-
1
-
-
0019137011
-
Correlation of succinylcholine duration of action with plasma cholinesterase activity in subjects with the genotypically normal enzyme
-
Viby-Mogensen J (1980) Correlation of succinylcholine duration of action with plasma cholinesterase activity in subjects with the genotypically normal enzyme. Anesthesiology 53:517-520
-
(1980)
Anesthesiology
, vol.53
, pp. 517-520
-
-
Viby-Mogensen, J.1
-
2
-
-
0026726182
-
Influence of plasma cholinesterase activity on recovery from mivacurium-induced neuromuscular blockade in phenotypically normal patients
-
Ostergaard D, Jensen FS, Jensen E, Skovgaard LT, Viby-Mogensen J (1992) Influence of plasma cholinesterase activity on recovery from mivacurium-induced neuromuscular blockade in phenotypically normal patients. Acta Anaesthesiol Scand 36:702-706
-
(1992)
Acta Anaesthesiol Scand
, vol.36
, pp. 702-706
-
-
Ostergaard, D.1
Jensen, F.S.2
Jensen, E.3
Skovgaard, L.T.4
Viby-Mogensen, J.5
-
3
-
-
0028958140
-
Plasma cholinesterase and abnormal reaction to succinylcholine: Twenty years' experience with the Danish Cholinesterase Research Unit
-
Jensen FS, Viby-Mogensen J (1995) Plasma cholinesterase and abnormal reaction to succinylcholine: twenty years' experience with the Danish Cholinesterase Research Unit. Acta Anaesthesiol Scand 39:150-156
-
(1995)
Acta Anaesthesiol Scand
, vol.39
, pp. 150-156
-
-
Jensen, F.S.1
Viby-Mogensen, J.2
-
4
-
-
0025294717
-
Genetic variants of human serum cholinesterase influence metabolism of the muscle relaxant succinylcholine
-
Lockridge O (1990) Genetic variants of human serum cholinesterase influence metabolism of the muscle relaxant succinylcholine. Pharmacol Ther 47:35-60
-
(1990)
Pharmacol Ther
, vol.47
, pp. 35-60
-
-
Lockridge, O.1
-
5
-
-
0030003649
-
Three different point mutations in the butyrylcholinesterase gene of three Japanese subjects with a silent phenotype: Possible Japanese type alleles
-
Sudo K, Maekawa M, Kanno T, Akizuki S, Magara T (1996) Three different point mutations in the butyrylcholinesterase gene of three Japanese subjects with a silent phenotype: possible Japanese type alleles. Clin Biochem 29:165-169
-
(1996)
Clin Biochem
, vol.29
, pp. 165-169
-
-
Sudo, K.1
Maekawa, M.2
Kanno, T.3
Akizuki, S.4
Magara, T.5
-
6
-
-
0029655692
-
Characterization of 12 silent alleles of the human butyrylcholinesterase (BCHE) gene
-
Primo-Parmo SL, Bartels CF, Wiersema B, van der Spek AF, Innis JW, La Du BN (1996) Characterization of 12 silent alleles of the human butyrylcholinesterase (BCHE) gene. Am J Hum Genet 58:52-64
-
(1996)
Am J Hum Genet
, vol.58
, pp. 52-64
-
-
Primo-Parmo, S.L.1
Bartels, C.F.2
Wiersema, B.3
Van Der Spek, A.F.4
Innis, J.W.5
La Du, B.N.6
-
7
-
-
0026659642
-
DNA mutations associated with the human butyrylcholinesterase J-variant
-
Bartels CF, James K, La Du BN (1992) DNA mutations associated with the human butyrylcholinesterase J-variant. Am J Hum Genet 50:1104-1114
-
(1992)
Am J Hum Genet
, vol.50
, pp. 1104-1114
-
-
Bartels, C.F.1
James, K.2
La Du, B.N.3
-
8
-
-
0017903667
-
Elk, another quantitative variant at cholinesterase locus 1
-
Rubinstein HM, Dietz AA, Lubrano T (1978) Elk, another quantitative variant at cholinesterase locus 1. J Med Genet 15:27-29
-
(1978)
J Med Genet
, vol.15
, pp. 27-29
-
-
Rubinstein, H.M.1
Dietz, A.A.2
Lubrano, T.3
-
9
-
-
0026695539
-
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 (1992) 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 50:1086-1103
-
(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
-
-
0022256704
-
Plasma cholinesterase variants: Family studies of the E1k gene
-
Whittaker M, Britten JJ (1985) Plasma cholinesterase variants: family studies of the E1k gene. Hum Hered 35:364-368
-
(1985)
Hum Hered
, vol.35
, pp. 364-368
-
-
Whittaker, M.1
Britten, J.J.2
-
11
-
-
0021324274
-
