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Central mimics of benign paroxysmal positional vertigo: an illustrative case series.
Published in:
2020
By:
- Joshi, Purwa;
- Mossman, Stuart;
- Luis, Leonel;
- Luxon, Linda M
Publication type:
journal article
A Māori specific RFC1 pathogenic repeat configuration in CANVAS, likely due to a founder allele.
Published in:
2020
By:
- Beecroft, Sarah J;
- Cortese, Andrea;
- Sullivan, Roisin;
- Yau, Wai Yan;
- Dyer, Zoe;
- Wu, Teddy Y;
- Mulroy, Eoin;
- Pelosi, Luciana;
- Rodrigues, Miriam;
- Taylor, Rachael;
- Mossman, Stuart;
- Leadbetter, Ruth;
- Cleland, James;
- Anderson, Tim;
- Ravenscroft, Gianina;
- Laing, Nigel G;
- Houlden, Henry;
- Reilly, Mary M;
- Roxburgh, Richard H
Publication type:
journal article
Cerebellar ataxia, neuropathy, vestibular areflexia syndrome due to RFC1 repeat expansion.
Published in:
2020
By:
- Cortese, Andrea;
- Tozza, Stefano;
- Yau, Wai Yan;
- Rossi, Salvatore;
- Beecroft, Sarah J;
- Jaunmuktane, Zane;
- Dyer, Zoe;
- Ravenscroft, Gianina;
- Lamont, Phillipa J;
- Mossman, Stuart;
- Chancellor, Andrew;
- Maisonobe, Thierry;
- Pereon, Yann;
- Cauquil, Cecile;
- Colnaghi, Silvia;
- Mallucci, Giulia;
- Curro, Riccardo;
- Tomaselli, Pedro J;
- Thomas-Black, Gilbert;
- Sullivan, Roisin
Publication type:
journal article
Cerebellar ataxia, neuropathy, vestibular areflexia syndrome (CANVAS): a review of the clinical features and video-oculographic diagnosis.
Published in:
Annals of the New York Academy of Sciences, 2011, v. 1233, n. 1, p. 139, doi. 10.1111/j.1749-6632.2011.06158.x
By:
- Szmulewicz, David J.;
- Waterston, John A.;
- MacDougall, Hamish G.;
- Mossman, Stuart;
- Chancellor, Andrew M.;
- McLean, Catriona A.;
- Merchant, Saumil;
- Patrikios, Peter;
- Halmagyi, G. Michael;
- Storey, Elsdon
Publication type:
Article
A Novel CACNA1A Nonsense Variant [c.4054C>T (p.Arg<sup>1352</sup>⁎)] Causing Episodic Ataxia Type 2.
Published in:
Case Reports in Neurological Medicine, 2018, p. 1, doi. 10.1155/2018/5802650
By:
- Lance, Sean;
- Mossman, Stuart;
- Poke, Gemma
Publication type:
Article
Peripheral nerve ultrasound in Friedreich ataxia.
Published in:
2018
By:
- Mulroy, Eoin;
- Pelosi, Luciana;
- Leadbetter, Ruth;
- Joshi, Purwa;
- Rodrigues, Miriam;
- Mossman, Stuart;
- Kilfoyle, Dean;
- Roxburgh, Richard
Publication type:
journal article
Peripheral nerve ultrasound in cerebellar ataxia neuropathy vestibular areflexia syndrome (CANVAS).
Published in:
2017
By:
- Pelosi, Luciana;
- Leadbetter, Ruth;
- Mulroy, Eoin;
- Chancellor, Andrew M.;
- Mossman, Stuart;
- Roxburgh, Richard
Publication type:
journal article
Immunological Heterogeneity and Cellular Mechanisms in Myasthenia Gravis<sup>a</sup>.
