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Your search keyword '"Pijnenburg, Yolande A. L."' showing total 40 results

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40 results on '"Pijnenburg, Yolande A. L."'

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1. X‐chromosome-wide association study for Alzheimer’s disease

2. Proteogenomic analysis of human cerebrospinal fluid identifies neurologically relevant regulation and implicates causal proteins for Alzheimer’s disease

3. Diagnosing primary lateral sclerosis: a clinico-pathological study

4. Rationale and design of the BeyeOMARKER study: prospective evaluation of blood- and eye-based biomarkers for early detection of Alzheimer’s disease pathology in the eye clinic

6. Cerebrospinal fluid proteomics in patients with Alzheimer’s disease reveals five molecular subtypes with distinct genetic risk profiles

16. The reporting of neuropsychiatric symptoms in electronic health records of individuals with Alzheimer’s disease: a natural language processing study

17. Author Correction: Common variants in Alzheimer’s disease and risk stratification by polygenic risk scores

19. CSF proteome profiling across the Alzheimer’s disease spectrum reflects the multifactorial nature of the disease and identifies specific biomarker panels

20. Genome-wide meta-analysis for Alzheimer’s disease cerebrospinal fluid biomarkers

21. New insights into the genetic etiology of Alzheimer’s disease and related dementias

22. The natural history of primary progressive aphasia: beyond aphasia

23. Elevated CSF and plasma complement proteins in genetic frontotemporal dementia: results from the GENFI study

24. Rationale and design of the “NEurodegeneration: Traumatic brain injury as Origin of the Neuropathology (NEwTON)” study: a prospective cohort study of individuals at risk for chronic traumatic encephalopathy

25. Cognitive composites for genetic frontotemporal dementia: GENFI-Cog

26. Letter to the editor on a paper by Kaivola et al. (2020): carriership of two copies of C9orf72 hexanucleotide repeat intermediate-length alleles is not associated with amyotrophic lateral sclerosis or frontotemporal dementia

31. Common variants in Alzheimer’s disease and risk stratification by polygenic risk scores

32. Genome-wide association study of frontotemporal dementia identifies a C9ORF72 haplotype with a median of 12-G4C2 repeats that predisposes to pathological repeat expansions

36. Early recognition and treatment of neuropsychiatric symptoms to improve quality of life in early Alzheimer’s disease: protocol of the BEAT-IT study

40. PLD3 variants in population studies

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