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2. Prodromal language impairment in genetic frontotemporal dementia within the GENFI cohort

3. Early neurotransmitters changes in prodromal frontotemporal dementia: A GENFI study

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

6. Examining empathy deficits across familial forms of frontotemporal dementia within the GENFI cohort

7. Social cognition impairment in genetic frontotemporal dementia within the GENFI cohort

8. Screening of dementia genes by whole-exome sequencing in Spanish patients with early-onset dementia: likely pathogenic, uncertain significance and risk variants

9. Age at symptom onset and death and disease duration in genetic frontotemporal dementia: an international retrospective cohort study

10. Serum neurofilament light chain in genetic frontotemporal dementia: a longitudinal, multicentre cohort study

12. Functional network resilience to pathology in presymptomatic genetic frontotemporal dementia

13. The inner fluctuations of the brain in presymptomatic Frontotemporal Dementia: The chronnectome fingerprint

16. Potential genetic modifiers of disease risk and age at onset in patients with frontotemporal lobar degeneration and GRN mutations: a genome-wide association study

17. Cerebral amyloid angiopathy in Down syndrome and sporadic and autosomal-dominant Alzheimer's disease

22. A unique common ancestor introduced P301L mutation in MAPT gene in frontotemporal dementia patients from Barcelona (Baix Llobregat, Spain)

24. 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]

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

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

31. The Alzheimer’s Association external quality control program for cerebrospinal fluid biomarkers

32. Assessing the role of TUBA4A gene in frontotemporal degeneration

33. Error in Article Information

34. Progression of Behavioral Disturbances and Neuropsychiatric Symptoms in Patients With Genetic Frontotemporal Dementia

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

37. Investigation of the role of rare TREM2 variants in frontotemporal dementia subtypes

44. A CEREBROSPINAL FLUID PANEL OF SYNAPTIC PROTEINS ACROSS THE ENTIRE ALZHEIMER’S DISEASE CONTINUUM

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