Risdiplam for the treatment of adults with spinal muscular atrophy: Experience of the Northern Ireland neuromuscular service von McCluskey, Gavin, Lamb, Siobhan, Mason, Sarah, NicFhirleinn, Grainne, Douglas, Isobel, Tirupathi, Sandya, Morrison, Karen E., McConville, John

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EFNS guidelines on the Clinical Management of Amyotrophic Lateral Sclerosis (MALS) - revised report of an EFNS task force von Andersen, Peter M., Abrahams, Sharon, Borasio, Gian D., de Carvalho, Mamede, Chio, Adriano, Van Damme, Philip, Hardiman, Orla, Kollewe, Katja, Morrison, Karen E., Petri, Susanne, Pradat, Pierre-Francois, Silani, Vincenzo, Tomik, Barbara, Wasner, Maria, Weber, Markus

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Exome sequencing in amyotrophic lateral sclerosis implicates a novel gene, DNAJC7, encoding a heat-shock protein von Farhan, Sali M. K., Howrigan, Daniel P., Abbott, Liam E., Klim, Joseph R., Topp, Simon D., Byrnes, Andrea E., Churchhouse, Claire, Phatnani, Hemali, Smith, Bradley N., Rampersaud, Evadnie, Wu, Gang, Wuu, Joanne, Shatunov, Aleksey, Iacoangeli, Alfredo, Al Khleifat, Ahmad, Mordes, Daniel A., Ghosh, Sulagna, Eggan, Kevin, Rademakers, Rosa, McCauley, Jacob L., Schüle, Rebecca, Züchner, Stephan, Benatar, Michael, Taylor, J. Paul, Nalls, Michael, Gotkine, Marc, Shaw, Pamela J., Morrison, Karen E., Al-Chalabi, Ammar, Traynor, Bryan, Shaw, Christopher E., Goldstein, David B., Harms, Matthew B., Daly, Mark J., Neale, Benjamin M.

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

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Mutations in CHMP2B in lower motor neuron predominant amyotrophic lateral sclerosis (ALS) von Cox, Laura E, Ferraiuolo, Laura, Goodall, Emily F, Heath, Paul R, Higginbottom, Adrian, Mortiboys, Heather, Hollinger, Hannah C, Hartley, Judith A, Brockington, Alice, Burness, Christine E, Morrison, Karen E, Wharton, Stephen B, Grierson, Andrew J, Ince, Paul G, Kirby, Janine, Shaw, Pamela J

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Two-stage association study and meta-analysis of mitochondrial DNA variants in Parkinson disease von Hudson, Gavin, Nalls, Mike, Evans, Jonathan R, Breen, David P, Winder-Rhodes, Sophie, Morrison, Karen E, Morris, Huw R, Williams-Gray, Caroline H, Barker, Roger A, Singleton, Andrew B, Hardy, John, Wood, Nicholas E, Burn, David J, Chinnery, Patrick F

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C9orf72 intermediate expansions of 24-30 repeats are associated with ALS von Iacoangeli, Alfredo, Al Khleifat, Ahmad, Jones, Ashley R, Sproviero, William, Shatunov, Aleksey, Opie-Martin, Sarah, Morrison, Karen E, Shaw, Pamela J, Shaw, Christopher E, Fogh, Isabella, Dobson, Richard J, Newhouse, Stephen J, Al-Chalabi, Ammar

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Deletions at 22q11.2 in idiopathic Parkinson's disease: a combined analysis of genome-wide association data von Mok, Kin Y, FRCP, Sheerin, Una, MRCP, Simón-Sánchez, Javier, PhD, Salaka, Afnan, PhD, Chester, Lucy, MPharm, Escott-Price, Valentina, PhD, Mantripragada, Kiran, PhD, Doherty, Karen M, MD, Noyce, Alastair J, MRCP, Mencacci, Niccolo E, MD, Lubbe, Steven J, PhD, Williams-Gray, Caroline H, PhD, Barker, Roger A, Prof, van Dijk, Karin D, MD, Berendse, Henk W, Prof, Heutink, Peter, Prof, Corvol, Jean-Christophe, Prof, Cormier, Florence, MD, Lesage, Suzanne, PhD, Brice, Alexis, Prof, Brockmann, Kathrin, MD, Schulte, Claudia, PhD, Gasser, Thomas, Prof, Foltynie, Thomas, PhD, Limousin, Patricia, Prof, Morrison, Karen E, Prof, Clarke, Carl E, Prof, Sawcer, Stephen, Prof, Warner, Tom T, Prof, Lees, Andrew J, Prof, Morris, Huw R, Prof, Nalls, Mike A, PhD, Singleton, Andrew B, PhD, Hardy, John, Prof, Abramov, Andrey Y, Prof, Plagnol, Vincent, PhD, Williams, Nigel M, Dr, Wood, Nicholas W, Prof

