Molecular analysis of prion strain variation and the aetiology of 'new variant' CJD von Collinge, John, Sidle, Katie C. L., Meads, Julie, Ironside, James, Hill, Andrew F.

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Tremor in motor neuron disease may be central rather than peripheral in origin von Latorre, A., Rocchi, L., Stamelou, M., Batla, A., Ciocca, M., Balint, B., Sidle, K., Berardelli, A., Rothwell, J. C., Bhatia, K. P.

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Profilin1 E117G is a moderate risk factor for amyotrophic lateral sclerosis von Fratta, Pietro, Charnock, James, Collins, Toby, Devoy, Anny, Howard, Robin, Malaspina, Andrea, Orrell, Richard, Sidle, Katie, Clarke, Jan, Shoai, Maryam, Lu, Ching-hua, Hardy, John, Plagnol, Vincent, Fisher, Elizabeth M C

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Review: Prion-like mechanisms of transactive response DNA binding protein of 43kDa (TDP-43) in amyotrophic lateral sclerosis (ALS) von Smethurst, Phillip, Sidle, Katie Claire Louise, Hardy, John

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Unaltered susceptibility to BSE in transgenic mice expressing human prion protein. [Addendum: Oct 2, 1997, v. 389 (6650), p. 526.] von Collinge, J, Palmer, M.S, Sidle, K.C, Hill, A.F, Gowland, I, Meads, J, Asante, E, Bradley, R, Doey, L.J, Lantos, P.L

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Myasthenia gravis and neuromyelitis opica: A causal link von Spillane, J, Christofi, G, Sidle, K.C, Kullmann, D.M, Howard, R.S

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Genetic basis of Creutzfeldt-Jakob disease in the United Kingdom : a systematic analysis of predisposing mutations and allelic variation in the PRNP gene von WINDL, O, DEMPSTER, M, PALMER, M. S, COLLINGE, J, ESTIBEIRO, J. P, LATHE, R, DE SILVA, R, ESMONDE, T, WILL, R, SPRINGBETT, A, CAMPBELL, T. A, SIDLE, K. C. L

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Molecular screening of sheep for bovine spongiform encephalopathy von Hill, Andrew F, Sidle, Katie C.L, Joiner, Susan, Keyes, Paula, Martin, Trevor C, Dawson, Michael, Collinge, John

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Transmission of Creutzfeldt-Jakob Disease from Humans to Transgenic Mice Expressing Chimeric Human-Mouse Prion Protein von Telling, Glenn C., Scott, Michael, Hsiao, Karen K., Foster, Dallas, Yang, Shu-Lian, Torchia, Marilyn, Katie C. L. Sidle, Collinge, John, DeArmond, Stephen J., Prusiner, Stanley B.

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Meta-analysis of pharmacogenetic interactions in amyotrophic lateral sclerosis clinical trials von van Eijk, Ruben P.A, Jones, Ashley R, Sproviero, William, Shatunov, Aleksey, Shaw, Pamela J, Leigh, P Nigel, Young, Carolyn A, Shaw, Christopher E, Mora, Gabriele, Mandrioli, Jessica, Borghero, Giuseppe, Volanti, Paolo, Diekstra, Frank P, van Rheenen, Wouter, Verstraete, Esther, Eijkemans, Marinus J.C, Veldink, Jan H, Chio, Adriano, Al-Chalabi, Ammar, van den Berg, Leonard H, van Es, Michael A

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The same prion strain causes vCJD and BSE von Hill, Andrew F., Desbruslais, Melanie, Joiner, Susan, Sidle, Katie C. L., Gowland, Ian, Collinge, John, Doey, Lawrence J., Lantos, Peter

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Rescue of neurophysiological phenotype seen in PrP null mice by transgene encoding human prion protein von Whittington, Miles A., Sidle, Katie C.L., Gowland, Ian, Meads, Julie, Hill, Andrew F., Palmer, Mark S., Jefferys, John G.R., Collinge, John

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Lithium in patients with amyotrophic lateral sclerosis (LiCALS): a phase 3 multicentre, randomised, double-blind, placebo-controlled trial von Morrison, K E, Dhariwal, S, Hornabrook, R, Savage, L, Burn, D J, Khoo, T K, Kelly, J, Murphy, C L, Al-Chalabi, A, Dougherty, A, Leigh, P N, Wijesekera, L, Thornhill, M, Ellis, C M, O'Hanlon, K, Panicker, J, Pate, L, Ray, P, Wyatt, L, Young, C A, Copeland, L, Ealing, J, Hamdalla, H, Leroi, I, Murphy, C, O'Keeffe, F, Oughton, E, Partington, L, Paterson, P, Rog, D, Sathish, A, Sexton, D, Smith, J, Vanek, H, Dodds, S, Williams, T L, Steen, I N, Clarke, J, Eziefula, C, Howard, R, Orrell, R, Sidle, K, Sylvester, R, Barrett, W, Merritt, C, Talbot, K, Turner, M R, Whatley, C, Williams, C, Williams, J, Cosby, C, Hanemann, C O, Iman, I, Philips, C, Timings, L, Crawford, S E, Hewamadduma, C, Hibberd, R, Hollinger, H, McDermott, C, Mils, G, Rafiq, M, Shaw, P J, Taylor, A, Waines, E, Walsh, T, Addison-Jones, R, Birt, J, Hare, M, Majid, T

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Fatal familial insomnia : a new Austrian family von ALMER, G, HAINFELLNER, J. A, COLLINGE, J, BUDKA, H, BRÜCKE, T, JELLINGER, K, KLEINERT, R, BAYER, G, WINDL, O, KRETZSCHMAR, H. A, HILL, A, SIDLE, K

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Prion protein is necessary for normal synaptic function von Collinge, John, Whittington, Miles A., Sidle, Katie C. L., Smith, Corinne J., Palmer, Mark S., Clarke, Anthony R., Jefferys, John G. R.

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Transmission of fatal familial insomnia to laboratory animals von Collinge, John, Palmer, MarkS, Sidle, KatieC.L., Gowland, Ian, Medori, Rosella, Ironside, James, Lantos, Peter

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Deletions in the prion protein gene are not associated with CJD von Palmer, Mark S., Mahal, Sukhvir P., Campbell, Tracy A., Hill, Andrew F., Sidle, Katie C.L., Laplanche, Jean-Louis, Collinge, John

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Typing prion isoforms von Parchi, P., Capellari, S., Chen, S. G., Petersen, R. B., Gambetti, P., Kopp, N., Brown, P., Kitamoto, T., Tateishi, J., Giese, A., Kretzschmar, H.

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Inherited prion disease (PrP lysine 200) in Britain: two case reports von Collinge, J, Palmer, M S, Campbell, T, Sidle, K C, Carroll, D, Harding, A

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Prion protein is necessary for normal synaptic function von COLLINGE, J, WHITTINGTON, M. A, SIDLE, K. C. L, SMITH, C. J, PALMER, M. S, CLARKE, A. R, JEFFERYS, J. G. R

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