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NEW ENGLAND JOURNAL OF MEDICINE (2020)
Oral levosimendan in amyotrophic lateral sclerosis: a phase II multicentre, randomised, double-blind, placebo-controlled trial
Ammar Al-Chalabi et al.
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY (2019)
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Carlo Rinaldi et al.
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Alex McCampbell et al.
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Amyotrophic lateral sclerosis
Michael A. van Es et al.
LANCET (2017)
Safety and efficacy of edaravone in well defined patients with amyotrophic lateral sclerosis: a randomised, double-blind, placebo-controlled trial
Koji Abe et al.
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Decoding ALS: from genes to mechanism
J. Paul Taylor et al.
NATURE (2016)
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Lars Toenges et al.
GLIA (2014)
State of play in amyotrophic lateral sclerosis genetics
Alan E. Renton et al.
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Jonne Doorduin et al.
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Mutations in UBQLN2 cause dominant X-linked juvenile and adult-onset ALS and ALS/dementia
Han-Xiang Deng et al.
NATURE (2011)
Prevention of Motor Neuron Degeneration by Novel Iron Chelators in SOD1(G93A) Transgenic Mice of Amyotrophic Lateral Sclerosis
Qian Wang et al.
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Safety, Tolerability, and Cerebrospinal Fluid Penetration of Ursodeoxycholic Acid in Patients With Amyotrophic Lateral Sclerosis
Gareth J. Parry et al.
CLINICAL NEUROPHARMACOLOGY (2010)
The Structure of Human Extracellular Copper-Zinc Superoxide Dismutase at 1.7 Å Resolution: Insights into Heparin and Collagen Binding
Svetlana V. Antonyuk et al.
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Smita Saxena et al.
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ALS-linked mutant SOD1 induces ER stress- and ASK1-dependent motor neuron death by targeting Derlin-1
Hideki Nishitoh et al.
GENES & DEVELOPMENT (2008)
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Koji Yamanaka et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2008)
Cognitive impairment in amyotrophic lateral sclerosis
Julie Phukan et al.
LANCET NEUROLOGY (2007)
Antisense oligonucleotide therapy for neurodegenerative disease
Richard A. Smith et al.
JOURNAL OF CLINICAL INVESTIGATION (2006)
Amyotrophic lateral sclerosis associated with mutations in the CuZn superoxide dismutase gene
Peter M. Andersen
CURRENT NEUROLOGY AND NEUROSCIENCE REPORTS (2006)
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GS Ralph et al.
NATURE MEDICINE (2005)
Focal dysfunction of the proteasome: a pathogenic factor in a mouse model of amyotrophic lateral sclerosis
E Kabashi et al.
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C Lomen-Hoerth et al.
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Medical progress: Amyotrophic lateral sclerosis.
LP Rowland et al.
NEW ENGLAND JOURNAL OF MEDICINE (2001)