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

Year Number of Results
1972 1
1977 1
1980 2
1981 1
1982 1
1983 2
1984 1
1985 2
1986 1
1987 6
1988 3
1989 3
1990 7
1991 9
1992 9
1993 6
1994 15
1995 16
1996 25
1997 20
1998 34
1999 58
2000 67
2001 83
2002 55
2003 77
2004 74
2005 92
2006 78
2007 147
2008 122
2009 114
2010 119
2011 165
2012 140
2013 203
2014 184
2015 219
2016 223
2017 217
2018 213
2019 209
2020 206
2021 245
2022 223
2023 221
2024 70

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3,523 results

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Page 1
Amyotrophic lateral sclerosis.
Hardiman O, Al-Chalabi A, Chio A, Corr EM, Logroscino G, Robberecht W, Shaw PJ, Simmons Z, van den Berg LH. Hardiman O, et al. Nat Rev Dis Primers. 2017 Oct 5;3:17071. doi: 10.1038/nrdp.2017.71. Nat Rev Dis Primers. 2017. PMID: 28980624 Free article. Review.
Amyotrophic lateral sclerosis (ALS), also known as motor neuron disease, is characterized by the degeneration of both upper and lower motor neurons, which leads to muscle weakness and eventual paralysis. ...
Amyotrophic lateral sclerosis (ALS), also known as motor neuron disease, is characterized by the degeneration of both u
Amyotrophic lateral sclerosis: a clinical review.
Masrori P, Van Damme P. Masrori P, et al. Eur J Neurol. 2020 Oct;27(10):1918-1929. doi: 10.1111/ene.14393. Epub 2020 Jul 7. Eur J Neurol. 2020. PMID: 32526057 Free PMC article. Review.
Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disorder affecting primarily the motor system, but in which extra-motor manifestations are increasingly recognized. ...In 10%-15% of patients, these problems are severe enough to meet the clinical cri
Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disorder affecting primarily the motor system, but in which
Frontotemporal dementia.
Bang J, Spina S, Miller BL. Bang J, et al. Lancet. 2015 Oct 24;386(10004):1672-82. doi: 10.1016/S0140-6736(15)00461-4. Lancet. 2015. PMID: 26595641 Free PMC article. Review.
Frontotemporal dementia is a common type of dementia, particularly in patients younger than 65 years. ...As the understanding of the molecular basis for frontotemporal dementia improves, rational therapies are beginning to emerge....
Frontotemporal dementia is a common type of dementia, particularly in patients younger than 65 years. ...As the underst
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.
Amyotrophic lateral sclerosis: disease state overview.
Hulisz D. Hulisz D. Am J Manag Care. 2018 Aug;24(15 Suppl):S320-S326. Am J Manag Care. 2018. PMID: 30207670 Free article. Review.
Amyotrophic lateral sclerosis (ALS) is a disease that results in the progressive deterioration and loss of function of the motor neurons in the brain and spinal cord, leading to paralysis. ALS affects approximately 16,000 individuals, with a prognosis for sur
Amyotrophic lateral sclerosis (ALS) is a disease that results in the progressive deterioration and loss of function of
Advances and controversies in frontotemporal dementia: diagnosis, biomarkers, and therapeutic considerations.
Boeve BF, Boxer AL, Kumfor F, Pijnenburg Y, Rohrer JD. Boeve BF, et al. Lancet Neurol. 2022 Mar;21(3):258-272. doi: 10.1016/S1474-4422(21)00341-0. Lancet Neurol. 2022. PMID: 35182511 Review.
Frontotemporal dementia comprises a group of clinical syndromes that are characterised by progressive changes in behaviour, executive function, or language. ...Accurate and early diagnosis of frontotemporal dementia is now a possibility due to developm
Frontotemporal dementia comprises a group of clinical syndromes that are characterised by progressive changes in behaviour, ex
Frontotemporal Dementia.
Olney NT, Spina S, Miller BL. Olney NT, et al. Neurol Clin. 2017 May;35(2):339-374. doi: 10.1016/j.ncl.2017.01.008. Neurol Clin. 2017. PMID: 28410663 Free PMC article. Review.
Frontotemporal dementia (FTD) is a heterogeneous disorder with distinct clinical phenotypes associated with multiple neuropathologic entities. ...The core FTD spectrum disorders include behavioral variant FTD, nonfluent/agrammatic variant primary progressive aphasia
Frontotemporal dementia (FTD) is a heterogeneous disorder with distinct clinical phenotypes associated with multiple neuropath
Biomarkers for amyotrophic lateral sclerosis.
Witzel S, Mayer K, Oeckl P. Witzel S, et al. Curr Opin Neurol. 2022 Oct 1;35(5):699-704. doi: 10.1097/WCO.0000000000001094. Epub 2022 Aug 4. Curr Opin Neurol. 2022. PMID: 35942674 Review.
PURPOSE OF REVIEW: Amyotrophic lateral sclerosis (ALS) is an incurable, devastating neurodegenerative disease. ...This review will discuss developments in ALS biomarker research and applications within the last 2 years and suggest future directions and …
PURPOSE OF REVIEW: Amyotrophic lateral sclerosis (ALS) is an incurable, devastating neurodegenerative disease. ...This …
Frontotemporal Dementia - Current Concepts.
Puppala GK, Gorthi SP, Chandran V, Gundabolu G. Puppala GK, et al. Neurol India. 2021 Sep-Oct;69(5):1144-1152. doi: 10.4103/0028-3886.329593. Neurol India. 2021. PMID: 34747778 Free article. Review.
Frontotemporal dementia (FTD) is an entity that includes a group of neurodegenerative disease with symptoms predominantly pertaining to deficits in behavior, executive function (or) language. ...We used the search terms "frontotemporal dementia," "Fron
Frontotemporal dementia (FTD) is an entity that includes a group of neurodegenerative disease with symptoms predominantly pert
The epidemiology of amyotrophic lateral sclerosis.
Talbott EO, Malek AM, Lacomis D. Talbott EO, et al. Handb Clin Neurol. 2016;138:225-38. doi: 10.1016/B978-0-12-802973-2.00013-6. Handb Clin Neurol. 2016. PMID: 27637961 Review.
Amyotrophic lateral sclerosis (ALS) is the most common motor neuron disease in adults and is characterized by neurodegeneration of motor neurons in the brain and spinal cord. The incidence of ALS is approximately 1-2.6 cases per 100 000 persons annuall
Amyotrophic lateral sclerosis (ALS) is the most common motor neuron disease in adults and is characterized by neurodege
3,523 results