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Times Cited: 1499
Times Cited: 1499
Times Cited
Times Co-cited
Similarity
El Escorial revisited: revised criteria for the diagnosis of amyotrophic lateral sclerosis.
B R Brooks, R G Miller, M Swash, T L Munsat. Amyotroph Lateral Scler Other Motor Neuron Disord 2000
B R Brooks, R G Miller, M Swash, T L Munsat. Amyotroph Lateral Scler Other Motor Neuron Disord 2000
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The ALSFRS-R: a revised ALS functional rating scale that incorporates assessments of respiratory function. BDNF ALS Study Group (Phase III).
J M Cedarbaum, N Stambler, E Malta, C Fuller, D Hilt, B Thurmond, A Nakanishi. J Neurol Sci 1999
J M Cedarbaum, N Stambler, E Malta, C Fuller, D Hilt, B Thurmond, A Nakanishi. J Neurol Sci 1999
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Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis.
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State of play in amyotrophic lateral sclerosis genetics.
Alan E Renton, Adriano Chiò, Bryan J Traynor. Nat Neurosci 2014
Alan E Renton, Adriano Chiò, Bryan J Traynor. Nat Neurosci 2014
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Ubiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis.
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A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD.
Alan E Renton, Elisa Majounie, Adrian Waite, Javier Simón-Sánchez, Sara Rollinson, J Raphael Gibbs, Jennifer C Schymick, Hannu Laaksovirta, John C van Swieten, Liisa Myllykangas,[...]. Neuron 2011
Alan E Renton, Elisa Majounie, Adrian Waite, Javier Simón-Sánchez, Sara Rollinson, J Raphael Gibbs, Jennifer C Schymick, Hannu Laaksovirta, John C van Swieten, Liisa Myllykangas,[...]. Neuron 2011
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Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS.
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Safety and efficacy of edaravone in well defined patients with amyotrophic lateral sclerosis: a randomised, double-blind, placebo-controlled trial.
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Decoding ALS: from genes to mechanism.
J Paul Taylor, Robert H Brown, Don W Cleveland. Nature 2016
J Paul Taylor, Robert H Brown, Don W Cleveland. Nature 2016
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Riluzole for amyotrophic lateral sclerosis (ALS)/motor neuron disease (MND).
Robert G Miller, J D Mitchell, Dan H Moore. Cochrane Database Syst Rev 2012
Robert G Miller, J D Mitchell, Dan H Moore. Cochrane Database Syst Rev 2012
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Electrodiagnostic criteria for diagnosis of ALS.
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A proposal for new diagnostic criteria for ALS.
Jeremy M Shefner, Ammar Al-Chalabi, Mark R Baker, Li-Ying Cui, Mamede de Carvalho, Andrew Eisen, Julian Grosskreutz, Orla Hardiman, Robert Henderson, Jose Manuel Matamala,[...]. Clin Neurophysiol 2020
Jeremy M Shefner, Ammar Al-Chalabi, Mark R Baker, Li-Ying Cui, Mamede de Carvalho, Andrew Eisen, Julian Grosskreutz, Orla Hardiman, Robert Henderson, Jose Manuel Matamala,[...]. Clin Neurophysiol 2020
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Riluzole and edaravone: A tale of two amyotrophic lateral sclerosis drugs.
Manoj Kumar Jaiswal. Med Res Rev 2019
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Amyotrophic lateral sclerosis.
Michael A van Es, Orla Hardiman, Adriano Chio, Ammar Al-Chalabi, R Jeroen Pasterkamp, Jan H Veldink, Leonard H van den Berg. Lancet 2017
Michael A van Es, Orla Hardiman, Adriano Chio, Ammar Al-Chalabi, R Jeroen Pasterkamp, Jan H Veldink, Leonard H van den Berg. Lancet 2017
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Genetic epidemiology of amyotrophic lateral sclerosis: a systematic review and meta-analysis.
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EFNS guidelines on the clinical management of amyotrophic lateral sclerosis (MALS)--revised report of an EFNS task force.
