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1,220 results

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Page 1
Did you mean diagnosis pick s disease of the brain (1,310 results)?
Frontotemporal Dementia, Where Do We Stand? A Narrative Review.
Antonioni A, Raho EM, Lopriore P, Pace AP, Latino RR, Assogna M, Mancuso M, Gragnaniello D, Granieri E, Pugliatti M, Di Lorenzo F, Koch G. Antonioni A, et al. Int J Mol Sci. 2023 Jul 21;24(14):11732. doi: 10.3390/ijms241411732. Int J Mol Sci. 2023. PMID: 37511491 Free PMC article. Review.
Here, we aim to provide a state of the art on the pathogenesis of this disease, starting with established findings and integrating them with more recent ones. ...Of note, the promising information provided by neurophysiological investigations, i.e., electroencephalography …
Here, we aim to provide a state of the art on the pathogenesis of this disease, starting with established findings and integrating th …
History of Pick's disease.
Mikol J. Mikol J. Clin Neuropathol. 2020 Jul/Aug;39(4):152-161. doi: 10.5414/NP301243. Clin Neuropathol. 2020. PMID: 32000890
After a short summary of Arnold Pick's biography, the history of how Pick's disease (PiD) was reported is presented, from its clinical symptoms to its molecular characterization. The macroscopic description of frontotemporal atrophy by Pick is recounte …
After a short summary of Arnold Pick's biography, the history of how Pick's disease (PiD) was reported is presented, fr …
Pick's disease.
Takeda N, Kishimoto Y, Yokota O. Takeda N, et al. Adv Exp Med Biol. 2012;724:300-16. doi: 10.1007/978-1-4614-0653-2_23. Adv Exp Med Biol. 2012. PMID: 22411252 Review.
Picks disease is a major clinicopathological disease having circumscribed atrophy in the frontotemporal lobe. ...In this chapter, recent findings regarding the distinct clinical and histopathological features of these pathological disease entities are present …
Picks disease is a major clinicopathological disease having circumscribed atrophy in the frontotemporal lobe. ...In this chapt …
[Argentinean Consensus on the Diagnosis and Treatment of Niemann- Pick Disease Type C].
Amartino H, Azcona C, Calandra C, Durand C, Fortini S, Kauffman M, Loos M, Maxit C, Menazzi S, Spécola N, Szlago M. Amartino H, et al. Medicina (B Aires). 2023;83(4):588-602. Medicina (B Aires). 2023. PMID: 37582133 Free article. Spanish.
Niemann-Pick type C (NPC) is a disorder of the lysosomal metabolism due to biallelic pathogenic variants in NPC1 or NPC2. ...This, in turn, is associated with a myriad of neurological / psychiatric and visceral symptoms, with wide variability in age of presentation, from p …
Niemann-Pick type C (NPC) is a disorder of the lysosomal metabolism due to biallelic pathogenic variants in NPC1 or NPC2. ...This, in …
Niemann-Pick type C disease: Case report and review of the literature.
Liu C, Li J, Xu T, Song M, Luo H. Liu C, et al. Neuro Endocrinol Lett. 2023 Apr 30;44(2):101-104. Neuro Endocrinol Lett. 2023. PMID: 37182232 Review.
Niemann-Pick type C (NPC) disease is an autosomal recessive disease of lysosomal lipid storage disorder caused by mutations in either the NPC1 (95%) or the NPC2 (5%) gene. ...The chest computed tomography (CT) incidentally showed splenomegaly. Brain ma …
Niemann-Pick type C (NPC) disease is an autosomal recessive disease of lysosomal lipid storage disorder caused by mutat …
Frontotemporal dementia: Past, present, and future.
Ulugut H, Pijnenburg YAL. Ulugut H, et al. Alzheimers Dement. 2023 Nov;19(11):5253-5263. doi: 10.1002/alz.13363. Epub 2023 Jun 28. Alzheimers Dement. 2023. PMID: 37379561 Review.
Overcoming these barriers involved revisiting early pioneers' approaches, focusing on focal impairment, establishing non-Alzheimer's disease cohorts, fostering collaboration, and developing diagnostic criteria. ...DISCUSSION: Independent multidisciplinary centers are essen …
Overcoming these barriers involved revisiting early pioneers' approaches, focusing on focal impairment, establishing non-Alzheimer's dise
Frontotemporal dementia.
Graff-Radford NR, Woodruff BK. Graff-Radford NR, et al. Semin Neurol. 2007 Feb;27(1):48-57. doi: 10.1055/s-2006-956755. Semin Neurol. 2007. PMID: 17226741 Review.
Frontotemporal dementia (FTD) is an uncommon but important form of degenerative disease. It may make up 50% of dementia cases presenting before age 60. ...The most common pathology found is frontotemporal degeneration with ubiquitin inclusions. In contrast, FTD with Pic
Frontotemporal dementia (FTD) is an uncommon but important form of degenerative disease. It may make up 50% of dementia cases present …
Study of Alzheimer's disease- and frontotemporal dementia-associated genes in the Cretan Aging Cohort.
Mathioudakis L, Dimovasili C, Bourbouli M, Latsoudis H, Kokosali E, Gouna G, Vogiatzi E, Basta M, Kapetanaki S, Panagiotakis S, Kanterakis A, Boumpas D, Lionis C, Plaitakis A, Simos P, Vgontzas A, Kafetzopoulos D, Zaganas I. Mathioudakis L, et al. Neurobiol Aging. 2023 Mar;123:111-128. doi: 10.1016/j.neurobiolaging.2022.07.002. Epub 2022 Jul 11. Neurobiol Aging. 2023. PMID: 36117051
Using exome sequencing, we analyzed 196 participants of the Cretan Aging Cohort (CAC; 95 with Alzheimer's disease [AD], 20 with mild cognitive impairment [MCI], and 81 cognitively normal controls). ...Also, we found the frontotemporal dementia (FTD)-associated TARDBP gene …
Using exome sequencing, we analyzed 196 participants of the Cretan Aging Cohort (CAC; 95 with Alzheimer's disease [AD], 20 with mild …
Changing perspectives on frontotemporal dementia: A review.
Snowden JS. Snowden JS. J Neuropsychol. 2023 Jun;17(2):211-234. doi: 10.1111/jnp.12297. Epub 2022 Oct 31. J Neuropsychol. 2023. PMID: 36315040 Review.
An absence of neurological signs is the hallmark of many FTD patients, but there is also an established association with motor neurone disease (MND), progressive supranuclear palsy (PSP) and corticobasal degeneration (CBD). ...Understanding the diverse nature of FTD is cru …
An absence of neurological signs is the hallmark of many FTD patients, but there is also an established association with motor neurone di
Accuracy of the clinical diagnosis of corticobasal degeneration: a clinicopathologic study.
Litvan I, Agid Y, Goetz C, Jankovic J, Wenning GK, Brandel JP, Lai EC, Verny M, Ray-Chaudhuri K, McKee A, Jellinger K, Pearce RK, Bartko JJ. Litvan I, et al. Neurology. 1997 Jan;48(1):119-25. doi: 10.1212/wnl.48.1.119. Neurology. 1997. PMID: 9008506 Review.
The accuracy of the clinical diagnosis of corticobasal degeneration (CBD) is unknown. To determine its diagnostic accuracy, we presented 105 cases with known neuropathologic diagnoses, including CBD (n = 10), progressive supranuclear palsy (PSP, n = 24), Parkinson's …
The accuracy of the clinical diagnosis of corticobasal degeneration (CBD) is unknown. To determine its diagnostic accuracy, we presen …
1,220 results