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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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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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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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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Coexistent hereditary and inflammatory neuropathy von Ginsberg, Lionel, Malik, Omar, Kenton, Anthony R., Sharp, David, Muddle, John R., Davis, Mary B., Winer, John B., Orrell, Richard W., King, Rosalind H. 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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Myelin and Axon Pathology in a Long-Term Study of PMP22-Overexpressing Mice von Verhamme, Camiel, King, Rosalind H.M, ten Asbroek, Anneloor L.M.A, Muddle, John R, Nourallah, Michelle, Wolterman, Ruud, Baas, Frank, van Schaik, Ivo N

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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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YAC transgenic mice carrying pathological alleles of the MJD1 locus exhibit a mild and slowly progressive cerebellar deficit von Cemal, Cemal K., Carroll, Christopher J., Lawrence, Lorraine, Lowrie, Margaret B., Ruddle, Piers, Al-Mahdawi, Sahar, King, Rosalind H.M., Pook, Mark A., Huxley, Clare, Chamberlain, Susan

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Chronic inflammatory demyelinating polyradiculoneuropathy with cholesterol deposits in a dog von Piñeyro, Pablo, Sponenberg, D. Philip, Pancotto, Theresa, King, Rosalind H. M., Jortner, Bernard S.

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Clinical spectrum of CMT4C disease in patients homozygous for the p.Arg1109X mutation in SH3TC2 von Colomer, Jaume, Gooding, Rebecca, Angelicheva, Dora, King, Rosalind H.M., Guillén-Navarro, Encarna, Parman, Yesim, Nascimento, Andres, Conill, Joan, Kalaydjieva, Luba

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Myotubularin-related 2 protein phosphatase and neurofilament light chain protein, both mutated in CMT neuropathies, interact in peripheral nerve von Previtali, Stefano C., Zerega, Barbara, Sherman, Diane L., Brophy, Peter J., Dina, Giorgia, King, Rosalind H.M., Salih, Mustafa M., Feltri, Laura, Quattrini, Angelo, Ravazzolo, Roberto, Wrabetz, Lawrence, Monaco, Anthony P., Bolino, Alessandra

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Hereditary motor and sensory neuropathy-russe: New autosomal recessive neuropathy in balkan gypsies von Thomas, P. K., Kalaydjieva, Luba, Youl, Brian, Rogers, Tamara, Angelicheva, Dora, King, Rosalind H. M., Guergueltcheva, Velina, Colomer, Jaume, Lupu, Constantin, Corches, Axinia, Popa, Gabriela, Merlini, Luciano, Shmarov, Alex, Muddle, John R., Nourallah, Michelle, Tournev, Ivailo

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N-myc Downstream-Regulated Gene 1 Is Mutated in Hereditary Motor and Sensory Neuropathy–Lom von Kalaydjieva, Luba, Gresham, David, Gooding, Rebecca, Heather, Lisa, Baas, Frank, de Jonge, Rosalein, Blechschmidt, Karin, Angelicheva, Dora, Chandler, David, Worsley, Penelope, Rosenthal, Andre, King, Rosalind H.M., Thomas, P.K.

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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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Pathological findings in a patient with ventilatory failure and chronic inflammatory demyelinating polyneuropathy von Kimber, Thomas E., Orrell, Richard W., King, Rosalind H. M., Ginsberg, Lionel

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Brachial plexus hypertrophy in chronic inflammatory demyelinating polyradiculoneuropathy von Bradley, Lloyd J., Wilhelm, Thomas, King, Rosalind H.M., Ginsberg, Lionel, Orrell, Richard W.

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Biomarkers of Nutrition for Development (BOND)-Zinc Review von King, Janet C, Brown, Kenneth H, Gibson, Rosalind S, Krebs, Nancy F, Lowe, Nicola M, Siekmann, Jonathan H, Raiten, Daniel J

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