Literature DB >> 13729348

Familial myoclonic epilepsy and its association with cerebellar disturbance.

K B NOAD, J W LANCE.   

Abstract

Entities:  

Keywords:  CEREBELLUM/diseases; EPILEPSY/genetics; MYOCLONUS/genetics

Mesh：

Year:  1960        PMID： 13729348     DOI： 10.1093/brain/83.4.618

Source DB:  PubMed          Journal:  Brain        ISSN： 0006-8950            Impact factor:   13.501


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  5 in total

1.  MYOCLONUS AND ATAXIA OCCURING IN A FAMILY.

Authors:  H JACOBS
Journal:  J Neurol Neurosurg Psychiatry       Date:  1965-06       Impact factor: 10.154

2.  Myoclonic dystonia.

Authors:  S M Pueschel; J H Friedman; T Shetty
Journal:  Childs Nerv Syst       Date:  1992-03       Impact factor: 1.475

3.  Progressive myoclonus and epilepsy with dentatorubral degeneration: a clinicopathological study of the Ramsay Hunt syndrome.

Authors:  T D Bird; C M Shaw
Journal:  J Neurol Neurosurg Psychiatry       Date:  1978-02       Impact factor: 10.154

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

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

5.  Autosomal recessive progressive myoclonus epilepsy with ataxia and mental retardation.

Authors:  Giovanni Coppola; Chiara Criscuolo; Giuseppe De Michele; Salvatore Striano; Fabrizio Barbieri; Pasquale Striano; Anna Perretti; Lucio Santoro; Vincenzo Brescia Morra; Francesco Saccà; Valentina Scarano; Adamo P D'Adamo; Sandro Banfi; Paolo Gasparini; Filippo M Santorelli; Anna E Lehesjoki; Alessandro Filla
Journal:  J Neurol       Date:  2005-03-08       Impact factor: 4.849
  5 in total

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