Sage Journals: Discover world-class research

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Brief report

First published 2013-5-21

GRN Thr272fs Clinical Heterogeneity: A Case with Atypical Late Onset Presenting with a Dementia with Lewy Bodies Phenotype

Beatrice Arosio, Carlo Abbate, Daniela Galimberti [...]

Journal of Alzheimer’s Disease

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Brief report

First published 2019-02-19

Monozygotic Twins with Frontotemporal Dementia Due To Thr272fs GRN Mutation Discordant for Age At Onset

Giorgio Giulio Fumagalli, Luca Sacchi, Paola Basilico [...]

Journal of Alzheimer’s Disease

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Research article

First published 2011-12-12

Cerebrospinal Fluid Biomarkers in Progranulin Mutations Carriers

Miryam Carecchio, Chiara Fenoglio, Francesca Cortini [...]

Journal of Alzheimer’s Disease

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Research article

First published 2012-12-17

Structural Brain Signature of FTLD Driven by Granulin Mutation

Marco Bozzali, Valentina Battistoni, Enrico Premi [...]

Journal of Alzheimer’s Disease

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Brief report

First published 2016-7-13

Plasma Screening for Progranulin Mutations in Patients with Progressive Supranuclear Palsy and Corticobasal Syndromes

Daniela Galimberti, Kelly Bertram, Alessandra Formica [...]

Journal of Alzheimer’s Disease

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Research article

First published 2011-12-12

From Genotype to Phenotype: Two Cases of Genetic Frontotemporal Lobar Degeneration with Premorbid Bipolar Disorder

Chiara Cerami, Alessandra Marcone, Daniela Galimberti [...]

Journal of Alzheimer’s Disease

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Research article

First published 2016-2-27

Looking for Neuroimaging Markers in Frontotemporal Lobar Degeneration Clinical Trials: A Multi-Voxel Pattern Analysis Study in Granulin Disease

Enrico Premi, Franco Cauda, Tommaso Costa [...]

Journal of Alzheimer’s Disease

Search results

GRN Thr272fs Clinical Heterogeneity: A Case with Atypical Late Onset Presenting with a Dementia with Lewy Bodies Phenotype

Monozygotic Twins with Frontotemporal Dementia Due To Thr272fs GRN Mutation Discordant for Age At Onset

Cerebrospinal Fluid Biomarkers in Progranulin Mutations Carriers

Structural Brain Signature of FTLD Driven by Granulin Mutation

Plasma Screening for Progranulin Mutations in Patients with Progressive Supranuclear Palsy and Corticobasal Syndromes

From Genotype to Phenotype: Two Cases of Genetic Frontotemporal Lobar Degeneration with Premorbid Bipolar Disorder

Looking for Neuroimaging Markers in Frontotemporal Lobar Degeneration Clinical Trials: A Multi-Voxel Pattern Analysis Study in Granulin Disease