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1. Age at symptom onset and death and disease duration in genetic frontotemporal dementia: an international retrospective cohort study. Issue 2 (February 2020)

2. 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)

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

4. Clinical, neuroimaging and neuropathological features of a new chromosome 9p-linked FTD-ALS family. Issue 2 (20th June 2010)

5. Early Neuropsychological Characteristics of Progranulin Mutation Carriers. (4th July 2014)

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

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

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)