Results 231 to 240 of about 93,643 (333)

Neuropathologic, Biochemical, and Molecular Characterization of the Frontotemporal Dementias [PDF]

, 2005
Ryan T. Mott, Dennis W. Dickson, John Q. Trojanowski, V Zhukareva, Virginia M. Lee, Mark S. Forman, Vivianna M. Van Deerlin, John F. Ervin, Deng-Shun Wang, Donald E. Schmechel, Christine M. Hulette   +10 more
openalex   +1 more source

Perspectives on Frontotemporal Dementias

The American Journal of Geriatric Psychiatry, 1994
Anand Kumar, Gary L. Gottlieb
openaire   +2 more sources

Multimodal Neuroimaging‐Guided Stratification in Amyotrophic Lateral Sclerosis Reveals Three Disease Subtypes: A Multi‐Cohort Analysis

Human Brain Mapping, Volume 46, Issue 14, 01 October 2025.
Amyotrophic lateral sclerosis (ALS) is recognized as a multifaceted disease with varying symptom profiles calling for a more comprehensive understanding of ALS. We demonstrate the feasibility of extracting personalized disease progression markers as well as distinct disease subtrajectories from in vivo multimodal neuroimaging data in a heterogeneous ...
Tobias R. Baumeister, Henk‐Jan Westeneng, Leonard van den Berg, Canadian ALS Neuroimaging Consortium (CALSNIC), Sanjay Kalra, Christopher Hanstock, Alan Wilman, Dean Eurich, Christian Beaulieu, Yee Hong Yang, Lawrence Korngut, Richard Frayne, Hannah Briemberg, Lorne Zinman, Agessandro Abrahao, Simon Graham, Angela Genge, Annie Dionne, Nicolas Dupré, Christen Shoesmith, Michael Benatar, Robert Welsh, Sanjay Kalra, Yasser Iturria‐Medina   +23 more
wiley   +1 more source

Functional neuroimaging and presenting psychiatric features in frontotemporal dementia [PDF]

, 2005
Mario F. Mendez
openalex   +1 more source

Incidence and Prevalence of Frontotemporal Dementia: A Systematic Review and Meta-Analysis.

JAMA Neurol
Urso D, Giannoni-Luza S, Brayne C, Ray N, Logroscino G.   +4 more
europepmc   +1 more source

Divergent Brain Network Activity in Asymptomatic C9orf72 and SOD1 Variant Carriers Compared With Established Amyotrophic Lateral Sclerosis

Human Brain Mapping, Volume 46, Issue 14, 01 October 2025.
Box A ‐ dynamic and time‐averaged (static) resting state MEG metrics extracted from four participant groups: symptomatic amyotrophic lateral sclerosis (ALS), asymptomatic C9orf72 expansion carriers, asymptomatic SOD1 variant carriers, and healthy controls. Box B ‐ summary of MEG‐de rived metric differences associated with each group compared to healthy
Michael Trubshaw, Chetan Gohil, Evan Edmond, Malcolm Proudfoot, Katie Yoganathan, Joanne Wuu, Alicia Northall, Oliver Kohl, Charlotte J. Stagg, Anna C. Nobre, Kevin Talbot, Alexander G. Thompson, Michael Benatar, Mark Woolrich, Martin R. Turner   +14 more
wiley   +1 more source

Comprehensive Segmentation of Deep Grey Nuclei From Structural MRI Data

Human Brain Mapping, Volume 46, Issue 14, 01 October 2025.
The proposed deep grey nuclei pipeline can either work on white‐matter‐nulled (WMn) MPRAGE or standard T1 data, which gets converted to WMn‐like contrast prior to segmentation, which uses a multi‐atlas framework. In addition to 12 thalamic nuclei, 8 other structures comprising the basal ganglia, red nucleus, claustrum, and amygdala are segmented ...
Manojkumar Saranathan, Giuseppina Cogliandro, Thomas Hicks, Dianne Patterson, Behroze Vachha, Asma Hader, Mohammed Salman Shazeeb, Alberto Cacciola   +7 more
wiley   +1 more source

