sakata Y, et al: Human glycine decarboxylase gene (GLDC) and its highly conserved processed pseudogene (psiGLDC): Their structure and expression, and the identification of a large deletion in a family with nonketotic hyperglycinemia. Hum Genet 2000;106:298-305.
    • (2000) Hum. Genet. , vol.106 , pp. 298-305
    • Takayanagi, M.1    Kure, S.2    Sakata, Y.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.