Search

Your search keyword '"Ghidoni, Roberta"' showing total 999 results

Search Constraints

Start Over You searched for: Author "Ghidoni, Roberta" Remove constraint Author: "Ghidoni, Roberta"
999 results on '"Ghidoni, Roberta"'

Search Results

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

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

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

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

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

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

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

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

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

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

13. Serum neurofilament light in professional soccer players: goal on safety

14. Clinical value of cerebrospinal fluid neurofilament light chain in semantic dementia.

15. Next Generation Sequencing Analysis in Early Onset Dementia Patients.

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

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

18. A C6orf10/LOC101929163 locus is associated with age of onset in C9orf72 carriers.

19. Downregulation of exosomal miR-204-5p and miR-632 as a biomarker for FTD: a GENFI study

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

21. Poly(GP), neurofilament and grey matter deficits in C9orf72 expansion carriers

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

42. Transferability of a European-derived Alzheimer’s Disease Genetic Risk Score across Multi-Ancestry Populations

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

45. C9orf72, AAO and ancestry help discriminating behavioural from language variants in FTLD cohorts

46. C9ORF72 repeat expansions in cases with previously identified pathogenic mutations

48. TheSORL1p.Y1816C variant causes impaired endosomal dimerization and autosomal dominant Alzheimer’s disease

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

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

Catalog

Books, media, physical & digital resources