Multiple Sclerosis: The History of a Disease

بواسطة Orrell, Richard W
منشور في 2005

Palliative care in amyotrophic lateral sclerosis

بواسطة Orrell, Richard W
منشور في 2007

Scapular fixation in muscular dystrophy

بواسطة Orrell, Richard W, Copeland, Stephen, Rose, Michael R
الحاوية / القاعدة Cochrane Database Syst Rev (2010)

Pharmacological treatments for Friedreich ataxia

بواسطة Kearney, Mary, Orrell, Richard W, Fahey, Michael, Brassington, Ruth, Pandolfo, Massimo
الحاوية / القاعدة Cochrane Database Syst Rev (2016)

β-catenin is central to DUX4-driven network rewiring in facioscapulohumeral muscular dystrophy

بواسطة Banerji, Christopher R. S., Knopp, Paul, Moyle, Louise A., Severini, Simone, Orrell, Richard W., Teschendorff, Andrew E., Zammit, Peter S.
الحاوية / القاعدة J R Soc Interface (2015)

Investigation of white matter pathology in ALS and PLS using tract‐based spatial statistics

بواسطة Ciccarelli, Olga, Behrens, Timothy E., Johansen‐Berg, Heidi, Talbot, Kevin, Orrell, Richard W., Howard, Robin S., Nunes, Rita G., Miller, David H., Matthews, Paul M., Thompson, Alan J., Smith, Stephen M.
الحاوية / القاعدة Hum Brain Mapp (2008)

Pathogenic VCP Mutations Induce Mitochondrial Uncoupling and Reduced ATP Levels

بواسطة Bartolome, Fernando, Wu, Hsiu-Chuan, Burchell, Victoria S., Preza, Elisavet, Wray, Selina, Mahoney, Colin J., Fox, Nick C., Calvo, Andrea, Canosa, Antonio, Moglia, Cristina, Mandrioli, Jessica, Chiò, Adriano, Orrell, Richard W., Houlden, Henry, Hardy, John, Abramov, Andrey Y., Plun-Favreau, Helene
منشور في 2013

A comprehensive analysis of rare genetic variation in amyotrophic lateral sclerosis in the UK

بواسطة Morgan, Sarah, Shatunov, Aleksey, Sproviero, William, Jones, Ashley R., Shoai, Maryam, Hughes, Deborah, Al Khleifat, Ahmad, Malaspina, Andrea, Morrison, Karen E., Shaw, Pamela J., Shaw, Christopher E., Sidle, Katie, Orrell, Richard W., Fratta, Pietro, Hardy, John, Pittman, Alan, Al-Chalabi, Ammar
الحاوية / القاعدة Brain (2017)

Homozygosity analysis in amyotrophic lateral sclerosis

بواسطة Mok, Kin, Laaksovirta, Hannu, Tienari, Pentti J, Peuralinna, Terhi, Myllykangas, Liisa, Chiò, Adriano, Traynor, Bryan J, Nalls, Michael A, Gurunlian, Nicole, Shatunov, Aleksey, Restagno, Gabriella, Mora, Gabriele, Nigel Leigh, P, Shaw, Chris E, Morrison, Karen E, Shaw, Pamela J, Al-Chalabi, Ammar, Hardy, John, Orrell, Richard W
منشور في 2013

The sex ratio in amyotrophic lateral sclerosis: A population based study

بواسطة Manjaly, Zita R., Scott, Kirsten M., Abhinav, Kumar, Wijesekera, Lokesh, Ganesalingam, Jeban, Goldstein, Laura H., Janssen, Anna, Dougherty, Andrew, Willey, Emma, Stanton, Biba R., Turner, Martin R., Ampong, Mary-Ann, Sakel, Mohammed, Orrell, Richard W., Howard, Robin, Shaw, Chris E., Leigh, P. Nigel, Al-Chalabi, Ammar
الحاوية / القاعدة Amyotroph Lateral Scler (2010)

Large C9orf72 Hexanucleotide Repeat Expansions Are Seen in Multiple Neurodegenerative Syndromes and Are More Frequent Than Expected in the UK Population

بواسطة Beck, Jon, Poulter, Mark, Hensman, Davina, Rohrer, Jonathan D., Mahoney, Colin J., Adamson, Gary, Campbell, Tracy, Uphill, James, Borg, Aaron, Fratta, Pietro, Orrell, Richard W., Malaspina, Andrea, Rowe, James, Brown, Jeremy, Hodges, John, Sidle, Katie, Polke, James M., Houlden, Henry, Schott, Jonathan M., Fox, Nick C., Rossor, Martin N., Tabrizi, Sarah J., Isaacs, Adrian M., Hardy, John, Warren, Jason D., Collinge, John, Mead, Simon
منشور في 2013

Safety, Pharmacokinetic, and Functional Effects of the Nogo-A Monoclonal Antibody in Amyotrophic Lateral Sclerosis: A Randomized, First-In-Human Clinical Trial

