Very late onset X-linked recessive bulbospinal neuronopathy: mild clinical features and a mild increase in the size of tandem CAG repeat in androgen receptor gene.-Reference-Cited by-同舟云学术

Very late onset X-linked recessive bulbospinal neuronopathy: mild clinical features and a mild increase in the size of tandem CAG repeat in androgen receptor gene.

Published:1993-07-01 Issue:7 Volume:56 Page:832-833
ISSN:0022-3050
Container-title:Journal of Neurology, Neurosurgery & Psychiatry
language:en
Short-container-title:Journal of Neurology, Neurosurgery & Psychiatry

Author:

Doyu M,Sobue G,Mitsuma T,Uchida M,Iwase T,Takahashi A

Publisher

BMJ

Subject

Psychiatry and Mental health,Clinical Neurology,Surgery

Reference15 articles.

1. Progressive proximal spinal and bulbar muscular atrophy of late onset: a sex-linked recessive trait;Kennedy, W.R.; Alter, M.; Sung, J.H.;Neurology,1968

2. X-linked recessive bulbospinal neuronopathy: a report of ten cases;Harding, A.E.; Thomas, P.K.; Baraister, M.; Bradbury, P.G.; Morgan-Hughes, J.A.; Ponsford, JR;J Neurol Neurosurg Psychiatty,1982

3. Endocrinological study of hypogonadism and feminization in patients with bulbar spinal muscular atrophy;Mukai, E.; Mitsuma, T.; Takahashi, A.; Sobue, I.;Clin Neurol (Tokyo),1984

4. X-linked recessive bulbospinal neuronopathy, a clinico-pathological study;Sobue, G.; Hashizume, Y.; Mukai, E.; Hirayama, M.; Mitsuma, T.; Takahashi, A.;Brain,1989

5. Clinical course and prognosis of bulbo-spinal muscular atrophy;Mukai, E.;Neurol Therapeut (Tokyo),1991

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