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Medrxiv : the Preprint Server for Health Sciences
|
June 22, 2026
Trajectories of brain structure and function in young adult carriers of genetic frontotemporal dementia variants
Isis So, Jolina Lombardi, Adam M Staffaroni, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association
|
April 25, 2025
Sex differences in clinical phenotypes of behavioral variant frontotemporal dementia
Xulin Liu, Sterre C M de Boer, Kasey Cortez, et al.
Brain : a Journal of Neurology
|
September 26, 2018
A C6orf10/LOC101929163 locus is associated with age of onset in C9orf72 carriers
Ming Zhang, Raffaele Ferrari, Maria Carmela Tartaglia, et al.
Human Molecular Genetics
|
May 5, 2012
Evidence for a role of the rare p.A152T variant in MAPT in increasing the risk for FTD-spectrum and Alzheimer's diseases
Giovanni Coppola, Subashchandrabose Chinnathambi, Jason JiYong Lee, et al.
Annals of Neurology
|
January 29, 2026
Individualized Atrophy-Based Prediction of Dementia Progression in Familial Frontotemporal Lobar Degeneration With Bayesian Linear Mixed-Effects Modeling
Shubir Dutt, Dana Leichter, Yann Cobigo, et al.
The Lancet. Neurology
|
December 8, 2019
Age at symptom onset and death and disease duration in genetic frontotemporal dementia: an international retrospective cohort study
Katrina M Moore, Jennifer Nicholas, Murray Grossman, et al.
Nature Medicine
|
September 22, 2022
Temporal order of clinical and biomarker changes in familial frontotemporal dementia
Adam M Staffaroni, Melanie Quintana, Barbara Wendelberger, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
January 28, 2024
Assessment of Mendelian and risk-factor genes in Alzheimer disease: A prospective nationwide clinical utility study and recommendations for genetic screening
Gaël Nicolas, Aline Zaréa, Morgane Lacour, 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 study
Cyril Pottier, Xiaolai Zhou, Ralph B Perkerson, et al.
The Lancet. Neurology
|
June 20, 2014
Frontotemporal dementia and its subtypes: a genome-wide association study
Raffaele Ferrari, Dena G Hernandez, Michael A Nalls, et al.
Page
of 48
Search research articles
Search
Showing results (461-470 of 473) with videos related to
Sort By:
Page
of 48
Medrxiv : the Preprint Server for Health Sciences
|
June 22, 2026
Trajectories of brain structure and function in young adult carriers of genetic frontotemporal dementia variants
Isis So, Jolina Lombardi, Adam M Staffaroni, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association
|
April 25, 2025
Sex differences in clinical phenotypes of behavioral variant frontotemporal dementia
Xulin Liu, Sterre C M de Boer, Kasey Cortez, et al.
Brain : a Journal of Neurology
|
September 26, 2018
A C6orf10/LOC101929163 locus is associated with age of onset in C9orf72 carriers
Ming Zhang, Raffaele Ferrari, Maria Carmela Tartaglia, et al.
Human Molecular Genetics
|
May 5, 2012
Evidence for a role of the rare p.A152T variant in MAPT in increasing the risk for FTD-spectrum and Alzheimer's diseases
Giovanni Coppola, Subashchandrabose Chinnathambi, Jason JiYong Lee, et al.
Annals of Neurology
|
January 29, 2026
Individualized Atrophy-Based Prediction of Dementia Progression in Familial Frontotemporal Lobar Degeneration With Bayesian Linear Mixed-Effects Modeling
Shubir Dutt, Dana Leichter, Yann Cobigo, et al.
The Lancet. Neurology
|
December 8, 2019
Age at symptom onset and death and disease duration in genetic frontotemporal dementia: an international retrospective cohort study
Katrina M Moore, Jennifer Nicholas, Murray Grossman, et al.
Nature Medicine
|
September 22, 2022
Temporal order of clinical and biomarker changes in familial frontotemporal dementia
Adam M Staffaroni, Melanie Quintana, Barbara Wendelberger, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
January 28, 2024
Assessment of Mendelian and risk-factor genes in Alzheimer disease: A prospective nationwide clinical utility study and recommendations for genetic screening
Gaël Nicolas, Aline Zaréa, Morgane Lacour, 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 study
Cyril Pottier, Xiaolai Zhou, Ralph B Perkerson, et al.
The Lancet. Neurology
|
June 20, 2014
Frontotemporal dementia and its subtypes: a genome-wide association study
Raffaele Ferrari, Dena G Hernandez, Michael A Nalls, et al.
Page
of 48