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Extracellular Vesicles in Amyotrophic Lateral Sclerosis von McCluskey, Gavin, Morrison, Karen E, Donaghy, Colette, Rene, Frederique, Duddy, William, Duguez, Stephanie

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Safety, pharmacokinetic, and functional effects of the nogo-a monoclonal antibody in amyotrophic lateral sclerosis: a randomized, first-in-human clinical trial von 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

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Systematic Review and UK-Based Study of PARK2 (parkin), PINK1, PARK7 (DJ-1) and LRRK2 in early-onset Parkinson's disease von Kilarski, Laura L., Pearson, Justin P., Newsway, Victoria, Majounie, Elisa, Knipe, M. Duleeka W., Misbahuddin, Anjum, Chinnery, Patrick F., Burn, David J., Clarke, Carl E., Marion, Marie-Helene, Lewthwaite, Alistair J., Nicholl, David J., Wood, Nicholas W., Morrison, Karen E., Williams-Gray, Caroline H., Evans, Jonathan R., Sawcer, Stephen J., Barker, Roger A., Wickremaratchi, Mirdhu M., Ben-Shlomo, Yoav, Williams, Nigel M., Morris, Huw R.

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Chromosome 9p21 in sporadic amyotrophic lateral sclerosis in the UK and seven other countries: a genome-wide association study von Shatunov, Aleksey, PhD, Mok, Kin, MSc, Newhouse, Stephen, PhD, Weale, Michael E, PhD, Smith, Bradley, PhD, Vance, Caroline, PhD, Johnson, Lauren, PhD, Veldink, Jan H, MD, van Es, Michael A, MD, van den Berg, Leonard H, Prof, Robberecht, Wim, Prof, Van Damme, Philip, MD, Hardiman, Orla, Prof, Farmer, Anne E, Prof, Lewis, Cathryn M, Prof, Butler, Amy W, PhD, Abel, Olubunmi, MSc, Andersen, Peter M, Prof, Fogh, Isabella, PhD, Silani, Vincenzo, Prof, Chiò, Adriano, MD, Traynor, Bryan J, MD, Melki, Judith, Prof, Meininger, Vincent, Prof, Landers, John E, PhD, McGuffin, Peter, Prof, Glass, Jonathan D, MD, Pall, Hardev, MD, Leigh, P Nigel, Prof, Hardy, John, Prof, Brown, Robert H, Prof, Powell, John F, DPhil, Orrell, Richard W, MD, Morrison, Karen E, Prof, Shaw, Pamela J, Prof, Shaw, Christopher E, Prof, Al-Chalabi, Ammar, Prof

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The contribution of Neanderthal introgression and natural selection to neurodegenerative diseases von Chen, Zhongbo, Reynolds, Regina H., Pardiñas, Antonio F., Gagliano Taliun, Sarah A., van Rheenen, Wouter, Lin, Kuang, Shatunov, Aleksey, Gustavsson, Emil K., Fogh, Isabella, Jones, Ashley R., Robberecht, Wim, Corcia, Philippe, Chiò, Adriano, Shaw, Pamela J., Morrison, Karen E., Veldink, Jan H., van den Berg, Leonard H., Shaw, Christopher E., Powell, John F., Silani, Vincenzo, Hardy, John A., Houlden, Henry, Owen, Michael J., Turner, Martin R., Ryten, Mina, Al-Chalabi, Ammar

