When should you order genetic testing for patients with cryptogenic neuropathy? Let the data do the talking-Reference-Cited by-同舟云学术

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When should you order genetic testing for patients with cryptogenic neuropathy? Let the data do the talking

Published:2019-01-23 Issue:3 Volume:59 Page:280-282
ISSN:0148-639X
Container-title:Muscle & Nerve
language:en
Short-container-title:Muscle Nerve

Author:

Pasnoor Mamatha¹,Gordon Smith A.¹²

Affiliation:

1. Department of NeurologyUniversity of Kansas Medical Center Kansas, City Kansas USA

2. Department of NeurologyVirginia Commonwealth University, 1101 East Marshall Street 6‐013 Richmond Virginia USA

Publisher

Wiley

Subject

Physiology (medical),Cellular and Molecular Neuroscience,Clinical Neurology,Physiology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/mus.26409

Reference17 articles.

1. North America and South America (NA-SA) neuropathy project

2. The diagnostic challenge of small fibre neuropathy: clinical presentations, evaluations, and causes

3. Enzyme replacement therapy for Fabry's disease

4. Inotersen Treatment for Patients with Hereditary Transthyretin Amyloidosis

5. Patisiran, an RNAi Therapeutic, for Hereditary Transthyretin Amyloidosis

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. Hereditary transthyretin amyloidosis overview;Neurological Sciences;2020-11-14

2. Screening for genetic mutations in patients with neuropathy without definite etiology is useful;Journal of Neurology;2020-05-12

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