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Provided with the increasing number of patients diagnosed with ALS and the improved societal awareness of the disease, more resources should be allocated to the research and care of ALS. Population-based studies, especially population-based disease registers, should be the priorities in ALS research, and more data from outside Europe are needed in gaining a better global perspective of the disease.
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Longinetti et al. (Tue,) studied this question.
synapsesocial.com/papers/69d84373617ce96c42ae372e — DOI: https://doi.org/10.1097/wco.0000000000000730
Elisa Longinetti
Karolinska University Hospital
Fang Fang
BGI Group (China)
Current Opinion in Neurology
Karolinska Institutet
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