Search

Your search keyword '"Ferreira, Catarina B"' showing total 113 results

Search Constraints

Start Over You searched for: Author "Ferreira, Catarina B" Remove constraint Author: "Ferreira, Catarina B"
113 results on '"Ferreira, Catarina B"'

Search Results

1. A small TAT-TrkB peptide prevents BDNF receptor cleavage and restores synaptic physiology in Alzheimer's disease

2. Author Correction: Common variants in Alzheimer’s disease and risk stratification by polygenic risk scores

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

4. 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. S327 phosphorylation of the presynaptic protein SEPTIN5 increases in the early stages of neurofibrillary pathology and alters the functionality of SEPTIN5

8. New insights into the genetic etiology of Alzheimer’s disease and related dementias

9. Differential early subcortical involvement in genetic FTD within the GENFI cohort

10. Disease-related cortical thinning in presymptomatic granulin mutation carriers

11. Challenges of BDNF-based therapies: From common to rare diseases

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

13. Extending the phenotypic spectrum assessed by the CDR plus NACC FTLD in genetic frontotemporal dementia

14. Common variants in Alzheimer’s disease and risk stratification by polygenic risk scores

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

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

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

18. White matter hyperintensities in progranulin-associated frontotemporal dementia: A longitudinal GENFI study

19. Loss of brainstem white matter predicts onset and motor neuron symptoms in C9orf72 expansion carriers: a GENFI study

20. Characterizing the Clinical Features and Atrophy Patterns of MAPT-Related Frontotemporal Dementia With Disease Progression Modeling

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

22. Early neurotransmitters changes in prodromal frontotemporal dementia

23. Language impairment in the genetic forms of behavioural variant frontotemporal dementia

24. Temporal order of clinical and biomarker changes in familial frontotemporal dementia

25. Structural MRI predicts clinical progression in presymptomatic genetic frontotemporal dementia: findings from the GENetic Frontotemporal dementia Initiative cohort

26. Genetic forms of primary progressive aphasia within the GENetic Frontotemporal dementia Initiative (GENFI) cohort

27. Neurodevelopmental effects of genetic frontotemporal dementia in young adult mutation carriers

28. Temporal dynamics predict symptom onset and cognitive decline in familial frontotemporal dementia

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

30. Anomia is present pre-symptomatically in frontotemporal dementia due to MAPT mutations

31. Data‐driven staging of genetic frontotemporal dementia using multi‐modal <scp>MRI</scp>

32. A small TAT-TrkB peptide prevents BDNF receptor cleavage and restores synaptic physiology in Alzheimer’s disease

33. A modified Camel and Cactus Test detects presymptomatic semantic impairment in genetic frontotemporal dementia within the GENFI cohort

34. Cognitive composites for genetic frontotemporal dementia: GENFI-Cog

35. Differential impairment of cerebrospinal fluid synaptic biomarkers in the genetic forms of frontotemporal dementia

36. Elevated CSF and plasma complement proteins in genetic frontotemporal dementia: results from the GENFI study

37. 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]

38. The CBI-R detects early behavioural impairment in genetic frontotemporal dementia

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

40. Development of a sensitive trial-ready poly(GP) CSF biomarker assay for C9orf72-associated frontotemporal dementia and amyotrophic lateral sclerosis

41. Network structure and transcriptomic vulnerability shape atrophy in frontotemporal dementia

42. Conceptual framework for the definition of preclinical and prodromal frontotemporal dementia

43. Hierarchical spectral clustering reveals brain size and shape changes in asymptomatic carriers of C9orf72

44. Practice effects in genetic frontotemporal dementia and at-risk individuals: a GENFI study

45. CSF glial markers are elevated in a subset of patients with genetic frontotemporal dementia

46. Comparison of clinical rating scales in genetic frontotemporal dementia within the GENFI cohort

47. Development of a sensitive trial-ready poly(GP) CSF biomarker assay for C9orf72-associated frontotemporal dementia and amyotrophic lateral sclerosis

48. Stratifying the Presymptomatic Phase of Genetic Frontotemporal Dementia by Serum NfL and pNfH: A Longitudinal Multicentre Study

49. Plasma glial fibrillary acidic protein is raised in progranulin-associated frontotemporal dementia

50. Faster Cortical Thinning and Surface Area Loss in Presymptomatic and Symptomatic C9orf72 Repeat Expansion Adult Carriers

Catalog

Books, media, physical & digital resources