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Brain and Language
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July 7, 2018
Prosodic and phonetic subtypes of primary progressive apraxia of speech
Rene L Utianski, Joseph R Duffy, Heather M Clark, et al.
Journal of Alzheimer'S Disease : JAD
|
February 5, 2015
Microbleeds in atypical presentations of Alzheimer's disease: a comparison to dementia of the Alzheimer's type
Jennifer L Whitwell, Kejal Kantarci, Stephen D Weigand, et al.
Movement Disorders Clinical Practice
|
August 9, 2019
An Evaluation of the Progressive Supranuclear Palsy Speech/Language Variant
Jennifer L Whitwell, Chase A Stevens, Joseph R Duffy, et al.
Journal of Alzheimer'S Disease : JAD
|
February 11, 2020
Longitudinal Amyloid-β PET in Atypical Alzheimer's Disease and Frontotemporal Lobar Degeneration
Jennifer L Whitwell, Nirubol Tosakulwong, Stephen D Weigand, et al.
Journal of Alzheimer'S Disease : JAD
|
October 21, 2015
Characterizing White Matter Tract Degeneration in Syndromic Variants of Alzheimer's Disease: A Diffusion Tensor Imaging Study
Ajay Madhavan, Christopher G Schwarz, Joseph R Duffy, et al.
Brain : a Journal of Neurology
|
June 15, 2019
Progressive agrammatic aphasia without apraxia of speech as a distinct syndrome
Katerina A Tetzloff, Joseph R Duffy, Heather M Clark, et al.
Annals of Neurology
|
December 4, 2020
Lewy Body Disease is a Contributor to Logopenic Progressive Aphasia Phenotype
Marina Buciuc, Jennifer L Whitwell, Koji Kasanuki, et al.
Nature Communications
|
June 9, 2021
A molecular pathology, neurobiology, biochemical, genetic and neuroimaging study of progressive apraxia of speech
Keith A Josephs, Joseph R Duffy, Heather M Clark, et al.
Nature Communications
|
February 17, 2019
Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language
Lot Snijders Blok, Justine Rousseau, Joanna Twist, et al.
Nature Communications
|
November 7, 2018
CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language
Lot Snijders Blok, Justine Rousseau, Joanna Twist, et al.
Page
of 10
Search research articles
Search
Showing results (81-90 of 91) with videos related to
Sort By:
Page
of 10
Brain and Language
|
July 7, 2018
Prosodic and phonetic subtypes of primary progressive apraxia of speech
Rene L Utianski, Joseph R Duffy, Heather M Clark, et al.
Journal of Alzheimer'S Disease : JAD
|
February 5, 2015
Microbleeds in atypical presentations of Alzheimer's disease: a comparison to dementia of the Alzheimer's type
Jennifer L Whitwell, Kejal Kantarci, Stephen D Weigand, et al.
Movement Disorders Clinical Practice
|
August 9, 2019
An Evaluation of the Progressive Supranuclear Palsy Speech/Language Variant
Jennifer L Whitwell, Chase A Stevens, Joseph R Duffy, et al.
Journal of Alzheimer'S Disease : JAD
|
February 11, 2020
Longitudinal Amyloid-β PET in Atypical Alzheimer's Disease and Frontotemporal Lobar Degeneration
Jennifer L Whitwell, Nirubol Tosakulwong, Stephen D Weigand, et al.
Journal of Alzheimer'S Disease : JAD
|
October 21, 2015
Characterizing White Matter Tract Degeneration in Syndromic Variants of Alzheimer's Disease: A Diffusion Tensor Imaging Study
Ajay Madhavan, Christopher G Schwarz, Joseph R Duffy, et al.
Brain : a Journal of Neurology
|
June 15, 2019
Progressive agrammatic aphasia without apraxia of speech as a distinct syndrome
Katerina A Tetzloff, Joseph R Duffy, Heather M Clark, et al.
Annals of Neurology
|
December 4, 2020
Lewy Body Disease is a Contributor to Logopenic Progressive Aphasia Phenotype
Marina Buciuc, Jennifer L Whitwell, Koji Kasanuki, et al.
Nature Communications
|
June 9, 2021
A molecular pathology, neurobiology, biochemical, genetic and neuroimaging study of progressive apraxia of speech
Keith A Josephs, Joseph R Duffy, Heather M Clark, et al.
Nature Communications
|
February 17, 2019
Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language
Lot Snijders Blok, Justine Rousseau, Joanna Twist, et al.
Nature Communications
|
November 7, 2018
CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language
Lot Snijders Blok, Justine Rousseau, Joanna Twist, et al.
Page
of 10