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Roos, Raymond P.Person Why?
Intrafamilial heterogeneity in hereditary motor neuron disease.Academic Article Why?
Diagnostic utility of the amyotrophic lateral sclerosis Functional Rating Scale-Revised to detect pharyngeal dysphagia in individuals with amyotrophic lateral sclerosis.Academic Article Why?
Familial amyotrophic lateral sclerosis.Academic Article Why?
Guanabenz, which enhances the unfolded protein response, ameliorates mutant SOD1-induced amyotrophic lateral sclerosis.Academic Article Why?
A molecular genetic approach to amyotrophic lateral sclerosis.Academic Article Why?
Amyotrophic lateral sclerosis and viruses.Academic Article Why?
Amyotrophic lateral sclerosis with antecedent poliomyelitis.Academic Article Why?
Amyotrophic lateral sclerosis.Academic Article Why?
Cerebro-cerebellar connectivity is increased in primary lateral sclerosis.Academic Article Why?
Dextromethorphan/quinidine for the treatment of bulbar impairment in amyotrophic lateral sclerosis.Academic Article Why?
Donation after cardiac death in amyotrophic lateral sclerosis: stepping forward into uncertain waters.Academic Article Why?
End of life decisions in amyotrophic lateral sclerosis: a cross-cultural perspective.Academic Article Why?
Failure to detect poliovirus genetic information in amyotrophic lateral sclerosis.Academic Article Why?
Familial amyotrophic lateral sclerosis.Academic Article Why?
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