|1.||Bekavac, Ivanka: 1 article (07/2014)|
|2.||Hafner, Tomislav: 1 article (07/2014)|
|3.||Mazul Sunko, Branka: 1 article (07/2014)|
|4.||Brozović, Gordana: 1 article (07/2014)|
|5.||Ok, Seong-Ho: 1 article (12/2013)|
|6.||Woo, Min-Kyu: 1 article (12/2013)|
|7.||Kim, Cheon-Gyu: 1 article (12/2013)|
|8.||Sohn, Ju-Tae: 1 article (12/2013)|
|9.||Hwang, Iljeong: 1 article (12/2013)|
|10.||Kostopanagiotou, Georgia: 1 article (03/2011)|
01/01/2002 - "Pseudocholinesterase deficiency is an uncommon occurrence but should be highly suspected in cases of prolonged paralysis following the administration of a short-acting muscle relaxant. "
04/01/1973 - "Prolonged paralysis in pseudocholinesterase deficiency."
12/01/2013 - "Delayed recovery from paralysis by succinylcholine in patient with preoperatively unrecognized and inherited pseudocholinesterase deficiency."
06/01/2005 - "The mild pseudocholinesterase deficiency necessitated a (50-75%) reduction in succinylcholine dosage, careful monitoring of the train of four, and postictal amnestic coverage to prevent paralysis upon waking. "
02/01/2005 - "Pseudocholinesterase deficiency is usually identified when an anesthetized patient has prolonged paralysis after receiving neuromuscular blocking agents dependent on pseudocholinesterase enzymes for hydrolysis. "
09/01/1967 - "Prolonged postoperative apnea with pseudocholinesterase deficiency."
09/01/1956 - "[Pseudocholinesterase deficiency; a complication in bronchoscopy in anesthesia and apnea]."
08/01/1982 - "Prolonged postoperative succinylcholine-induced apnea with pseudocholinesterase deficiency."
07/01/1978 - "The present report represents the 1st case in which a peripheral nerve stimulator has been used to substantiate the increased succinylcholine sensitivity of a patient heterozygous for the silent and the fluoride-resistant gene, and the 2nd published case of prolonged apnea following succinylcholine in a patient carrying the Ef1 Es1 genotype for abnormal serum cholinesterase."
|3.||Muscular Diseases (Myopathy)
11/01/1969 - "Myopathy and succinylcholine sensitivity."
10/01/2010 - "We screened for mutations responsible for four relatively frequent autosomal recessive conditions in Persian Jews in which effective interventions are available for each: Pseudocholinesterase deficiency (butyryl cholinesterase deficiency); Congenital hypoaldosteronism (corticosterone methyl oxidase II); Autoimmune polyendocrinopathy (autoimmune regulatory element); and Hereditary Inclusion Body myopathy. "
|1.||Succinylcholine (Suxamethonium Chloride)
|4.||Neuromuscular Blocking Agents
|8.||rocuronium (rocuronium bromide)
|9.||cyclo(cysteinyl- tyrosyl- norleucyl- glycyl- tryptophyl- cysteinyl)- aspartyl- phenylalaninamide (Es1)
|10.||corticosterone methyl oxidase II
|2.||Cesarean Section (Caesarean Section)