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You searched for: Author/Creator Cruts, Marc

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1. A Pan‐European Study of the C9orf72 Repeat Associated with FTLD: Geographic Prevalence, Genomic Instability, and Intermediate Repeats. Issue 2 (4th January 2013)

2. DT‐02‐01: Loss‐of‐function mutations in TBK1 are frequently associated with frontotemporal lobar degeneration in a belgian patient cohort. (1st July 2015)

3. Familial primary lateral sclerosis or dementia associated with Arg573Gly TBK1 mutation. Issue 11 (1st April 2017)

5. Loss of TBK1 is a frequent cause of frontotemporal dementia in a Belgian cohort. (15th December 2015)

7. O3‐13‐03: Massive parallel gene panel sequencing in a belgian ftld cohort of causal genes associated with diverse neurodegenerative brain diseases. (1st July 2015)

8. P1‐053: OLFACTORY RECEPTOR COPY NUMBER VARIATION INVOLVED IN ALZHEIMER'S DISEASE. (1st July 2014)