Lewy body pathology in familial Alzheimer disease: evidence for disease- and mutation-specific pathologic phenotype.
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Summary
It is suggested that there are genetic influences on the presence of LBP in familial AD as demonstrated by the differences between PSEN 1 and PSEN 2 mutation cases.
- Type
- article
- Published
- 2006-03-01
- Cited by
- 136
- References
- 53
- Access
- Open access
- OpenAlex
- https://openalex.org/W2012635225
- Semantic Scholar
- https://api.semanticscholar.org/CorpusID:1387910
Keywords
Pathology, Medicine, Mutation, Biology, Genetics
References
- Regional distribution of alpha-synuclein pathology in unimpaired aging and Alzheimer disease.
- CHARACTERISTICS OF FAMILIAL ALZHEIMER'S DISEASE IN NINE KINDREDS OF VOLGA GERMAN ANCESTRY
- Aggregation of alpha-synuclein in Lewy bodies of sporadic Parkinson's disease and dementia with Lewy bodies.
- Familial alzheimer's disease in american descendants of the volga germans: Probable genetic founder effect
- Amyloid angiopathy in a volga german family with Alzheimer's disease and a presenilin‐2 mutation (N141I)
- Accuracy of the clinical diagnoses of Lewy body disease, Parkinson disease, and dementia with Lewy bodies: a clinicopathologic study.
- Lewy body and Alzheimer pathology in a family with the amyloid-β precursor protein APP717 gene mutation
- Neuropathologic and clinical features of Parkinson's disease in Alzheimer's disease patients
- Parkinson's disease in patients with Alzheimer's disease.
- Lewy Bodies in Alzheimer's Disease: A Neuropathological Review of 145 Cases Using α‐Synuclein Immunohistochemistry
- Amyloid (Aβ) deposition in chromosome 1–linked Alzheimer's disease: The volga german families
- Hippocampal degeneration differentiates diffuse Lewy body disease (DLBD) from Alzheimer's disease
- Sensitivity and specificity of three clinical criteria for dementia with Lewy bodies in an autopsy‐verified sample
- The Lewy-Body Variant of Alzheimer's Disease
- Genetic linkage evidence for a familial Alzheimer's disease locus on chromosome 14.
- Novel antibodies to synuclein show abundant striatal pathology in Lewy body diseases
- A novel presenilin-1 mutation: increased beta-amyloid and neurofibrillary changes.
- α-Synuclein in filamentous inclusions of Lewy bodies from Parkinson’s disease and dementia with Lewy bodies
- Neuropathological stageing of Alzheimer-related changes
- A familial Alzheimer's disease locus on chromosome 1
Cited by
- The 7th Leonard Berg Symposium, Part 3
- Neuropathology of Autosomal Dominant Alzheimer Disease in the National Alzheimer Coordinating Center Database
- Apport de l'analyse multidisciplinaire dans la compréhension des mécanismes physiopathologiques des démences
- Genetic mouse models of neurodegenerative diseases.
- Frequency and Clinicopathological Characteristics of Presenilin 1 Gly206Ala Mutation in Puerto Rican Hispanics with Dementia
- The French Series of Autosomal Dominant Early Onset Alzheimer's Disease Cases: Mutation Spectrum and Cerebrospinal Fluid Biomarkers
- Empiric refinement of the pathologic assessment of Lewy-related pathology in the dementia patient.
- Genetics Underlying Atypical Parkinsonism and Related Neurodegenerative Disorders
- The Genetics and Neuropathology of Alzheimer’s Disease
- A novel PSEN2 mutation associated with a peculiar phenotype
- AUTISM SPECTRUM DISORDERS FOLLOWING IN UTERO EXPOSURE TO ANTIEPILEPTIC DRUGS
- Correlating familial Alzheimer's disease gene mutations with clinical phenotype
- Recent advances in the genetics of dementia with Lewy bodies
- Confluence of α-synuclein, tau, and β-amyloid pathologies in dementia with Lewy bodies.
- INTRAFAMILIAL DIVERSITY OF PHENOTYPE ASSOCIATED WITH APP DUPLICATION
- Leucine-rich repeat kinase 1: a paralog of LRRK2 and a candidate gene for Parkinson’s disease
- Strategizing the Development of Alzheimer’s Therapeutics
- Classification and basic pathology of Alzheimer disease
- The Expanding Role of Genetics in the Lewy Body Diseases: The Glucocerebrosidase Gene
- Alzheimer's disease phenotypes and genotypes associated with mutations in presenilin 2.
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