Relapse Patterns in NMOSD: Evidence for Earlier Occurrence of Optic Neuritis and Possible Seasonal Variation

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

Publikováno v: Frontiers in Neurology, Vol 11 (2020)

Neuromyelitis optica spectrum disorders (NMOSD) and multiple sclerosis (MS) show overlap in their clinical features. We performed an analysis of relapses with the aim of determining differences between the two conditions. Cases of NMOSD and age- and

Externí odkaz: https://doaj.org/article/9368fd0e4b594e0a86dbfe7d5222074a

Relapse Patterns in NMOSD: Evidence for Earlier Occurrence of Optic Neuritis and Possible Seasonal Variation

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

Publikováno v: Frontiers in Neurology
Frontiers in Neurology, Vol 11 (2020)

Neuromyelitis optica spectrum disorders (NMOSD) and multiple sclerosis (MS) show overlap in their clinical features. We performed an analysis of relapses with the aim of determining differences between the two conditions. Cases of NMOSD and age- and

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d4a6b26c4c797f44ed9b0250893369de

Incidence and prevalence of NMOSD in Australia and New Zealand

Autor: Mark Woodhall, Wajih Bukhari, Trevor Killpatrick, Stephen W. Reddel, Ming-Wei Lin, Karyn Boundy, Michael Walsh, Ernest Willoughby, Alan Coulthard, Robert Heard, Christopher Kneebone, Helmut Butzkueven, Richard C. W. Wong, Mark Slee, Jim Stankovich, Laura Clarke, Sofia Jimenez-Sanchez, Robert Wilson, Michael P. Pender, Cullen O'Gorman, Marzena J. Fabis-Pedrini, Keith Dear, David A. Fulcher, Christpher Lynch, Judith M. Spies, Deborah F. Mason, Jeannette Lechner-Scott, John D. Pollard, Allan G. Kermode, Bruce V. Taylor, Ian Sutton, John King, Kerri Prain, Mike Boggild, Russell C. Dale, William M. Carroll, Christine Bundell, David Abernethy, John Parratt, Stefan Blum, Andrew J. Kornberg, Michael Barnett, Chandi Das, Mark Marriott, Sandeep Bhuta, Simon Broadley, Richard A L Macdonell, Pamela A. McCombe, Eppie M. Yiu, Matthew A. Brown, David Gillis, Steve Vucic, Bruce J. Brew, Patrick Waters, Simon Hawke, Cameron Shaw, Jennifer Pereira, Saman Heshmat, Celia Chen, Wallace J Brownlee, Roger Silvestrini, Angela Vincent, Suzanne Hodgkinson, Andrew P.D. Henderson

Objectives We have undertaken a clinic-based survey of neuromyelitis optica spectrum disorders (NMOSDs) in Australia and New Zealand to establish incidence and prevalence across the region and in populations of differing ancestry. Background NMOSD is

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0ca8a4b7fe5e330c78f7bd1c11917593
https://ora.ox.ac.uk/objects/uuid:58050765-0835-4384-9f31-1eb4484571a4

Prevalence and Predictors of Burden in Caregivers of People with Dementia

Autor: Karyn Boundy, Henry Brodaty, David Ames, Michael M Woodward, Robert Balshaw

Publikováno v: The American Journal of Geriatric Psychiatry. 22:756-765

Objective To examine prevalence and predictors of burden in caregivers of people with dementia attending memory clinics. Methods This Prospective cohort study conducted at nine memory clinics in Australia rated 732 outpatient attendees and their prim

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::083fa3e3461c40f246704de3baf3a36d
https://doi.org/10.1016/j.jagp.2013.05.004

