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[Muscle energy metabolism in children with progressive muscular dystrophy type Duchenne. Metabolites of the Embden-Meyerhof pathway, the citric acid cycle and high energy phosphates and enzyme activity of alpha-glycerol-oxidase, succinate-dehydrogenase and 6-phospho-gluconate-dehydrogenase (author's transl)].

作者信息

Stengel-Rutkowski L, Barthelmai W

出版信息

Klin Wochenschr. 1973 Oct 1;51(19):957-68. doi: 10.1007/BF01468251.

DOI:10.1007/BF01468251
PMID:4762584
Abstract
摘要

相似文献

1
[Muscle energy metabolism in children with progressive muscular dystrophy type Duchenne. Metabolites of the Embden-Meyerhof pathway, the citric acid cycle and high energy phosphates and enzyme activity of alpha-glycerol-oxidase, succinate-dehydrogenase and 6-phospho-gluconate-dehydrogenase (author's transl)].杜兴氏进行性肌营养不良症患儿的肌肉能量代谢。糖酵解途径、柠檬酸循环的代谢产物及高能磷酸盐，以及α-甘油氧化酶、琥珀酸脱氢酶和6-磷酸葡萄糖酸脱氢酶的酶活性（作者译）
Klin Wochenschr. 1973 Oct 1;51(19):957-68. doi: 10.1007/BF01468251.
2
Energy metabolism of the skeletal muscle of genetically dystrophic hamster.遗传性营养不良仓鼠骨骼肌的能量代谢
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Z Med Labortech. 1976 Dec 6;17(6):291-9.
4
[Metabolic characteristics of the skeletal muscles in the Duchenne form of progressive muscular dystrophy].[杜氏进行性肌营养不良症中骨骼肌的代谢特征]
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Glycogen, glycolytic intermediates and high-energy phosphates determined in biopsy samples of musculus quadriceps femoris of man at rest. Methods and variance of values.在静息状态下人体股四头肌活检样本中测定糖原、糖酵解中间产物和高能磷酸化合物。方法及数值的方差。
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Metabolic control of rat heart glycolysis after acute ischaemia. Fluoracetate treatment and thyroid interactions.急性缺血后大鼠心脏糖酵解的代谢调控。氟乙酸处理与甲状腺的相互作用。
J Mol Cell Cardiol. 1971 Aug;2(3):193-210. doi: 10.1016/0022-2828(71)90053-8.
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Duchenne muscular dystrophy.
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Muscle ATP content in rheumatoid arthritis--a biopsy study.类风湿关节炎患者肌肉中的三磷酸腺苷含量——一项活检研究
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[Comparative study of energy metabolism of the skeletal muscles in man, dogs and rats during long-term ischemia].[人、狗和大鼠骨骼肌在长期缺血期间能量代谢的比较研究]
Chir Forum Exp Klin Forsch. 1977 Apr:135-9.
10
Histochemical fibre "types" in Duchenne muscular dystrophy.
J Neurol Sci. 1970 Feb;10(2):163-71. doi: 10.1016/0022-510x(70)90015-8.

引用本文的文献

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Clinical applications of nuclear magnetic resonance spectroscopy: a review.核磁共振波谱的临床应用：综述
J R Soc Med. 1984 Sep;77(9):774-9. doi: 10.1177/014107688407700913.
2
[Comparative biochemical and electrophysiologic studies in skeletal muscle in alcoholism (author's transl)].酒精中毒时骨骼肌的比较生物化学和电生理学研究（作者译）
Arch Psychiatr Nervenkr (1970). 1977 May 16;223(3):249-63. doi: 10.1007/BF00342342.
3
The value of enzyme histochemical techniques in the classification of fibre types of human skeletal muscle. 3. Human skeletal muscles with inherited or acquired disease of the neuromuscular system.

本文引用的文献

1
Microestimation of non-protein nitrogen in serum, plasma, or blood.
Lancet. 1947 Aug 2;2(6466):171. doi: 10.1016/s0140-6736(47)92176-4.
2
THE CHEMICAL COMPOSITION OF VOLUNTARY MUSCLE IN MUSCLE DISEASE: A COMPARISON OF PROGRESSIVE MUSCULAR DYSTROPHY WITH OTHER DISEASES TOGETHER WITH A STUDY OF EFFECTS OF GLYCINE AND CREATINE THERAPY.肌肉疾病中随意肌的化学成分：进行性肌营养不良与其他疾病的比较以及甘氨酸和肌酸治疗效果的研究
J Clin Invest. 1938 Jul;17(4):377-83. doi: 10.1172/JCI100963.
3
Comparative chemical studies in skeletal muscle following neurotomy and tenotomy.神经切断术和肌腱切断术后骨骼肌的比较化学研究。
Histochemistry. 1977 Aug 1;53(2):97-105. doi: 10.1007/BF00498485.
Am J Physiol. 1950 Jun 1;161(3):406-12. doi: 10.1152/ajplegacy.1950.161.3.406.
4
Studies in disorders of muscle. VI. Is progressive muscular dystrophy an endocrine or metabolic disorder?肌肉疾病研究。VI. 进行性肌营养不良是一种内分泌或代谢紊乱疾病吗？
AMA Arch Intern Med. 1951 Aug;88(2):175-90. doi: 10.1001/archinte.1951.03810080043005.
5
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.
6
DISTURBANCES OF THE COMBUSTION PROCESSES IN MUSCULAR DISORDERS.肌肉疾病中燃烧过程的紊乱
J Neurol Neurosurg Psychiatry. 1965 Feb;28(1):19-22. doi: 10.1136/jnnp.28.1.19.
7
[CLINICAL AND BIOCHEMICAL STUDIES IN MYOPATHIES. I. SERUM ENZYMES IN PROGRESSIVE MUSCULAR DYSTROPHY (TYPE I, II, IIIA)].[肌病的临床与生化研究。I. 进行性肌营养不良（I型、II型、IIIA型）中的血清酶]
Klin Wochenschr. 1965 Feb 1;43:144-50. doi: 10.1007/BF01484506.
8
BIOCHEMICAL CHANGES IN PROGRESSIVE MUSCULAR DYSTROPY. II. PHOSPHORUS METABOLISM IN NORMAL, NUTRITIONAL AND HEREDITARY DYSTROPHIC MUSCLES, LIVERS AND BRAINS OF ANIMALS.进行性肌营养不良的生化变化。II. 动物正常、营养性及遗传性营养不良的肌肉、肝脏和大脑中的磷代谢
J Nutr. 1964 Jul;83(3):193-201. doi: 10.1093/jn/83.3.193.
9
GLYCOGEN, CREATINE, AND HIGH ENERGY PHOSPHATE IN HUMAN MUSCLE DISEASE.人类肌肉疾病中的糖原、肌酸和高能磷酸盐
J Lab Clin Med. 1963 Oct;62:579-90.
10
Studies on the "pentose phosphate pathway" in hereditary muscular distrophy in mice.
Med Exp Int J Exp Med. 1962;7:26-31.