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You searched for: Author/Creator Gavrilova, Ralitza H

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1. Application of whole exome sequencing in undiagnosed inherited polyneuropathies. Issue 11 (6th March 2014)

2. Demographic and psychosocial factors associated with the decision to learn mutation status in familial frontotemporal dementia and the impact of disclosure on mood. (1st February 2022)

3. Demographic and psychosocial factors associated with the decision to learn mutation status in familial frontotemporal dementia and the impact of disclosure on mood. (December 2021)

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)