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The ataxic form of Creutzfeldt-Jakob disease.

作者信息

Gomori A J, Partnow M J, Horoupian D S, Hirano A

出版信息

Arch Neurol. 1973 Nov;29(5):318-23. doi: 10.1001/archneur.1973.00490290058006.

DOI:10.1001/archneur.1973.00490290058006
PMID:4582819
Abstract
摘要

相似文献

1
The ataxic form of Creutzfeldt-Jakob disease.克雅氏病的共济失调型
Arch Neurol. 1973 Nov;29(5):318-23. doi: 10.1001/archneur.1973.00490290058006.
2
Familial clustering of the ataxic form of Creutzfeldt-Jakob disease with Hirano bodies.伴有 Hirano 小体的克雅氏病共济失调型的家族聚集性。
J Neurol Neurosurg Psychiatry. 1985 Mar;48(3):234-8. doi: 10.1136/jnnp.48.3.234.
3
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.
4
Sporadic Creutzfeldt-Jakob disease with cerebellar ataxia at onset in the UK.英国散发性克雅氏病发病时伴有小脑共济失调
J Neurol Neurosurg Psychiatry. 2006 Nov;77(11):1273-5. doi: 10.1136/jnnp.2006.088930. Epub 2006 Jul 11.
5
Creutzfeldt-Jakob's disease presenting with ataxia and a movement disorder.以共济失调和运动障碍为表现的克雅氏病。
Mov Disord. 1991;6(2):157-62. doi: 10.1002/mds.870060212.
6
[Progressive myoclonic cerebellar ataxia as a manifestation of Creutzfeldt-Jakob disease].
Rev Neurol. 2003;37(6):535-8.
7
Superficial bedside brain biopsy can be a safe and practical approach to confirm a rare form of prion disease in cerebellar ataxia: A case study.
J Neurol Sci. 2017 Apr 15;375:73-75. doi: 10.1016/j.jns.2017.01.047. Epub 2017 Jan 16.
8
Ataxia, dementia, and death in a 68-year-old woman.
Am J Med. 1984 Jun;76(6):1087-96. doi: 10.1016/0002-9343(84)90863-5.
9
[Corticocerebellar form of Creutzfeldt-Jakob disease. Anatomo-clinical study].
Pathologica. 1983 Jul-Aug;75(1038):577-81.
10
Clinical Reasoning: A 57-year-old woman with progressive ataxia and falls.临床推理：一名57岁进行性共济失调和跌倒的女性。
Neurology. 2020 Oct 6;95(14):650-656. doi: 10.1212/WNL.0000000000010464. Epub 2020 Aug 4.

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Agent strain variation in human prion disease: insights from a molecular and pathological review of the National Institutes of Health series of experimentally transmitted disease.人类朊病毒病中的病原体毒株变异：来自美国国立卫生研究院系列实验性传播疾病分子与病理学综述的见解
Brain. 2010 Oct;133(10):3030-42. doi: 10.1093/brain/awq234. Epub 2010 Sep 7.
2
Review. The origin of the prion agent of kuru: molecular and biological strain typing.综述：库鲁病朊病毒病原体的起源：分子和生物学毒株分型
Philos Trans R Soc Lond B Biol Sci. 2008 Nov 27;363(1510):3747-53. doi: 10.1098/rstb.2008.0069.
3
[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.
4
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.
5
Cerebellar plaques in familial Alzheimer's disease (Gerstmann-Sträussler-Scheinker variant?).家族性阿尔茨海默病中的小脑斑块（格斯特曼-施特劳斯勒-谢因克变异型？）
Acta Neuropathol. 1985;65(3-4):235-46. doi: 10.1007/BF00687003.
6
Abnormal arborizations of Purkinje cell dendrites in Creutzfeldt-Jakob disease: a manifestation of neuronal plasticity?克雅氏病中浦肯野细胞树突的异常分支：神经元可塑性的一种表现？
J Neurol Neurosurg Psychiatry. 1986 May;49(5):581-4. doi: 10.1136/jnnp.49.5.581.
7
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.
8
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.