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Lack of evidence of monomer/misfolded superoxide dismutase-1 in sporadic amyotrophic lateral sclerosis
Annals of Neurology , 08/18/09

Liu HN et al. – Although SEDI antibody does not necessarily label all misfolded forms of SOD1, these findings show a distinct difference between fALS1 and sALS, and do not support that monomer/misfolded SOD1 is a common disease entity linking all types of ALS. This is important to the understanding of ALS disease pathogenesis and to considerations of the applicability of using therapeutics that target misfolded SOD1 to non–SOD1–related cases.

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Cervical spondylotic amyotrophy presenting as dropped head syndrome
Clinical Neurology and Neurosurgery, 11/13/09 Relevance Score: 66%

Progression in primary lateral sclerosis: A prospective analysis
Amyotrophic Lateral Sclerosis, 10/19/09 Relevance Score: 65%

Matrix metalloproteinases and their tissue inhibitors in serum and cerebrospinal fluid of patients with amyotrophic lateral sclerosis
European Journal of Neurology, 10/12/09 Relevance Score: 65%

Multidisciplinary care for adults with amyotrophic lateral sclerosis or motor neuron disease
Cochrane Reviews, 10/09/09 Relevance Score: 65%

In vitro neurotoxic properties and excitatory aminoacids concentration in the cerebrospinal fluid of amyotrophic lateral sclerosis patients. Relationship with the degree of certainty of disease diagnoses
Acta Neurologica Scandinavica, 10/08/09 Relevance Score: 65%