بواسطة Meininger, Vincent, Pradat, Pierre-François, Corse, Andrea, Al-Sarraj, Safa, Rix Brooks, Benjamin, Caress, James B., Cudkowicz, Merit, Kolb, Stephen J., Lange, Dale, Leigh, P. Nigel, Meyer, Thomas, Milleri, Stefano, Morrison, Karen E., Orrell, Richard W., Peters, Gary, Rothstein, Jeffrey D., Shefner, Jeremy, Lavrov, Arseniy, Williams, Nicola, Overend, Phil, Price, Jeffrey, Bates, Stewart, Bullman, Jonathan, Krull, David, Berges, Alienor, Abila, Bams, Meno-Tetang, Guy, Wurthner, Jens
منشور في 2014

Analysis of amyotrophic lateral sclerosis as a multistep process: a population-based modelling study

بواسطة Al-Chalabi, Ammar, Calvo, Andrea, Chio, Adriano, Colville, Shuna, Ellis, Cathy M, Hardiman, Orla, Heverin, Mark, Howard, Robin S, Huisman, Mark H B, Keren, Noa, Leigh, P Nigel, Mazzini, Letizia, Mora, Gabriele, Orrell, Richard W, Rooney, James, Scott, Kirsten M, Scotton, William J, Seelen, Meinie, Shaw, Christopher E, Sidle, Katie S, Swingler, Robert, Tsuda, Miho, Veldink, Jan H, Visser, Anne E, van den Berg, Leonard H, Pearce, Neil
منشور في 2014

Screening a UK amyotrophic lateral sclerosis cohort provides evidence of multiple origins of the C9orf72 expansion()

بواسطة Fratta, Pietro, Polke, James M., Newcombe, Jia, Mizielinska, Sarah, Lashley, Tammaryn, Poulter, Mark, Beck, Jon, Preza, Elisavet, Devoy, Anny, Sidle, Katie, Howard, Robin, Malaspina, Andrea, Orrell, Richard W., Clarke, Jan, Lu, Ching-Hua, Mok, Kin, Collins, Toby, Shoaii, Maryam, Nanji, Tina, Wray, Selina, Adamson, Gary, Pittman, Alan, Renton, Alan E., Traynor, Bryan J., Sweeney, Mary G., Revesz, Tamas, Houlden, Henry, Mead, Simon, Isaacs, Adrian M., Fisher, Elizabeth M.C.
الحاوية / القاعدة Neurobiol Aging (2015)

The chromosome 9 ALS and FTD locus is probably derived from a single founder

بواسطة Mok, Kin, Traynor, Bryan J., Schymick, Jennifer, Tienari, Pentti J., Laaksovirta, Hannu, Peuralinna, Terhi, Myllykangas, Liisa, Chiò, Adriano, Shatunov, Aleksey, Boeve, Bradley F., Boxer, Adam L., DeJesus-Hernandez, Mariely, Mackenzie, Ian R., Waite, Adrian, Williams, Nigel, Morris, Huw R., Simón-Sánchez, Javier, van Swieten, John C., Heutink, Peter, Restagno, Gabriella, Mora, Gabriele, Morrison, Karen E., Shaw, Pamela J., Rollinson, Pamela Sara, Al-Chalabi, Ammar, Rademakers, Rosa, Pickering-Brown, Stuart, Orrell, Richard W., Nalls, Michael A., Hardy, John
منشور في 2012

DiPALS: Diaphragm Pacing in patients with Amyotrophic Lateral Sclerosis - a randomised controlled trial.

بواسطة McDermott, Christopher J, Bradburn, Mike J, Maguire, Chin, Cooper, Cindy L, Baird, Wendy O, Baxter, Susan K, Cohen, Judith, Cantrill, Hannah, Dixon, Simon, Ackroyd, Roger, Baudouin, Simon, Bentley, Andrew, Berrisford, Richard, Bianchi, Stephen, Bourke, Stephen C, Darlison, Roy, Ealing, John, Elliott, Mark, Fitzgerald, Patrick, Galloway, Simon, Hamdalla, Hisham, Hanemann, C Oliver, Hughes, Philip, Imam, Ibrahim, Karat, Dayalan, Leek, Roger, Maynard, Nick, Orrell, Richard W, Sarela, Abeezar, Stradling, John, Talbot, Kevin, Taylor, Lyn, Turner, Martin, Simonds, Anita K, Williams, Tim, Wedzicha, Wisia, Young, Carolyn, Shaw, Pamela J
الحاوية / القاعدة Health Technol Assess (2016)

Chromosome 9p21 in sporadic amyotrophic lateral sclerosis in the UK and seven other countries: a genome-wide association study

بواسطة Shatunov, Aleksey, Mok, Kin, Newhouse, Stephen, Weale, Michael E, Smith, Bradley, Vance, Caroline, Johnson, Lauren, Veldink, Jan H, van Es, Michael A, van den Berg, Leonard H, Robberecht, Wim, Van Damme, Philip, Hardiman, Orla, Farmer, Anne E, Lewis, Cathryn M, Butler, Amy W, Abel, Olubunmi, Andersen, Peter M, Fogh, Isabella, Silani, Vincenzo, Chiò, Adriano, Traynor, Bryan J, Melki, Judith, Meininger, Vincent, Landers, John E, McGuffin, Peter, Glass, Jonathan D, Pall, Hardev, Leigh, P Nigel, Hardy, John, Brown, Robert H, Powell, John F, Orrell, Richard W, Morrison, Karen E, Shaw, Pamela J, Shaw, Christopher E, Al-Chalabi, Ammar
منشور في 2010

