[关于进行性肌营养不良的研究。V. 杜兴型进行性肌营养不良临床前期的组织学发现] - Suppr

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[Contribution on progressive muscular dystrophy. V. Histological findings in the preclinical stage of Duchenne-type progressive muscular dystrophy].

作者信息

Heyck H, Lüders C J, Laudahn G

出版信息

Klin Wochenschr. 1966 Jul 15;44(14):813-8. doi: 10.1007/BF01711498.

DOI:10.1007/BF01711498

PMID:5994678

Abstract

摘要

相似文献

[Contribution on progressive muscular dystrophy. V. Histological findings in the preclinical stage of Duchenne-type progressive muscular dystrophy].[关于进行性肌营养不良的研究。V. 杜兴型进行性肌营养不良临床前期的组织学发现]

Klin Wochenschr. 1966 Jul 15;44(14):813-8. doi: 10.1007/BF01711498.

[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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Histopathological changes in Duchenne muscular dystrophy.杜氏肌营养不良症的组织病理学变化。

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Regeneration in Duchenne muscular dystrophy. A histological electron-microscopic and histochemical study.杜兴氏肌营养不良症的再生。一项组织学、电子显微镜和组织化学研究。

Proc Aust Assoc Neurol. 1969;6:93-106.

An appraisal of histochemical fiber types in Duchenne muscular dystrophy.杜氏肌营养不良症中组织化学纤维类型的评估。

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Maturational defect of regenerating muscle fibers in cases with Duchenne and congenital muscular dystrophies.杜兴氏肌营养不良症和先天性肌营养不良症病例中再生肌纤维的成熟缺陷。

Muscle Nerve. 1983 Oct;6(8):545-52. doi: 10.1002/mus.880060802.

引用本文的文献

[Morphological findings in dermatomyositis].[皮肌炎的形态学表现]

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Acta Neuropathol. 1971;18(2):173-89. doi: 10.1007/BF00687605.

[Creatine phosphokinase activity in serum of carriers of progressive muscular dystrophy of Duchenne type].[杜兴氏型进行性肌营养不良携带者血清中的肌酸磷酸激酶活性]

Humangenetik. 1969 Oct;8(2):115-33. doi: 10.1007/BF00295835.

[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.

本文引用的文献

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.

Abnormalities of muscle protein metabolism in mice with muscular dystrophy.患有肌肉萎缩症的小鼠肌肉蛋白质代谢异常。

J Clin Invest. 1960 Jul;39(7):1180-4. doi: 10.1172/JCI104132.

HISTOCHEMISTRY OF MUSCLE IN INFANTILE SPINAL MUSCULAR ATROPHY.婴儿型脊髓性肌萎缩症的肌肉组织化学

Neurology. 1963 Dec;13:1059-66. doi: 10.1212/wnl.13.12.1059.

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.

[ON THE NEUROLOGICAL SIGNIFICANCE OF MUSCLE BIOPSY STUDIES].[论肌肉活检研究的神经学意义]

Acta Morphol Acad Sci Hung. 1963;12:163-80.

Evidence of regeneration in repeat biopsies of dystrophic human muscle.营养不良性人类肌肉重复活检中的再生证据。

Neurology. 1962 Jun;12:381-4. doi: 10.1212/wnl.12.6.381.

Biochemical and histological features of early muscular dystrophy.早期肌肉营养不良的生化和组织学特征。

Rev Can Biol. 1962 Sep-Dec;21:533-42.

[The myopathies and the muscular biopsy].[肌病与肌肉活检]

Rev Med Liege. 1961 Sep 1;16:490-6.

Pattern of regeneration of muscle from progressive muscular dystrophy patients cultivated in vitro as compared to normal human skeletal muscle.与正常人骨骼肌相比，进行性肌营养不良患者体外培养的肌肉再生模式。

J Neuropathol Exp Neurol. 1957 Oct;16(4):523-43.

The nature of muscular diseases.肌肉疾病的本质。

Can Med Assoc J. 1952 Jul;67(1):1-6.

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