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You searched for: Author/Creator Cras, Patrick

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1. [O2–08–06]: CONTRIBUTION OF RARE DELETERIOUS ABCA7 MUTATIONS TO A BELGIAN EARLY‐ONSET ALZHEIMER's DISEASE COHORT. (1st July 2017)

2. [O2–13–05]: DELETERIOUS ABCA7 MUTATIONS CONTRIBUTE TO EARLY‐ONSET ALZHEIMER's DISEASE AND ARE SUBJECT TO TRANSCRIPT RESCUE MECHANISMS. (1st July 2017)

3. [P4–069]: A PROSPECTIVE NEUROGENETIC STUDY ON EARLY‐ONSET DEMENTIA IN PATIENTS WITH UNCLEAR INITIAL DIAGNOSIS OF DEGENERATIVE DEMENTIA. (1st July 2017)

4. [P4–075]: THE MAPT P.ARG406TRP IS A FOUNDER MUTATION IN BELGIUM AND PRESENTS WITH AN ALZHEIMER DISEASE DEMENTIA‐LIKE PHENOTYPE. (1st July 2017)

5. A family‐based genetic study identifies mutations in TLR9 impairing receptor activation: A role for innate immunity in AD pathogenesis: Developing topics. (7th December 2020)

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

7. ABCA7 PTC mutation carriers present with Alzheimer's disease pathology and cerebral amyloid angiopathy: Basic science and pathogenesis: Genetics and omics of AD. (7th December 2020)

8. Abnormal Pain Response to Visual Feedback During Cervical Movements in Chronic Whiplash: An Experimental Study. Issue 2 (23rd February 2016)

10. Automated PGP9.5 immunofluorescence staining: a valuable tool in the assessment of small fiber neuropathy?. (December 2016)