在277例对照者的薄束核中所见的一种独特类型的轴突改变（所谓的轴突营养不良）。对衰老过程病理学的一项贡献。 - Suppr

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超能文献

AN UNIQUE TYPE OF AXONAL ALTERATION (so-called axonal dystrophy) as seen in Goll's nucleus of 277 cases of controls. A contribution to the pathology of aging process.

作者信息

Fujisawa K

出版信息

Acta Neuropathol. 1967 May 5;8(3):255-75. doi: 10.1007/BF00688827.

DOI:10.1007/BF00688827

PMID:4166363

Abstract

摘要

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AN UNIQUE TYPE OF AXONAL ALTERATION (so-called axonal dystrophy) as seen in Goll's nucleus of 277 cases of controls. A contribution to the pathology of aging process.在277例对照者的薄束核中所见的一种独特类型的轴突改变（所谓的轴突营养不良）。对衰老过程病理学的一项贡献。

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Acta Neuropathol. 1963 Sep 2;3:16-28. doi: 10.1007/BF00684016.

AXON SWELLINGS PRODUCED IN VIVO IN ISOLATED SEGMENTS OF NERVES.体内神经孤立节段产生的轴突肿胀

Acta Neuropathol. 1964 Jan 2;3:229-37. doi: 10.1007/BF00684398.

ELECTROPHORETIC PRODUCTION OF "REACTIVE" AXON SWELLINGS IN VITRO AND THEIR HISTOCHEMICAL PROPERTIES.体外电泳产生“反应性”轴突肿胀及其组织化学特性

Acta Neuropathol. 1964 Jan 2;3:217-28. doi: 10.1007/BF00684397.

AN ELECTRON MICROSCOPIC STUDY OF DYSTROPHIC AXONS IN THE GRACILE AND CUNEATE NUCLEI OF VITAMIN E-DEFICIENT RATS.维生素E缺乏大鼠薄束核和楔束核中营养不良性轴突的电子显微镜研究

J Neuropathol Exp Neurol. 1964 Jan;23:60-77. doi: 10.1097/00005072-196401000-00005.

Infantile neuroaxonal dystrophy.婴儿神经轴索性营养不良

J Neuropathol Exp Neurol. 1963 Apr;22:175-236. doi: 10.1097/00005072-196304000-00001.

[Late infantile form of Hallervorden-Spatz disease. II. Histochemical findings; discussion on nosology].

Dtsch Z Nervenheilkd. 1957;176(1):104-25.

[Late infantile form of the Hallervorden-Spatz disease. I. Clinical and anatomical findings].

Dtsch Z Nervenheilkd. 1957;176(1):77-103.

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Prog Brain Res. 1966;21:373-425. doi: 10.1016/s0079-6123(08)64238-7.

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