Associated Papers
Progranulin Gene Mutations in Chinese Patients with Frontotemporal Dementia: A Case Report and Literature Review.
Chu M et al.
Journal of Alzheimer's Disease : Jad, 2023
36970912 (PubMed )
Supplement: jad-93-jad230052-s001.pdf
Progression of Behavioral Disturbances and Neuropsychiatric Symptoms in Patients With Genetic Frontotemporal Dementia.
Benussi A et al.
Jama Network Open, 2021
33404617 (PubMed )
Supplement: jamanetwopen-e2030194-s001.pdf
Age at symptom onset and death and disease duration in genetic frontotemporal dementia: an international retrospective cohort study.
Moore KM et al.
The Lancet. Neurology, 2020
31810826 (PubMed )
Supplement: NIHMS1067362-supplement-Supplement.pdf
The multiple phenotypes of corticobasal syndrome and corticobasal degeneration: implications for further study.
Boeve BF
Journal of Molecular Neuroscience : Mn, 2011
Clinical and neuroanatomical signatures of tissue pathology in frontotemporal lobar degeneration.
Rohrer JD et al.
Brain : a Journal of Neurology, 2011
Corticobasal syndrome associated with a novel 1048_1049insG progranulin mutation.
Rohrer JD et al.
Journal of Neurology, Neurosurgery, and Psychiatry, 2009
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