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You searched for: Author/Creator Pearlman, Rodney

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1. An 8‐week, open‐label, dose‐finding study of nimodipine for the treatment of progranulin insufficiency from GRN gene mutations. Issue 4 (30th August 2017)

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. Gearing up for the future: Exploring facilitators and barriers to inform clinical trial design in frontotemporal lobar degeneration. (1st February 2022)

5. Gearing up for the future: Exploring facilitators and barriers to inform clinical trial design in frontotemporal lobar degeneration. (December 2021)

6. Genetic screening of a large series of North American sporadic and familial frontotemporal dementia cases. Issue 1 (8th January 2020)

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

8. New directions in clinical trials for frontotemporal lobar degeneration: Methods and outcome measures. Issue 1 (6th January 2020)

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

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