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Globular neuropathy. A disorder of axons and Schwann cells.

作者信息

Dayan A D, Graveson G S, Robinson P K, Woodhouse M A

出版信息

J Neurol Neurosurg Psychiatry. 1968 Dec;31(6):552-60. doi: 10.1136/jnnp.31.6.552.

DOI:10.1136/jnnp.31.6.552
PMID:4303801
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC496422/
Abstract
摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a69c/496422/1d2153bb0854/jnnpsyc00234-0025-c.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a69c/496422/1fa45ccabbc5/jnnpsyc00234-0019-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a69c/496422/0faf55572a2d/jnnpsyc00234-0020-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a69c/496422/45f142653192/jnnpsyc00234-0020-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a69c/496422/d406b536ef75/jnnpsyc00234-0021-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a69c/496422/b337c2363a06/jnnpsyc00234-0021-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a69c/496422/63003cb6a4b9/jnnpsyc00234-0022-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a69c/496422/1bde658d0958/jnnpsyc00234-0023-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a69c/496422/2fe3be7117a4/jnnpsyc00234-0025-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a69c/496422/4bd5c8465fdb/jnnpsyc00234-0025-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a69c/496422/1d2153bb0854/jnnpsyc00234-0025-c.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a69c/496422/1fa45ccabbc5/jnnpsyc00234-0019-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a69c/496422/0faf55572a2d/jnnpsyc00234-0020-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a69c/496422/45f142653192/jnnpsyc00234-0020-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a69c/496422/d406b536ef75/jnnpsyc00234-0021-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a69c/496422/b337c2363a06/jnnpsyc00234-0021-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a69c/496422/63003cb6a4b9/jnnpsyc00234-0022-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a69c/496422/1bde658d0958/jnnpsyc00234-0023-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a69c/496422/2fe3be7117a4/jnnpsyc00234-0025-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a69c/496422/4bd5c8465fdb/jnnpsyc00234-0025-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a69c/496422/1d2153bb0854/jnnpsyc00234-0025-c.jpg

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Dejerine-Sottas syndrome grown to maturity: overview of genetic and morphological heterogeneity and follow-up of 25 patients.成人型德热里纳-索塔斯综合征:遗传和形态学异质性概述及25例患者随访
J Anat. 2002 Apr;200(4):341-56. doi: 10.1046/j.1469-7580.2002.00043.x.
3
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本文引用的文献

1
Severe sensory changes, and trophic disorder, in peroneal muscular atrophy (Charcot-Marie-Tooth type).
AMA Arch Neurol Psychiatry. 1952 Jan;67(1):1-22. doi: 10.1001/archneurpsyc.1952.02320130007001.
2
DIPHTHERITIC NEUROPATHY IN THE CHICKEN: AN ELECTRON-MICROSCOPE STUDY.鸡白喉性神经病:一项电子显微镜研究
J Pathol Bacteriol. 1965 Apr;89:591-8. doi: 10.1002/path.1700890218.
3
CHANGES IN NERVE CONDUCTION IN EXPERIMENTAL ALLERGIC NEURITIS.实验性变应性神经炎中神经传导的变化
J Neurol Neurosurg Psychiatry. 2000 Apr;68(4):483-8. doi: 10.1136/jnnp.68.4.483.
4
Atypical hereditary neuropathy with liability to pressure palsies (HNPP): the value of direct DNA diagnosis.遗传性压力易感性周围神经病(HNPP):直接DNA诊断的价值
J Med Genet. 1997 Nov;34(11):889-92. doi: 10.1136/jmg.34.11.889.
5
Dominantly inherited motor and sensory neuropathy with excessive myelin folding complex.伴有髓鞘过度折叠复合体的显性遗传性运动和感觉神经病
Acta Neuropathol. 1993;86(6):602-8. doi: 10.1007/BF00294299.
6
Clinical spectrum of the tomaculous neuropathies. Report of 60 cases and review of the literature.腊肠样神经病的临床谱。60例报告及文献复习。
Ital J Neurol Sci. 1993 Dec;14(9):609-17. doi: 10.1007/BF02339245.
7
Autosomal recessive hypermyelinating neuropathy.常染色体隐性遗传性高髓鞘性神经病
Acta Neuropathol. 1994;87(4):337-42. doi: 10.1007/BF00313601.
8
Tomaculous neuropathy in chromosome 1 Charcot-Marie-Tooth syndrome.1型遗传性运动感觉神经病中的腊肠样神经病
Acta Neuropathol. 1994;87(1):91-7. doi: 10.1007/BF00386259.
9
Sural nerve biopsies from workers with a history of chronic exposure to organic solvents and from normal control cases. Morphometric and ultrastructural studies.对有慢性有机溶剂接触史的工人和正常对照者进行腓肠神经活检。形态测量和超微结构研究。
Acta Neuropathol. 1983;62(1-2):73-86. doi: 10.1007/BF00684923.
10
Hereditary motor and sensory neuropathy of demyelinating and remyelinating type in children. Ultrastructural and morphometric studies on sural nerve biopsy specimens from ten sporadic cases.儿童脱髓鞘和再髓鞘化型遗传性运动和感觉神经病。对10例散发病例腓肠神经活检标本的超微结构和形态计量学研究。
Acta Neuropathol. 1984;65(1):1-9. doi: 10.1007/BF00689822.
J Neurol Neurosurg Psychiatry. 1964 Apr;27(2):106-15. doi: 10.1136/jnnp.27.2.106.
4
Changes due to age in internodal length in the sural nerve in man.人类腓肠神经节间长度随年龄的变化。
J Neurol Neurosurg Psychiatry. 1966 Feb;29(1):40-4. doi: 10.1136/jnnp.29.1.40.
5
The significance of the "dying back" process in experimental and human neurological disease.“逆行性”过程在实验性和人类神经疾病中的意义。
Int Rev Exp Pathol. 1964;3:219-67.
6
Acid phosphatase and lysosome activity in diphtheritic neuropathy and Wallerian degeneration.白喉性神经病和华勒氏变性中的酸性磷酸酶及溶酶体活性
Br J Exp Pathol. 1966 Oct;47(5):425-34.
7
Histologic and teased-fiber measurements of sural nerve in disorders of lower motor and primary sensory neurons.
Mayo Clin Proc. 1968 Feb;43(2):81-123.
8
Peripheral neuropathy of metachromatic leucodystrophy: observations on segmental demyelination and remyelination and the intracellular distribution of sulphatide.异染性脑白质营养不良的周围神经病:节段性脱髓鞘和再髓鞘形成以及硫脂细胞内分布的观察
J Neurol Neurosurg Psychiatry. 1967 Aug;30(4):311-8. doi: 10.1136/jnnp.30.4.311.