无Lafora小体的进行性肌阵挛癫痫 - Suppr | 超能文献

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无Lafora小体的进行性肌阵挛癫痫 - Suppr | 超能文献

Progressive myoclonus epilepsy without Lafora bodies.

作者信息

Matthews W B, Howell D A, Stevens D L

出版信息

J Neurol Neurosurg Psychiatry. 1969 Apr;32(2):116-22. doi: 10.1136/jnnp.32.2.116.

DOI:10.1136/jnnp.32.2.116

原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC496452/

Abstract

摘要

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eec7/496452/44b94efa408b/jnnpsyc00224-0047-b.jpg

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eec7/496452/536a0e43302a/jnnpsyc00224-0045-a.jpg

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eec7/496452/052962bbe5cb/jnnpsyc00224-0046-a.jpg

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eec7/496452/c90c3eac8663/jnnpsyc00224-0047-a.jpg

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eec7/496452/44b94efa408b/jnnpsyc00224-0047-b.jpg

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eec7/496452/536a0e43302a/jnnpsyc00224-0045-a.jpg

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eec7/496452/052962bbe5cb/jnnpsyc00224-0046-a.jpg

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eec7/496452/c90c3eac8663/jnnpsyc00224-0047-a.jpg

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eec7/496452/44b94efa408b/jnnpsyc00224-0047-b.jpg

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1

Progressive myoclonus epilepsy without Lafora bodies.无Lafora小体的进行性肌阵挛癫痫

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Progressive myoclonic epilepsy due to Gaucher's disease in an adult.一名成人因戈谢病导致的进行性肌阵挛癫痫。

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3

Myoclonus epilepsy with cerebellar Lafora bodies. Report of a case.伴有小脑拉福拉小体的肌阵挛性癫痫。病例报告。

本文引用的文献

1

[On a hereditary dementia with dementia, epilepsy-myocloma and arachnodactyly].[关于一种伴有痴呆、癫痫 - 肌阵挛及蜘蛛指的遗传性痴呆]

Monatsschr Psychiatr Neurol. 1949 Dec;118(6):364-78.

2

A CASE OF LATE INFANTILE AMAUROTIC IDIOCY OF THE MYOCLONUS TYPE.一例肌阵挛型晚期婴儿黑蒙性白痴

Acta Neurol Scand. 1965;41(2):172-86. doi: 10.1111/j.1600-0404.1965.tb04290.x.

3

LAFORA'S DISEASE. DISTINCT CLINICO-PATHOLOGIC FORM OF UNVERRICHT'S SYNDROME.

Arch Neurol. 1965 Feb;12:172-88. doi: 10.1001/archneur.1965.00460260062008.

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4

Urinary glycosaminoglycans in patients with progressive myoclonus epilepsy.进行性肌阵挛癫痫患者的尿糖胺聚糖

J Neurol. 1979 Jan 5;220(4):291-5. doi: 10.1007/BF00314153.

4

[THE MYOCLONUS BODY DISEASE. A CONGENITAL DISORDER OF THE CARBOHYDRATE METABOLISM. CLINICOPATHOLOGICAL STUDY OF 5 CASES].[肌阵挛身体疾病。一种碳水化合物代谢的先天性疾病。5例临床病理研究]

Fortschr Neurol Psychiatr Grenzgeb. 1964 Jul;32:305-45.

5

AMAUROTIC IDIOCY AND EPILEPSY.黑蒙性白痴与癫痫

Epilepsia. 1963 Dec;4:241-60. doi: 10.1111/j.1528-1157.1963.tb05224.x.

6

PROGRESSIVE MYOCLONUS EPILEPSY WITH LAFORA BODIES. CLINICAL-PATHOLOGICAL FEATURES.伴有拉福拉小体的进行性肌阵挛癫痫。临床病理特征。

Epilepsia. 1963 Jun;4:95-119. doi: 10.1111/j.1528-1157.1963.tb05214.x.

7

The detection of carriers in hereditary myoclonic epilepsy.遗传性肌阵挛性癫痫携带者的检测

Acta Genet Med Gemellol (Roma). 1960 Oct;9:466-71. doi: 10.1017/s1120962300018199.

8

[On myoclonic cerebellar dyssynergy].[关于肌阵挛性小脑协同障碍]

Rev Neurol (Paris). 1958 Jun;98(6):695-9.

9

[Latent senile cerebellar atrophy with the clinical aspects of epilepsy and progressive myoclonus with mental deficiency].[伴有癫痫临床症状及进行性肌阵挛伴智力缺陷的潜在性老年小脑萎缩]

Acta Neurol Psychiatr Belg. 1958 Mar;58(3):270-5.

10

[Dys-synergia cerebellaris myoclonica of Ramsay Hunt; anatomical study of a case].

Rev Neurol (Paris). 1956 Oct;95(4):297-309.