36 results on '"Cuijt, Ivy"'
Search Results
2. 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
3. TDP-43 Transgenic Mice Develop Spastic Paralysis and Neuronal Inclusions Characteristic of ALS and Frontotemporal Lobar Degeneration
4. Overexpression of ALS-Associated p.M337V Human TDP-43 in Mice Worsens Disease Features Compared to Wild-type Human TDP-43 Mice
5. Intraneuronal amyloid β and reduced brain volume in a novel APP T714I mouse model for Alzheimer's disease
6. Cellular ageing, increased mortality and FTLD-TDP-associated neuropathology in progranulin knockout mice
7. Identification of 2 Loci at Chromosomes 9 and 14 in a Multiplex Family With Frontotemporal Lobar Degeneration and Amyotrophic Lateral Sclerosis
8. Progranulin expression correlates with dense-core amyloid plaque burden in Alzheimer disease mouse models
9. Alzheimer and Parkinson Diagnoses in Progranulin Null Mutation Carriers in an Extended Founder Family
10. Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21
11. Characterization of Ubiquitinated Intraneuronal Inclusions in a Novel Belgian Frontotemporal Lobar Degeneration Family
12. Clinical variability and onset age modifiers in an extended Belgian GRN founder family.
13. Clinical variability and onset age modifiers in an extended Belgian GRN founder family
14. Additional file 1: Supplementary tables. of Investigating the role of filamin C in Belgian patients with frontotemporal dementia linked to GRN deficiency in FTLD-TDP brains
15. Additional file 2: Supplementary figures. of Investigating the role of filamin C in Belgian patients with frontotemporal dementia linked to GRN deficiency in FTLD-TDP brains
16. Drosophila screen connects nuclear transport genes to DPR pathology in c9ALS/FTD
17. Loss ofTBK1is a frequent cause of frontotemporal dementia in a Belgian cohort
18. Loss ofTBK1is a frequent cause of frontotemporal dementia in a Belgian cohort
19. DT-02-01: Loss-of-function mutations in TBK1 are frequently associated with frontotemporal lobar degeneration in a belgian patient cohort
20. Gene expression profiling to identify microvascular changes in Alzheimer's disease mouse models
21. Loss of TBK1 is a frequent cause of frontotemporal dementia in a Belgian cohort.
22. S4-04-02: Overexpression of Wild-type TDP-43 Leads to Motor Neuron Degeneration and Spastic Quadriplegia in Germline Transgenic Mice
23. O4-03-03: Biochemical characterization of FTLD-TDP overexpression and knockout mouse models
24. Reduced brain volumes in mice expressing APP-Austrian mutation but not in mice expressing APP-Swedish–Austrian mutations
25. P2‐184: Identification of a novel chromosomal locus in a Belgian FTLD‐MND family
26. P2-191: Neuropathological and biochemical characterization of GRN mutation carriers and GRN conditional mice
27. P4‐300: Gene expression profiling to identify microvascular changes in Alzheimer's disease mouse models
28. P1-044: Intraneuronal amyloid-β does not cause reduced brain volumes in novel mouse models with Austrian Alzheimer mutation
29. Investigating the role of filamin C in Belgian patients with frontotemporal dementia linked to GRN deficiency in FTLD-TDP brains.
30. P3–196: Characterization of ubiquitinated intraneuronal inclusions in a novel Belgian FTD (FTLD–U) family
31. P1-045: Intraneuronal amyloid β and reduced brain volume in a novel APP ‘Austrian’ mouse model for Alzheimer's disease
32. Loss of TBK1is a frequent cause of frontotemporal dementia in a Belgian cohort
33. Overexpression of Wild-type TDP-43 Leads to Motor Neuron Degeneration and Spastic Quadriplegia in Germline Transgenic Mice
34. Biochemical characterization of FTLD-TDP overexpression and knockout mouse models
35. Loss-of-function mutations in TBK1 are frequently associated with frontotemporal lobar degeneration in a belgian patient cohort.
36. Clinical variability and onset age modifiers in an extended Belgian GRN founder family
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