On the identification and frequency of the J and K cholinesterase phenotypes in a Caucasian population
-
Evans RT, Wardell J (1984) On the identification and frequency of the J and K cholinesterase phenotypes in a Caucasian population. J Med Genet 21:99-102
-
(1984)
J Med Genet
, vol.21
, pp. 99-102
-
-
Evans, R.T.1
Wardell, J.2
-
13
-
-
0030030131
-
Detection of the plasma cholinesterase K-variant by PCR using an amplification-created restriction site
-
Jensen FS, Nielsen LR, Schwartz M (1996) Detection of the plasma cholinesterase K-variant by PCR using an amplification-created restriction site. Hum Hered 46:26-31
-
(1996)
Hum Hered
, vol.46
, pp. 26-31
-
-
Jensen, F.S.1
Nielsen, L.R.2
Schwartz, M.3
-
14
-
-
0025571392
-
Frequency of the CHE1*K allele of serum cholinesterase in a sample from southern Brazil
-
Alcantara VM, Chautard-Freire-Maia EA, Picheth G, Vieria MM (1990) Frequency of the CHE1*K allele of serum cholinesterase in a sample from southern Brazil. Hum Hered 40:386-390
-
(1990)
Hum Hered
, vol.40
, pp. 386-390
-
-
Alcantara, V.M.1
Chautard-Freire-Maia, E.A.2
Picheth, G.3
Vieria, M.M.4
-
15
-
-
0033043013
-
Failure to confirm a synergistic effect between the K-variant of the butyrylcholinesterase gene and the epsilon4 allele of the apolipoprotein gene in Japanese patients with Alzheimer's disease
-
Yamamoto Y, Yasuda M, Mori E, Maeda K (1999) Failure to confirm a synergistic effect between the K-variant of the butyrylcholinesterase gene and the epsilon4 allele of the apolipoprotein gene in Japanese patients with Alzheimer's disease. J Neurol Neurosurg Psychiatry 67:94-96
-
(1999)
J Neurol Neurosurg Psychiatry
, vol.67
, pp. 94-96
-
-
Yamamoto, Y.1
Yasuda, M.2
Mori, E.3
Maeda, K.4
-
16
-
-
0028946233
-
Identification of human plasma cholinesterase variants in 6,688 individuals using biochemical analysis
-
Jensen FS, Skovgaard LT, Viby-Mogensen J (1995) Identification of human plasma cholinesterase variants in 6,688 individuals using biochemical analysis. Acta Anaesthesiol Scand 39:157-162
-
(1995)
Acta Anaesthesiol Scand
, vol.39
, pp. 157-162
-
-
Jensen, F.S.1
Skovgaard, L.T.2
Viby-Mogensen, J.3
-
17
-
-
0019521054
-
Succinylcholine neuromuscular blockade in subjects homozygous for atypical plasma cholinesterase
-
Viby-Mogensen J (1981) Succinylcholine neuromuscular blockade in subjects homozygous for atypical plasma cholinesterase. Anesthesiology 55:429-434
-
(1981)
Anesthesiology
, vol.55
, pp. 429-434
-
-
Viby-Mogensen, J.1
-
18
-
-
0033707060
-
Prolonged duration of neuromuscular block with rapacuronium in the presence of sevoflurane
-
Cara DM, Armory P, Mahajan RP (2000) Prolonged duration of neuromuscular block with rapacuronium in the presence of sevoflurane. Anesth Analg 91:1392-1393
-
(2000)
Anesth Analg
, vol.91
, pp. 1392-1393
-
-
Cara, D.M.1
Armory, P.2
Mahajan, R.P.3
-
19
-
-
0033369663
-
Acquired pseudocholinesterase deficiency after high-dose cyclophosphamide
-
Koseoglu V, Chiang J, Chan KW (1999) Acquired pseudocholinesterase deficiency after high-dose cyclophosphamide. Bone Marrow Transplant 24:1367-1368
-
(1999)
Bone Marrow Transplant
, vol.24
, pp. 1367-1368
-
-
Koseoglu, V.1
Chiang, J.2
Chan, K.W.3
-
20
-
-
0021059489
-
Plasma cholinesterase and trophoblastic disease. Gestational trophoblastic disease and reduced activity of plasma cholinesterase
-
Davies JM, Carmichael D, Dymond C (1983) Plasma cholinesterase and trophoblastic disease. Gestational trophoblastic disease and reduced activity of plasma cholinesterase. Anaesthesia 38:1071-1074
-
(1983)
Anaesthesia
, vol.38
, pp. 1071-1074
-
-
Davies, J.M.1
Carmichael, D.2
Dymond, C.3
-
21
-
-
0024369927
-
Prolongation of succinylcholine block by metoclopramide
-
Kao YJ, Turner DR (1989) Prolongation of succinylcholine block by metoclopramide. Anesthesiology 70:905-908
-
(1989)
Anesthesiology
, vol.70
, pp. 905-908
-
-
Kao, Y.J.1
Turner, D.R.2
|