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

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

5. Genome sequencing analysis identifies new loci associated with Lewy body dementia and provides insights into its genetic architecture

6. Clear cell meningiomas are defined by a highly distinct DNA methylation profile and mutations in SMARCE1

10. The Boston criteria version 2.0 for cerebral amyloid angiopathy: a multicentre, retrospective, MRI–neuropathology diagnostic accuracy study

13. Prion protein monoclonal antibody (PRN100) therapy for Creutzfeldt–Jakob disease: evaluation of a first-in-human treatment programme

14. Single-cell somatic copy number variants in brain using different amplification methods and reference genomes.

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

17. Tau filaments with the Alzheimer fold in cases with MAPT mutations V337M and R406W

21. Genetic determinants of survival in progressive supranuclear palsy: a genome-wide association study

22. Cleaved TMEM106B forms amyloid aggregates in central and peripheral nervous systems

23. Genetic, transcriptomic, histological, and biochemical analysis of progressive supranuclear palsy implicates glial activation and novel risk genes

25. Nerve biopsy in T-cell lymphoma with neurolymphomatosis: where and when.

26. Pathology of neurodegenerative disease for the general neurologist.

27. Identification of novel risk loci and causal insights for sporadic Creutzfeldt-Jakob disease: a genome-wide association study

28. Potential human transmission of amyloid β pathology: surveillance and risks

30. Large-scale visualisation of α-synuclein oligomers in Parkinson's disease brain tissue

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

32. Letter to the editor on: Hornerin deposits in neuronal intranuclear inclusion disease: direct identification of proteins with compositionally biased regions in inclusions by Park et al. (2022)

33. Sarcoma classification by DNA methylation profiling

34. The white matter is a pro-differentiative niche for glioblastoma

38. Fulminant corticobasal degeneration: a distinct variant with predominant neuronal tau aggregates

39. Isomorphic diffuse glioma is a morphologically and molecularly distinct tumour entity with recurrent gene fusions of MYBL1 or MYB and a benign disease course

47. Biallelic expansion of an intronic repeat in RFC1 is a common cause of late-onset ataxia

48. Disease-related patterns of in vivo pathology in Corticobasal syndrome

49. Single-cell somatic copy number variants in brain using different amplification methods and reference genomes

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