Published in:
Annals of the New York Academy of Sciences, 1987, v. 505, n. 1, p. 12, doi. 10.1111/j.1749-6632.1987.tb51279.x
By:
- NEWSOM-DAVIS, JOHN;
- WILLCOX, NICK;
- SCHLUEP, MYRIAM;
- HARCOURT, GILLIAN;
- VINCENT, ANGELA;
- MOSSMAN, STUART;
- WRAY, DENNIS;
- BURGES, JUDITH
Publication type:
Article
Autonomic dysfunction is a major feature of cerebellar ataxia, neuropathy, vestibular areflexia ‘CANVAS’ syndrome.
Published in:
Brain: A Journal of Neurology, 2014, v. 137, n. 10, p. 2649, doi. 10.1093/brain/awu196
By:
- Wu, Teddy Y.;
- Taylor, Jennifer M.;
- Kilfoyle, Dean H.;
- Smith, Andrew D.;
- McGuinness, Ben J.;
- Simpson, Mark P.;
- Walker, Elizabeth B.;
- Bergin, Peter S.;
- Cleland, James C.;
- Hutchinson, David O.;
- Anderson, Neil E.;
- Snow, Barry J.;
- Anderson, Tim J.;
- Paermentier, Laura A. F.;
- Cutfield, Nick J.;
- Chancellor, Andrew M.;
- Mossman, Stuart S.;
- Roxburgh, Richard H.
Publication type:
Article
Autonomic dysfunction is a major feature of cerebellar ataxia, neuropathy, vestibular areflexia 'CANVAS' syndrome.
Published in:
2014
By:
- Wu, Teddy Y;
- Taylor, Jennifer M;
- Kilfoyle, Dean H;
- Smith, Andrew D;
- McGuinness, Ben J;
- Simpson, Mark P;
- Walker, Elizabeth B;
- Bergin, Peter S;
- Cleland, James C;
- Hutchinson, David O;
- Anderson, Neil E;
- Snow, Barry J;
- Anderson, Tim J;
- Paermentier, Laura A F;
- Cutfield, Nick J;
- Chancellor, Andrew M;
- Mossman, Stuart S;
- Roxburgh, Richard H
Publication type:
Journal Article
Inherited RORB pathogenic variants: Overlap of photosensitive genetic generalized and occipital lobe epilepsy.
Published in:
Epilepsia (Series 4), 2020, v. 61, n. 4, p. e23, doi. 10.1111/epi.16475
By:
- Sadleir, Lynette G.;
- de Valles‐Ibáñez, Guillem;
- King, Chontelle;
- Coleman, Matthew;
- Mossman, Stuart;
- Paterson, Sarah;
- Nguyen, John;
- Berkovic, Samuel F.;
- Mullen, Saul;
- Bahlo, Melanie;
- Hildebrand, Michael S.;
- Mefford, Heather C.;
- Scheffer, Ingrid E.
Publication type:
Article
The p.Ala510Val mutation in the SPG7 (paraplegin) gene is the most common mutation causing adult onset neurogenetic disease in patients of British ancestry.
Published in:
Journal of Neurology, 2013, v. 260, n. 5, p. 1286, doi. 10.1007/s00415-012-6792-z
By:
- Roxburgh, Richard;
- Marquis-Nicholson, Renate;
- Ashton, Fern;
- George, Alice;
- Lea, Rod;
- Eccles, David;
- Mossman, Stuart;
- Bird, Thomas;
- Gassen, Koen;
- Kamsteeg, Erik-Jan;
- Love, Donald
Publication type:
Article
Occult peripheral neuropathy in an elite hockey player.
Published in:
2012
By:
- PEARSON, JAKE N.;
- MOSSMAN, STUART
Publication type:
Case Study
Age dependent normal horizontal VOR gain of head impulse test as measured with video-oculography.
Published in:
Journal of Otolaryngology -- Head & Neck Surgery, 2015, v. 44, n. 1, p. 1, doi. 10.1186/s40463-015-0081-7
By:
- Mossman, Benjamin;
- Mossman, Stuart;
- Purdie, Gordon;
- Schneider, Erich
Publication type:
Article

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