X-linked recessive bulbospinal neuronopathy: a report of ten cases.

Author:

Harding A E,Thomas P K,Baraitser M,Bradbury P G,Morgan-Hughes J A,Ponsford J R

Publisher

BMJ

Subject

Psychiatry and Mental health,Neurology (clinical),Surgery

Reference20 articles.

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2. A clinical and genetic study;J Neurol Sci,1978

3. A clinical and genetic study of adult onset spinal muscular atrophy. The autosomal recessive form as a discrete disease entity. Brain 1978; 101: 591-606. 4 McLeod JG, Prineas JW. Distal type of chronic spinal muscular atrophy-clinical, electrophysiological and pathological studies;Peam, J.H.; Hudgson, P.; Walton, J.N.;Brain,1971

4. Hereditary distal spinal muscular atrophy. A report on 34 cases and a review of the literature;Harding, A.E.; Thomas, P.K.;J Neurol Sci,1980

5. Scapuloperoneal muscular atrophy;Kaeser, H.E.;Brain,1965

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