Literature DB >> 13904687

Myoclonus epilepsy (Univerricht-Lundborg) in Finland.

A Harenko, E I Toivakka.   

Abstract

Entities:  

Keywords:  EPILEPSY/statistics; MYOCLONUS/statistics

Mesh：

Year:  1961        PMID： 13904687     DOI： 10.1111/j.1600-0404.1961.tb01068.x

Source DB:  PubMed          Journal:  Acta Neurol Scand        ISSN： 0001-6314            Impact factor:   3.209


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  5 in total

1.  Progressive myoclonus epilepsy. A variant with probable X-linked inheritance.

Authors:  T F Wienker; G M von Reutern; H H Ropers
Journal:  Hum Genet       Date:  1979-05-23       Impact factor: 4.132

Review 2.  The Finnish Disease Heritage III: the individual diseases.

Authors:  Reijo Norio
Journal:  Hum Genet       Date:  2003-03-08       Impact factor: 4.132

3.  [Four genetic and clinical types of progressive myoclonus epilepsies].

Authors:  K Diebold
Journal:  Arch Psychiatr Nervenkr (1970)       Date:  1972

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

Authors:  D Klein; M Mumenthaler; R Kraus-Ruppert; E Rallo
Journal:  Humangenetik       Date:  1968

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

Authors:  F Vogel; H Häfner; K Diebold
Journal:  Humangenetik       Date:  1965
  5 in total

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