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Electron-microscopic heterogeneity of onion-bulb neuropathies of the Déjerine-Sottas type. Two patients in one family with the variant described by Lyon (1969).

作者信息

Joosten E, Gabreëls F, Gabrèèls-Festen A, Vrensen G, Korten J, Notermans S

出版信息

Acta Neuropathol. 1974 Feb 28;27(2):105-18. doi: 10.1007/BF00687161.

DOI:10.1007/BF00687161
PMID:4152255
Abstract
摘要

相似文献

1
Electron-microscopic heterogeneity of onion-bulb neuropathies of the Déjerine-Sottas type. Two patients in one family with the variant described by Lyon (1969).德热里纳 - 索塔斯型洋葱球样神经病的电子显微镜下异质性。一个家族中有两名患者患有里昂（1969年）描述的变异型。
Acta Neuropathol. 1974 Feb 28;27(2):105-18. doi: 10.1007/BF00687161.
2
[Formation of "onion bulbs" in Charcot-Marie-Tooth and Dejerine-Sottas hypertrophic neuropathies].[夏科-马里-图思病和德热里纳-索塔斯肥厚性神经病中“洋葱球”的形成]
Neuropatol Pol. 1975 Jan-Mar;13(1):93-106.
3
[Renaut's bodies and familial neuropathy of the Dejerine-Sottas type. Apropos of 2 anatomo-clinical cases].[勒诺氏小体与德热里纳 - 索塔斯型家族性神经病。关于2例解剖临床病例]
Sem Hop. 1975;51(31-34):2103-7.
4
Histologic and lipid studies of sural nerves in inherited hypertrophic neuropathy: preliminary report of a lipid abnormality in nerve and liver in Dejerine-Sottas disease.遗传性肥厚性神经病腓肠神经的组织学和脂质研究：德热里纳 - 索塔斯病神经和肝脏脂质异常的初步报告
Mayo Clin Proc. 1970 Apr;45(4):286-327.
5
[Electron microscopic study of a peripheral nerve biopsy specimen in four cases of Dejerine-Sottas hypertrophic neuritis].
Rev Neurol (Paris). 1966 Nov;115(5):917-32.
6
Onion bulb neuropathy in the trembler mouse: a model of hypertrophic interstitial neuropathy (Dejerine-Sottas) in man.震颤小鼠的洋葱球样神经病：人类肥厚性间质性神经病（德热里纳 - 索塔斯病）的一种模型
Acta Neuropathol. 1973 Jun 26;25(1):54-70. doi: 10.1007/BF00686858.
7
A case of Déjerine-Sottas disease with schizophrenic symptoms. A clinical and pathological study.一例伴有精神分裂症症状的德热里纳 - 索塔斯病。一项临床与病理研究。
Folia Psychiatr Neurol Jpn. 1975;29(1):13-24. doi: 10.1111/j.1440-1819.1975.tb02319.x.
8
Histochemical and electron microscopic observations on "onion bulb" formations in a case of hypertrophic neuritis of 25 years duration with onset in childhood.
Acta Neuropathol. 1968 Sep 2;11(2):157-73. doi: 10.1007/BF00690218.
9
Ataxia-telangiectasia (Louis Bar syndrome): with special reference to findings in the peripheral nervous system.
Psychiatr Neurol Neurochir. 1973 Nov-Dec;76(6):459-72.
10
Endoneurial space and its constituents in the sural nerve of patients with neuropathy.神经病变患者腓肠神经的神经内膜间隙及其组成成分
Brain. 1974 Dec;97(4):773-84. doi: 10.1093/brain/97.1.773.