CCNF mutations in amyotrophic lateral sclerosis and frontotemporal dementia

Autor: John B.J. Kwok, Ronald C. Petersen, Natalie E. Farrawell, Kelly L. Williams, Jack W. Miller, Athina Soragia Gkazi, Annie Levert, Jun Mitsui, Alberto García-Redondo, Simon Topp, José Luis Muñoz-Blanco, Jason E. Kost, Ian P. Blair, Hussein Daoud, Cinzia Gellera, Xun Hu, Jun Goto, Robert H. Brown, Guy A. Rouleau, Justin J. Yerbury, Claire S. Leblond, Bradley N. Smith, John Landers, Meraida Polak, Vinod Sundaramoorthy, Shoji Tsuji, Julie D. Atkin, Hiroyuki Ishiura, William S. Brooks, Joanne D. Stockton, Karen E. Morrison, Jonathan D. Glass, Claire Winnick, Patrick A. Dion, Nicholas J. Cole, Neill R. Graff-Radford, Aaron D. Gitler, Katharine Y. Zhang, Dennis W. Dickson, Albert Lee, Cyril Pottier, Karyn Boundy, Sadaf T. Warraich, Carol Dobson-Stone, Emily P. McCann, Caroline Vance, Garth A. Nicholson, Marka van Blitterswijk, Jacqueline de Belleroche, Jesús Esteban-Pérez, Stephanie L. Rayner, Alberto Rábano, Shu Yang, Yuji Takahashi, Jennifer A. Fifita, Mark P. Molloy, Alessandra Chesi, Melissa E. Murray, Rosa Rademakers, Bradley F. Boeve, Roger S. Chung, Alison L. Hogan, Vincenzo Silani, Nicola Ticozzi, Orla Hardiman, Christopher Shaw, Emily K. Don, Gilles J. Guillemin

Publikováno v: Repositorio Institucional de la Consejería de Sanidad de la Comunidad de Madrid
Consejería de Sanidad de la Comunidad de Madrid
Williams, K L, Topp, S, Yang, S, Smith, B, Fifita, J A, Warraich, S T, Zhang, K Y, Farrawell, N, Vance, C, Hu, X, Chesi, A, Leblond, C S, Lee, A, Rayner, S L, Sundaramoorthy, V, Dobson-Stone, C, Molloy, M P, van Blitterswijk, M, Dickson, D W, Petersen, R C, Graff-Radford, N R, Boeve, B F, Murray, M E, Pottier, C, Don, E, Winnick, C, McCann, E P, Hogan, A, Daoud, H, Levert, A, Dion, P A, Mitsui, J, Ishiura, H, Takahashi, Y, Goto, J, Kost, J, Gellera, C, Gkazi, A S, Miller, J, Stockton, J, Brooks, W S, Boundy, K, Polak, M, Muñoz-Blanco, J L, Esteban-Pérez, J, Rábano, A, Hardiman, O, Morrison, K E, Ticozzi, N, Silani, V, de Belleroche, J, Glass, J D, Kwok, J B J, Guillemin, G J, Chung, R S, Tsuji, S, Brown, R H, García-Redondo, A, Rademakers, R, Landers, J E, Gitler, A D, Rouleau, G A, Cole, N J, Yerbury, J J, Atkin, J D, Shaw, C E, Nicholson, G A & Blair, I P 2016, ' CCNF mutations in amyotrophic lateral sclerosis and frontotemporal dementia ', Nature Communications, vol. 7, 11256 . https://doi.org/10.1038/ncomms11253
Nature communications
Williams, K L, Topp, S, Yang, S, Smith, B, Fifita, J A, Warraich, S T, Zhang, K Y, Farrawell, N, Vance, C, Hu, X, Chesi, A, Leblond, C S, Lee, A, Rayner, S L, Sundaramoorthy, V, Dobson-Stone, C, Molloy, M P, van Blitterswijk, M, Dickson, D W, Petersen, R C, Graff-Radford, N R, Boeve, B F, Murray, M E, Pottier, C, Don, E, Winnick, C, McCann, E P, Hogan, A, Daoud, H, Levert, A, Dion, P A, Mitsui, J, Ishiura, H, Takahashi, Y, Goto, J, Kost, J, Gellera, C, Gkazi, A S, Miller, J, Stockton, J, Brooks, W S, Boundy, K, Polak, M, Muñoz-Blanco, J L, Esteban-Pérez, J, Rábano, A, Hardiman, O, Morrison, K E, Ticozzi, N, Silani, V, De Belleroche, J, Glass, J D, Kwok, J B J, Guillemin, G J, Chung, R S, Tsuji, S, Brown, R H, García-Redondo, A, Rademakers, R, Landers, J E, Gitler, A D, Rouleau, G A, Cole, N J, Yerbury, J J, Atkin, J D, Shaw, C E, Nicholson, G A & Blair, I P 2016, ' CCNF mutations in amyotrophic lateral sclerosis and frontotemporal dementia ', Nature Communications, vol. 7, 11253 . https://doi.org/10.1038/ncomms11253
Nature Communications
Nature Communications, Vol 7, Iss 1, Pp 1-8 (2016)

Amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD) are overlapping, fatal neurodegenerative disorders in which the molecular and pathogenic basis remains poorly understood. Ubiquitinated protein aggregates, of which TDP-43 is a maj

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2742f08a78bf057bb8af1cef05775251
https://hdl.handle.net/20.500.12530/26848