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

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Serum Neurofilaments in Motor Neuron Disease and Their Utility in Differentiating ALS, PMA and PLS von McCluskey, Gavin, Morrison, Karen E, Donaghy, Colette, McConville, John, McCarron, Mark O, McVerry, Ferghal, Duddy, William, Duguez, Stephanie

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Genetic variants of the alpha-synuclein gene SNCA are associated with multiple system atrophy von Al-Chalabi, Ammar, Dürr, Alexandra, Wood, Nicholas W, Parkinson, Michael H, Camuzat, Agnes, Hulot, Jean-Sébastien, Morrison, Karen E, Renton, Alan, Sussmuth, Sigurd D, Landwehrmeyer, Bernhard G, Ludolph, Albert, Agid, Yves, Brice, Alexis, Leigh, P Nigel, Bensimon, Gilbert

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An evaluation of a SVA retrotransposon in the FUS promoter as a transcriptional regulator and its association to ALS von Savage, Abigail L, Wilm, Thomas P, Khursheed, Kejhal, Shatunov, Aleksey, Morrison, Karen E, Shaw, Pamela J, Shaw, Christopher E, Smith, Bradley, Breen, Gerome, Al-Chalabi, Ammar, Moss, Diana, Bubb, Vivien J, Quinn, John P

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Large-scale analyses of CAV1 and CAV2 suggest their expression is higher in post-mortem ALS brain tissue and affects survival von Adey, Brett N, Cooper-Knock, Johnathan, Al Khleifat, Ahmad, Fogh, Isabella, van Damme, Philip, Corcia, Philippe, Couratier, Philippe, Hardiman, Orla, McLaughlin, Russell, Gotkine, Marc, Drory, Vivian, Silani, Vincenzo, Ticozzi, Nicola, Veldink, Jan H, van den Berg, Leonard H, de Carvalho, Mamede, Pinto, Susana, Mora Pardina, Jesus S, Povedano Panades, Mónica, Andersen, Peter M, Weber, Markus, Başak, Nazli A, Shaw, Christopher E, Shaw, Pamela J, Morrison, Karen E, Landers, John E, Glass, Jonathan D, Vourc'h, Patrick, Dobson, Richard J B, Breen, Gerome, Al-Chalabi, Ammar, Jones, Ashley R, Iacoangeli, Alfredo

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Amyotrophic lateral sclerosis (motor neuron disease): proposed mechanisms and pathways to treatment von Goodall, Emily F., Morrison, Karen E.

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Mutations in the tail and rod domains of the neurofilament heavy‐chain gene increase the risk of ALS von Marriott, Heather, Spargo, Thomas P., Al Khleifat, Ahmad, Andersen, Peter M, Başak, Nazli A., Cooper‐Knock, Johnathan, Corcia, Philippe, Couratier, Philippe, Carvalho, Mamede, Drory, Vivian, Gotkine, Marc, Landers, John E., McLaughlin, Russell, Pardina, Jesús S. Mora, Morrison, Karen E., Pinto, Susana, Shaw, Christopher E., Shaw, Pamela J., Silani, Vincenzo, Ticozzi, Nicola, Damme, Philip, Berg, Leonard H., Vourc'h, Patrick, Weber, Markus, Veldink, Jan H., Al Khleifat, Ahmad, Al‐Chalabi, Ammar, Andersen, Peter M, Başak, Nazli A., Cooper‐Knock, Johnathan, Corcia, Philippe, Couratier, Philippe, Carvalho, Mamede, Drory, Vivian, Glass, Jonathan D., Gotkine, Marc, Hardiman, Orla, Iacoangeli, Alfredo, Landers, John E., McLaughlin, Russell, Pardina, Jesús S. Mora, Morrison, Karen E., Pinto, Susana, Povedano, Monica, Shaw, Christopher E., Shaw, Pamela J., Silani, Vincenzo, Ticozzi, Nicola, Damme, Philip, Berg, Leonard H., Vourc'h, Patrick, Weber, Markus, Veldink, Jan H., Dobson, Richard J., Schwab, Patrick, Al‐Chalabi, Ammar, Iacoangeli, Alfredo

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