克雅氏病的共济失调（小脑）型 - Suppr

Suppr

超能文献

The ataxic (cerebellar) form of Creutzfeldt-Jakob disease.

作者信息

Jellinger K, Heiss W D, Deisenhammer E

出版信息

J Neurol. 1974;207(4):289-305. doi: 10.1007/BF00312583.

DOI:10.1007/BF00312583

PMID:4138140

Abstract

摘要

相似文献

The ataxic (cerebellar) form of Creutzfeldt-Jakob disease.克雅氏病的共济失调（小脑）型

J Neurol. 1974;207(4):289-305. doi: 10.1007/BF00312583.

Ataxic Creutzfeldt-Jakob disease: diagnostic techniques and neuropathologic observations in early disease.

Neurology. 1985 Feb;35(2):254-7. doi: 10.1212/wnl.35.2.254.

[An autopsy case of ataxic form of Creutzfeldt-Jakob disease].

No To Shinkei. 1992 Feb;44(2):177-81.

[Ataxic form of Jakob-Creutzfeldt syndrome].

Neurol Neurochir Pol. 1981 Jan-Feb;15(1):91-5.

An autopsy case of Creutzfeldt-Jakob disease accompanying prominent status spongiosus.

Acta Pathol Jpn. 1974 Sep;24(5):673-91. doi: 10.1111/j.1440-1827.1974.tb01243.x.

Crossed cerebellar diaschisis: a clue to the mechanism of ataxic hemiparesis in Creutzfeldt-Jakob disease?交叉性小脑失联络：克雅氏病中共济失调性偏瘫机制的线索？

J Neurol. 2001 Dec;248(12):1093-5. doi: 10.1007/pl00007828.

Creutzfeldt-Jakob disease: further similarities with kuru.克雅氏病：与库鲁病的更多相似之处。

J Neurol Neurosurg Psychiatry. 1974 Feb;37(2):195-200. doi: 10.1136/jnnp.37.2.195.

Subacute spongioform encephalopathy--a clinical and pathological study with attention to liver involvement.

Proc Aust Assoc Neurol. 1973;9:111-9.

Creutzfeldt-Jakob disease. Some unusual morphological features reminiscent of kuru.

Z Neurol. 1973 Dec 31;206(1):1-24.

[Subacute spongiform encephalopathy (Jakob-Cretzfeldt syndrome). Clinico-pathological evaluation of 9 cases].

Arch Psychiatr Nervenkr (1970). 1971;214(3):207-27. doi: 10.1007/BF00342625.

引用本文的文献

Primary progressive aphasia with focal periodic sharp wave complexes: An unusual manifestation of Creutzfeldt-Jakob disease.伴有局灶性周期性锐波复合波的原发性进行性失语：克雅氏病的一种不寻常表现。

Clin Neurophysiol Pract. 2023 Dec 18;9:21-26. doi: 10.1016/j.cnp.2023.12.002. eCollection 2024.

Severe cerebellar atrophy in the panencephalopathic type of Creutzfeldt-Jakob disease: a case report.

J Neurol. 1995 May;242(5):348-50. doi: 10.1007/BF00878880.

[Subacute spongiform encephalopathy with multiform plaque formation. "Peculiar familial-hereditary disease of CNS [spinocerebellar atrophy with dementia, plaques, and plaque-like deposits in cerebellum and cerebrum" (Gerstmann, Sträussler, Scheinker)] (author's transl)].伴有多形性斑块形成的亚急性海绵状脑病。“中枢神经系统的特殊家族遗传性疾病[脊髓小脑萎缩伴痴呆，小脑和大脑中有斑块及斑块样沉积物”（格斯特曼、施特劳斯勒、申克）]（作者译）

Acta Neuropathol. 1980;49(3):205-12. doi: 10.1007/BF00707108.

[Morbus Gerstmann-Sträussler-Scheinker. The Sch. family-a report of three cases (author's transl)].[格斯特曼-施特劳斯勒-申克病。施氏家族——三例报告（作者译）]

Arch Psychiatr Nervenkr (1970). 1981;230(3):179-96. doi: 10.1007/BF00344444.

Unusual EEG findings in a case of Creutzfeldt-Jakob disease.

J Neurol. 1987 Jan;234(1):55-8. doi: 10.1007/BF00314011.

Creutzfeldt-Jakob disease with severe involvement of cerebral white matter and cerebellum.

Virchows Arch A Pathol Anat Histopathol. 1990;417(6):533-8. doi: 10.1007/BF01625735.

Acute ascending polyradiculoneuritis in a case of Creutzfeldt-Jakob disease.

J Neurol Neurosurg Psychiatry. 1977 Feb;40(2):149-55. doi: 10.1136/jnnp.40.2.149.

本文引用的文献

AN ATAXIC FORM OF SUBACUTE PRESENILE POLIOENCEPHALOPATHY (CREUTZFELDT-JAKOB DISEASE).一种亚急性早老性脑脊髓病（克雅氏病）的共济失调型

J Neurol Neurosurg Psychiatry. 1965 Aug;28(4):350-61. doi: 10.1136/jnnp.28.4.350.

NEURONAL ENZYMATIC FAILURE IN CREUTZFELDT-JAKOB DISEASE; A FAMILIAL STUDY.

Arch Neurol. 1964 Feb;10:181-95. doi: 10.1001/archneur.1964.00460140067009.

CREUTZFELDT-JAKOB'S DISEASE. CLINICOPATHOLOGIC REPORT OF 15 CASES AND REVIEW OF THE LITERATURE (WITH SPECIAL REFERENCE TO A RELATED DISORDER DESIGNATED AS SUBACUTE SPONGIFORM ENCEPHALOPATHY).

J Neuropathol Exp Neurol. 1963 Jul;22:381-402.

Degenerative disease of the central nervous system in New Guinea; the endemic occurrence of kuru in the native population.新几内亚的中枢神经系统退行性疾病；当地人群中库鲁病的地方性流行。

N Engl J Med. 1957 Nov 14;257(20):974-8. doi: 10.1056/NEJM195711142572005.

A subacute progressive encephalopathy with mutism, hypokinesia, rigidity, and myoclonus.

Q J Med. 1957 Jul;26(103):349-73.

Myxedema and ataxia. Cerebellar alterations and "neural myxedema bodies".黏液性水肿与共济失调。小脑改变及“神经黏液性水肿小体”

Neurology. 1966 Oct;16(10):957-62. doi: 10.1212/wnl.16.10.957.

Subacute cerebellar degeneration associated with neoplasms.与肿瘤相关的亚急性小脑变性

Brain. 1965 Sep;88(3):465-78. doi: 10.1093/brain/88.3.465.

[The subacute encephalopathy Creutzfeldt-Jakob, an abiotrophic degeneration during the presenium].[亚急性克雅氏病性脑病，一种早老期的营养缺失性变性]

Dtsch Z Nervenheilkd. 1968 Jun 5;193(4):351-69.

Creutzfeldt-Jakob disease (spongiform encephalopathy): transmission to the chimpanzee.克雅氏病（海绵状脑病）：传播至黑猩猩。

Science. 1968 Jul 26;161(3839):388-9. doi: 10.1126/science.161.3839.388.

Kuru--a subacute cerebellar degeneration. The natural history and clinical features.

Brain. 1968 Mar;91(1):53-74. doi: 10.1093/brain/91.1.53.

文献AI研究员

20分钟写一篇综述，助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型，支持多种主流文档格式。

立即体验