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1. Identifying latent disease factors differently expressed in patient subgroups using group factor analysis

2. Diagnostic accuracy of research criteria for prodromal frontotemporal dementia

4. Identifying healthy individuals with Alzheimer’s disease neuroimaging phenotypes in the UK Biobank

5. Network structure and transcriptomic vulnerability shape atrophy in frontotemporal dementia

6. Uncovering spatiotemporal patterns of atrophy in progressive supranuclear palsy using unsupervised machine learning.

7. Temporal order of clinical and biomarker changes in familial frontotemporal dementia

8. Inflammatory plasma profile in genetic symptomatic and presymptomatic Frontotemporal Dementia − A GENFI study

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

12. Altered plasma protein profiles in genetic FTD – a GENFI study

15. MAPT H2 haplotype and risk of Pick's disease in the Pick's disease International Consortium: a genetic association study

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

18. Language impairment in the genetic forms of behavioural variant frontotemporal dementia

19. Loss of brainstem white matter predicts onset and motor neuron symptoms in C9orf72 expansion carriers: a GENFI study

20. Motor symptoms in genetic frontotemporal dementia: developing a new module for clinical rating scales

21. Evidence and implications of abnormal predictive coding in dementia

22. Separating vascular and neuronal effects of age on fMRI BOLD signals

23. Plasma Neurofilament Light for Prediction of Disease Progression in Familial Frontotemporal Lobar Degeneration

24. Gene Expression Imputation Across Multiple Tissue Types Provides Insight Into the Genetic Architecture of Frontotemporal Dementia and Its Clinical Subtypes

27. Pathogenic Huntingtin Repeat Expansions in Patients with Frontotemporal Dementia and Amyotrophic Lateral Sclerosis

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

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

32. Age at symptom onset and death and disease duration in genetic frontotemporal dementia: an international retrospective cohort study.

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

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

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

37. Dementia

39. Anomia is present pre-symptomatically in frontotemporal dementia due to MAPT mutations

42. Locus coeruleus imaging as a biomarker for noradrenergic dysfunction in neurodegenerative diseases.

43. How to apply the movement disorder society criteria for diagnosis of progressive supranuclear palsy.

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

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

49. Differential impairment of cerebrospinal fluid synaptic biomarkers in the genetic forms of frontotemporal dementia

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