Determination of a positive malignant hyperthermia (MH) disposition without the in vitro contracture test in families carrying the RYR1 Arg614Cys mutation
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1034/j.1399-0004.2001.600205.x/fullpdf
Reference42 articles.
1. Prediction of malignant hyperthermia susceptibility by clinical signs;Larach;Anesthesiology,1987
2. Inheritance of Malignant Hyperthermia—A Review of Published Data
3. A protocol for the investigation of malignant hyperpyrexia (MH) susceptibility;The European Malignant Hyperpyrexia Group;Br J Anaesth,1984
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1. Mild clinical and histopathological features in patients who carry the frequent and causative malignant hyperthermia RyR1 mutation p.Thr2206Met;CLIN NEUROPATHOL;2009
2. Spontaneous Occurrence of the Disposition to Malignant Hyperthermia;Anesthesiology;2004-03-01
3. Severe prognosis in a large family with hypokalemic periodic paralysis;Muscle & Nerve;2003-01-23
4. Screening for Mutations in the RYR1 Gene in Families with Malignant Hyperthermia;Journal of Molecular Neuroscience;2003
5. Evidence for a spontaneous C1840-T mutation in the RYR1 gene after DNA fingerprinting in a malignant hyperthermia susceptible family;Naunyn-Schmiedeberg's Archives of Pharmacology;2002-10-01
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