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Neurology|May 7, 2020
Revised Self-Monitoring Scale: A potential endpoint for frontotemporal dementia clinical trialsGianina Toller, Kamalini Ranasinghe, Yann Cobigo, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|May 27, 2023
Learning slopes in early-onset Alzheimer's diseaseDustin B Hammers, Sára Nemes, Taylor Diedrich, et al.
Acta Neuropathologica|November 1, 2021
Genome-wide association study and functional validation implicates JADE1 in tauopathyKurt Farrell, SoongHo Kim, Natalia Han, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|January 2, 2023
Multisite ALLFTD study modeling progressive empathy loss from the earliest stages of behavioral variant frontotemporal dementiaGianina Toller, Yann Cobigo, Patrick Callahan, et al.
Alzheimer'S Research & Therapy|August 18, 2022
Italian adaptation of the Uniform Data Set Neuropsychological Test Battery (I-UDSNB 1.0): development and normative dataFrancesca Conca, Valentina Esposito, Francesco Rundo, et al.
Cortex; a Journal Devoted to the Study of the Nervous System and Behavior|April 15, 2021
Recognition memory and divergent cognitive profiles in prodromal genetic frontotemporal dementiaMegan S Barker, Masood Manoochehri, Sandra J Rizer, et al.
Archives of Neurology|April 13, 2011
Genetic and clinical features of progranulin-associated frontotemporal lobar degenerationAlice S Chen-Plotkin, Maria Martinez-Lage, Patrick M A Sleiman, et al.
Acta Neuropathologica|February 11, 2019
Genome-wide analyses as part of the international FTLD-TDP whole-genome sequencing consortium reveals novel disease risk factors and increases support for immune dysfunction in FTLDCyril Pottier, Yingxue Ren, Ralph B Perkerson, et al.
Communications Medicine|December 12, 2025
Clinical recognition of frontotemporal dementia with right temporal predominance: a consensus statement from the International Working GroupHulya Ulugut, Kyan Younes, Maxime Montembeault, et al.
The Lancet. Neurology|May 5, 2018
Potential genetic modifiers of disease risk and age at onset in patients with frontotemporal lobar degeneration and GRN mutations: a genome-wide association studyCyril Pottier, Xiaolai Zhou, Ralph B Perkerson, et al.
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