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Article

Mivacurium sensitivity in a patient heterozygous for the atypical and silent genes for plasma cholinesterase.

Annals of clinical biochemistry - 1 Jul 1995

Robertson W S, Shaikh J, Purdie D W

Abstract excerpt

No abstract is available from the source.

Topics

Adult
Cholinesterases
Drug Hypersensitivity
Female
Genetic Markers
Heterozygote
Humans
Isoquinolines
Mivacurium
Neostigmine
Neuromuscular Nondepolarizing Agents
Phenotype

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 7486808
DOI: 10.1177/000456329503200416

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 30 Aug 2026.

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Related research

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Click a neighbor to travelStep 1 · 12 closest

Mivacurium sensitivity in a patient heterozygous for the atypical and silent genes for plasma cholinesterase.PMID 7486808Read ↗

Markedly prolonged paralysis after mivacurium in a patient apparently heterozygous for the atypical and usual pseudocholinesterase alleles by conventional biochemical testing.Semantic proximity Read ↗

Prolonged mivacurium neuromuscular block in children.Semantic proximity Read ↗

Mivacurium-induced neuromuscular blockade in patients with atypical plasma cholinesterase.Semantic proximity Read ↗

Pharmacokinetics and pharmacodynamics of mivacurium in patients phenotypically heterozygous for the usual and atypical plasma cholinesterase variants (UA).Semantic proximity Read ↗

Pharmacokinetics and pharmacodynamics of mivacurium in patients phenotypically homozygous for the atypical plasma cholinesterase variant: effect of injection of human cholinesterase.Semantic proximity Read ↗

Response to mivacurium in a patient compound heterozygous for a novel and a known silent mutation in the butyrylcholinesterase gene: genotyping by sequencing.Semantic proximity Read ↗

Congenital myasthenic syndrome due to a novel missense mutation in the gene encoding choline acetyltransferaseSemantic proximity Read ↗

Identification of a heterozygote for the silent and Kalow alleles of cholinesterase using a polymerase chain reaction technique.Semantic proximity Read ↗

Butyrylcholinesterase Atypical Mutation in a Patient Undergoing Electroconvulsive Therapy.Semantic proximity Read ↗

Rapid identification of atypical variant of plasma butyrylcholinesterase by PCR.Semantic proximity Read ↗

[Succinylcholine apnea in a patient homozygotic for atypical cholinesterase gene].Semantic proximity Read ↗

[Prolonged succinylcholine-induced apnoea associated with cholinesterase silent plasma variant].Semantic proximity Read ↗

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