Gears for electric motor von Desaidamle, Sonia, Macleod, Blair, Reps, Christopher, Chalabi, Christopher, Deas, Johnathan, Foresti, Stefano, Gottesfeld, Samuel, Robinson, Michiro

Volltext bestellen

Gears for Electric Motor von FORESTI, Stefano, MACLEOD, Blair, DEAS, Johnathan, DESAIDAMLE, Sonia, GOTTESFELD, Samuel, ROBINSON, Michiro, REPS, Christopher, CHALABI, Christopher

Volltext bestellen

GEARS FOR ELECTRIC MOTOR von FORESTI, Stefano, MACLEOD, Blair, DEAS, Johnathan, DESAIDAMLE, Sonia, GOTTESFELD, Samuel, ROBINSON, Michiro, REPS, Christopher, CHALABI, Christopher

Volltext bestellen

GEARS FOR ELECTRIC MOTOR von FORESTI, Stefano, MACLEOD, Blair, DEAS, Johnathan, DESAIDAMLE, Sonia, GOTTESFELD, Samuel, ROBINSON, Michiro, REPS, Christopher, CHALABI, Christopher

Volltext bestellen

Weyl anomalies of four dimensional conformal boundaries and defects von Chalabi, Adam, Herzog, Christopher P., O’Bannon, Andy, Robinson, Brandon, Sisti, Jacopo

Volltext

An estimate of amyotrophic lateral sclerosis heritability using twin data von Al-Chalabi, A, Fang, F, Hanby, M F, Leigh, P N, Shaw, C E, Ye, W, Rijsdijk, F

Volltext

Mutations in FUS, an RNA Processing Protein, Cause Familial Amyotrophic Lateral Sclerosis Type 6 von Vance, Caroline, Rogelj, Boris, Hortobágyi, Tibor, De Vos, Kurt J, Nishimura, Agnes Lumi, Sreedharan, Jemeen, Hu, Xun, Smith, Bradley, Ruddy, Deborah, Wright, Paul, Ganesalingam, Jeban, Williams, Kelly L, Tripathi, Vineeta, Al-Saraj, Safa, Al-Chalabi, Ammar, Leigh, P. Nigel, Blair, Ian P, Nicholson, Garth, de Belleroche, Jackie, Gallo, Jean-Marc, Miller, Christopher C, Shaw, Christopher E

Volltext

TDP-43 Mutations in Familial and Sporadic Amyotrophic Lateral Sclerosis von Sreedharan, Jemeen, Blair, Ian P, Tripathi, Vineeta B, Hu, Xun, Vance, Caroline, Rogelj, Boris, Ackerley, Steven, Durnall, Jennifer C, Williams, Kelly L, Buratti, Emanuele, Baralle, Francisco, de Belleroche, Jacqueline, Mitchell, J. Douglas, Leigh, P. Nigel, Al-Chalabi, Ammar, Miller, Christopher C, Nicholson, Garth, Shaw, Christopher E

Volltext

European Academy of Neurology (EAN) guideline on the management of amyotrophic lateral sclerosis in collaboration with European Reference Network for Neuromuscular Diseases (ERN EU... von Van Damme, Philip, Al‐Chalabi, Ammar, Andersen, Peter M., Chiò, Adriano, Couratier, Philippe, De Carvalho, Mamede, Hardiman, Orla, Kuźma‐Kozakiewicz, Magdalena, Ludolph, Albert, McDermott, Christopher J., Mora, Jesus S., Petri, Susanne, Probyn, Katrin, Reviers, Evy, Salachas, François, Silani, Vincenzo, Tysnes, Ole‐Bjørn, Berg, Leonard H., Villanueva, Gemma, Weber, Markus

Volltext

p62 positive, TDP-43 negative, neuronal cytoplasmic and intranuclear inclusions in the cerebellum and hippocampus define the pathology of C9orf72-linked FTLD and MND/ALS von Al-Sarraj, Safa, King, Andrew, Troakes, Claire, Smith, Bradley, Maekawa, Satomi, Bodi, Istvan, Rogelj, Boris, Al-Chalabi, Ammar, Hortobágyi, Tibor, Shaw, Christopher E.

