Kennedy病一例_《華西醫學》

作者：

張波 ,  方登富 , 張運偉 , 喻明 , 蔣世杰 , 聶本剛

關鍵詞：

Kennedy病神經遺傳疾病病例報告

DOI：

10.7507/1002-0179.20130354

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引用本文： 張波,方登富,張運偉,喻明,蔣世杰,聶本剛. Kennedy病一例. 華西醫學, 2013, 28(7): 1141-1142. doi: 10.7507/1002-0179.20130354 復制

1.	Kennedy WR, Alter M. Progressive proximal spinal and bulbar muscular atrophy of late onset: a sex-linked recessive trait[J]. Neurology, 2000, 2(1): 3-5.
2.	Guidetti D, Sabadini R, Ferlini A, et al. Epidemiological survey of X-linked bulbar and spinal muscular atrophy, or Kennedy disease, in the province of Reggio Emilia, Italy[J]. Eur J Epidemiol, 2001, 17(6): 587-591.
3.	Montie HL, Merry DE. Autophagy and access: understanding the role of androgen receptor subcellular localization in SBMA[J]. Autophagy, 2009, 5(8): 1194-1197.
4.	Finsterer J. Perspectives of kennedy’s disease[J]. J Neurol Sci, 2010, 298(1-2): 1-10.
5.	Merry DE. Molecular pathogenesis of spinal and bulbar muscular atrophy[J]. Brain Res Bull, 2001, 56(3-4): 203-207.
6.	Greenland KJ, Beilin J, Castro J, et al. Polymorphic CAG repeat length in the androgen receptor gene and association with neurodegeneration in a heterozygous female carrier of Kennedy’s disease[J]. J Neurol, 2004, 251(1): 35-41.
7.	Atsuta N, Watanabe H, Ito M, et al. Natural history of spinal and bulbar muscular atrophy (SBMA): a study of 223 Japanese patients[J]. Brain, 2006, 129(6): 1446-1455.
8.	Sperfeld AD, Karitzky J, Brummer D, et al. X-linked bulbospinal neuronopathy:Kennedy disease[J]. Arch Neurol, 2002, 59(12): 1921-1926.
9.	Banno H, Katsuno M, Suzuki K, et al. Neuropathology and therapeutic intervention in spinal and bulbar muscular atrophy[J]. Int J Mol Sci, 2009, 10(3): 1000-1012.

1. 　Kennedy WR, Alter M. Progressive proximal spinal and bulbar muscular atrophy of late onset: a sex-linked recessive trait[J]. Neurology, 2000, 2(1): 3-5.
2. 　Guidetti D, Sabadini R, Ferlini A, et al. Epidemiological survey of X-linked bulbar and spinal muscular atrophy, or Kennedy disease, in the province of Reggio Emilia, Italy[J]. Eur J Epidemiol, 2001, 17(6): 587-591.
3. 　Montie HL, Merry DE. Autophagy and access: understanding the role of androgen receptor subcellular localization in SBMA[J]. Autophagy, 2009, 5(8): 1194-1197.
4. 　Finsterer J. Perspectives of kennedy’s disease[J]. J Neurol Sci, 2010, 298(1-2): 1-10.
5. 　Merry DE. Molecular pathogenesis of spinal and bulbar muscular atrophy[J]. Brain Res Bull, 2001, 56(3-4): 203-207.
6. 　Greenland KJ, Beilin J, Castro J, et al. Polymorphic CAG repeat length in the androgen receptor gene and association with neurodegeneration in a heterozygous female carrier of Kennedy’s disease[J]. J Neurol, 2004, 251(1): 35-41.
7. 　Atsuta N, Watanabe H, Ito M, et al. Natural history of spinal and bulbar muscular atrophy (SBMA): a study of 223 Japanese patients[J]. Brain, 2006, 129(6): 1446-1455.
8. 　Sperfeld AD, Karitzky J, Brummer D, et al. X-linked bulbospinal neuronopathy:Kennedy disease[J]. Arch Neurol, 2002, 59(12): 1921-1926.
9. 　Banno H, Katsuno M, Suzuki K, et al. Neuropathology and therapeutic intervention in spinal and bulbar muscular atrophy[J]. Int J Mol Sci, 2009, 10(3): 1000-1012.