“ALS reversals”: demographics, disease characteristics, treatments, and co-morbidities-Reference-Cited by-同舟云学术

“ALS reversals”: demographics, disease characteristics, treatments, and co-morbidities

Published:2018-04-02 Issue:7-8 Volume:19 Page:495-499
ISSN:2167-8421
Container-title:Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration
language:en
Short-container-title:Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration

Author:

Harrison Daniel¹^ORCID,Mehta Paul²,van Es Michael A.³,Stommel Elijah⁴,Drory Vivian E.⁵,Nefussy Beatrice⁵,van den Berg Leonard H.³,Crayle Jesse¹,Bedlack Richard⁶,

Affiliation:

1. School of Medicine, Duke University, Durham, NC, USA,

2. Agency for Toxic Substances and Disease Registry, National ALS Registry, Atlanta, GA, USA,

3. Department of Neurology, University Medical Center Utrecht, Utrecht, The Netherlands,

4. Department of Neurology, Geisel School of Medicine at Dartmouth, Hanover, NH, USA,

5. Department of Neurology, Tel-Aviv Medical Center, Tel-Aviv, Israel, and

6. Department of Neurology, Duke University and Durham VA Medical Center, Durham, NC, USA

Funder

LVH ALS Foundation

Publisher

Informa UK Limited

Subject

Clinical Neurology,Neurology

Link

https://www.tandfonline.com/doi/pdf/10.1080/21678421.2018.1457059

Reference23 articles.

1. El Escorial revisited: Revised criteria for the diagnosis of amyotrophic lateral sclerosis

2. Awaji Criteria for the Diagnosis of Amyotrophic Lateral Sclerosis

3. Progressive muscular atrophy and other lower motor neuron syndromes of adults

4. Study of 962 patients indicates progressive muscular atrophy is a form of ALS

5. Amyotrophic lateral sclerosis and myasthenia gravis: association or chance occurrence?

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