Back to Authors

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

Teaching Neuro Images : “Pancake-like” gadolinium enhancement suggests compressive myelopathy due to spondylosis
Flanagan, Eoin P. , Marsh, Richard W., Weinshenker, Brian G. , Flanagan, E P , Weinshenker, Brian G

Neurology | May 20, 2013 | Volume: 80 | Issue: 21 | Pages: No page available

10.1212/wnl.0b013e318293e346 Get It

TNFRSF1A polymorphisms and MS
Weinshenker, Brian, Tienari, Pentti J. , Weinshenker, Brian G. , Weinshenker, Brian G

Neurology | April 27, 2013 | Volume: 80 | Issue: 22 | Pages: 2002-2003

10.1212/wnl.0b013e318294b4ab Get It

Industrial pharmaceutical drug research has done more for the health of people with MS than academic neurologists: No
Weinshenker, Brian G. , Weinshenker, Brian G

Multiple Sclerosis Journal | August 30, 2012 | Volume: 18 | Issue: 9 | Pages: 1211-1212

10.1177/1352458512458043 Get It

Onset of progressive phase is an age-dependent clinical milestone in multiple sclerosis
Tütüncü, Melih , Tang, Junger, Zeid, Nuhad Abou, Kale, Nilüfer , Crusan, D. J., Atkinson, Elizabeth J. , Sıva, Aksel , Pittock, Sean J. , Pirko, Istvan, Lucchinetti, Claudia F. , Noseworthy, John H., Rodriguez, Moses , Weinshenker, Brian G. , Kantarci, Orhun H. , Crusan, Daniel J. , Keegan, B. Mark , Pittock, S J , Weinshenker, Brian G , Rodriguez, Moses , Siva, Aksel

Multiple Sclerosis Journal | June 27, 2012 | Volume: 19 | Issue: 2 | Pages: 188-198

10.1177/1352458512451510 Get It

Background: It is unclear if all patients with relapsing–remitting multiple sclerosis (RRMS) ultimately develop progressive MS. Onset of progressive disease course seems to be age- rather than disease duration-dependent. Some forms of progressive MS (e.g. primary progressive MS (PPMS)) are uncommon in population-based studies. Ascertainment of patients with PPMS from clinic-based populations can facilitate a powerful comparison of age at progression onset between secondary progressive MS (SPMS) and PPMS but may introduce unclear biases. Objective: Our aim is to confirm that onset of progressive disease course is more relevant to the patient’s age than the presence or duration of a pre-progression relapsing disease course in MS. Methods: We studied a population-based MS cohort ( n =210, RRMS n =109, progressive MS n =101) and a clinic-based progressive MS cohort ( n =754). Progressive course was classified as primary (PPMS; n =322), single attack (SAPMS; n =112) and secondary progressive (SPMS; n =421). We studied demographics (chi 2 or t -test), age-of-progression-onset ( t -test) and time to Expanded Disability Status Scale of 6 (EDSS6) (Kaplan–Meier analyses). Results: Sex ratio ( p =0.58), age at progression onset ( p =0.37) and time to EDSS6 ( p =0.16) did not differ between the cohorts. Progression had developed before age 75 in 99% of patients with known progressive disease course; 38% with RRMS did not develop progression by age 75. Age at progression onset did not differ between SPMS (44.9±9.6), SAPMS (45.5±9.6) and PPMS (45.7±10.8). In either cohort, only 2% of patients had reached EDSS6 before onset of progression. Conclusions: Patients with RRMS do not inevitably develop a progressive disease course. Onset of progression is more dependent on age than the presence or duration of a pre-progression symptomatic disease course. Moderate disability is sustained predominantly after the onset of a progressive disease course in MS.
Interferon beta-1b in secondary progressive MS
Kappos, Ludwig , Weinshenker, Brian G. , Pozzilli, Carlo , Thompson, Alan J. , Beckmann, K., Polman, Chris H. , McFarland, Henry F. , Dahlke, Frank , Weinshenker, Brian G , Pozzilli, Carlo

Neurology | May 13, 2012 | Volume: 63 | Issue: 10 | Pages: 1779-1787

10.1212/01.wnl.0000145561.08973.4f Get It

Association of APOE polymorphisms with disease severity in MS is limited to women
Kantarci, Orhun H. , Hebrink, David D., Achenbach, Sara J., Pittock, S J , Altıntaş, Ayşe , Schaefer-Klein, Janet, Atkinson, Elizabeth J. , McMurray, Cynthia T. , Weinshenker, Brian G. , Pittock, Sean J. , Andrade, Mariza de , Rodriguez, Moses , Weinshenker, Brian G

Neurology | May 13, 2012 | Volume: 62 | Issue: 5 | Pages: 811-814

10.1212/01.wnl.0000113721.83287.83 Get It

Change in MS-related disability in a population-based cohort
Pittock, Sean J. , Mayr, William T., McClelland, Robyn L. , Jorgensen, Neal W. , Weigand, Stephen D. , Noseworthy, John H., Weinshenker, Brian G. , Rodriguez, Moses , Pittock, S J , Weinshenker, Brian G

Neurology | May 13, 2012 | Volume: 62 | Issue: 1 | Pages: 51-59

10.1212/01.wnl.0000101724.93433.00 Get It

Contrasting effects of IFNβ and IVIG in children with central and peripheral demyelination
Pirko, Istvan, Kuntz, Nancy L. , Patterson, Marc C. , Weinshenker, B. G., Weinshenker, Brian G. , Keegan, B. Mark , Rodriguez, Moses , Weinshenker, Brian G , Patterson, Marc

Neurology | May 13, 2012 | Volume: 60 | Issue: 10 | Pages: 1697-1699

10.1212/01.wnl.0000064163.94122.eb Get It

Plasma exchange for severe attacks of CNS demyelination: Predictors of response
Keegan, Mark , Pineda, Alvaro A., McClelland, Robyn L. , Darby, C. H., Weinshenker, Brian G. , Rodriguez, Moses , Weinshenker, Brian G

Neurology | May 13, 2012 | Volume: 58 | Issue: 1 | Pages: 143-146

10.1212/wnl.58.1.143 Get It