116 related articles for article (PubMed ID: 12387584)
1. Rapid simultaneous genotyping of the frequent butyrylcholinesterase variants Asp70Gly and Ala539Thr with fluorescent hybridization probes.
Gätke MR; Viby-Mogensen J; Bundgaard JR
Scand J Clin Lab Invest; 2002; 62(5):375-83. PubMed ID: 12387584
[TBL] [Abstract][Full Text] [Related]
2. Two novel mutations in the BCHE gene in patients with prolonged duration of action of mivacurium or succinylcholine during anaesthesia.
Gätke MR; Bundgaard JR; Viby-Mogensen J
Pharmacogenet Genomics; 2007 Nov; 17(11):995-9. PubMed ID: 18075469
[TBL] [Abstract][Full Text] [Related]
3. Characterization of a novel BCHE "silent" allele: point mutation (p.Val204Asp) causes loss of activity and prolonged apnea with suxamethonium.
Delacour H; Lushchekina S; Mabboux I; Bousquet A; Ceppa F; Schopfer LM; Lockridge O; Masson P
PLoS One; 2014; 9(7):e101552. PubMed ID: 25054547
[TBL] [Abstract][Full Text] [Related]
4. Timing of blood sampling for butyrylcholinesterase phenotyping in patients with prolonged neuromuscular block after mivacurium or suxamethonium.
Mintjens N; Brummans R; Soetens F; Claes KBM; Vanlinthout LE
Acta Anaesthesiol Scand; 2021 Feb; 65(2):182-187. PubMed ID: 33010031
[TBL] [Abstract][Full Text] [Related]
5. Genotyping the butyrylcholinesterase in patients with prolonged neuromuscular block after succinylcholine.
Levano S; Ginz H; Siegemund M; Filipovic M; Voronkov E; Urwyler A; Girard T
Anesthesiology; 2005 Mar; 102(3):531-5. PubMed ID: 15731589
[TBL] [Abstract][Full Text] [Related]
6. Frequency of butyrylcholinesterase gene mutations in individuals with abnormal inhibition numbers: an Italian-population study.
Lando G; Mosca A; Bonora R; Azzario F; Penco S; Marocchi A; Panteghini M; Patrosso MC
Pharmacogenetics; 2003 May; 13(5):265-70. PubMed ID: 12724618
[TBL] [Abstract][Full Text] [Related]
7. Biochemical and genetic analysis of butyrylcholinesterase (BChE) in a family, due to prolonged neuromuscular blockade after the use of succinylcholine.
Garcia DF; Oliveira TG; Molfetta GA; Garcia LV; Ferreira CA; Marques AA; Silva WA
Genet Mol Biol; 2011 Jan; 34(1):40-4. PubMed ID: 21637541
[TBL] [Abstract][Full Text] [Related]
8. [Rapid detection of BCHE atypical variant (p.Asp70Gly) by high resolution melting curve analysis].
Mabboux I; Dos Santos M; Courcelle S; Hary B; Ceppa F; Delacour H
Ann Biol Clin (Paris); 2014; 72(5):543-8. PubMed ID: 25336127
[TBL] [Abstract][Full Text] [Related]
9. Rapid and accurate detection of atypical and Kalow variants in the butyrylcholinesterase gene using denaturing high performance liquid chromatography.
Levano S; Keller D; Schobinger E; Urwyler A; Girard T
Anesth Analg; 2008 Jan; 106(1):147-51, table of contents. PubMed ID: 18165570
[TBL] [Abstract][Full Text] [Related]
10. Patients with prolonged effect of succinylcholine or mivacurium had novel mutations in the butyrylcholinesterase gene.
Wichmann S; Færk G; Bundgaard JR; Gätke MR
Pharmacogenet Genomics; 2016 Jul; 26(7):351-6. PubMed ID: 27031121
[TBL] [Abstract][Full Text] [Related]
11. Butyrylcholinesterase (BCHE) genotyping for post-succinylcholine apnea in an Australian population.
Yen T; Nightingale BN; Burns JC; Sullivan DR; Stewart PM
Clin Chem; 2003 Aug; 49(8):1297-308. PubMed ID: 12881446
[TBL] [Abstract][Full Text] [Related]
12. Cholinesterase: phenotyping and genotyping.
Goodall R;
Ann Clin Biochem; 2004 Mar; 41(Pt 2):98-110. PubMed ID: 15025799
[TBL] [Abstract][Full Text] [Related]
13. Large-scale studies of the functional K variant of the butyrylcholinesterase gene in relation to Type 2 diabetes and insulin secretion.
Johansen A; Nielsen EM; Andersen G; Hamid YH; Jensen DP; Glümer C; Drivsholm T; Borch-Johnsen K; Jørgensen T; Hansen T; Pedersen O
Diabetologia; 2004 Aug; 47(8):1437-41. PubMed ID: 15258737
[TBL] [Abstract][Full Text] [Related]
14. Screening patients with prolonged neuromuscular blockade after succinylcholine and mivacurium.
Cerf C; Mesguish M; Gabriel I; Amselem S; Duvaldestin P
Anesth Analg; 2002 Feb; 94(2):461-6, table of contents. PubMed ID: 11812719
[TBL] [Abstract][Full Text] [Related]
15. Naturally occurring mutation, Asp70his, in human butyrylcholinesterase.
Boeck AT; Fry DL; Sastre A; Lockridge O
Ann Clin Biochem; 2002 Mar; 39(Pt 2):154-6. PubMed ID: 11928765
[TBL] [Abstract][Full Text] [Related]
16. Response to succinylcholine in patients carrying the K-variant of the butyrylcholinesterase gene.
Bretlau C; Sørensen MK; Vedersoe AL; Rasmussen LS; Gätke MR
Anesth Analg; 2013 Mar; 116(3):596-601. PubMed ID: 23400986
[TBL] [Abstract][Full Text] [Related]
17. Rapid detection of the 46C --> T polymorphism in the factor XII gene, a novel genetic risk factor for thrombosis, by melting peak analysis using fluorescence hybridization probes.
Tirado I; Fontcuberta J; Soria JM
Genet Test; 2003; 7(4):295-301. PubMed ID: 15000805
[TBL] [Abstract][Full Text] [Related]
18. Rapid triplex asymmetric real-time PCR hybridization probe assay for the joint genotyping of F2, F5 and F12.
Martínez-Serra J; Gutierrez A; Amat JC; Galmés B; Vila A; Julia M; López H; Bautista AM; Truyols C; Ros T; Navarro M; Canaro M; Díaz M; Besalduch J
Clin Biochem; 2009 Aug; 42(12):1317-24. PubMed ID: 19422815
[TBL] [Abstract][Full Text] [Related]
19. [Prolonged neuromuscular block in a patient with butyrylcholinesterase deficiency].
Mabboux I; Hary B; Courcelle S; Ceppa F; Delacour H
Arch Pediatr; 2016 May; 23(5):497-500. PubMed ID: 27017361
[TBL] [Abstract][Full Text] [Related]
20. Response to mivacurium in a patient compound heterozygous for a novel and a known silent mutation in the butyrylcholinesterase gene: genotyping by sequencing.
Gätke MR; Ostergaard D; Bundgaard JR; Varin F; Viby-Mogensen J
Anesthesiology; 2001 Sep; 95(3):600-6. PubMed ID: 11575530
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
