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Mario Masellis

Showing results (191-200 of 368) with videos related to

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Neurobiology of Aging|November 25, 2017
Patterns of gray matter atrophy in genetic frontotemporal dementia: results from the GENFI studyDavid M Cash, Martina Bocchetta, David L Thomas, et al.
Neuroimage. Clinical|May 23, 2017
White matter hyperintensities are seen only in <i>GRN</i> mutation carriers in the GENFI cohortCarole H Sudre, Martina Bocchetta, David Cash, et al.
Neuroinformatics|February 2, 2021
Improved Segmentation of the Intracranial and Ventricular Volumes in Populations with Cerebrovascular Lesions and Atrophy Using 3D CNNsEmmanuel E Ntiri, Melissa F Holmes, Parisa M Forooshani, et al.
Neuroimage|December 12, 2018
Spatiotemporal analysis for detection of pre-symptomatic shape changes in neurodegenerative diseases: Initial application to the GENFI cohortClaire Cury, Stanley Durrleman, David M Cash, et al.
Gene|June 29, 2024
Vascular calcification in chronic kidney disease associated with pathogenic variants in ABCC6Clara Schott, Allison A Dilliott, Jian Wang, et al.
Molecular Neurodegeneration|November 28, 2021
A panel of CSF proteins separates genetic frontotemporal dementia from presymptomatic mutation carriers: a GENFI studySofia Bergström, Linn Öijerstedt, Julia Remnestål, et al.
The Journal of Clinical Psychiatry|March 23, 2026
Neuropsychiatric Symptom Clusters and Their Association With Brain Structure in Alzheimer DiseaseDaniel Kapustin, Neda Rashidi-Ranjbar, Wei Wang, et al.
Journal of Visualized Experiments : Jove|April 24, 2018
Targeted Next-generation Sequencing and Bioinformatics Pipeline to Evaluate Genetic Determinants of Constitutional DiseaseAllison A Dilliott, Sali M K Farhan, Mahdi Ghani, et al.
Neurology|October 4, 2019
Ventricular volume expansion in presymptomatic genetic frontotemporal dementiaTamara P Tavares, Derek G V Mitchell, Kristy Coleman, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|June 24, 2020
Parkinson's Disease, NOTCH3 Genetic Variants, and White Matter HyperintensitiesJoel Ramirez, Allison A Dilliott, Malcolm A Binns, et al.
Pageof 37

Showing results (191-200 of 368) with videos related to

Sort By:
Pageof 37
Neurobiology of Aging|November 25, 2017
Patterns of gray matter atrophy in genetic frontotemporal dementia: results from the GENFI studyDavid M Cash, Martina Bocchetta, David L Thomas, et al.
Neuroimage. Clinical|May 23, 2017
White matter hyperintensities are seen only in <i>GRN</i> mutation carriers in the GENFI cohortCarole H Sudre, Martina Bocchetta, David Cash, et al.
Neuroinformatics|February 2, 2021
Improved Segmentation of the Intracranial and Ventricular Volumes in Populations with Cerebrovascular Lesions and Atrophy Using 3D CNNsEmmanuel E Ntiri, Melissa F Holmes, Parisa M Forooshani, et al.
Neuroimage|December 12, 2018
Spatiotemporal analysis for detection of pre-symptomatic shape changes in neurodegenerative diseases: Initial application to the GENFI cohortClaire Cury, Stanley Durrleman, David M Cash, et al.
Gene|June 29, 2024
Vascular calcification in chronic kidney disease associated with pathogenic variants in ABCC6Clara Schott, Allison A Dilliott, Jian Wang, et al.
Molecular Neurodegeneration|November 28, 2021
A panel of CSF proteins separates genetic frontotemporal dementia from presymptomatic mutation carriers: a GENFI studySofia Bergström, Linn Öijerstedt, Julia Remnestål, et al.
The Journal of Clinical Psychiatry|March 23, 2026
Neuropsychiatric Symptom Clusters and Their Association With Brain Structure in Alzheimer DiseaseDaniel Kapustin, Neda Rashidi-Ranjbar, Wei Wang, et al.
Journal of Visualized Experiments : Jove|April 24, 2018
Targeted Next-generation Sequencing and Bioinformatics Pipeline to Evaluate Genetic Determinants of Constitutional DiseaseAllison A Dilliott, Sali M K Farhan, Mahdi Ghani, et al.
Neurology|October 4, 2019
Ventricular volume expansion in presymptomatic genetic frontotemporal dementiaTamara P Tavares, Derek G V Mitchell, Kristy Coleman, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|June 24, 2020
Parkinson's Disease, NOTCH3 Genetic Variants, and White Matter HyperintensitiesJoel Ramirez, Allison A Dilliott, Malcolm A Binns, et al.
Pageof 37