Autosomal dominant congenital spinal muscular atrophy: a true form of spinal muscular atrophy caused by early loss of anterior horn cells von OATES, Emily C, REDDEL, Stephen, RODRIGUEZ, Michael L, GANDOLFO, Luke C, BAHLO, Melanie, HAWKE, Simon H, LAMANDE, Shireen R, CLARKE, Nigel F, NORTH, Kathryn N

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Fatal reversible cerebral vasoconstriction syndrome von Kunchok, Amy, Castley, Helen C., Aldous, Lucie, Hawke, Simon H., Torzillo, Emma, Parker, Geoffrey D., Halmagyi, G. Michael

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Immunotherapy as a therapeutic treatment for neurodegenerative disorders von White, Anthony R., Hawke, Simon H.

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Protein Conformation Significantly Influences Immune Responses to Prion Protein von Khalili-Shirazi, Azadeh, Quaratino, Sonia, Londei, Marco, Summers, Linda, Tayebi, Mourad, Clarke, Anthony R, Hawke, Simon H, Jackson, Graham S, Collinge, John

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Sjögren’s syndrome–associated myelopathy:: Response to immunosuppressive treatment von Vincent, Tonia L, Richardson, Mark P, Mackworth-Young, Charles G, Hawke, Simon H, Venables, Patrick J.W

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β-PrP form of human prion protein stimulates production of monoclonal antibodies to epitope 91–110 that recognise native PrPSc von Khalili-Shirazi, Azadeh, Kaisar, Maria, Mallinson, Gary, Jones, Samantha, Bhelt, Daljit, Fraser, Carol, Clarke, Anthony R., Hawke, Simon H., Jackson, Graham S., Collinge, John

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beta -PrP form of human prion protein stimulates production of monoclonal antibodies to epitope 91-110 that recognise native PrP super(Sc) von Khalili-Shirazi, Azadeh, Kaisar, Maria, Mallinson, Gary, Jones, Samantha, Bhelt, Daljit, Fraser, Carol, Clarke, Anthony R, Hawke, Simon H, Jackson, Graham S, Collinge, John

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β-PrP form of human prion protein stimulates production of monoclonal antibodies to epitope 91–110 that recognise native PrP Sc von Khalili-Shirazi, Azadeh, Kaisar, Maria, Mallinson, Gary, Jones, Samantha, Bhelt, Daljit, Fraser, Carol, Clarke, Anthony R., Hawke, Simon H., Jackson, Graham S., Collinge, John

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Sjögren’s syndrome–associated myelopathy von Vincent, Tonia L, Richardson, Mark P, Mackworth-Young, Charles G, Hawke, Simon H, Venables, Patrick J.W

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Exosomal microRNA signatures in multiple sclerosis reflect disease status von Ebrahimkhani, Saeideh, Vafaee, Fatemeh, Young, Paul E., Hur, Suzy S. J., Hawke, Simon, Devenney, Emma, Beadnall, Heidi, Barnett, Michael H., Suter, Catherine M., Buckland, Michael E.

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Circulating Memory B Cells in Early Multiple Sclerosis Exhibit Increased IgA + Cells, Globally Decreased BAFF-R Expression and an EBV-Related IgM + Cell Signature von Leffler, Jonatan, Trend, Stephanie, Ward, Natalie C, Grau, Georges E, Hawke, Simon, Byrne, Scott N, Kermode, Allan G, French, Martyn A, Hart, Prue H

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RFC1 expansions can mimic hereditary sensory neuropathy with cough and Sjögren syndrome von Kumar, Kishore R, Cortese, Andrea, Tomlinson, Susan E, Efthymiou, Stephanie, Ellis, Melina, Zhu, Danqing, Stoll, Marion, Dominik, Natalia, Tisch, Stephen, Tchan, Michel, Wu, Kathy H C, Devery, Sophie, Spring, Penelope J, Hawke, Simon, Cremer, Phillip, Ng, Karl, Reilly, Mary M, Nicholson, Garth A, Houlden, Henry, Kennerson, Marina

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Peripheral B‐cell dysregulation is associated with relapse after long‐term quiescence in patients with multiple sclerosis von Marsh‐Wakefield, Felix, Juillard, Pierre, Ashhurst, Thomas M, Juillard, Annette, Shinko, Diana, Putri, Givanna H, Read, Mark N, McGuire, Helen M, Byrne, Scott N, Hawke, Simon, Grau, Georges E

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Plasma levels of endothelial and B-cell-derived microparticles are restored by fingolimod treatment in multiple sclerosis patients von Zinger, Anna, Latham, Sharissa L, Combes, Valery, Byrne, Scott, Barnett, Michael H, Hawke, Simon, Grau, Georges E

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IgG3+ B cells are associated with the development of multiple sclerosis von Marsh‐Wakefield, Felix, Ashhurst, Thomas, Trend, Stephanie, McGuire, Helen M, Juillard, Pierre, Zinger, Anna, Jones, Anderson P, Kermode, Allan G, Hawke, Simon, Grau, Georges E, Hart, Prue H, Byrne, Scott N

