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

Year Number of Results
1971 1
1977 1
1979 1
1982 1
1985 1
1987 3
1988 1
1989 1
1990 2
1991 1
1992 2
1993 3
1994 4
1995 10
1996 16
1997 11
1998 25
1999 39
2000 48
2001 49
2002 40
2003 48
2004 47
2005 55
2006 58
2007 104
2008 86
2009 78
2010 89
2011 114
2012 98
2013 140
2014 127
2015 155
2016 169
2017 163
2018 156
2019 159
2020 164
2021 180
2022 167
2023 151
2024 70

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2,545 results

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Page 1
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. ...The most common genetic cause is a hexanucleotide repeat expansion in the C9orf72
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
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 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
Clinical Neurology and Epidemiology of the Major Neurodegenerative Diseases.
Erkkinen MG, Kim MO, Geschwind MD. Erkkinen MG, et al. Cold Spring Harb Perspect Biol. 2018 Apr 2;10(4):a033118. doi: 10.1101/cshperspect.a033118. Cold Spring Harb Perspect Biol. 2018. PMID: 28716886 Free PMC article. Review.
This review summarizes and highlights clinical aspects of several of the most commonly encountered neurodegenerative diseases, including AD, frontotemporal dementia (FTD) and its variants, progressive supranuclear palsy (PSP), corticobasal degeneration (CBD), Parkin …
This review summarizes and highlights clinical aspects of several of the most commonly encountered neurodegenerative diseases, including AD, …
Systematic Review of Therapeutic Physical Exercise in Patients with Amyotrophic Lateral Sclerosis over Time.
Ortega-Hombrados L, Molina-Torres G, Galán-Mercant A, Sánchez-Guerrero E, González-Sánchez M, Ruiz-Muñoz M. Ortega-Hombrados L, et al. Int J Environ Res Public Health. 2021 Jan 26;18(3):1074. doi: 10.3390/ijerph18031074. Int J Environ Res Public Health. 2021. PMID: 33530383 Free PMC article. Review.
BACKGROUND: the main objective of this study was to analyze the potential short-, medium- and long-term effects of a therapeutic physical exercise (TFE) programme on the functionality of amyotrophic lateral sclerosis (ALS) patients, measured with the Revised …
BACKGROUND: the main objective of this study was to analyze the potential short-, medium- and long-term effects of a therapeutic physical ex …
TDP-43 and FUS in amyotrophic lateral sclerosis and frontotemporal dementia.
Mackenzie IR, Rademakers R, Neumann M. Mackenzie IR, et al. Lancet Neurol. 2010 Oct;9(10):995-1007. doi: 10.1016/S1474-4422(10)70195-2. Lancet Neurol. 2010. PMID: 20864052 Review.
Abnormal intracellular protein aggregates comprise a key characteristic in most neurodegenerative diseases, including amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD). The seminal discoveries of accumulation of TDP-43 in mos …
Abnormal intracellular protein aggregates comprise a key characteristic in most neurodegenerative diseases, including amyotrophic
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
Recent Updates on the Genetics of Amyotrophic Lateral Sclerosis and Frontotemporal Dementia.
Kirola L, Mukherjee A, Mutsuddi M. Kirola L, et al. Mol Neurobiol. 2022 Sep;59(9):5673-5694. doi: 10.1007/s12035-022-02934-z. Epub 2022 Jun 30. Mol Neurobiol. 2022. PMID: 35768750 Review.
Amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD) primarily affect the motor and frontotemporal areas of the brain, respectively. ...
Amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD) primarily affect the motor and f
2,545 results