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6 in total

Review 1. The history of progressive myoclonus epilepsies.

Authors: Pierre Genton; Pasquale Striano; Berge A Minassian
Journal: Epileptic Disord Date: 2016-09-01 Impact factor: 1.819

2. Autosomal dominant late onset cerebellar ataxia with myoclonus, peripheral neuropathy and sensorineural deafness: a clinicopathological report.

Authors: M Baraitser; W Gooddy; A M Halliday; A E Harding; P Rudge; F Scaravilli
Journal: J Neurol Neurosurg Psychiatry Date: 1984-01 Impact factor: 10.154

3. Dyssynergia cerebellaris myoclonica (Ramsay Hunt syndrome): a condition unrelated to mitochondrial encephalomyopathies.

Authors: C A Tassinari; R Michelucci; P Genton; J F Pellissier; J Roger
Journal: J Neurol Neurosurg Psychiatry Date: 1989-02 Impact factor: 10.154

4. Treatment of myoclonus with pheneturide.

Authors: C D Ward
Journal: J Neurol Neurosurg Psychiatry Date: 1978-07 Impact factor: 10.154

5. Normal muscle mitochondrial function in Ramsay-Hunt syndrome.

Authors: T Sacquegna; P Montagna; M Moggio; P De Carolis; R Agati; N Bresolin
Journal: Ital J Neurol Sci Date: 1989-02

6. PME of Unverricht-Lundborg type in the Mediterranean region: linkage and linkage disequilibrium confirm the assignment to the EPM1 locus.

Authors: A E Lehesjoki; C A Tassinari; G Avanzini; R Michelucci; S Franceschetti; A Antonelli; G Rubboli; A de la Chapelle
Journal: Hum Genet Date: 1994-06 Impact factor: 4.132

6 in total