Dentatorubral-pallidoluysian atrophy. Clinical features of a five-generation danish family
Author:
Publisher
Wiley
Subject
Clinical Neurology,Neurology
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2. Hereditary dentatorubral-pallidoluysian atrophy: clinical and pathologic variants in a family;Takahashi;Neurology,1988
3. Dentato-rubro-pallidoluysian atrophy: a clinico-pathological study;Iizuka;J Neurol Neurosurg Psychiatry,1984
4. Familial myoclonus epilepsy and choreoathetosis: hereditary dentatorubral-pallidoluysian atrophy;Naito;Neurology,1982
5. Autosomal dominant dentatorubropallidoluysian atrophy in the United Kingdom;Warner;Mov Disord,1994
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3. Myoclonic occipital photosensitive epilepsy with dystonia (MOPED): A familial epilepsy syndrome;Epilepsy Research;2015-08
4. Clinical and genetic characteristics of non-Asian dentatorubral-pallidoluysian atrophy: A systematic review;Movement Disorders;2009-08-15
5. Clinical and molecular findings in the first identified Italian family with dentatorubral-pallidoluysian atrophy;Acta Neurologica Scandinavica;2009-01-29
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