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Your search keyword '"De Mendonça, Alexandre"' showing total 17 results

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17 results on '"De Mendonça, Alexandre"'

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1. Structural brain splitting is a hallmark of Granulin-related frontotemporal dementia

2. Dissemination in time and space in presymptomatic granulin mutation carriers: a GENFI spatial chronnectome study

3. Patterns of gray matter atrophy in genetic frontotemporal dementia: results from the GENFI study

4. The frequency and influence of dementia risk factors in prodromal Alzheimer's disease

5. Corrigendum to “Dissemination in time and space in presymptomatic granulin mutation carriers: A spatial chronnectome study” [Neurobiology of Aging Volume 108, December 2021, Pages 155–167]

6. Genetic and biochemical markers in patients with Alzheimer's disease support a concerted systemic iron homeostasis dysregulation

7. Corrigendum to “Dissemination in time and space in presymptomatic granulin mutation carriers: A spatial chronnectome study” [Neurobiology of Aging Volume 108, December 2021, Pages 155–167]

8. Rare nonsynonymous variants in SORT1 are associated with increased risk for frontotemporal dementia

9. Common and rare TBK1 variants in early-onset Alzheimer disease in a European cohort

10. Progranulin plasma levels predict the presence of GRN mutations in asymptomatic subjects and do not correlate with brain atrophy: results from the GENFI study

11. Structural brain splitting is a hallmark of Granulin-related frontotemporal dementia

12. Genetic variability in SQSTM1 and risk of early-onset Alzheimer dementia: a European early-onset dementia consortium study

13. No supportive evidence for TIA1 gene mutations in a European cohort of ALS-FTD spectrum patients

14. Patterns of gray matter atrophy in genetic frontotemporal dementia: results from the GENFI study

15. Progranulin plasma levels predict the presence of GRN mutations in asymptomatic subjects and do not correlate with brain atrophy: results from the GENFI study

16. Common and rare TBK1 variants in early-onset Alzheimer disease in a European cohort

17. No supportive evidence for TIA1 gene mutations in a European cohort of ALS-FTD spectrum patients

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