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1. Assessment of executive function declines in presymptomatic and mildly symptomatic familial frontotemporal dementia: NIH‐EXAMINER as a potential clinical trial endpoint. Issue 1 (8th January 2020)

2. Brain MR Spectroscopy Changes Precede Frontotemporal Lobar Degeneration Phenoconversion in Mapt Mutation Carriers. Issue 5 (7th June 2019)

3. Clinical and volumetric changes with increasing functional impairment in familial frontotemporal lobar degeneration. Issue 1 (6th January 2020)

4. Frontal lobe 1H MR spectroscopy in asymptomatic and symptomatic MAPT mutation carriers. (20th August 2019)

5. Individualized atrophy scores predict dementia onset in familial frontotemporal lobar degeneration. Issue 1 (6th January 2020)

6. Nonlinear Z‐score modeling for improved detection of cognitive abnormality. Issue 1 (1st December 2019)

7. O1‐08‐01: THE NIH‐EXAMINER IS SENSITIVE TO COGNITIVE CHANGES IN ASYMPTOMATIC AND MILDLY SYMPTOMATIC FAMILIAL FRONTOTEMPORAL DEMENTIA. (1st July 2006)

8. O2‐14‐01: CHARACTERISTICS AND PROGRESS OF 320 SUBJECTS IN THE LONGITUDINAL EVALUATION OF FAMILIAL FRONTOTEMPORAL DEMENTIA SUBJECTS (LEFFTDS) PROTOCOL. (1st July 2006)

9. P1‐281: NONLINEAR N‐SCORE ESTIMATION FOR ESTABLISHING COGNITIVE NORMS FROM THE NATIONAL ALZHEIMER'S COORDINATING CENTER (NACC) DATASET. (1st July 2006)

10. P1‐419: USING A BRAIN NETWORK APPROACH TO PREDICT GENETIC MUTATION IN INDIVIDUAL PATIENTS WITH FAMILIAL FRONTOTEMPORAL DEMENTIA. (1st July 2006)