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You searched for: Record Type Journal Article Author/Creator Serpente, Maria

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1. A case of bipolar disorder developing into atypical parkinsonism and presenting with frontotemporal asymmetrical brain degeneration. A TREDEM Registry Case Report. (18th February 2020)

2. C9ORF72 hexanucleotide repeat expansion as a rare cause of bipolar disorder. (16th December 2013)

3. C9orf72, age at onset, and ancestry help discriminate behavioral from language variants in FTLD cohorts. (15th December 2020)

4. Evidence of CNS β-amyloid deposition in Nasu-Hakola disease due to the TREM2 Q33X mutation. (12th December 2017)

5. P1‐043: CIRCULATING AND INTRATHECAL MIRNAS AS POTENTIAL BIOMARKERS FOR ALZHEIMER'S DISEASE. (1st July 2014)

6. P1‐044: TREM2 GENETIC VARIABILITY IN PATIENTS WITH ALZHEIMER'S DISEASE AND FRONTOTEMPORAL LOBAR DEGENERATION. (1st July 2014)

7. Phenotypic heterogeneity of the rare R377W PSEN1 mutation: Late‐onset presentation with mixed Alzheimer's and frontotemporal dementia features: Genetics/genetic factors of Alzheimer's disease. (7th December 2020)

8. Progranulin gene variability influences the risk for bipolar I disorder, but not bipolar II disorder. (6th February 2014)

9. Rapidly progressive primary progressive aphasia and parkinsonism with novel GRN mutation. Issue 3 (15th November 2016)