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1. Clinical recognition of frontotemporal dementia with right anterior temporal predominance: A multicenter retrospective cohort study

2. Genome-wide analyses reveal a potential role for the MAPT, MOBP, and APOE loci in sporadic frontotemporal dementia.

3. Amyloid pathology and vascular risk are associated with distinct patterns of cerebral white matter hyperintensities: A multicenter study in 3132 memory clinic patients

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

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

8. Spatial distributions of white matter hyperintensities on brain MRI: A pooled analysis of individual participant data from 11 memory clinic cohorts

10. Social dysfunction relates to shifts within socioaffective brain systems among Schizophrenia and Alzheimer's disease patients

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

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

24. Demographic, clinical, biomarker, and neuropathological correlates of posterior cortical atrophy: an international cohort study and individual participant data meta-analysis

27. Heterogeneous distribution of tau pathology in the behavioural variant of Alzheimer’s disease

29. C9orf72, age at onset, and ancestry help discriminate behavioral from language variants in FTLD cohorts

30. Investigating the clinico-anatomical dissociation in the behavioral variant of Alzheimer disease

31. Prodromal language impairment in genetic frontotemporal dementia within the GENFI cohort

32. Latent atrophy factors related to phenotypical variants of posterior cortical atrophy.

33. Recommendations to distinguish behavioural variant frontotemporal dementia from psychiatric disorders

34. Correction to: A nonsynonymous mutation in PLCG2 reduces the risk of Alzheimer's disease, dementia with Lewy bodies and frontotemporal dementia, and increases the likelihood of longevity.

35. Prioritization of Drug Targets for Neurodegenerative Diseases by Integrating Genetic and Proteomic Data From Brain and Blood

37. Early neurotransmitters changes in prodromal frontotemporal dementia: A GENFI study

38. The Benson Complex Figure Test detects deficits in visuoconstruction and visual memory in symptomatic familial frontotemporal dementia: A GENFI study

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

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

41. Clinical value of cerebrospinal fluid neurofilament light chain in semantic dementia.

42. A nonsynonymous mutation in PLCG2 reduces the risk of Alzheimer's disease, dementia with Lewy bodies and frontotemporal dementia, and increases the likelihood of longevity.

43. Structural brain splitting is a hallmark of Granulin-related frontotemporal dementia

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

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

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

47. 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

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

50. 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

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