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164 results

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Quoted phrase not found in phrase index: "Malignant hyperthermia, susceptibility to, 5"
Page 1
Malignant hyperthermia: a review.
Rosenberg H, Pollock N, Schiemann A, Bulger T, Stowell K. Rosenberg H, et al. Orphanet J Rare Dis. 2015 Aug 4;10:93. doi: 10.1186/s13023-015-0310-1. Orphanet J Rare Dis. 2015. PMID: 26238698 Free PMC article. Review.
Malignant hyperthermia (MH) is a pharmacogenetic disorder of skeletal muscle that presents as a hypermetabolic response to potent volatile anesthetic gases such as halothane, sevoflurane, desflurane, isoflurane and the depolarizing muscle relaxant succinylcholine, a
Malignant hyperthermia (MH) is a pharmacogenetic disorder of skeletal muscle that presents as a hypermetabolic response to pot
Malignant hyperthermia 2020: Guideline from the Association of Anaesthetists.
Hopkins PM, Girard T, Dalay S, Jenkins B, Thacker A, Patteril M, McGrady E. Hopkins PM, et al. Anaesthesia. 2021 May;76(5):655-664. doi: 10.1111/anae.15317. Epub 2021 Jan 5. Anaesthesia. 2021. PMID: 33399225 Free article.
Malignant hyperthermia is defined in the International Classification of Diseases as a progressive life-threatening hyperthermic reaction occurring during general anaesthesia. Malignant hyperthermia has an underlying genetic basis, and genetically s
Malignant hyperthermia is defined in the International Classification of Diseases as a progressive life-threatening hypertherm
Malignant Hyperthermia Update.
Ellinas H, Albrecht MA. Ellinas H, et al. Anesthesiol Clin. 2020 Mar;38(1):165-181. doi: 10.1016/j.anclin.2019.10.010. Anesthesiol Clin. 2020. PMID: 32008650 Review.
Malignant hyperthermia (MH) is a rare but potentially lethal skeletal muscle disorder affecting calcium release channels. ...Current data suggest that mortality has improved to less than 5%. The gold standard for ruling out MH is the contracture test. ...
Malignant hyperthermia (MH) is a rare but potentially lethal skeletal muscle disorder affecting calcium release channels. ...C
Malignant hyperthermia.
Rosenberg H, Davis M, James D, Pollock N, Stowell K. Rosenberg H, et al. Orphanet J Rare Dis. 2007 Apr 24;2:21. doi: 10.1186/1750-1172-2-21. Orphanet J Rare Dis. 2007. PMID: 17456235 Free PMC article. Review.
Malignant hyperthermia (MH) is a pharmacogenetic disorder of skeletal muscle that presents as a hypermetabolic response to potent volatile anesthetic gases such as halothane, sevoflurane, desflurane and the depolarizing muscle relaxant succinylcholine, and rarely, i
Malignant hyperthermia (MH) is a pharmacogenetic disorder of skeletal muscle that presents as a hypermetabolic response to pot
Malignant hyperthermia.
Ali SZ, Taguchi A, Rosenberg H. Ali SZ, et al. Best Pract Res Clin Anaesthesiol. 2003 Dec;17(4):519-33. doi: 10.1016/j.bpa.2003.09.012. Best Pract Res Clin Anaesthesiol. 2003. PMID: 14661655 Review.
Malignant hyperthermia (MH) is an uncommon, life-threatening, acute pharmacogenetic disorder of the skeletal muscle cell. ...The ryanodine receptor, the calcium-release channel of the sarcoplasmic reticulum, is the primary locus for malignant hypothermia s
Malignant hyperthermia (MH) is an uncommon, life-threatening, acute pharmacogenetic disorder of the skeletal muscle cell. ...T
Malignant hyperthermia.
Halliday NJ. Halliday NJ. J Craniofac Surg. 2003 Sep;14(5):800-2. doi: 10.1097/00001665-200309000-00039. J Craniofac Surg. 2003. PMID: 14501352
Malignant Hyperthermia (MH) has been a recognized complication of general anesthesia after the first case reports in the 1940's. ...The caffeine/halothane testing of muscle biopsies is currently the most definitive test for malignant hyperthermia su
Malignant Hyperthermia (MH) has been a recognized complication of general anesthesia after the first case reports in the 1940'
Malignant hyperthermia.
Gronert GA. Gronert GA. Anesthesiology. 1980 Nov;53(5):395-423. doi: 10.1097/00000542-198011000-00007. Anesthesiology. 1980. PMID: 6999950 Free article. Review.
Sympathetic involvement in MH, while controversial, is probably a response to stress that affects blood flow, heat loss, and myocardial function, rather than a direct sympathetic activation of susceptible muscle. Diagnosis is based upon extraordinary temperature and acid-b …
Sympathetic involvement in MH, while controversial, is probably a response to stress that affects blood flow, heat loss, and myocardial func …
Malignant hyperthermia when dantrolene is not readily available.
Gong X. Gong X. BMC Anesthesiol. 2021 Apr 16;21(1):119. doi: 10.1186/s12871-021-01328-3. BMC Anesthesiol. 2021. PMID: 33863282 Free PMC article.
BACKGROUND: Malignant hyperthermia is a rare but life-threatening pharmacogenetic muscle disorder characterized by abnormal hypermetabolic reactions and commonly triggered in susceptible individuals by volatile anesthetics or succinylcholine, or both. ...METH …
BACKGROUND: Malignant hyperthermia is a rare but life-threatening pharmacogenetic muscle disorder characterized by abnormal hy …
Pharmacogenetics and pathophysiology of CACNA1S mutations in malignant hyperthermia.
Beam TA, Loudermilk EF, Kisor DF. Beam TA, et al. Physiol Genomics. 2017 Feb 1;49(2):81-87. doi: 10.1152/physiolgenomics.00126.2016. Epub 2016 Dec 23. Physiol Genomics. 2017. PMID: 28011884 Review.
A review of the pharmacogenetics (PGt) and pathophysiology of calcium voltage-gated channel subunit alpha1 S (CACNA1S) mutations in malignant hyperthermia susceptibility type 5 (MHS5; MIM #60188) is presented. Malignant hyperthermia (MH) …
A review of the pharmacogenetics (PGt) and pathophysiology of calcium voltage-gated channel subunit alpha1 S (CACNA1S) mutations in malig
Congenital myopathies: not only a paediatric topic.
Jungbluth H, Voermans NC. Jungbluth H, et al. Curr Opin Neurol. 2016 Oct;29(5):642-50. doi: 10.1097/WCO.0000000000000372. Curr Opin Neurol. 2016. PMID: 27538056 Review.
PURPOSE OF REVIEW: This article reviews adult presentations of the major congenital myopathies - central core disease, multiminicore disease, centronuclear myopathy and nemaline myopathy - with an emphasis on common genetic backgrounds, typical clinicopathological f …
PURPOSE OF REVIEW: This article reviews adult presentations of the major congenital myopathies - central core disease, multiminicore …
164 results