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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1959 2
1962 1
1963 3
1964 1
1965 4
1967 4
1968 3
1969 2
1970 1
1971 4
1972 9
1973 4
1974 2
1975 3
1976 7
1977 8
1978 5
1979 3
1980 4
1981 2
1982 5
1983 5
1984 5
1985 11
1986 9
1987 29
1988 12
1989 21
1990 24
1991 53
1992 34
1993 48
1994 49
1995 101
1996 89
1997 74
1998 78
1999 128
2000 141
2001 127
2002 98
2003 118
2004 151
2005 143
2006 220
2007 217
2008 213
2009 217
2010 254
2011 304
2012 280
2013 361
2014 401
2015 432
2016 464
2017 528
2018 523
2019 548
2020 655
2021 783
2022 728
2023 710
2024 762
2025 906
2026 469

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10,453 results

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Page 1
Amyotrophic lateral sclerosis.
Feldman EL, Goutman SA, Petri S, Mazzini L, Savelieff MG, Shaw PJ, Sobue G. Feldman EL, et al. Lancet. 2022 Oct 15;400(10360):1363-1380. doi: 10.1016/S0140-6736(22)01272-7. Epub 2022 Sep 15. Lancet. 2022. PMID: 36116464 Free PMC article. Review.
Amyotrophic lateral sclerosis is a fatal CNS neurodegenerative disease. Despite intensive research, current management of amyotrophic lateral sclerosis remains suboptimal from diagnosis to prognosis. ...This Seminar will outline these ins …
Amyotrophic lateral sclerosis is a fatal CNS neurodegenerative disease. Despite intensive research, current management …
Amyotrophic Lateral Sclerosis.
Brown RH, Al-Chalabi A. Brown RH, et al. N Engl J Med. 2017 Jul 13;377(2):162-172. doi: 10.1056/NEJMra1603471. N Engl J Med. 2017. PMID: 28700839 Free article. Review. No abstract available.
Understanding Amyotrophic Lateral Sclerosis: Pathophysiology, Diagnosis, and Therapeutic Advances.
Rizea RE, Corlatescu AD, Costin HP, Dumitru A, Ciurea AV. Rizea RE, et al. Int J Mol Sci. 2024 Sep 15;25(18):9966. doi: 10.3390/ijms25189966. Int J Mol Sci. 2024. PMID: 39337454 Free PMC article. Review.
This review offers an in-depth examination of amyotrophic lateral sclerosis (ALS), addressing its epidemiology, pathophysiology, clinical presentation, diagnostic techniques, and current as well as emerging treatments. ...Emerging treatments, such as g …
This review offers an in-depth examination of amyotrophic lateral sclerosis (ALS), addressing its epidemiology, …
Narrative review of diagnosis, management and treatment of dysphagia and sialorrhea in amyotrophic lateral sclerosis.
Bjelica B, Petri S. Bjelica B, et al. J Neurol. 2024 Oct;271(10):6508-6513. doi: 10.1007/s00415-024-12657-x. Epub 2024 Aug 29. J Neurol. 2024. PMID: 39207520 Free PMC article. Review.
The degenerative motor neuron disorder amyotrophic lateral sclerosis (ALS) frequently leads bulbar symptoms like dysarthria, dysphagia, and sialorrhea, in approximately one-third of cases being the initial symptom. ...Early discussion of potential treatments …
The degenerative motor neuron disorder amyotrophic lateral sclerosis (ALS) frequently leads bulbar symptoms like dysart …
Amyotrophic lateral sclerosis.
Younger DS, Brown RH Jr. Younger DS, et al. Handb Clin Neurol. 2023;196:203-229. doi: 10.1016/B978-0-323-98817-9.00031-4. Handb Clin Neurol. 2023. PMID: 37620070 Review.
The scientific landscape surrounding amyotrophic lateral sclerosis has shifted immensely with a number of well-defined ALS disease-causing genes, each with related phenotypical and cellular motor neuron processes that have come to light. ...This chapter provi …
The scientific landscape surrounding amyotrophic lateral sclerosis has shifted immensely with a number of well-defined …
Clinical Spectrum of Amyotrophic Lateral Sclerosis (ALS).
Grad LI, Rouleau GA, Ravits J, Cashman NR. Grad LI, et al. Cold Spring Harb Perspect Med. 2017 Aug 1;7(8):a024117. doi: 10.1101/cshperspect.a024117. Cold Spring Harb Perspect Med. 2017. PMID: 28003278 Free PMC article. Review.
Amyotrophic lateral sclerosis (ALS) is primarily characterized by progressive loss of motor neurons, although there is marked phenotypic heterogeneity between cases. Typical, or "classical," ALS is associated with simultaneous upper motor neuron (UMN) and low …
Amyotrophic lateral sclerosis (ALS) is primarily characterized by progressive loss of motor neurons, although there is …
Advances in molecular pathology, diagnosis, and treatment of amyotrophic lateral sclerosis.
Ilieva H, Vullaganti M, Kwan J. Ilieva H, et al. BMJ. 2023 Oct 27;383:e075037. doi: 10.1136/bmj-2023-075037. BMJ. 2023. PMID: 37890889 Free PMC article. Review.
Although the past two decades have produced exciting discoveries in the genetics and pathology of amyotrophic lateral sclerosis (ALS), progress in developing an effective therapy remains slow. This review summarizes the critical discoveries and outline …
Although the past two decades have produced exciting discoveries in the genetics and pathology of amyotrophic lateral scler …
Amyotrophic lateral sclerosis.
Kiernan MC, Vucic S, Cheah BC, Turner MR, Eisen A, Hardiman O, Burrell JR, Zoing MC. Kiernan MC, et al. Lancet. 2011 Mar 12;377(9769):942-55. doi: 10.1016/S0140-6736(10)61156-7. Epub 2011 Feb 4. Lancet. 2011. PMID: 21296405 Free article. Review.
Amyotrophic lateral sclerosis (ALS) is an idiopathic, fatal neurodegenerative disease of the human motor system. ...
Amyotrophic lateral sclerosis (ALS) is an idiopathic, fatal neurodegenerative disease of the human motor system. ...
Amyotrophic Lateral Sclerosis: Pathophysiological Mechanisms and Treatment Strategies (Part 2).
Tolochko C, Shiryaeva O, Alekseeva T, Dyachuk V. Tolochko C, et al. Int J Mol Sci. 2025 May 29;26(11):5240. doi: 10.3390/ijms26115240. Int J Mol Sci. 2025. PMID: 40508048 Free PMC article. Review.
Amyotrophic lateral sclerosis (ALS) is a progressive neurodegenerative disease associated with damage to motor neurons and leading to severe muscle weakness and, eventually, death. Over the past decade, understanding of the key pathogenetic links of ALS, incl …
Amyotrophic lateral sclerosis (ALS) is a progressive neurodegenerative disease associated with damage to motor neurons …
Respiratory Failure in Amyotrophic Lateral Sclerosis.
Niedermeyer S, Murn M, Choi PJ. Niedermeyer S, et al. Chest. 2019 Feb;155(2):401-408. doi: 10.1016/j.chest.2018.06.035. Epub 2018 Jul 7. Chest. 2019. PMID: 29990478 Review.
Amyotrophic lateral sclerosis is a progressive neuromuscular disease characterized by both lower motor neuron and upper motor neuron dysfunction. ...Standard of care for patients with ALS includes treatment from multidisciplinary teams, but many patients do n …
Amyotrophic lateral sclerosis is a progressive neuromuscular disease characterized by both lower motor neuron and upper …
10,453 results
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