Abstract:
:Antibodies to myelin-associated glycoprotein (MAG) are found in patients with both monoclonal gammopathy and sensorimotor peripheral neuropathy but almost never in patients with amyotrophic lateral sclerosis (ALS). Ninety percent of patients with anti-MAG activity also have antibodies to sulfated glucuronic acid paragloboside (SGPG). We studied a patient with autopsy-proven ALS who had high titers of anti-SGPG but normal anti-MAG--one more unexplained immunologic abnormality in ALS.
journal_name
Neurologyjournal_title
Neurologyauthors
Rowland LP,Sherman WL,Hays AP,Lange DJ,Latov N,Trojaborg W,Younger DSdoi
10.1212/wnl.45.4.827subject
Has Abstractpub_date
1995-04-01 00:00:00pages
827-9issue
4eissn
0028-3878issn
1526-632Xjournal_volume
45pub_type
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