Progressive myoclonus epilepsies: an electroclinical, biochemical, morphological and molecular genetic study of 17 cases

Author:

Franceschetti S.,Antozzi C.,Binelli S.,Carrara F.,Nardocci N.,Zeviani M.,Avanzini G.

Publisher

Wiley

Subject

Clinical Neurology,Neurology,General Medicine

Reference28 articles.

1. Viewpoints on the Ramsay Hunt syndrome. I. The Ramsay Hunt syndrome is a useful clinical entity;MARSDEN;Movement Disorders,1989

2. Viewpoints on the Ramsay Hunt syndrome. II. The Ramsay Hunt syndrome is no longer a useful diagnostic category;ANDERMANN;Movement Disorders,1989

3. Ramsay Hunt syndrome, Unverricht-Lundborg disease, or what;HARDING;Movement Disorders,1989

4. Progressive myoclonus epilepsies: specific causes and diagnosis;BERKOVIC;N Engl J Med,1986

5. Mitochondrial Encephalomyopathies: a solution to the enigma of the Ramsay Hunt syndrome;BERKOVIC;Neurology,1987

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1. Mitochondrial Neurodegeneration;Cells;2022-02-11

2. Long-term evolution of EEG in Unverricht-Lundborg disease;Neurophysiologie Clinique/Clinical Neurophysiology;2016-04

3. Complex single gene disorders and epilepsy;Epilepsia;2012-09

4. Ataxia in mitochondrial disorders;Handbook of Clinical Neurology;2012

5. Unverricht–Lundborg Disease (EPM1);Atlas of Epilepsies;2010

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