An adult onset hexosaminidase A deficiency syndrome with sensory neuropathy and internuclear ophthalmoplegia.

Author:

Barnes D,Misra V P,Young E P,Thomas P K,Harding A E

Publisher

BMJ

Subject

Psychiatry and Mental health,Clinical Neurology,Surgery

Reference8 articles.

1. The clinical spectrum of hexosaminidase deficiency diseases;Johnson, W.G.;Neurology,1981

2. Adult onset supranuclear ophthalmoplegia, cerebellar ataxia, and neurogenic proximal muscle weakness in a brother and sister: another hexosaminidase A deficiency syndrome;Harding, A.E.; Young, E.P.; Schon, F.;J Neurol Neurosurg Psychiatry,1987

3. Hexosaminidase A activity and amyotrophic lateral sclerosis;Gudesblatt, M.; Ludman, M.D.; Cohen, J.A.;Muscle Nerve,1988

4. Hexosaminidase A deficiency presenting as juvenile progressive dystonia;Hardie, R.J.; Young, E.P.; Morgan-Hughes, J.A.;J Neurol Neurosurg Psychiatry,1988

5. The juvenile and chronic forms of GM, gangliosidosis;Specola, N.; Vanier, M.T.; Goutieres, F.; Mikol, J.; Aicardi, J.;Neurology,1990

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