脑脂褐质（类蜡样质）贮积病的神经病理学和神经化学研究 - Suppr

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超能文献

Lipofuscin (ceroid) storage disease of the brain neuropathological and neurochemical studies.

作者信息

Ryan G B, Anderson M, Menkes J H, Dennett X

出版信息

Brain. 1970;93(3):617-28. doi: 10.1093/brain/93.3.617.

DOI:10.1093/brain/93.3.617

PMID:5507017

Abstract

摘要

相似文献

Lipofuscin (ceroid) storage disease of the brain neuropathological and neurochemical studies.脑脂褐质（类蜡样质）贮积病的神经病理学和神经化学研究

Brain. 1970;93(3):617-28. doi: 10.1093/brain/93.3.617.

Infantile form of so-called neuronal ceroid lipofuscinosis: lipid biochemical studies, fatty acid analysis of cerebroside sulfatides and sphingomyelin, myelin density profile and lipid composition.所谓神经元蜡样脂褐质沉积症的婴儿型：脂质生化研究、脑硫脂和鞘磷脂的脂肪酸分析、髓磷脂密度分布及脂质组成

Eur Neurol. 1979;18(5):312-21. doi: 10.1159/000115095.

[Neuronal ceroidolipofuscinosis. Apropos of a new case].[神经元蜡样脂褐质沉积症。关于一例新病例]

Rev Clin Esp. 1981 Nov 30;163(4):279-83.

[Ceroidolipofuscinosis (Jansky-Bielchowsky type). Report of a new case with electroencephalographic and anatomopathologic clinical diagnosis].[蜡样脂褐质沉积症（扬斯基－比尔绍斯基型）。一例经脑电图及解剖病理学临床诊断的新病例报告]

Rev Clin Esp. 1981 Nov 15;163(3):213-6.

The neurophysiological features of various diseases with NCL storage.各种伴有NCL蓄积疾病的神经生理学特征。

Riv Patol Nerv Ment. 1976 Aug;97(4):186-90.

[Atypical ceroid-lipofuscinosis in the adult or atypical spinocerebellar degeneration with intracytoplasmic inclusions? (author's transl)].成人非典型蜡样脂褐质沉积症还是伴有胞浆内包涵体的非典型脊髓小脑变性？（作者译）

Rev Otoneuroophtalmol. 1981 Mar-Apr;53(2):111-20.

Infantile Gaucher's disease: A biochemical study.婴儿型戈谢病：一项生化研究。

Neurology. 1974 Feb;24(2):162-7. doi: 10.1212/wnl.24.2.162.

The development of the neutral lipids and fatty acids in the brain of man, whales and dolphins.人类、鲸鱼和海豚大脑中中性脂质和脂肪酸的发育情况。

Clin Chim Acta. 1969 Aug;25(2):269-82. doi: 10.1016/0009-8981(69)90265-4.

Isolation and chemical characterization of metachromatic granules from a brain with metachromatic leukodystrophy.从患有异染性脑白质营养不良的大脑中分离并进行异染粒的化学特性分析。

J Neuropathol Exp Neurol. 1967 Oct;26(4):537-50. doi: 10.1097/00005072-196710000-00002.

Late infantile neurovisceral storage disease with curvilinear bodies.伴有曲线体的晚发性婴儿神经内脏贮积病

Neurology. 1971 Mar;21(3):207-17. doi: 10.1212/wnl.21.3.207.

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Acta Neuropathol Commun. 2025 Jul 23;13(1):160. doi: 10.1186/s40478-025-02059-z.

Gene therapy ameliorates bowel dysmotility and enteric neuron degeneration and extends survival in lysosomal storage disorder mouse models.基因治疗可改善肠道运动障碍和肠神经元变性，并延长溶酶体贮积症小鼠模型的生存期。

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Pathological changes in the thyroid gland in crush asphyxia.挤压性窒息时甲状腺的病理变化。

Forensic Sci Med Pathol. 2013 Dec;9(4):568-72. doi: 10.1007/s12024-013-9462-2. Epub 2013 Aug 13.

Infantile type of so-called neuronal ceroid-lipofuscinosis. Histological and electron microscopic studies.所谓婴儿型神经元蜡样脂褐质沉积症。组织学和电子显微镜研究。

Acta Neuropathol. 1973 Oct 11;26(2):157-70. doi: 10.1007/BF00697751.

[Clinical and ultrastructural observations in a case of juvenile amaurotic idiocy with protracted course (author's transl)].[一例病程迁延的青少年黑蒙性白痴的临床及超微结构观察（作者译）]

Arch Psychiatr Nervenkr (1970). 1973 Nov 27;218(1):79-91. doi: 10.1007/BF00347090.

A black thyroid and minocycline treatment.黑色甲状腺与米诺环素治疗

Br Med J. 1976 Nov 6;2(6044):1109-10. doi: 10.1136/bmj.2.6044.1109.

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