Search Results - Shanmugarajah, Priya
- Showing 1 - 10 results of 10
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The Significance of Low Titre Antigliadin Antibodies in the Diagnosis of Gluten Ataxia by Hadjivassiliou, Marios, Grünewald, Richard A, Sanders, David S, Zis, Panagiotis, Croall, Iain, Shanmugarajah, Priya D, Sarrigiannis, Ptolemaios G, Trott, Nick, Wild, Graeme, Hoggard, Nigel
Published 2018Text -
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Alcohol-related cerebellar degeneration: not all down to toxicity? by Shanmugarajah, Priya D., Hoggard, Nigel, Currie, Stuart, Aeschlimann, Daniel P., Aeschlimann, Pascale C., Gleeson, Dermot C., Karajeh, Mohammed, Woodroofe, Nicola, Grünewald, Richard A., Hadjivassiliou, Marios
Published 2016Text -
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Consensus Paper: Neuroimmune Mechanisms of Cerebellar Ataxias by Mitoma, Hiroshi, Adhikari, Keya, Aeschlimann, Daniel, Chattopadhyay, Partha, Hadjivassiliou, Marios, Hampe, Christiane S., Honnorat, Jérôme, Joubert, Bastien, Kakei, Shinji, Lee, Jongho, Manto, Mario, Matsunaga, Akiko, Mizusawa, Hidehiro, Nanri, Kazunori, Shanmugarajah, Priya, Yoneda, Makoto, Yuki, Nobuhiro
Published 2015Text -
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Novel genotype-phenotype and MRI correlations in a large cohort of patients with SPG7 mutations by Hewamadduma, Channa A., Hoggard, Nigel, O'Malley, Ronan, Robinson, Megan K., Beauchamp, Nick J., Segamogaite, Ruta, Martindale, Jo, Rodgers, Tobias, Rao, Ganesh, Sarrigiannis, Ptolemaios, Shanmugarajah, Priya, Zis, Panagiotis, Sharrack, Basil, McDermott, Christopher J., Shaw, Pamela J., Hadjivassiliou, Marios
Published 2018Text -
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Expanding the FDXR-Associated Disease Phenotype: Retinal Dystrophy Is a Recurrent Ocular Feature by Jurkute, Neringa, Shanmugarajah, Priya D., Hadjivassiliou, Marios, Higgs, Jenny, Vojcic, Miodrag, Horrocks, Iain, Nadjar, Yann, Touitou, Valerie, Lenaers, Guy, Poh, Roy, Acheson, James, Robson, Anthony G., Raymond, F. Lucy, Reilly, Mary M., Yu-Wai-Man, Patrick, Moore, Anthony T., Webster, Andrew R., Arno, Gavin
Published 2021Text