Genomic architecture of human 17q21 linked to frontotemporal dementia uncovers a highly homologous family of low-copy repeats in the tau region [PDF]

, 2005
Marc Cruts, Rosa Rademakers, Ilse Gijselinck, Julie van der Zee, Bart Dermaut, Tim De Pooter, Peter De Rijk, Jurgen Del‐Favero, Christine Van Broeckhoven   +8 more
openalex   +1 more source

Thyroid Cancer Surgery in a Patient With Frontotemporal Dementia: Balancing Oncologic and Neurocognitive Challenges. [PDF]

Cureus
Bontozis A, Makris A, Tzanakis N, Politopoulos C, Giannopoulos G.   +4 more
europepmc   +1 more source

Apolipoprotein E and Alzheimer’s disease: The influence of apolipoprotein E on amyloid- and other amyloidogenic proteins [PDF]

, 2017
Agosta, Alata, Albert A. Davis, Aleshkov, Allen, Alzheimer, Anderson, Atagi, Bailey, Bales, Bales, Bales, Basak, Bateman, Beffert, Beffert, Beffert, Bell, Bell, Benilova, Benjamin, Bernardi, Bertram, Bien-Ly, Bien-Ly, Biere, Brecht, Brunden, Bu, Caselli, Castellano, Castellano, Cedazo-Mínguez, Cheng, Cirrito, Cirrito, Cole, Cooper, Corder, Corder, Cotman, David M. Holtzman, de la Torre, Deane, Deane, DeMattos, Drory, Emamzadeh, Engelborghs, Esparza, Evans, Fabre, Fagan, Fagan, Farrer, Fryer, Fryer, Funato, Gallardo, Gallyas, Games, Gao, Garai, Govone, Greenberg, Grehan, Guerreiro, Gustafson, Halliday, Hardy, Harris, Harris, Heinonen, Hirsch-Reinshagen, Hirsch-Reinshagen, Holtzman, Holtzman, Holtzman, Holtzman, Hone, Hong, Hu, Huang, Huang, Huang, Hughes, Irizarry, Irwin, Irwin, Irwin, Iwai, Jakes, Jarrett, Jason D. Ulrich, Jellinger, Ji, Jiang, Jonsson, Josephs, Kanekiyo, Kehoe, Kim, Kim, Kim, Klunk, Klunk, Koistinaho, Koldamova, Korczyn, Kotzbauer, Lacomblez, LaDu, LaDu, Lashuel, Lee, Li, Li, Li, Li, Liao, Lill, Lippa, Liu, Liu, Ma, Mahley, Mahley, Mak, Mandrekar, Marchesi, Marder, Martin, Masliah, Mathis, Mattila, Mauch, McKee, Mikolaenko, Morris, Mui, Nalivaeva, Namba, Narita, Nathan, Nelson, Nielsen, Ohm, Panegyres, Paresce, Paresce, Pfeifer, Pfrieger, Pitas, Poirier, Praline, Rebeck, Rebeck, Reiman, Riemenschneider, Rockenstein, Roses, Roychaudhuri, Saavedra, Sabbagh, Saito, Sanan, Schmechel, Shaffer, Shibata, Siderowf, Srinivasan, Strittmatter, Strittmatter, Strittmatter, Sullivan, Sunderland, Szaruga, Tamamizu-Kato, Tesseur, Thal, Theendakara, Tien-Phat V. Huynh, Tiraboschi, Tokuda, Tsuang, Ulrich, Van Gool, van Horssen, Verghese, Wahrle, Wahrle, Wakabayashi, Wang, Watanabe, Wilson, Wisniewski, Wisniewski, Withers, Wood, Wyss-Coray, Yang, Ye, Yeh, Yuan, Zerbinatti, Zhang, Zhang, Zlokovic   +207 more
core   +2 more sources