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Volumn 58, Issue 3, 2012, Pages 496-500

A patient with prolonged paralysis

Author keywords

[No Author keywords available]

Indexed keywords

SUXAMETHONIUM; VECURONIUM;

EID: 84857826162     PISSN: 00099147     EISSN: 15308561     Source Type: Journal    
DOI: 10.1373/clinchem.2011.163782     Document Type: Article
Times cited : (4)

References (12)
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    • A method for the detection of atypical forms of human serum cholinesterase; determination of dibucaine numbers
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    • (1955) Can J Biochem Physiol , vol.33 , pp. 568-574
    • Kalow, W.1    Lindsay, H.A.2
  • 6
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    • The familial incidence of low pseudocholinesterase level
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    • Lehmann, H.1    Ryan, E.2
  • 7
    • 0001738098 scopus 로고
    • Differential inhibition of human serum cholinesterase with fluoride: Recognition of two new phenotypes
    • Harris H, Whittaker M. Differential inhibition of human serum cholinesterase with fluoride: recognition of two new phenotypes. Nature 1961; 191:496-8.
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  • 8
    • 0009549759 scopus 로고
    • Complete pseudocholinesterase deficiency: Genetic and immunologic characterization
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  • 9
    • 0026695539 scopus 로고
    • DNA mutation associated with the human butyrylcholinesterase K-variant and its linkage to the atypical variant mutation and other polymorphic sites
    • Bartels CF, Jensen FS, Lockridge O, van der Spek AF, Rubinstein HM, Lubrano T, La Du BN. DNA mutation associated with the human butyrylcholinesterase K-variant and its linkage to the atypical variant mutation and other polymorphic sites. Am J Hum Genet 1992;50: 1086-103.
    • (1992) Am J Hum Genet , vol.50 , pp. 1086-1103
    • Bartels, C.F.1    Jensen, F.S.2    Lockridge, O.3    Van Der Spek, A.F.4    Rubinstein, H.M.5    Lubrano, T.6    La Du, B.N.7
  • 10
    • 0041866793 scopus 로고    scopus 로고
    • Butyrylcholinesterase (BCHE) genotyping for post-succinylcholine apnea in an Australian population
    • DOI 10.1373/49.8.1297
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    • A mutation linked with autism reveals a common mechanism of endoplasmic reticulum retention for the alpha,beta-hydrolase fold protein family
    • DOI 10.1074/jbc.M510262200
    • De Jaco A, Comoletti D, Kovarik Z, Gaietta G, Radic Z, Lockridge O, et al. A mutation linked with autism reveals a common mechanism of endoplasmic reticulum retention for the alpha,beta-hydrolase fold protein family. J Biol Chem 2006;281:9667-76. (Pubitemid 43864685)
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.