Silver diagnosis in neuropathology: principles, practice and revised interpretation
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Summary
Four major silver-staining methods are outlined with respect to their principles, basic protocols and interpretations, thereby providing neuropathologists, technicians and neuroscientists with a common basis for comparing findings and identifying the issues that still need to be clarified.
- Type
- review
- Published
- 2007-03-31
- Cited by
- 195
- References
- 138
- Access
- Open access
- OpenAlex
- https://openalex.org/W2010751802
- Semantic Scholar
- https://api.semanticscholar.org/CorpusID:2871001
Keywords
Pathology, Progressive supranuclear palsy, Corticobasal degeneration, Lesion, Staining
References
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- The Impregnation of Neurofibrils
- Diffuse type of senile plaques in the brains of Alzheimer-type dementia
- The Diagnosis of Alzheimer's Disease
- New temperature modification makes the Bielschowsky silver stain reproducible
- Different conformation of neuronal tau deposits distinguished by double immunofluorescence with AT8 and thiazin red combined with Gallyas method
- Cytological technique : the principles underlying routine methods
- Argyrophilic Grain Disease Is a Sporadic 4‐Repeat Tauopathy
- Neurofibrillary Degeneration in Progressive Supranuclear Palsy and Corticobasal Degeneration
- Absence of Abnormal Hyperphosphorylation of Tau in Intracellular Tangles in Alzheimer's Disease
- Familial tauopathy mimicking corticobasal degeneration an autopsy study on three siblings.
Cited by
- Pale Neurites, Premature α‐Synuclein Aggregates with Centripetal Extension from Axon Collaterals
- Aging African green monkeys manifest transcriptional, pathological, and cognitive hallmarks of human Alzheimer's disease.
- A common antigenic motif recognized by naturally occurring human VH5–51/VL4–1 anti-tau antibodies with distinct functionalities
- Neuropathology of Pick body disease.
- Limbic and Nigral Lewy Bodies and Alzheimer's Disease Pathology Mimicking Progressive Supranuclear Palsy in a 75-Year-Old Man with Preserved Cardiac Uptake of MIBG
- Pretangles and neurofibrillary changes: Similarities and differences between AD and CBD based on molecular and morphological evolution
- Monitoring autophagy in Alzheimer's disease and related neurodegenerative diseases.
- Where, when, and in what form does sporadic Alzheimer's disease begin?
- Combined Treatment of an Amyotrophic Lateral Sclerosis Rat Model with Recombinant GOT1 and Oxaloacetic Acid: A Novel Neuroprotective Treatment
- Expanding morphological dimensions in neuropathology, from sequence biology to pathological sequences and clinical consequences
- Factors patogènics convergents en taupaties
- An 85-Year Old Male with Levodopa-Responsive Parkinsonism Followed by Dementia and Supranuclear Ophthalmoplegia Caused by Alzheimer-Type Pathology without Lewy Bodies
- Technique: Imaging Earliest Tooth Development in 3D Using a Silver‐Based Tissue Contrast Agent
- Propagation of alpha-synuclein pathology: hypotheses, discoveries, and yet unresolved questions from experimental and human brain studies
- Imaging fibres in the brain
- Invited review: Neuropathology of tauopathies: principles and practice
- The preclinical phase of the pathological process underlying sporadic Alzheimer's disease.
- Sporadic four-repeat tauopathy with frontotemporal lobar degeneration, Parkinsonism, and motor neuron disease: a distinct clinicopathological and biochemical disease entity
- Correspondence regarding: selective deposition of 4-repeat tau in cerebral infarcts. J Neuropathol Exp Neurol 2009;68:1029-36.
- Alzheimer-type tau pathology in advanced aged nonhuman primate brains harboring substantial amyloid deposition.
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