Ndrg1 in development and maintenance of the myelin sheath von King, Rosalind H.M, Chandler, David, Lopaticki, Sash, Huang, Dexing, Blake, Julian, Muddle, John R, Kilpatrick, Trevor, Nourallah, Michelle, Miyata, Toshiyuki, Okuda, Tomohiko, Carter, Kim W, Hunter, Michael, Angelicheva, Dora, Morahan, Grant, Kalaydjieva, Luba

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The phenotype of Charcot–Marie–Tooth disease type 4C due to SH3TC2 mutations and possible predisposition to an inflammatory neuropathy von Houlden, Henry, Laura, Matilde, Ginsberg, Lionel, Jungbluth, Heinz, Robb, Stephanie A, Blake, Julian, Robinson, Susan, King, Rosalind H.M, Reilly, Mary M

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A novel RAB7 mutation associated with ulcero-mutilating neuropathy von Houlden, Henry, King, Rosalind H. M., Muddle, John R., Warner, Thomas T., Reilly, Mary M., Orrell, Richard W., Ginsberg, Lionel

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Proteasomal inhibition causes loss of nigral tyrosine hydroxylase neurons von Schapira, Anthony H. V., Cleeter, Michael W. J., Muddle, John R., Workman, Jane M., Cooper, J. Mark, King, Rosalind H. M.

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The stretcher spontaneous neurodegenerative mutation models Charcot-Marie-Tooth disease type 4D [version 1; peer review: 3 approved] von Chandler, David, Lopaticki, Sash, Huang, Dexing, Hunter, Michael, Angelicheva, Dora, Kilpatrick, Trevor, King, Rosalind HM, Kalaydjieva, Luba, Morahan, Grant

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High Incidence of Spontaneous Disease in an HLA-DR15 and TCR Transgenic Multiple Sclerosis Model von Ellmerich, Stephan, Mycko, Marcin, Takacs, Katalin, Waldner, Hanspeter, Wahid, Faisal N, Boyton, Rosemary J, King, Rosalind H. M, Smith, Paul A, Amor, Sandra, Herlihy, Amy H, Hewitt, Rachel E, Jutton, Mark, Price, David A, Hafler, David A, Kuchroo, Vijay K, Altmann, Daniel M

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Professor P. K. Thomas: clinician, investigator, editor and leader--a retrospective appreciation von Asbury, Arthur K, King, Rosalind H M, Reilly, Mary M, Dyck, Peter J, Said, Gerard, Compston, Alastair

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The phagocytic capacity of neurones von Bowen, Samantha, Ateh, Davidson D., Deinhardt, Katrin, Bird, Margaret M., Price, Karen M., Baker, Cathy S., Robson, Joanna C., Swash, Michael, Shamsuddin, Wassim, Kawar, Shalini, El-Tawil, Tariq, Roos, Jesper, Hoyle, Andrew, Nickols, Carole D., Knowles, Charles H., Pullen, Anthony H., Luthert, Phillip J., Weller, Roy O., Hafezparast, Majid, Franklin, Robin J. M., Revesz, Tamas, King, Rosalind H. M., Berninghausen, Otto, Fisher, Elizabeth M. C., Schiavo, Giampietro, Martin, Joanne E.

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Increased axonal ribosome numbers in CMT diseases von Verheijen, Mark H. G., Lammens, Martin, Ceuterick-de Groote, Chantal, Timmerman, Vincent, De Jonghe, Peter, King, Rosalind H. M., Smit, August B., van Minnen, Jan

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