206 results on '"Peeters, Karin"'
Search Results
2. Unraveling the Immune Signature of Herpes Zoster: Insights Into the Pathophysiology and Human Leukocyte Antigen Risk Profile.
3. Clinical variability and onset age modifiers in an extended Belgian GRN founder family
4. Loss of DPP6 in neurodegenerative dementia: a genetic player in the dysfunction of neuronal excitability
5. Unraveling the immune signature of herpes zoster: Insights into pathophysiology and the HLA risk profile
6. Rare nonsynonymous variants in SORT1 are associated with increased risk for frontotemporal dementia
7. A C9orf72 promoter repeat expansion in a Flanders-Belgian cohort with disorders of the frontotemporal lobar degeneration-amyotrophic lateral sclerosis spectrum: a gene identification study
8. GIGYF2 has no major role in Parkinson genetic etiology in a Belgian population
9. Rare mutations in SQSTM1 modify susceptibility to frontotemporal lobar degeneration
10. Clinical features of TBK1 carriers compared with C9orf72, GRN and non-mutation carriers in a Belgian cohort
11. Distinct Clinical Characteristics of C9orf72 Expansion Carriers Compared With GRN, MAPT, and Nonmutation Carriers in a Flanders-Belgian FTLD Cohort
12. Guanosine Triphosphate Cyclohydrolase 1 Promoter Deletion Causes Dopa-Responsive Dystonia
13. Investigating the role of rare heterozygous TREM2 variants in Alzheimer's disease and frontotemporal dementia
14. TMEM106B is associated with frontotemporal lobar degeneration in a clinically diagnosed patient cohort
15. ABCA7 mutations are major contributors to Alzheimer’s disease in Belgian patients
16. ABCA7 PTC mutation carriers present with Alzheimer’s disease pathology and cerebral amyloid angiopathy
17. Highly Frequent MAPT p.R406W Carriers with a Nonconforming FTD Phenotype in the Belgian Flemish Population (1127)
18. In a Large Belgian AD Cohort Loss of ABCA7 Mutations Are Associated with Alzheimer’s Disease and Cerebral Amyloid Angiopathy. (1779)
19. Identification of 2 Loci at Chromosomes 9 and 14 in a Multiplex Family With Frontotemporal Lobar Degeneration and Amyotrophic Lateral Sclerosis
20. Genetic Variability in the Mitochondrial Serine Protease HTRA2 Contributes to Risk for Parkinson Disease
21. CHMP2B C-truncating mutations in frontotemporal lobar degeneration are associated with an aberrant endosomal phenotype in vitro
22. Alzheimer and Parkinson Diagnoses in Progranulin Null Mutation Carriers in an Extended Founder Family
23. A novel locus for dementia with Lewy bodies: a clinically and genetically heterogeneous disorder
24. Mutations Other Than Null Mutations Producing a Pathogenic Loss of Progranulin in Frontotemporal Dementia
25. Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21
26. A Belgian ancestral haplotype harbours a highly prevalent mutation for 17q21-linked tau-negative FTLD
27. C9orf72 G4C2 repeat expansions in Alzheimer's disease and mild cognitive impairment
28. Loss of DPP6 in neurodegenerative dementia: a genetic player in the dysfunction of neuronal excitability.
29. Contribution of VPS35 genetic variability to LBD in the Flanders-Belgian population
30. DLB and PDD: a role for mutations in dementia and Parkinson disease genes?
31. Both common variations and rare non-synonymous substitutions and small insertion/deletions in CLU are associated with increased Alzheimer risk
32. Clinical variability and onset age modifiers in an extended Belgian GRN founder family.
33. Clinical variability and onset age modifiers in an extended Belgian GRN founder family
34. Clinical Evidence of Disease Anticipation in Families Segregating aC9orf72Repeat Expansion
35. Krimpcafé
36. Clinical characteristics of loss-of function mutations in TBK1 in Belgian FTD and ALS patients
37. Clinical characteristics of loss-of-function mutations in ABCA7 in Belgian Alzheimer disease patients and families
38. The C9orf72 repeat size correlates with onset age of disease, DNA methylation and transcriptional downregulation of the promoter
39. Clinical features of TBK1 carriers compared with C9orf72, GRN and non-mutation carriers in a Belgian cohort
40. Mutations in glucocerebrosidase are a major genetic risk factor for Parkinson’s disease and increase susceptibility to dementia in a Flanders-Belgian cohort
41. Clinical Evidence for Disease Anticipation in Families Segregating a C9orf72 Repeat Expansion (S21.006)
42. Clinical Features of TBK1 Carriers and Comparison with C9orf72, GRN and Nonmutation Carriers in a Belgian Patient Cohort (S21.007)
43. Phenotypic characteristics of Alzheimer patients carrying an ABCA7 mutation
44. Loss ofTBK1is a frequent cause of frontotemporal dementia in a Belgian cohort
45. Clinical features ofTBK1carriers compared withC9orf72,GRNand non-mutation carriers in a Belgian cohort
46. Loss ofTBK1is a frequent cause of frontotemporal dementia in a Belgian cohort
47. Mutations in ABCA7 in a Belgian cohort of Alzheimer's disease patients: a targeted resequencing study
48. P4-194: The identification of high-penetrant loss-of-function mutations in abca7 in Alzheimer's disease
49. DT-02-01: Loss-of-function mutations in TBK1 are frequently associated with frontotemporal lobar degeneration in a belgian patient cohort
50. Clinical evidence for genetic anticipation in C9orf72 pedigrees
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