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

Year Number of Results
1987 2
1991 1
1992 1
1993 1
1994 1
1995 5
1996 10
1997 7
1998 19
1999 34
2000 40
2001 39
2002 35
2003 40
2004 44
2005 48
2006 42
2007 92
2008 69
2009 69
2010 73
2011 99
2012 79
2013 131
2014 114
2015 135
2016 146
2017 137
2018 131
2019 145
2020 133
2021 147
2022 145
2023 131
2024 43

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2,129 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.
In 10%-15% of patients, these problems are severe enough to meet the clinical criteria of frontotemporal dementia (FTD). In 10% of ALS patients, the family history suggests an autosomal dominant inheritance pattern. ...The most common genetic cause is a hexanucleoti …
In 10%-15% of patients, these problems are severe enough to meet the clinical criteria of frontotemporal dementia (FTD). In 10 …
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
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, …
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 most cases of ALS and th …
Abnormal intracellular protein aggregates comprise a key characteristic in most neurodegenerative diseases, including amyotrophic lateral sc …
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 frontotemporal are …
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
Progranulin as a therapeutic target in neurodegenerative diseases.
Rhinn H, Tatton N, McCaughey S, Kurnellas M, Rosenthal A. Rhinn H, et al. Trends Pharmacol Sci. 2022 Aug;43(8):641-652. doi: 10.1016/j.tips.2021.11.015. Epub 2022 Jan 15. Trends Pharmacol Sci. 2022. PMID: 35039149 Free article. Review.
GRN loss-of-function mutations cause neuronal ceroid lipofuscinosis or frontotemporal dementia-GRN (FTD-GRN) in a gene dosage-dependent manner. ...
GRN loss-of-function mutations cause neuronal ceroid lipofuscinosis or frontotemporal dementia-GRN (FTD-GRN) in a gene dosage- …
Frontotemporal Dementia: A Clinical Review.
Sivasathiaseelan H, Marshall CR, Agustus JL, Benhamou E, Bond RL, van Leeuwen JEP, Hardy CJD, Rohrer JD, Warren JD. Sivasathiaseelan H, et al. Semin Neurol. 2019 Apr;39(2):251-263. doi: 10.1055/s-0039-1683379. Epub 2019 Mar 29. Semin Neurol. 2019. PMID: 30925617 Review.
Frontotemporal dementias are a clinically, neuroanatomically, and pathologically diverse group of diseases that collectively constitute an important cause of young-onset dementia. ...Predicting molecular pathology from clinical and radiological phenotypes remains ch
Frontotemporal dementias are a clinically, neuroanatomically, and pathologically diverse group of diseases that collectively constitu
2,129 results