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Characterization of the human myelin oligodendrocyte glycoprotein antibody response in demyelination von Tea, Fiona, Lopez, Joseph A, Ramanathan, Sudarshini, Merheb, Vera, Lee, Fiona X Z, Zou, Alicia, Pilli, Deepti, Patrick, Ellis, van der Walt, Anneke, Monif, Mastura, Tantsis, Esther M, Yiu, Eppie M, Vucic, Steve, Henderson, Andrew P D, Fok, Anthony, Fraser, Clare L, Lechner-Scott, Jeanette, Reddel, Stephen W, Broadley, Simon, Barnett, Michael H, Brown, David A, Lunemann, Jan D, Dale, Russell C, Brilot, Fabienne

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NMOSD and MS prevalence in the Indigenous populations of Australia and New Zealand von Bukhari, Wajih, Khalilidehkordi, Elham, Mason, Deborah F., Barnett, Michael H., Taylor, Bruce V., Fabis-Pedrini, Marzena, Kermode, Allan G., Subramanian, Sankar, Waters, Patrick, Broadley, Simon A.

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Relapse Patterns in NMOSD: Evidence for Earlier Occurrence of Optic Neuritis and Possible Seasonal Variation von Khalilidehkordi, Elham, Clarke, Laura, Arnett, Simon, Bukhari, Wajih, Jimenez Sanchez, Sofia, O'Gorman, Cullen, Sun, Jing, Prain, Kerri M., Woodhall, Mark, Silvestrini, Roger, Bundell, Christine S., Abernethy, David, Bhuta, Sandeep, Blum, Stefan, Boggild, Mike, Boundy, Karyn, Brew, Bruce J., Brown, Matthew, Brownlee, Wallace, Butzkueven, Helmut, Carroll, William M., Chen, Celia, Coulthard, Alan, Dale, Russell C., Das, Chandi, Fabis-Pedrini, Marzena J., Fulcher, David, Gillis, David, Hawke, Simon, Heard, Robert, Henderson, Andrew P. D., Heshmat, Saman, Hodgkinson, Suzanne, Kilpatrick, Trevor J., King, John, Kneebone, Chris, Kornberg, Andrew J., Lechner-Scott, Jeannette, Lin, Ming-Wei, Lynch, Christopher, Macdonell, Richard A. L., Mason, Deborah F., McCombe, Pamela A., Pereira, Jennifer, Pollard, John D., Ramanathan, Sudarshini, Reddel, Stephen W., Shaw, Cameron, Spies, Judith, Stankovich, James, Sutton, Ian, Vucic, Steve, Walsh, Michael, Wong, Richard C., Yiu, Eppie M., Barnett, Michael H., Kermode, Allan G., Marriott, Mark P., Parratt, John, Slee, Mark, Taylor, Bruce V., Willoughby, Ernest, Brilot, Fabienne, Vincent, Angela, Waters, Patrick, Broadley, Simon A.

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MRI Patterns Distinguish AQP4 Antibody Positive Neuromyelitis Optica Spectrum Disorder From Multiple Sclerosis von Clarke, Laura, Arnett, Simon, Bukhari, Wajih, Khalilidehkordi, Elham, Jimenez Sanchez, Sofia, O'Gorman, Cullen, Sun, Jing, Prain, Kerri M., Woodhall, Mark, Silvestrini, Roger, Bundell, Christine S., Abernethy, David A., Bhuta, Sandeep, Blum, Stefan, Boggild, Mike, Boundy, Karyn, Brew, Bruce J., Brownlee, Wallace, Butzkueven, Helmut, Carroll, William M., Chen, Cella, Coulthard, Alan, Dale, Russell C., Das, Chandi, Fabis-Pedrini, Marzena J., Gillis, David, Hawke, Simon, Heard, Robert, Henderson, Andrew P. D., Heshmat, Saman, Hodgkinson, Suzanne, Kilpatrick, Trevor J., King, John, Kneebone, Christopher, Kornberg, Andrew J., Lechner-Scott, Jeannette, Lin, Ming-Wei, Lynch, Christopher, Macdonell, Richard A. L., Mason, Deborah F., McCombe, Pamela A., Pereira, Jennifer, Pollard, John D., Ramanathan, Sudarshini, Reddel, Stephen W., Shaw, Cameron P., Spies, Judith M., Stankovich, James, Sutton, Ian, Vucic, Steve, Walsh, Michael, Wong, Richard C., Yiu, Eppie M., Barnett, Michael H., Kermode, Allan G. K., Marriott, Mark P., Parratt, John D. E., Slee, Mark, Taylor, Bruce V., Willoughby, Ernest, Brilot, Fabienne, Vincent, Angela, Waters, Patrick, Broadley, Simon A.

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Assessment of the bioequivalence of a generic cyclosporine A by a randomized controlled trial in stable renal recipients von HIBBERD, Adrian D, TREVILLIAN, Paul R, ROGER, Simon D, WLODARCZYK, John H, STEIN, Ann M, BOHRINGER, Elizabeth G, MILSON-HAWKE, Sally M

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