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1. Age at onset in genetic prion disease and the design of preventive clinical trials. (9th July 2019)

2. Brain volumetric deficits in MAPT mutation carriers: a multisite study. Issue 1 (28th November 2020)

3. Brain volumetric deficits in MAPT mutation carriers: a multisite study. Issue 1 (28th November 2020)

4. Clinical value of CSF tau, p‐tau181, neurogranin and neurofilaments in familial frontotemporal lobar degeneration. (1st February 2022)

5. Clinical value of CSF tau, p‐tau181, neurogranin and neurofilaments in familial frontotemporal lobar degeneration. (December 2021)

6. Diagnostic value of plasma P‐tau217 in frontotemporal dementia spectrum disorders. (1st February 2022)

7. Diagnostic value of plasma P‐tau217 in frontotemporal dementia spectrum disorders. (December 2021)

8. Genetic prion disease: Experience of a rapidly progressive dementia center in the United States and a review of the literature. Issue 1 (12th December 2016)

9. Genome Sequencing in the Parkinson Disease Clinic. (9th August 2022)