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[Liver in progressive myoclonus epilepsy (Lafora's disease) (author's transl)].

作者信息

Huchzermeyer H, Gerhard L

出版信息

Klin Wochenschr. 1974 Jun 15;52(12):559-67. doi: 10.1007/BF01468496.

DOI:10.1007/BF01468496
PMID:4368175
Abstract
摘要

相似文献

1
[Liver in progressive myoclonus epilepsy (Lafora's disease) (author's transl)].
Klin Wochenschr. 1974 Jun 15;52(12):559-67. doi: 10.1007/BF01468496.
2
Ultrastructural studies in myoclonus epilepsy. (Clinical Unverricht-Lafora's disease).
Neurology. 1968 May;18(5):427-38. doi: 10.1212/wnl.18.5.427.
3
[Myoclonic epilepsy with inclusion bodies (Lafora's disease)--(clinico-pathologic case report)].
Neuropsihijatrija. 1971;19(3):133-40.
4
[Histochemical study of Lafora's bodies].[拉福拉小体的组织化学研究]
Acta Neuropathol. 1969;12(3):205-17. doi: 10.1007/BF00687645.
5
The myocardium in Lafora disease.拉福拉病中的心肌。
Acta Neuropathol. 1975 Dec 30;33(4):343-9. doi: 10.1007/BF00686166.
6
Lafora's disease in the dog. A comparative study.
Am J Pathol. 1970 Mar;58(3):509-30.
7
An autopsy case of glycogen and non-glycogen polysaccharide storage disease with cardiomegaly.一例伴有心脏肥大的糖原与非糖原多糖贮积病尸检病例。
Acta Pathol Jpn. 1973 Feb;23(1):189-209. doi: 10.1111/j.1440-1827.1973.tb00785.x.
8
Lafora's disease. An ultrastructural and histochemical study.
Acta Neuropathol. 1974;30(3):189-96. doi: 10.1007/BF00688920.
9
[Intracytoplasmic inclusions in the liver in myoclonus epilepsy].[肌阵挛性癫痫患者肝脏中的胞质内包涵体]
Zentralbl Allg Pathol. 1970;113(4):448-50.
10
Presenile dementia with "Lafora-like" intraneuronal inclusions.
Arch Neurol. 1971 Jul;25(1):69-80. doi: 10.1001/archneur.1971.00490010079011.

引用本文的文献

1
Polyglucosan bodies in the digestive tract of the aged dog.老年犬消化道中的多聚葡萄糖体。
Acta Neuropathol. 1983;60(3-4):297-300. doi: 10.1007/BF00691880.
2
Atypical myoclonus body epilepsy (adult variant).非典型肌阵挛性全身性癫痫（成人型）
Acta Neuropathol. 1975;31(3):201-6. doi: 10.1007/BF00684559.

本文引用的文献

1
A MYOPATHY PRESENTING IN ADULT LIFE WITH FEATURES SUGGESTIVE OF GLYCOGEN STORAGE DISEASE.一种在成人期出现、具有提示糖原贮积病特征的肌病。
J Neurol Neurosurg Psychiatry. 1960 Nov;23(4):302-11. doi: 10.1136/jnnp.23.4.302.
2
[Clinical and biochemical studies of family with progressive familial myoclonic epilepsy (Lafora type)].
Seishin Shinkeigaku Zasshi. 1961 Oct;63:1105-16.
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.
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
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.
6
PROGRESSIVE MYOCLONUS EPILEPSY AS AN INBORN ERROR OF METABOLISM COMPARABLE TO STORAGE DISEASE.进行性肌阵挛癫痫作为一种与贮积病类似的先天性代谢缺陷。
Epilepsia. 1963 Jun;4:120-37. doi: 10.1111/j.1528-1157.1963.tb05215.x.
7
Progressive familial myoclonic epilepsy in three families: its clinical features and pathological basis.
Brain. 1955 Sep;78(3):325-49. doi: 10.1093/brain/78.3.325.
8
Progressive myoclonus epilepsy with Lafora inclusion bodies. II. Studies of ultrastructure.伴有拉福拉包涵体的进行性肌阵挛癫痫。II. 超微结构研究
Arch Neurol. 1967 Jun;16(6):583-94. doi: 10.1001/archneur.1967.00470240021002.
9
Progressive myoclonus epilepsy with Lafora inclusion bodies. I. Clinical, genetic, histopathologic, and biochemical aspects.
Arch Neurol. 1967 Jun;16(6):565-82. doi: 10.1001/archneur.1967.00470240003001.
10
Atypical inclusion bodies with myoclonic epilepsy.伴有肌阵挛性癫痫的非典型包涵体
Acta Neuropathol. 1966 Sep 1;7(1):16-25. doi: 10.1007/BF00686606.