Primary lateral sclerosis and hereditary spastic paraplegia in sporadic patients. An important distinction in descriptive studies.

Author:

Vázquez-Costa Juan F.123,Bataller Luis123,Vílchez Juan J.1234

Affiliation:

1. Neuromuscular Diseases and Ataxias Research Unit, La Fe Research Institute; University of Valencia; Valencia Spain

2. Department of Neurology; La Fe University and Polytechnic Hospital, University of Valencia; Valencia Spain

3. Center for Biomedical Network Research on Rare Diseases (CIBERER); University of Valencia; Valencia Spain

4. Department of Medicine; University of Valencia; Valencia Spain

Funder

Instituto de Investigación Sanitaria La Fe

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Cited by 5 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. Presenilin-1 Mutations Are a Cause of Primary Lateral Sclerosis-Like Syndrome;Frontiers in Molecular Neuroscience;2021-08-30

2. Challenges and Controversies in the Genetic Diagnosis of Hereditary Spastic Paraplegia;Current Neurology and Neuroscience Reports;2021-02-28

3. Hereditary primary lateral sclerosis and progressive nonfluent aphasia;Journal of Neurology;2019-03-05

4. A case series of PLS patients with frontotemporal dementia and overview of the literature;Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration;2017-07-26

5. What's in the Literature?;Journal of Clinical Neuromuscular Disease;2016-09

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