ALS genetic epidemiology ‘How simplex is the genetic epidemiology of ALS?’
Author:
Publisher
BMJ
Subject
Psychiatry and Mental health,Clinical Neurology,Surgery
Reference8 articles.
1. Rate of familial amyotrophic lateral sclerosis: a systematic review and meta-analysis;Byrne;J Neurol Neurosurg Psychiatry,2011
2. An estimate of amyotrophic lateral sclerosis heritability using twin data;Al-Chalabi;J Neurol Neurosurg Psychiatry,2010
3. Genetic epidemiology of amyotrophic lateral sclerosis: a systematic review and meta-analysis;Zou;J Neurol Neurosurg Psychiatry,2017
4. Proposed criteria for familial amyotrophic lateral sclerosis;Byrne;Amyotroph Lateral Scler,2011
5. The C9ORF72 expansion mutation is a common cause of ALS+/-FTD in Europe and has a single founder;Smith;Eur J Hum Genet,2013
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2. Transcriptomic profiling of cerebrospinal fluid identifies ALS pathway enrichment and RNA biomarkers in MND individuals;Experimental Biology and Medicine;2023-11-24
3. A Medicinal Chemistry Perspective on Excitatory Amino Acid Transporter 2 Dysfunction in Neurodegenerative Diseases;Journal of Medicinal Chemistry;2023-02-14
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5. ALS/FTD: Evolution, Aging, and Cellular Metabolic Exhaustion;Frontiers in Neurology;2022-05-27
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