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Weinshenker, Brian G

0000-0001-5806-6203

Mayo Clinic

From the Department of Neurology (S.S.S., M.B., D.T., B.G.W., S.J.P., E.P.F., M.T.B., J.J.C.), and Center for Multiple Sclerosis and Autoimmune Neurology (S.S.S., M.B., D.M.W., B.G.W., S.J.P., E.P.F., J.J.C.), Mayo Clinic, Rochester, MN; Department of Neur

Citations 140

Western vs optic-spinal MS

Neurology | June 14, 2011 | Volume: 64 | Issue: 4 | Pages: 594-595

10.1212/01.wnl.0000154673.37555.6f | PMID 15728277

Paraneoplastic isolated myelopathy

Neurology | June 14, 2011 | Volume: 76 | Issue: 24 | Pages: 2089-2095

10.1212/wnl.0b013e31821f468f | PMID 21670438

Neuromyelitis optica unique area postrema lesions

Neurology | March 3, 2011 | Volume: 76 | Issue: 14 | Pages: 1229-1237

10.1212/wnl.0b013e318214332c | PMID 21368286

Do old HLA and mitochondrial DNA variants associate with demyelination types in young patients?

Neurology | February 3, 2011 | Volume: 76 | Issue: 9 | Pages: 768-769

10.1212/wnl.0b013e31820e7bfc | PMID 21288985

Pearls & Oy-sters: Clues for spinal dural arteriovenous fistulae

Neurology | January 17, 2011 | Volume: 76 | Issue: 3 | Pages: No page available

10.1212/wnl.0b013e3182074a42 | PMID 21242488

Association of IL2RA p olymorphisms with susceptibility to multiple sclerosis is not explained by missense mutations in IL2RA

Multiple Sclerosis Journal | January 14, 2011 | Volume: 17 | Issue: 5 | Pages: 634-636

10.1177/1352458510394703 | PMID 21239413

Genome-wide association studies have identified an association between two intronic single nucleotide polymorphisms (SNPs), rs12722489 and rs2104286, in the interleukin-2 receptor alpha-chain gene ( IL2RA) and susceptibility to multiple sclerosis (MS). We studied these SNPs in association with susceptibility to and severity of MS in a population-based cohort of 220 patients from Olmsted County, Minnesota, compared with 442 matched controls. We sequenced the exons, splice sites and 5’ and 3’ untranslated regions in 27 randomly selected MS patients (powered for allele frequency ≥0.04) to search for mutations. No novel missense mutation was identified. Two patients (7.5%) had an exon 2 SNP ( rs4308625) and two patients had an exon 4 SNP ( rs2228149), both synonymous.
Absence of cortical demyelination in neuromyelitis optica

Neurology | December 6, 2010 | Volume: 75 | Issue: 23 | Pages: 2103-2109

10.1212/wnl.0b013e318200d80c | PMID 21135384

Approach to acute or subacute myelopathy

Neurology | November 4, 2010 | Volume: 75 | Issue: 18_supplement_1 | Pages: No page available

10.1212/wnl.0b013e3181fb3638 | PMID 21041766

Japanese optic-spinal MS

Neurology | September 9, 2010 | Volume: 75 | Issue: 16 | Pages: 1404-1405

10.1212/wnl.0b013e3181f88382 | PMID 20826710

Familial neuromyelitis optica

Neurology | July 26, 2010 | Volume: 75 | Issue: 4 | Pages: 310-315

10.1212/wnl.0b013e3181ea9f15 | PMID 20660861