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[Limited anesthetic possibilities in patients with hereditary muscular diseases].

作者信息

Althoff H

出版信息

Z Rechtsmed. 1973 Apr 30;72(2):128-39. doi: 10.1007/BF02077217.

DOI:10.1007/BF02077217
PMID:4733606
Abstract
摘要

相似文献

1
[Limited anesthetic possibilities in patients with hereditary muscular diseases].[遗传性肌肉疾病患者麻醉选择有限]
Z Rechtsmed. 1973 Apr 30;72(2):128-39. doi: 10.1007/BF02077217.
2
Malignant hyperpyrexia myopathy.恶性高热性肌病
Q J Med. 1973 Oct;42(168):639-64.
3
Malignant hyperthermia.恶性高热
Proc R Soc Med. 1970 Feb;63(2):178-80. doi: 10.1177/003591577006300228.
4
[Death from malignant hyperthermia. Etiology, pathophysiology, epidemiology and pathomorphology].[恶性高热致死。病因、病理生理学、流行病学及病理形态学]
Med Welt. 1978 Mar 31;29(13):522-31.
5
[Malignant hyperthermia--clinical aspects and treatment of life-endangering complications of anesthesia].
Chirurg. 1974 Oct;45(10):472-6.
6
Pathology of malignant hyperpyrexia.恶性高热的病理学
Br Med J. 1973 Feb 3;1(5848):249.
7
[Malignant hyperthermia during general anesthesia with rigor, myoglobinuria and disturbance of the blood coagulation mechanism].
Anaesthesist. 1971 Aug;20(8):315-22.
8
[Heart arrest during general anesthesia in a child with unrecognized Duchenne's dystrophy].[一名未被识别出患有杜氏肌营养不良症的儿童在全身麻醉期间发生心脏骤停]
Ann Fr Anesth Reanim. 1986;5(6):612-4. doi: 10.1016/s0750-7658(86)80073-9.
9
Rhabdomyolysis, myoglobinuria and hyperpyrexia caused by suxamethonium in a child with increased serum creatine kinase concentrations.一名血清肌酸激酶浓度升高的儿童因琥珀酰胆碱导致横纹肌溶解、肌红蛋白尿和高热。
Br J Anaesth. 1981 Sep;53(9):981-4. doi: 10.1093/bja/53.9.981.
10
Hyperthermia associated with ophthalmic surgery.与眼科手术相关的体温过高。
Am J Ophthalmol. 1974 Jan;77(1):76-9.

引用本文的文献

1
[Malignant hyperthermia following an old gunshot head injury].[陈旧性头部枪伤后发生恶性高热]
Z Rechtsmed. 1983;90(1):71-80. doi: 10.1007/BF01886069.
2
[Death from malignant hyperthermia during anaesthesia (author's transl)].麻醉期间恶性高热致死（作者译）
Z Rechtsmed. 1975 Nov 11;76(2):131-9. doi: 10.1007/BF00200559.

本文引用的文献

1
A modification of the masson trichrome technique for routine laboratory purposes.一种用于常规实验室目的的改良马森三色染色技术。
Am J Pathol. 1938 Mar;14(2):237-43.
2
Progressive Muscular Dystrophy. V. The Identification of the Carrier State in the Duchenne Type by Serum Creatine Kinase Determination.进行性肌营养不良症。五、通过血清肌酸激酶测定识别杜氏型携带者状态
Am J Hum Genet. 1963 Jun;15(2):133-54.
3
[Current views of the pathogenesis of Erb's progressive muscular dystrophy, with special consideration of the excretion of all neutral C-17-ketosteroids].
[关于埃尔布进行性肌营养不良发病机制的当前观点，特别考虑所有中性C-17-酮类固醇的排泄情况]
Klin Wochenschr. 1952 May 15;30(19-20):465-9. doi: 10.1007/BF01471631.
4
Histopathological features of muscle in the preclinical stages of muscular dystrophy.肌肉营养不良临床前期阶段肌肉的组织病理学特征。
Brain. 1962 Mar;85:109-20. doi: 10.1093/brain/85.1.109.
5
Serum enzymes in carriers of muscular dystrophy.肌营养不良携带者的血清酶
Br Med J. 1962 Oct 13;2(5310):963-4. doi: 10.1136/bmj.2.5310.963.
6
[Creatine metabolism in children with Erb's progressive muscular dystrophy].[埃尔布氏进行性肌营养不良患儿的肌酸代谢]
Klin Wochenschr. 1955 Jun 15;33(23-24):556-62. doi: 10.1007/BF01473765.
7
Glycogenolytic enzymes in human progressive muscular dystrophy.人类进行性肌营养不良中的糖原分解酶
Am J Phys Med. 1955 Feb;34(1):313-9.
8
[Enzymopathy in dystrophia musculorum progressiva Erb].[进行性肌营养不良症（埃尔布型）中的酶病]
Klin Wochenschr. 1955 Feb 15;33(7-8):179-82. doi: 10.1007/BF01467298.
9
MUSCULAR DYSTROPHY. REVIEW AND RECENT OBSERVATIONS.肌肉萎缩症。综述与近期观察
Am J Med. 1963 Nov;35:632-45. doi: 10.1016/0002-9343(63)90135-9.
10
STUDIES OF HUMAN MYOGLOBIN IN SEVERAL DISEASES OF MUSCLE.
N Engl J Med. 1964 Feb 6;270:263-9. doi: 10.1056/NEJM196402062700601.