Volltext

Cost‐effectiveness of acceptance and commitment therapy for people living with motor neuron disease, and their health‐related quality of life von Keetharuth, Anju D., Gould, Rebecca L., McDermott, Christopher J., Thompson, Benjamin J., Rawlinson, Charlotte, Bradburn, Mike, Bursnall, Matt, Kumar, Pavithra, Turton, Emily J., Tappenden, Paul, White, David, Howard, Robert J., Serfaty, Marc A., McCracken, Lance M., Graham, Christopher D., Al‐Chalabi, Ammar, Goldstein, Laura H., Lawrence, Vanessa, Cooper, Cindy, Young, Tracey

Volltext

Loss and gain of Drosophila TDP-43 impair synaptic efficacy and motor control leading to age-related neurodegeneration by loss-of-function phenotypes von Diaper, Danielle C, Adachi, Yoshitsugu, Sutcliffe, Ben, Humphrey, Dickon M, Elliott, Christopher J H, Stepto, Alan, Ludlow, Zoe N, Vanden Broeck, Lies, Callaerts, Patrick, Dermaut, Bart, Al-Chalabi, Ammar, Shaw, Christopher E, Robinson, Iain M, Hirth, Frank

Volltext

Is language impairment more common than executive dysfunction in amyotrophic lateral sclerosis? von Taylor, Lorna J, Brown, Richard G, Tsermentseli, Stella, Al-Chalabi, Ammar, Shaw, Christopher E, Ellis, Catherine M, Leigh, P Nigel, Goldstein, Laura H

Volltext

Analysis of amyotrophic lateral sclerosis as a multistep process: a population-based modelling study von Al-Chalabi, Ammar, Prof, Calvo, Andrea, MD, Chio, Adriano, Prof, Colville, Shuna, MPH, Ellis, Cathy M, PhD, Hardiman, Orla, Prof, Heverin, Mark, MSc, Howard, Robin S, PhD, Huisman, Mark H B, MD, Keren, Noa, MBBS, Leigh, P Nigel, Prof, Mazzini, Letizia, MD, Mora, Gabriele, MD, Orrell, Richard W, MD, Rooney, James, MSc, Scott, Kirsten M, MBBS, Scotton, William J, MBioch, Seelen, Meinie, MD, Shaw, Christopher E, Prof, Sidle, Katie S, PhD, Swingler, Robert, MD, Tsuda, Miho, MBChB, Veldink, Jan H, Prof, Visser, Anne E, MD, van den Berg, Leonard H, Prof, Pearce, Neil, Prof

Volltext

Boundaries in free higher derivative conformal field theories von Chalabi, Adam, Herzog, Christopher P., Ray, Krishnendu, Robinson, Brandon, Sisti, Jacopo, Stergiou, Andreas

Volltext

ALS-specific cognitive and behavior changes associated with advancing disease stage in ALS von Crockford, Christopher, Newton, Judith, Lonergan, Katie, Chiwera, Theresa, Booth, Tom, Chandran, Siddharthan, Colville, Shuna, Heverin, Mark, Mays, Iain, Pal, Suvankar, Pender, Niall, Pinto-Grau, Marta, Radakovic, Ratko, Shaw, Christopher E, Stephenson, Laura, Swingler, Robert, Vajda, Alice, Al-Chalabi, Ammar, Hardiman, Orla, Abrahams, Sharon

Volltext

Improving clinical trial outcomes in amyotrophic lateral sclerosis von Kiernan, Matthew C., Vucic, Steve, Talbot, Kevin, McDermott, Christopher J., Hardiman, Orla, Shefner, Jeremy M., Al-Chalabi, Ammar, Huynh, William, Cudkowicz, Merit, Talman, Paul, Van den Berg, Leonard H., Dharmadasa, Thanuja, Wicks, Paul, Reilly, Claire, Turner, Martin R.

Volltext

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

Volltext

An MND/ALS phenotype associated with C9orf72 repeat expansion: Abundant p62-positive, TDP-43-negative inclusions in cerebral cortex, hippocampus and cerebellum but without associat... von Troakes, Claire, Maekawa, Satomi, Wijesekera, Lokesh, Rogelj, Boris, Siklós, László, Bell, Christopher, Smith, Bradley, Newhouse, Stephen, Vance, Caroline, Johnson, Lauren, Hortobágyi, Tibor, Shatunov, Aleksey, Al-Chalabi, Ammar, Leigh, Nigel, Shaw, Christopher E., King, Andrew, Al-Sarraj, Safa

Volltext

PRECISION ALS-an integrated pan European patient data platform for ALS von McFarlane, R, Galvin, M, Heverin, M, Mac Domhnaill, E, Murray, D, Meldrum, D, Bede, P, Bolger, A, Hederman, L, Impey, S, Stephens, G, O'Meara, C, Wade, V, Al Chalabi, A, Chio, A, Corcia, P, van Damme, P, Ingre, C, McDermott, C, Povedanos, M, Van den Berg, L, Hardiman, O

Volltext