Resultados de procura - Shanmugarajah, Priya
- Mostrando 1 - 10 Resultados de 10
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The Significance of Low Titre Antigliadin Antibodies in the Diagnosis of Gluten Ataxia por Hadjivassiliou, Marios, Grünewald, Richard A, Sanders, David S, Zis, Panagiotis, Croall, Iain, Shanmugarajah, Priya D, Sarrigiannis, Ptolemaios G, Trott, Nick, Wild, Graeme, Hoggard, Nigel
Publicado 2018Text -
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Alcohol-related cerebellar degeneration: not all down to toxicity? por 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
Publicado 2016Text -
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Consensus Paper: Neuroimmune Mechanisms of Cerebellar Ataxias por 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
Publicado 2015Text -
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Novel genotype-phenotype and MRI correlations in a large cohort of patients with SPG7 mutations por 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
Publicado 2018Text -
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Expanding the FDXR-Associated Disease Phenotype: Retinal Dystrophy Is a Recurrent Ocular Feature por 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
Publicado 2021Text