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A study of the late form (type Lundborg) of progressive myoclonic epilepsy.

作者信息

Kraus-Ruppert R, Ostertag B, Häfner H

出版信息

J Neurol Sci. 1970 Jul;11(1):1-15. doi: 10.1016/0022-510x(70)90037-7.

DOI:10.1016/0022-510x(70)90037-7
PMID:4194907
Abstract
摘要

相似文献

1
A study of the late form (type Lundborg) of progressive myoclonic epilepsy.进行性肌阵挛癫痫迟发型（伦德伯格型）的一项研究。
J Neurol Sci. 1970 Jul;11(1):1-15. doi: 10.1016/0022-510x(70)90037-7.
2
Presenile dementia with "Lafora-like" intraneuronal inclusions.
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A histochemical study on myoclonus-epilepsy (Lafora-body type).肌阵挛性癫痫（拉福拉体病型）的组织化学研究。
Folia Psychiatr Neurol Jpn. 1966;20(1):33-43. doi: 10.1111/j.1440-1819.1966.tb00057.x.
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[Liver in progressive myoclonus epilepsy (Lafora's disease) (author's transl)].
Klin Wochenschr. 1974 Jun 15;52(12):559-67. doi: 10.1007/BF01468496.
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[The basic hereditary myoclonus-epilepsy-dementia syndromes. Progressive myoclonus epilepsies--myoclonic cerebellar dyssynergia--myoclonic variants of the 3 postinfantile types of amaurotic idiocy].[基本遗传性肌阵挛-癫痫-痴呆综合征。进行性肌阵挛癫痫——肌阵挛性小脑协同失调——3种婴儿后期黑蒙性白痴类型的肌阵挛变异型]
Monogr Gesamtgeb Psychiatr Psychiatry Ser. 1973;8:1-254.
6
[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.
7
[Unverricht-Lundborg progressive epilepsy-myoclonus and the problem of progressive encephalopathies combining epilepsy and myoclonia].
Rev Neurol (Paris). 1968 Jul;119(1):47-57.
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Progressive familial myoclonic epilepsy with Lafora bodies. Electron microscopic and histochemical study of a cerebral biopsy.
Acta Neuropathol. 1967 Feb 3;7(4):315-36. doi: 10.1007/BF00688087.
9
[2 autopsy cases of myoclonus epilepsy of the degenerative type in siblings].
No To Shinkei. 1968 Nov;20(11):1177-83.
10
[Tapetoretinal degeneration, deafness, myoclonus, dementia, epilepsy with the presence of excess alpha-amino-n-butyric acid. Contribution to the study of leptomeningeal angiomatosis with leukodystrophy sudanophil and abiotrophic complexes].[视锥视杆细胞营养不良、耳聋、肌阵挛、痴呆、伴有过量α-氨基丁酸的癫痫。对伴有嗜苏丹性脑白质营养不良和营养障碍性复合体的软脑膜血管瘤病研究的贡献]
J Neurol Sci. 1968 Mar-Apr;6(2):217-36. doi: 10.1016/0022-510x(68)90092-0.

引用本文的文献

1
A type of adult polyglucosan body disease.一种成人多聚葡萄糖体病。
Acta Neuropathol. 1982;58(1):73-7. doi: 10.1007/BF00692701.
2
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.
3
[Liver in progressive myoclonus epilepsy (Lafora's disease) (author's transl)].
Klin Wochenschr. 1974 Jun 15;52(12):559-67. doi: 10.1007/BF01468496.
4
[Recessive hereditary amyotrophic lateral sclerosis with "Lafora bodies" (author's transl)].伴有“拉福拉小体”的隐性遗传性肌萎缩侧索硬化症（作者译）
Arch Psychiatr Nervenkr (1970). 1973 Oct 25;217(4):387-412. doi: 10.1007/BF02552701.
5
Progressive myoclonic epilepsy (Unverricht type) with atypical Lafora bodies. Case report.
Eur Arch Psychiatry Neurol Sci. 1986;235(4):259-62. doi: 10.1007/BF00379982.
6
Polyglucosan bodies in intramuscular motor nerves.
Acta Neuropathol. 1989;77(6):629-33. doi: 10.1007/BF00687891.
7
Polyglucosan bodies in sural nerve biopsies.
Acta Neuropathol. 1990;80(5):554-7. doi: 10.1007/BF00294618.
8
Early detection of skin and muscular involvement in Lafora disease.
J Neurol. 1991 Jul;238(4):217-20. doi: 10.1007/BF00314784.