1,226 results on '"Holton, Janice"'
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2. Author Correction: Development and validation of an expanded antibody toolset that captures alpha-synuclein pathological diversity in Lewy body diseases
3. Demographic, clinical, biomarker, and neuropathological correlates of posterior cortical atrophy: an international cohort study and individual participant data meta-analysis
4. Development and validation of an expanded antibody toolset that captures alpha-synuclein pathological diversity in Lewy body diseases
5. The genetic and clinico-pathological profile of early-onset progressive supranuclear palsy.
6. LATE to the PART-y
7. Recommendations of the Global Multiple System Atrophy Research Roadmap Meeting
8. Prominent astrocytic alpha-synuclein pathology with unique post-translational modification signatures unveiled across Lewy body disorders
9. Association of clusterin with the BRI2-derived amyloid molecules ABri and ADan
10. Development of parkinsonism after long-standing cervical dystonia – A cohort
11. Genetic determinants of survival in progressive supranuclear palsy: a genome-wide association study
12. Results of an open label feasibility study of sodium valproate in people with McArdle disease
13. Demographic, clinical, biomarker, and neuropathological correlates of posterior cortical atrophy: an international cohort study and individual participant data meta-analysis
14. A genome-wide association study in multiple system atrophy
15. Fulminant corticobasal degeneration: a distinct variant with predominant neuronal tau aggregates
16. Early presentation of urinary retention in multiple system atrophy: can the disease begin in the sacral spinal cord?
17. White matter DNA methylation profiling reveals deregulation of HIP1, LMAN2, MOBP, and other loci in multiple system atrophy
18. Assembly of α-synuclein and neurodegeneration in the central nervous system of heterozygous M83 mice following the peripheral administration of α-synuclein seeds
19. Genetic and phenotypic characterisation of inherited myopathies in a tertiary neuromuscular centre
20. Heritability and genetic variance of dementia with Lewy bodies
21. Antibody-Mediated Muscle Disease?
22. A Treatable Systemic Muscle Disease
23. A Blood Vessel Disease Causing Weakness
24. A Common Cause of Progressive Proximal Weakness…
25. Atypical Phenotype, MRI and Histology
26. Typical Phenotype, MRI and Histology
27. Investigating the genetic architecture of dementia with Lewy bodies: a two-stage genome-wide association study
28. Expanding the molecular and phenotypic spectrum of truncating MT-ATP6 mutations
29. FUS pathology defines the majority of tau- and TDP-43-negative frontotemporal lobar degeneration.
30. When the Wind Comes Back
31. and the Other Common Cause
32. A multimodal computational pipeline for 3D histology of the human brain
33. Transcriptional profiling of multiple system atrophy cerebellar tissue highlights differences between the parkinsonian and cerebellar sub-types of the disease
34. Epigenomics and transcriptomics analyses of multiple system atrophy brain tissue supports a role for inflammatory processes in disease pathogenesis
35. Analysis of neurodegenerative disease-causing genes in dementia with Lewy bodies
36. A Decamer Duplication in the 3 ′ Region of the BRI Gene Originates an Amyloid Peptide that Is Associated with Dementia in a Danish Kindred
37. Disease-related patterns of in vivo pathology in Corticobasal syndrome
38. Clinical phenotype and genetic associations in autosomal dominant familial Alzheimer’s disease: a case series
39. CAV3 mutations causing exercise intolerance, myalgia and rhabdomyolysis: Expanding the phenotypic spectrum of caveolinopathies
40. Cryptic Amyloidogenic Elements in the 3′ UTRs of Neurofilament Genes Trigger Axonal Neuropathy
41. Loss of VPS13C Function in Autosomal-Recessive Parkinsonism Causes Mitochondrial Dysfunction and Increases PINK1/Parkin-Dependent Mitophagy
42. Idiopathic inflammatory myopathy: Interrater variability in muscle biopsy reading
43. Neuroaxonal Dystrophy/Neurodegeneration with Brain Iron Accumulation
44. Investigation of somatic CNVs in brains of synucleinopathy cases using targeted SNCA analysis and single cell sequencing
45. Luminescent conjugated oligothiophenes distinguish between α-synuclein assemblies of Parkinson’s disease and multiple system atrophy
46. Silver staining (Campbell-Switzer) of neuronal α-synuclein assemblies induced by multiple system atrophy and Parkinson’s disease brain extracts in transgenic mice
47. Cerebral mitochondrial electron transport chain dysfunction in multiple system atrophy and Parkinson’s disease
48. Alzheimer's disease pathology concomitant with memory impairment in late‐onset multiple system atrophy
49. C9orf72 expansions in frontotemporal dementia and amyotrophic lateral sclerosis
50. 205th ENMC International Workshop: Pathology diagnosis of idiopathic inflammatory myopathies Part II 28–30 March 2014, Naarden, The Netherlands
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