Spinobulbar muscular atrophy combined with atypical hereditary neuropathy with liability to pressure palsy-Reference-Cited by-同舟云学术

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Spinobulbar muscular atrophy combined with atypical hereditary neuropathy with liability to pressure palsy

Published:2018-02 Issue: Volume:48 Page:90-92
ISSN:0967-5868
Container-title:Journal of Clinical Neuroscience
language:en
Short-container-title:Journal of Clinical Neuroscience

Author:

Choi Kyomin,Ahn So Hyun,Baek Seol-Hee,Kim Jun-Soon,Choi Seok-Jin,Shin Je-Young,Kim Sung-Min,Hong Yoon-Ho,Sung Jung-Joon

Publisher

Elsevier BV

Subject

Physiology (medical),Neurology (clinical),Neurology,General Medicine,Surgery

Reference15 articles.

1. Loss of endogenous androgen receptor protein accelerates motor neuron degeneration and accentuates androgen insensitivity in a mouse model of X-linked spinal and bulbar muscular atrophy;Thomas;Hum Mol Genet,2006

2. Hereditary neuropathy with liability to pressure palsy: the electrophysiology fits the name;Li;Neurology,2002

3. Phenotypic variability leads to under-recognition of HNPP;Kumar;J Clin Neuromuscul Dis,2002

4. Spectrum of clinical and electrophysiologic features in HNPP patients with the 17p11.2 deletion;Mouton;Neurology,1999

5. Progressive proximal spinal and bulbar muscular atrophy of late onset. A sex-linked recessive trait;Kennedy;Neurology,1968

Cited by 2 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Atypical Presentation of Hereditary Neuropathy with Liability to Pressure Palsy: A Case Report;Journal of Electrodiagnosis and Neuromuscular Diseases;2021-04-30

2. Congenital nephrotic syndrome associated with 22q11.2 duplication syndrome in a Chinese family and functional analysis of the intronic NPHS1 c. 3286 + 5G > A mutation;Italian Journal of Pediatrics;2019-08-23

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