Malignant hyperthermia: relationship to other diseases.
نویسنده
چکیده
s of the 4th International Malignant Hyperpyrexia Workshop, Leeds, England. 22. Leeds DE, Gadde PL, Macnamara TE. Malignanthyperthermia in association with Burkett's lymphoma:Report of a third case. Anesthesia and Analgesia 1980; 59,514-515. 23. Linter SPK, Thomas PR, Withington PS, Hall MG.Suxamethonium associated hypertonicity and cardiacarrest in suspected pseudohypertrophic muscular dystro-phy. British Journal of Anaesthesia 1982; 4: 1331-1332. 24. Lotstra F, Linkowski P, Mendlewicz J. General anesthesiaafter neuroleptic malignant syndrome. Biological Psych-iatry 1983; 18: 243-247. 25. Mabuchi K, Sreter FA. The use of cryostat sectioning formeasurement of Ca uptake by sarcoplasmic reticulum.Analytical Biochemistry 1978; 86: 733-742. 26. McPherson EW, and Taylor CA. The King Syndrome:Malignant hyperthermia, myopathy, and multiple anomalies. American Journal of Medical Genetics 1981; 8: 159-165.27. Nagarajan K, Fishbein WN, Carlin HM, Pezeshkpour G,Muldoon SM. Frozen section calcium-uptake versushalothane and caffeine contracture tests on human muscle.Anesthesiology 1985; 83: A307. 28. Nakazota A, Shime H, Morooka K, Nonaka K. Anes-thesia-induced rhabdomyolysis in a patient with Fuku-yama-type muscular dystrophy. Brain and Development1983;5: 243. 29. Ohtani Y, Miike T, Ishitsu T, Matsuda I, Tamari H. Acase of malignant hyperthermia with mitochondrial dys-function. Brain and Development 1985; 7: 249. 30. Oka S, Igarashi Y, Takagi A, Nishida M, Sato K, NakadaK, Ikeda K. Malignant hyperpyrexia and Duchennemuscular dystrophy: a case report. Canadian AnaesthetistsSociety Journal 1982; 29: 627-629. 31. Ording H. Incidence of malignant hyperthermia inDenmark. Anesthesia and Analgesia 1985; 64: 700-704. 32. Rampton AJ, Kelly DA, Shanahan EC, Ingram GS.Occurrence of malignant hyperpyrexia in a patient with osteogenesis imperfecta. British Journal of Anaesthesia 1984; 56: 1443-1446. 33. Rosenberg H, Fisher CA, Reed SB, Addonizio P. Plateletaggregation in patients susceptible to malignant hyper-thermia. Anesthesiology 1981; 55: 621-624. 34. Scarlett JD, Zimmerman R, Berkovic SF. Neuroleptic malignant syndrome. Australian and New Zealand Journal of Medicine 1983; 13: 70-73. 35. Seay AR, Ziter FA, Thompson JA. Cardiac arrest duringinduction of anesthesia in Duchenne muscular dystrophy.Journal of Pediatrics 1978; 93: 88-90. 36. Seay AR, Ziter FA. Malignant hyperpyrexia in a patientwith Schwartz-Jampel syndrome. Journal of Pediatrics1978; 93: 83-84. 37. Shuaib A, Paasuke RT, Brownell AKW. Central coredisease: A reappraisal of its clinical features and newmanagement recommendations. Medicine (Baltimore)1987; 66: 389-396.38. Solomons CC, Masson NC. Platelet model for halothane-induced effects on nucleotide metabolism applied to malignant hyperthermia. Acta Anaesthesiologica Scandinavica 1984; 28: 185-190. 39. Takagi A, Sunohara N, Ishihara T, Nonaka I, Sugita H.Malignant hyperthermia and related neuromuscular di-seases : caffeine contracture of the skinned muscle fibers.Muscle and Nerve 1983; 6: 510-514. 40. Thach BT. Sudden infant death syndrome. New EnglandJournal of Medicine 1986; 315: 126-128. 41. Tollefson G. A case of neuroleptic malignant syndrome:in vitro muscle comparison with malignant hyperthermia.Journal of Clinical Psychopharmacology 1982; 2: 266-270.42. Tsueda K, Dubick MN, Wright BD, Sachatello CR.Intraoperative hyperthermic crisis in two children withundifferentiated lymphoma. Anesthesia and Analgesia1978; 57: 511-514.
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Malignant Hyperthermia
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عنوان ژورنال:
- British journal of anaesthesia
دوره 60 3 شماره
صفحات -
تاریخ انتشار 1988