[A large family of Valais affected with progressive myoclonic epilepsy and retinitis pigmentosa. A clinical, genetical and anatomo-pathological study].

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作者信息

Klein D, Mumenthaler M, Kraus-Ruppert R, Rallo E

出版信息

Humangenetik. 1968;6(3):237-52. doi: 10.1007/BF00291867.

DOI:10.1007/BF00291867

PMID:5709082

Abstract

摘要

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Myoclonus epilepsy (Univerricht-Lundborg) in Finland.

Acta Neurol Scand. 1961;37(4):282-96. doi: 10.1111/j.1600-0404.1961.tb01068.x.

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.

[On genetics of progressive myoclonic epilepsies (Unverricht-Lundborg)].

Humangenetik. 1965;1(5):437-75.

Lafora's disease--a distinct genetically determined form of Unverricht's syndrome.

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The clinical incidence of myoclonus.肌阵挛的临床发病率。

Mod Trends Neurol. 1967;4(0):69-105.

[Progressive malignant myoclonic epilepsy (Lafora's disease). Clinical and biochemical study of a case].[进行性恶性肌阵挛性癫痫（拉福拉病）。1例临床及生化研究]

Acta Neurol Psychiatr Belg. 1968 May;68(5):356-69.

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