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Peter M Andersen, Sharon Abrahams, Gian D Borasio, Mamede de Carvalho, Adriano Chio, Philip Van Damme, Orla Hardiman, Katja Kollewe, Karen E Morrison, Susanne Petri,[...]. Eur J Neurol 2012
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Risk factors for amyotrophic lateral sclerosis.
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Incidence of amyotrophic lateral sclerosis in Europe.
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Giancarlo Logroscino, Bryan J Traynor, Orla Hardiman, Adriano Chiò, Douglas Mitchell, Robert J Swingler, Andrea Millul, Emma Benn, Ettore Beghi. J Neurol Neurosurg Psychiatry 2010
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ALS Clinical Trials Review: 20 Years of Failure. Are We Any Closer to Registering a New Treatment?
Dmitry Petrov, Colin Mansfield, Alain Moussy, Olivier Hermine. Front Aging Neurosci 2017
Dmitry Petrov, Colin Mansfield, Alain Moussy, Olivier Hermine. Front Aging Neurosci 2017
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A revision of the El Escorial criteria - 2015.
Albert Ludolph, Vivian Drory, Orla Hardiman, Imaharu Nakano, John Ravits, Wim Robberecht, Jeremy Shefner. Amyotroph Lateral Scler Frontotemporal Degener 2015
Albert Ludolph, Vivian Drory, Orla Hardiman, Imaharu Nakano, John Ravits, Wim Robberecht, Jeremy Shefner. Amyotroph Lateral Scler Frontotemporal Degener 2015
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Amyotrophic Lateral Sclerosis: An Update for 2018.
Björn Oskarsson, Tania F Gendron, Nathan P Staff. Mayo Clin Proc 2018
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Controversies and priorities in amyotrophic lateral sclerosis.
Martin R Turner, Orla Hardiman, Michael Benatar, Benjamin R Brooks, Adriano Chio, Mamede de Carvalho, Paul G Ince, Cindy Lin, Robert G Miller, Hiroshi Mitsumoto,[...]. Lancet Neurol 2013
Martin R Turner, Orla Hardiman, Michael Benatar, Benjamin R Brooks, Adriano Chio, Mamede de Carvalho, Paul G Ince, Cindy Lin, Robert G Miller, Hiroshi Mitsumoto,[...]. Lancet Neurol 2013
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Mutations in FUS, an RNA processing protein, cause familial amyotrophic lateral sclerosis type 6.
Caroline Vance, Boris Rogelj, Tibor Hortobágyi, Kurt J De Vos, Agnes Lumi Nishimura, Jemeen Sreedharan, Xun Hu, Bradley Smith, Deborah Ruddy, Paul Wright,[...]. Science 2009
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Unraveling the mechanisms involved in motor neuron degeneration in ALS.
Lucie I Bruijn, Timothy M Miller, Don W Cleveland. Annu Rev Neurosci 2004
Lucie I Bruijn, Timothy M Miller, Don W Cleveland. Annu Rev Neurosci 2004
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Motor neuron degeneration in mice that express a human Cu,Zn superoxide dismutase mutation.
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Global epidemiology of amyotrophic lateral sclerosis: a systematic review of the published literature.
A Chiò, G Logroscino, B J Traynor, J Collins, J C Simeone, L A Goldstein, L A White. Neuroepidemiology 2013
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Amyotrophic lateral sclerosis.
Orla Hardiman, Ammar Al-Chalabi, Adriano Chio, Emma M Corr, Giancarlo Logroscino, Wim Robberecht, Pamela J Shaw, Zachary Simmons, Leonard H van den Berg. Nat Rev Dis Primers 2017
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Phase 1-2 Trial of Antisense Oligonucleotide Tofersen for SOD1 ALS.
Timothy Miller, Merit Cudkowicz, Pamela J Shaw, Peter M Andersen, Nazem Atassi, Robert C Bucelli, Angela Genge, Jonathan Glass, Shafeeq Ladha, Albert L Ludolph,[...]. N Engl J Med 2020
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The epidemiology of ALS: a conspiracy of genes, environment and time.
