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- W2912136011 abstract "Amyotrophic lateral sclerosis (ALS) represents the major adult-onset motor neuron disease. Both human and animal studies reveal the critical implication of muscle and neuromuscular junctions (NMJs) in the initial phase of this disease. Despite the common efforts, ALS diagnosis remains particularly challenging since many other disorders can overlap yielding similar clinical phenotypic features. A combination of further research on the NMJ parameters that are specific for this disease and laboratory tests are crucial for the early determination of specific changes in the muscle, as well as in motor neuron and the prediction of ALS progression. Also, it could provide a powerful tool in the discrimination of particular ALS and ALS-mimic cases and increase the efficacy of therapeutic treatments." @default.
- W2912136011 created "2019-02-21" @default.
- W2912136011 creator A5016934486 @default.
- W2912136011 creator A5029972870 @default.
- W2912136011 creator A5091192587 @default.
- W2912136011 date "2019-02-06" @default.
- W2912136011 modified "2023-10-18" @default.
- W2912136011 title "Diagnostic Challenge and Neuromuscular Junction Contribution to ALS Pathogenesis" @default.
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