Kennedy’s disease (spinal and bulbar muscular atrophy): a clinically oriented review of a rare disease
Author:
Publisher
Springer Science and Business Media LLC
Subject
Neurology (clinical),Neurology
Link
http://link.springer.com/article/10.1007/s00415-018-8968-7/fulltext.html
Reference74 articles.
1. La Spada AR, Wilson EM, Lubahn DB et al (1991) Androgen receptor gene mutations in X-linked spinal and bulbar muscular atrophy. Nature 352:77–79. https://doi.org/10.1038/352077a0
2. Pennuto M, Rinaldi C (2017) From gene to therapy in spinal and bulbar muscular atrophy: are we there yet? Mol Cell Endocrinol. https://doi.org/10.1016/j.mce.2017.07.005
3. Kennedy WR, Alter M, Sung JH (1968) Progressive proximal spinal and bulbar muscular atrophy of late onset. Neurology 18
4. Harding AE, Thomas PK, Baraitser M et al (1982) X-linked recessive bulbospinal neuronopathy: a report of ten cases. J Neurol Neurosurg Psychiatry 45:1012–1019. https://doi.org/10.1136/jnnp.45.11.1012
5. Koutsis G, Kladi A, Breza M et al (2015) Spinobulbar muscular atrophy (Kennedy’s disease): a rare diagnosis in the Greek population. J Neurol Sci 359:450–451. https://doi.org/10.1016/j.jns.2015.10.021
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