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Annals of Neurology
|
September 27, 2018
Prevalence of amyloid-β pathology in distinct variants of primary progressive aphasia
David Bergeron, Maria L Gorno-Tempini, Gil D Rabinovici, et al.
Alzheimer'S Research & Therapy
|
March 28, 2024
A systematic review of progranulin concentrations in biofluids in over 7,000 people-assessing the pathogenicity of GRN mutations and other influencing factors
Imogen J Swift, Rosa Rademakers, NiCole Finch, 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.
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 FTLD
Cyril Pottier, Yingxue Ren, Ralph B Perkerson, et al.
Nature Genetics
|
February 16, 2010
Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusions
Vivianna M Van Deerlin, Patrick M A Sleiman, Maria Martinez-Lage, et al.
Medrxiv : the Preprint Server for Health Sciences
|
July 9, 2024
Deciphering Distinct Genetic Risk Factors for FTLD-TDP Pathological Subtypes via Whole-Genome Sequencing
Cyril Pottier, Fahri Küçükali, Matt Baker, et al.
Nature Communications
|
April 25, 2025
Deciphering distinct genetic risk factors for FTLD-TDP pathological subtypes via whole-genome sequencing
Cyril Pottier, Fahri Küçükali, Matt Baker, et al.
Nature Genetics
|
March 13, 2026
A repeat expansion in GOLGA8A is a major risk factor for atypical frontotemporal lobar degeneration with ubiquitin-positive inclusions
Wouter De Coster, Marleen Van den Broeck, Matt Baker, 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.
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of 49
Search research articles
Search
Showing results (471-480 of 483) with videos related to
Sort By:
Page
of 49
Annals of Neurology
|
September 27, 2018
Prevalence of amyloid-β pathology in distinct variants of primary progressive aphasia
David Bergeron, Maria L Gorno-Tempini, Gil D Rabinovici, et al.
Alzheimer'S Research & Therapy
|
March 28, 2024
A systematic review of progranulin concentrations in biofluids in over 7,000 people-assessing the pathogenicity of GRN mutations and other influencing factors
Imogen J Swift, Rosa Rademakers, NiCole Finch, 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.
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 FTLD
Cyril Pottier, Yingxue Ren, Ralph B Perkerson, et al.
Nature Genetics
|
February 16, 2010
Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusions
Vivianna M Van Deerlin, Patrick M A Sleiman, Maria Martinez-Lage, et al.
Medrxiv : the Preprint Server for Health Sciences
|
July 9, 2024
Deciphering Distinct Genetic Risk Factors for FTLD-TDP Pathological Subtypes via Whole-Genome Sequencing
Cyril Pottier, Fahri Küçükali, Matt Baker, et al.
Nature Communications
|
April 25, 2025
Deciphering distinct genetic risk factors for FTLD-TDP pathological subtypes via whole-genome sequencing
Cyril Pottier, Fahri Küçükali, Matt Baker, et al.
Nature Genetics
|
March 13, 2026
A repeat expansion in GOLGA8A is a major risk factor for atypical frontotemporal lobar degeneration with ubiquitin-positive inclusions
Wouter De Coster, Marleen Van den Broeck, Matt Baker, 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.
Page
of 49