Twenty two cases of canine neural angiostronglyosis in eastern Australia (2002-2005) and a review of the literature von Lunn, Julian A, Lee, Rogan, Smaller, Joanna, MacKay, Bruce M, King, Terry, Hunt, Geraldine B, Martin, Patricia, Krockenberger, Mark B, Spielman, Derek, Malik, Richard

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Computed tomography findings of nasal cryptococcosis in Australia (2008-2020): 12 dogs and 9 cats von Wong, Samantha A, Jacobson, Else, Podadera, Juan, Siow, Jia Wen, Woerde, Dennis J, Tebb, Anna, Thompson, Mary, Colins, Dave, Lunn, Julian, Malik, Richard

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Twenty two cases of canine neural angiostrongylosis in eastern Australia (2002-2005) and a review of the literature von Lunn, Julian A, Lee, Rogan, Smaller, Joanna, MacKay, Bruce M, King, Terry, Hunt, Geraldine B, Martin, Patricia, Krockenberger, Mark B, Spielman, Derek, Malik, Richard

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Canine Neural Angiostrongyliasis von Lunn, Julian Alexander

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Charcot–Marie–Tooth disease: frequency of genetic subtypes and guidelines for genetic testing von Murphy, Sinead M, Laura, Matilde, Fawcett, Katherine, Pandraud, Amelie, Liu, Yo-Tsen, Davidson, Gabrielle L, Rossor, Alexander M, Polke, James M, Castleman, Victoria, Manji, Hadi, Lunn, Michael P T, Bull, Karen, Ramdharry, Gita, Davis, Mary, Blake, Julian C, Houlden, Henry, Reilly, Mary M

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Plasma neurofilament light chain concentration is increased and correlates with the severity of neuropathy in hereditary transthyretin amyloidosis von Kapoor, Mahima, Foiani, Martha, Heslegrave, Amanda, Zetterberg, Henrik, Lunn, Michael P., Malaspina, Andrea, Gillmore, Julian D., Rossor, Alexander M., Reilly, Mary M.

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A Partial C4 Photosynthetic Biochemical Pathway in Rice von Lin, HsiangChun, Arrivault, Stéphanie, Coe, Robert A., Karki, Shanta, Covshoff, Sarah, Bagunu, Efren, Lunn, John E., Stitt, Mark, Furbank, Robert T., Hibberd, Julian M., Quick, William Paul

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Pain and small fiber function in charcot-marie-tooth disease type 1A von Laurà, Matilde, Hutton, Elspeth J., Blake, Julian, Lunn, Michael P., Fox, Zoe, Pareyson, Davide, Solari, Alessandra, Radice, Davide, Koltzenburg, Martin, Reilly, Mary M.

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Development of a risk assessment profile tool to determine appropriate use of SARS-CoV-2 rapid antigen detection tests for different activities and events in Ireland, since October... von Mallon, Patrick Wg, Horgan, Mary, McAloon, Conor G, Lunn, Peter D, Little, Julian, Beck, Andrew, Bennett, Alexandria, Shaver, Nicole, Conway, Aileen, O'Regan, Rhea, Whelan, Barbara

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Unusual upper limb features in SORD neuropathy von Record, Christopher J, Pipis, Menelaos, Blake, Julian, Curro, Riccardo, Lunn, Michael P, Rossor, Alexander M, Laura, Matilde, Cortese, Andrea, Reilly, Mary M

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Genetic dysfunction of MT-ATP6 causes axonal Charcot-Marie-Tooth disease von Pitceathly, Robert D S, Murphy, Sinéad M, Cottenie, Ellen, Chalasani, Annapurna, Sweeney, Mary G, Woodward, Cathy, Mudanohwo, Ese E, Hargreaves, Iain, Heales, Simon, Land, John, Holton, Janice L, Houlden, Henry, Blake, Julian, Champion, Michael, Flinter, Frances, Robb, Stephanie A, Page, Rupert, Rose, Michael, Palace, Jacqueline, Crowe, Carol, Longman, Cheryl, Lunn, Michael P, Rahman, Shamima, Reilly, Mary M, Hanna, Michael G

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Posthospitalization COVID-19 cognitive deficits at 1 year are global and associated with elevated brain injury markers and gray matter volume reduction von Wood, Greta K, Sargent, Brendan F, Ahmad, Zain-Ul-Abideen, Tharmaratnam, Kukatharmini, Dunai, Cordelia, Egbe, Franklyn N, Martin, Naomi H, Facer, Bethany, Pendered, Sophie L, Rogers, Henry C, Hübel, Christopher, van Wamelen, Daniel J, Bethlehem, Richard A I, Giunchiglia, Valentina, Hellyer, Peter J, Trender, William, Kalsi, Gursharan, Needham, Edward, Easton, Ava, Jackson, Thomas A, Cunningham, Colm, Upthegrove, Rachel, Pollak, Thomas A, Hotopf, Matthew, Solomon, Tom, Pett, Sarah L, Shaw, Pamela J, Wood, Nicholas, Harrison, Neil A, Miller, Karla L, Jezzard, Peter, Williams, Guy, Duff, Eugene P, Williams, Steven, Zelaya, Fernando, Smith, Stephen M, Keller, Simon, Broome, Matthew, Kingston, Nathalie, Husain, Masud, Vincent, Angela, Bradley, John, Chinnery, Patrick, Menon, David K, Aggleton, John P, Nicholson, Timothy R, Taylor, John-Paul, David, Anthony S, Carson, Alan, Bullmore, Ed, Breen, Gerome, Hampshire, Adam, Michael, Benedict D, Paddick, Stella-Maria, Leek, E Charles

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Asymmetric sensory ganglionopathy: A case series von Marquez-Infante, Celedonio, Murphy, Sinéad M., Mathew, Liberty, Alsanousi, Ali, Lunn, Michael P., Brandner, Sebastian, Yousry, Tarek A., Blake, Julian, Reilly, Mary M.

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THE NEUROPATHY SPECTRUM IN WALDENSTRöM'S MACROGLOBULINAEMIA von Carr, Aisling, Jaunmuktane, Zane, Brandner, Sebastian, Kothari, J, Blake, Julian, D'Sa, Shirley, Lunn, Mike

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Anti Ma2-associated myeloradiculopathy: expanding the phenotype of anti-Ma2 associated paraneoplastic syndromes von Murphy, Sinéad M, Khan, Usman, Alifrangis, Constantine, Hazell, Steven, Hrouda, David, Blake, Julian, Ball, Joanna, Gabriel, Carolyn, Markarian, Pierre, Rees, Jeremy, Karim, Abid, Seckl, Michael J, Lunn, Michael P, Reilly, Mary M

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Optineurin mutations in Japanese amyotrophic lateral sclerosis von Iida, Aritoshi, Hosono, Naoya, Sano, Motoki, Kamei, Tetsumasa, Oshima, Shuichi, Tokuda, Torao, Kubo, Michiaki, Nakamura, Yusuke, Ikegawa, Shiro

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