Rezultati - 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 od Hadjivassiliou, Marios, Grünewald, Richard A, Sanders, David S, Zis, Panagiotis, Croall, Iain, Shanmugarajah, Priya D, Sarrigiannis, Ptolemaios G, Trott, Nick, Wild, Graeme, Hoggard, Nigel
Izdano 2018Text -
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Alcohol-related cerebellar degeneration: not all down to toxicity? od 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
Izdano 2016Text -
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Consensus Paper: Neuroimmune Mechanisms of Cerebellar Ataxias od 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
Izdano 2015Text -
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Novel genotype-phenotype and MRI correlations in a large cohort of patients with SPG7 mutations od 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
Izdano 2018Text -
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Expanding the FDXR-Associated Disease Phenotype: Retinal Dystrophy Is a Recurrent Ocular Feature od 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
Izdano 2021Text