Ammar Al-Chalabi, Orla Hardiman. Nat Rev Neurol 2013
Ammar Al-Chalabi, Orla Hardiman. Nat Rev Neurol 2013
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Proposed criteria for familial amyotrophic lateral sclerosis.
Susan Byrne, Peter Bede, Marwa Elamin, Kevin Kenna, Catherine Lynch, Russell McLaughlin, Orla Hardiman. Amyotroph Lateral Scler 2011
Susan Byrne, Peter Bede, Marwa Elamin, Kevin Kenna, Catherine Lynch, Russell McLaughlin, Orla Hardiman. Amyotroph Lateral Scler 2011
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TDP-43 mutations in familial and sporadic amyotrophic lateral sclerosis.
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Novel genes associated with amyotrophic lateral sclerosis: diagnostic and clinical implications.
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Improving clinical trial outcomes in amyotrophic lateral sclerosis.
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Matthew C Kiernan, Steve Vucic, Kevin Talbot, Christopher J McDermott, Orla Hardiman, Jeremy M Shefner, Ammar Al-Chalabi, William Huynh, Merit Cudkowicz, Paul Talman,[...]. Nat Rev Neurol 2021
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Genome-wide Analyses Identify KIF5A as a Novel ALS Gene.
Aude Nicolas, Kevin P Kenna, Alan E Renton, Nicola Ticozzi, Faraz Faghri, Ruth Chia, Janice A Dominov, Brendan J Kenna, Mike A Nalls, Pamela Keagle,[...]. Neuron 2018
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ALS Genetics, Mechanisms, and Therapeutics: Where Are We Now?
Rita Mejzini, Loren L Flynn, Ianthe L Pitout, Sue Fletcher, Steve D Wilton, P Anthony Akkari. Front Neurosci 2019
Rita Mejzini, Loren L Flynn, Ianthe L Pitout, Sue Fletcher, Steve D Wilton, P Anthony Akkari. Front Neurosci 2019
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Effects of gender in amyotrophic lateral sclerosis.
Pamela A McCombe, Robert D Henderson. Gend Med 2010
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Global, regional, and national burden of motor neuron diseases 1990-2016: a systematic analysis for the Global Burden of Disease Study 2016.
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Refining eligibility criteria for amyotrophic lateral sclerosis clinical trials.
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Practice parameter update: the care of the patient with amyotrophic lateral sclerosis: drug, nutritional, and respiratory therapies (an evidence-based review): report of the Quality Standards Subcommittee of the American Academy of Neurology.
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C9orf72-mediated ALS and FTD: multiple pathways to disease.
Rubika Balendra, Adrian M Isaacs. Nat Rev Neurol 2018
Rubika Balendra, Adrian M Isaacs. Nat Rev Neurol 2018
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Mutations in UBQLN2 cause dominant X-linked juvenile and adult-onset ALS and ALS/dementia.
Han-Xiang Deng, Wenjie Chen, Seong-Tshool Hong, Kym M Boycott, George H Gorrie, Nailah Siddique, Yi Yang, Faisal Fecto, Yong Shi, Hong Zhai,[...]. Nature 2011
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4
Exome sequencing in amyotrophic lateral sclerosis identifies risk genes and pathways.
Elizabeth T Cirulli, Brittany N Lasseigne, Slavé Petrovski, Peter C Sapp, Patrick A Dion, Claire S Leblond, Julien Couthouis, Yi-Fan Lu, Quanli Wang, Brian J Krueger,[...]. Science 2015
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Selective vulnerability and pruning of phasic motoneuron axons in motoneuron disease alleviated by CNTF.
San Pun, Alexandre Ferrão Santos, Smita Saxena, Lan Xu, Pico Caroni. Nat Neurosci 2006
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Microglia centered pathogenesis in ALS: insights in cell interconnectivity.
Dora Brites, Ana R Vaz. Front Cell Neurosci 2014
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4
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