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Brain : a Journal of Neurology|December 16, 1997
Clinical and neurophysiological features of tick paralysisP J Grattan-Smith, J G Morris, H M Johnston, et al.
Human Mutation|January 1, 1995
Déjérine-Sottas neuropathy is associated with a de novo PMP22 mutationL J Valentijn, R A Ouvrier, N H van den Bosch, et al.
Neuropediatrics|February 1, 1989
Kinetic study of catecholamine metabolism in hereditary progressive dystoniaA P de Jong, E A Haan, J I Manson, et al.
Neurology|May 7, 2008
Severe early-onset axonal neuropathy with homozygous and compound heterozygous MFN2 mutationsG A Nicholson, C Magdelaine, D Zhu, et al.
Nature Genetics|November 1, 1993
De novo mutation of the myelin P0 gene in Dejerine-Sottas disease (hereditary motor and sensory neuropathy type III)K Hayasaka, M Himoro, Y Sawaishi, et al.
The Medical Journal of Australia|March 20, 1989
Japanese encephalitis after a two-week holiday in BaliW B Macdonald, A R Tink, R A Ouvrier, et al.
American Journal of Human Genetics|September 16, 1999
A novel syndrome of episodic muscle weakness maps to xp22.3M M Ryan, P Taylor, J A Donald, et al.
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