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1. Early pathological gambling in co-occurrence with semantic variant primary progressive aphasia: a case report

2. Protein network analysis reveals selectively vulnerable regions and biological processes in FTD

3. The diagnostic accuracy of late-life depression is influenced by subjective memory complaints and educational level in an older population in Southern Italy

4. Genetic architecture of sporadic frontotemporal dementia and overlap with Alzheimerʼs and Parkinsonʼs diseases

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

8. Correction to:A nonsynonymous mutation in PLCG2 reduces the risk of Alzheimer’s disease, dementia with Lewy bodies and frontotemporal dementia, and increases the likelihood of longevity (Acta Neuropathologica, (2019), 138, 2, (237-250), 10.1007/s00401-019-02026-8)

9. Correction to: A nonsynonymous mutation in PLCG2 reduces the risk of Alzheimer’s disease, dementia with Lewy bodies and frontotemporal dementia, and increases the likelihood of longevity (Acta Neuropathologica, (2019), 138, 2, (237-250), 10.1007/s00401-019-02026-8)

10. Mendelian randomization implies no direct causal association between leukocyte telomere length and amyotrophic lateral sclerosis

14. Correction to: A nonsynonymous mutation in PLCG2 reduces the risk of Alzheimer’s disease, dementia with Lewy bodies and frontotemporal dementia, and increases the likelihood of longevity

15. Genetic variation across RNA metabolism and cell death gene networks is implicated in the semantic variant of primary progressive aphasia

16. Genetic variation across RNA metabolism and cell death gene networks is implicated in the semantic variant of primary progressive aphasia

17. Promising therapies for the treatment of frontotemporal dementia clinical phenotypes: from symptomatic to disease-modifying drugs

18. CXCR4involvement in neurodegenerative diseases

19. Genetic risk for neurodegenerative disorders, and its overlap with cognitive ability and physical function

20. Protein network analysis reveals selectively vulnerable regions and biological processes in FTD

21. Genetic architecture of sporadic frontotemporal dementia and overlap with Alzheimer’s and Parkinson’s diseases

22. Immune-related genetic enrichment in frontotemporal dementia: An analysis of genome-wide association studies

23. Susceptible genes and disease mechanisms identified in frontotemporal dementia and frontotemporal dementia with Amyotrophic Lateral Sclerosis by DNA-methylation and GWAS

24. Immune-related genetic enrichment in frontotemporal dementia

25. Shared genetic risk between corticobasal degeneration, progressive supranuclear palsy, and frontotemporal dementia

26. Genetic architecture of sporadic frontotemporal dementia and overlap with Alzheimer's and Parkinson's diseases

27. Gene-based association studies report genetic links for clinical subtypes of frontotemporal dementia

29. Physical activity and amyotrophic lateral sclerosis: A European population-based case-control study

30. Educational level influenced the gold standard diagnosis of late-life depression in the GreatAGE study

31. Swallowing Disturbances and Psychiatric Profile in Older Adults: The GreatAGE Study

32. Trauma and amyotrophic lateral sclerosis: a case-control study from a population-based registry

34. Validity of the Geriatric Depression Scale-30 against the gold standard diagnosis of depression in older age: The GreatAGE Study

35. Coffee and Amyotrophic Lateral Sclerosis: A Possible Preventive Role

37. Frontotemporal dementia and its subtypes: A genome-wide association study

40. Trauma and amyotrophic lateral sclerosis: a case-control study from a population-based registry

44. Genetic analysis suggests lysosomal and immune system involvement in frontotemporal dementia

45. More than two-hundred and fifty FTD patients looking for genes: results from Italian FTD Network

46. Genetic variation across RNA metabolism and cell death gene networks is implicated in the semantic variant of primary progressive aphasia

47. Frontotemporal dementia and its subtypes: A genome-wide association study

48. Mitochondrial genome aberrations in skeletal muscle of patients with motor neuron disease

49. Early and severe autonomic failure: broadening the clinical phenotype of type-2 spinocerebellar ataxia. A case report

50. Mitochondrial genome large rearrangements in the skeletal muscle of a patient with PMA

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