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

2. Octapeptide repeat insertions in the prion protein gene and early onset dementia

4. Prospective Belgian study of neurodegenerative and vascular dementia: APOE genotype effects

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

18. CXCR4involvement in neurodegenerative diseases

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

22. Identification of evolutionarily conserved gene networks mediating neurodegenerative dementia

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

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

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

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

27. Immune-related genetic enrichment in frontotemporal dementia

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

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

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

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

33. Unraveling the genetic role of SORT1 in the Belgian frontotemporal dementia population

34. The C9orf72 repeat size correlates with onset age of disease, DNA methylation and transcriptional downregulation of the promoter

35. Transcriptome analysis in FTD patients: genes, pathways and networks

36. Clinical evidence for disease anticipation in C9orf72 families

39. Chromosome 17 linked dementia in the absence of tau mutations

41. C9orf72-Related Amyotrophic Lateral Sclerosis and Frontotemporal Dementia

42. Loss-of-Function Mutations in TBK1 Are Frequently Associated with Frontotemporal Lobar Degeneration in a Belgian Patient Cohort

43. TBK1 loss-of function and dominant-negative mutations in an extended European cohort of FTD and ALS patients

45. A pan-European study of the C9orf72 repeat associated with FTLD: geographic prevalence, genomic instability, and intermediate repeats

47. Genomic characterization of the C9orf72 promoter repeat in FTLD and ALS patients

50. Serum progranulin is a noninvasive biomarker for frontotemporal lobar degeneration

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