Mutations in the Matrin 3 gene cause familial amyotrophic lateral sclerosis

بواسطة Johnson, Janel O., Pioro, Erik P., Boehringer, Ashley, Chia, Ruth, Feit, Howard, Renton, Alan E., Pliner, Hannah A., Abramzon, Yevgeniya, Marangi, Giuseppe, Winborn, Brett J., Gibbs, J Raphael, Nalls, Michael A., Morgan, Sarah, Shoai, Maryam, Hardy, John, Pittman, Alan, Orrell, Richard W., Malaspina, Andrea, Sidle, Katie C., Fratta, Pietro, Harms, Matthew B., Baloh, Robert H., Pestronk, Alan, Weihl, Conrad C., Rogaeva, Ekaterina, Zinman, Lorne, Drory, Vivian E., Borghero, Giuseppe, Mora, Gabriele, Calvo, Andrea, Rothstein, Jeffrey D., Drepper, Carsten, Sendtner, Michael, Singleton, Andrew B., Taylor, J. Paul, Cookson, Mark R., Restagno, Gabriella, Sabatelli, Mario, Bowser, Robert, Chiò, Adriano, Traynor, Bryan J.
منشور في 2014

Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study

بواسطة Majounie, Elisa, Renton, Alan E, Mok, Kin, Dopper, Elise GP, Waite, Adrian, Rollinson, Sara, Chiò, Adriano, Restagno, Gabriella, Nicolaou, Nayia, Simon-Sanchez, Javier, van Swieten, John C, Abramzon, Yevgeniya, Johnson, Janel O, Sendtner, Michael, Pamphlett, Roger, Orrell, Richard W, Mead, Simon, Sidle, Katie C, Houlden, Henry, Rohrer, Jonathan D, Morrison, Karen E, Pall, Hardev, Talbot, Kevin, Ansorge, Olaf, Hernandez, Dena G, Arepalli, Sampath, Sabatelli, Mario, Mora, Gabriele, Corbo, Massimo, Giannini, Fabio, Calvo, Andrea, Englund, Elisabet, Borghero, Giuseppe, Floris, Gian Luca, Remes, Anne M, Laaksovirta, Hannu, McCluskey, Leo, Trojanowski, John Q, Van Deerlin, Vivianna M, Schellenberg, Gerard D, Nalls, Michael A, Drory, Vivian E, Lu, Chin-Song, Yeh, Tu-Hsueh, Ishiura, Hiroyuki, Takahashi, Yuji, Tsuji, Shoji, Le Ber, Isabelle, Brice, Alexis, Drepper, Carsten, Williams, Nigel, Kirby, Janine, Shaw, Pamela, Hardy, John, Tienari, Pentti J, Heutink, Peter, Morris, Huw R, Pickering-Brown, Stuart, Traynor, Bryan J
منشور في 2012

A two-stage genome-wide association study of sporadic amyotrophic lateral sclerosis

بواسطة Chiò, Adriano, Schymick, Jennifer C., Restagno, Gabriella, Scholz, Sonja W., Lombardo, Federica, Lai, Shiao-Lin, Mora, Gabriele, Fung, Hon-Chung, Britton, Angela, Arepalli, Sampath, Gibbs, J. Raphael, Nalls, Michael, Berger, Stephen, Kwee, Lydia Coulter, Oddone, Eugene Z., Ding, Jinhui, Crews, Cynthia, Rafferty, Ian, Washecka, Nicole, Hernandez, Dena, Ferrucci, Luigi, Bandinelli, Stefania, Guralnik, Jack, Macciardi, Fabio, Torri, Federica, Lupoli, Sara, Chanock, Stephen J., Thomas, Gilles, Hunter, David J., Gieger, Christian, Wichmann, H. Erich, Calvo, Andrea, Mutani, Roberto, Battistini, Stefania, Giannini, Fabio, Caponnetto, Claudia, Mancardi, Giovanni Luigi, La Bella, Vincenzo, Valentino, Francesca, Monsurrò, Maria Rosaria, Tedeschi, Gioacchino, Marinou, Kalliopi, Sabatelli, Mario, Conte, Amelia, Mandrioli, Jessica, Sola, Patrizia, Salvi, Fabrizio, Bartolomei, Ilaria, Siciliano, Gabriele, Carlesi, Cecilia, Orrell, Richard W., Talbot, Kevin, Simmons, Zachary, Connor, James, Pioro, Erik P., Dunkley, Travis, Stephan, Dietrich A., Kasperaviciute, Dalia, Fisher, Elizabeth M., Jabonka, Sibylle, Sendtner, Michael, Beck, Marcus, Bruijn, Lucie, Rothstein, Jeffrey, Schmidt, Silke, Singleton, Andrew, Hardy, John, Traynor, Bryan J.
منشور في 2009