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364 results on '"Ghidoni, Roberta"'

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1. X‐chromosome-wide association study for Alzheimer’s disease

2. Physical Activity in young female outpatients with BORderline personality Disorder (PABORD): a study protocol for a randomized controlled trial (RCT)

3. A systematic review of progranulin concentrations in biofluids in over 7,000 people—assessing the pathogenicity of GRN mutations and other influencing factors

5. Genome-wide analyses reveal a potential role for the MAPT, MOBP, and APOE loci in sporadic frontotemporal dementia

7. Prioritization of Drug Targets for Neurodegenerative Diseases by Integrating Genetic and Proteomic Data From Brain and Blood

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

9. Association of rs3027178 polymorphism in the circadian clock gene PER1 with susceptibility to Alzheimer’s disease and longevity in an Italian population

10. Gene Expression Imputation Across Multiple Tissue Types Provides Insight Into the Genetic Architecture of Frontotemporal Dementia and Its Clinical Subtypes

11. Pathogenic Huntingtin Repeat Expansions in Patients with Frontotemporal Dementia and Amyotrophic Lateral Sclerosis

12. The SORL1 p.Y1816C variant causes impaired endosomal dimerization and autosomal dominant Alzheimer's disease.

13. Serum Beta-Secretase 1 Activity Is a Potential Marker for the Differential Diagnosis between Alzheimer's Disease and Frontotemporal Dementia: A Pilot Study.

14. Unveiling New Genetic Variants Associated with Age at Onset in Alzheimer's Disease and Frontotemporal Lobar Degeneration Due to C9orf72 Repeat Expansions.

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

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

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

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

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

23. Spatiotemporal analysis for detection of pre-symptomatic shape changes in neurodegenerative diseases: Initial application to the GENFI cohort

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

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

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

28. White matter hyperintensities are seen only in GRN mutation carriers in the GENFI cohort

29. Distribution of the C9orf72 hexanucleotide repeat expansion in healthy subjects: a multicenter study promoted by the Italian IRCCS network of neuroscience and neurorehabilitation.

30. Autophagy Markers Are Altered in Alzheimer's Disease, Dementia with Lewy Bodies and Frontotemporal Dementia.

31. CCR5 deficiency: Decreased neuronal resilience to oxidative stress and increased risk of vascular dementia.

32. Incidence of young‐onset dementia in Italy: The Brescia register study.

33. C9orf72, age at onset, and ancestry help discriminate behavioral from language variants in FTLD cohorts

34. Genetic variation in APOE, GRN, and TP53 are phenotype modifiers in frontotemporal dementia

35. Progranulin Deficiency Promotes Circuit-Specific Synaptic Pruning by Microglia via Complement Activation

36. Loss of exosomes in progranulin-associated frontotemporal dementia

38. Role for ATXN1, ATXN2, and HTT intermediate repeats in frontotemporal dementia and Alzheimer's disease

40. Survival in Incident Cases with Frontotemporal Lobar Degeneration: A Registry-Based Study.

41. Presymptomatic cognitive and neuroanatomical changes in genetic frontotemporal dementia in the Genetic Frontotemporal dementia Initiative (GENFI) study: a cross-sectional analysis

42. Deleterious ABCA7 mutations and transcript rescue mechanisms in early onset Alzheimer’s disease

43. Frontotemporal dementia and its subtypes: a genome-wide association study

45. A Multimodal Approach for Clinical Diagnosis and Treatment of Primary Progressive Aphasia (MAINSTREAM): A Study Protocol.

47. A comprehensive study of the genetic impact of rare variants in SORL1 in European early-onset Alzheimer’s disease

48. The SIRT2 polymorphism rs10410544 and risk of Alzheimer’s disease in two Caucasian case–control cohorts

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

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