引用本文的文献

1
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.
2
Study on the gene and phenotypic characterisation of autosomal recessive demyelinating motor and sensory neuropathy (Charcot-Marie-Tooth disease) with a gene locus on chromosome 5q23-q33.5q23 - q33染色体基因位点的常染色体隐性脱髓鞘运动和感觉神经病（夏科 - 马里 - 图斯病）的基因及表型特征研究
J Neurol Neurosurg Psychiatry. 1999 May;66(5):569-74. doi: 10.1136/jnnp.66.5.569.
3

本文引用的文献

1
THE EFFECTS OF EXPERIMENTAL DEMYELINATION ON CONDUCTION IN PERIPHERAL NERVE: A HISTOLOGICAL AND ELECTROPHYSIOLOGICAL STUDY. I. CLINICAL AND HISTOLOGICAL OBSERVATIONS.实验性脱髓鞘对周围神经传导的影响：一项组织学和电生理学研究。I. 临床和组织学观察
Brain. 1963 Sep;86:481-500. doi: 10.1093/brain/86.3.481.
2
Mitochondrial localization of oxidative enzymes: staining results with two tetrazolium salts.氧化酶的线粒体定位：两种四唑盐的染色结果
J Biophys Biochem Cytol. 1961 Jan;9(1):47-61. doi: 10.1083/jcb.9.1.47.
3
The cytochemical localization of oxidative enzymes. I. Diphosphopyridine nucleotide diaphorase and triphosphopyridine nucleotide diaphorase.
Neuroaxonal pathology of central and peripheral nervous systems in cerebrotendinous xanthomatosis (CTX).
脑腱黄瘤病（CTX）中枢和周围神经系统的神经轴突病变
Acta Neuropathol. 1984;64(3):259-64. doi: 10.1007/BF00688117.
4
A case report of congenital hypomyelination.先天性髓鞘形成低下一例报告
Eur J Pediatr. 1982 May;138(3):265-70. doi: 10.1007/BF00441215.
5
Refsum disease. Clinical and morphological report on a case.雷夫叙姆病。一例病例的临床及形态学报告。
Ital J Neurol Sci. 1982 Oct;3(3):241-5. doi: 10.1007/BF02043317.
6
Hypertrophy of peripheral nerves in the syndrome of multiple mucosal neuromas, endocrine tumours and Marfanoid habitus. Autonomic disturbances and sural nerve findings.多发性黏膜神经瘤、内分泌肿瘤及马方综合征体型综合征中周围神经的肥大。自主神经功能障碍及腓肠神经检查结果。
Acta Neuropathol. 1974;30(3):251-61. doi: 10.1007/BF00688925.
7
Variability of morphological features in early infantile polyneuropathy with defective myelination.早期婴儿脱髓鞘性多神经病形态学特征的变异性
Acta Neuropathol. 1987;73(3):295-300. doi: 10.1007/BF00686625.
氧化酶的细胞化学定位。I. 二磷酸吡啶核苷酸黄递酶和三磷酸吡啶核苷酸黄递酶。
J Biophys Biochem Cytol. 1958 Nov 25;4(6):747-52. doi: 10.1083/jcb.4.6.747.
4
The normal sural nerve in man. I. Ultrastructure and numbers of fibres and cells.人类正常的腓肠神经。I. 纤维和细胞的超微结构及数量
Acta Neuropathol. 1969;13(3):197-216. doi: 10.1007/BF00690642.
5
Quantitative teased-fiber and histologic studies of human sural nerve during postnatal development.人腓肠神经在出生后发育过程中的定量 teased 纤维和组织学研究。
J Comp Neurol. 1970 Jan;138(1):117-29. doi: 10.1002/cne.901380109.
6
[Ultrastructure of experimental allergic neuritis in the rabbit].[兔实验性过敏性神经炎的超微结构]
Acta Neuropathol. 1970;14(4):261-83. doi: 10.1007/BF00685783.
7
Spinocerebellar ataxia with neural myatrophy.伴神经肌萎缩的脊髓小脑性共济失调
Neuropadiatrie. 1971 Jul;3(1):97-105. doi: 10.1055/s-0028-1091802.
8
A brief review of inherited hypertrophic neuropathy.
Birth Defects Orig Artic Ser. 1971 Feb;7(2):66-71.
9
Experimental hypertrophic neuropathy. Pathogenesis of onion-bulb formations produced by repeated tourniquet applications.
Arch Neurol. 1969 Jul;21(1):73-95. doi: 10.1001/archneur.1969.00480130087010.
10
Necrotizing angiopathic neuropathy. Three-dimensional morphology of fiber degeneration related to sites of occluded vessels.坏死性血管病性神经病。与闭塞血管部位相关的纤维变性的三维形态。
Mayo Clin Proc. 1972 Jul;47(7):461-75.