8 results on '"Vercelletto, Martine"'
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2. DCTN1 Mutation Analysis in Families With Progressive Supranuclear Palsy–Like Phenotypes
3. General practice-based intervention for suspecting and detecting dementia in France A cluster randomized controlled trial
4. Phenotype variability in progranulin mutation carriers: a clinical, neuropsychological, imaging and genetic study
5. Progranulin Null Mutations in Both Sporadic and Familial Frontotemporal Dementia
6. Mutations Other Than Null Mutations Producing a Pathogenic Loss of Progranulin in Frontotemporal Dementia
7. Demographic, neurological and behavioural characteristics and brain perfusion SPECT in frontal variant of frontotemporal dementia
8. Phenotype associated with APP duplication in five families
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