Neuronal Intranuclear and Neuropil Inclusions for Pathological Assessment of Huntington?s Disease-Reference-Cited by-同舟云学术

Neuronal Intranuclear and Neuropil Inclusions for Pathological Assessment of Huntington?s Disease

Published:2007-01 Issue:1 Volume:17 Page:31-37
ISSN:1015-6305
Container-title:Brain Pathology
language:en
Short-container-title:Brain Pathology

Author:

Maat-Schieman Marion,Roos Raymund,Losekoot Monique,Dorsman Josephine,Welling-Graafland Corrie,Hegeman-Kleinn Ingrid,Broeyer Freerk,Breuning Martijn,van Duinen Sjoerd

Publisher

Wiley

Subject

Neurology (clinical),Pathology and Forensic Medicine,General Neuroscience

Reference51 articles.

1. Trinucleotide repeat expansion in SCA17/TBP in white patients with Huntington's disease-like phenotype

2. Dentatorubral and pallidoluysian atrophy (DRPLA) Clinical and neuropathological findings in genetically confirmed north american and european pedigrees

3. Intranuclear Neuronal Inclusions in Huntington's Disease and Dentatorubral and Pallidoluysian Atrophy: Correlation between the Density of Inclusions andIT15CAG Triplet Repeat Length

4. Stages in the development of Parkinson’s disease-related pathology

5. Behavioral Disorder, Dementia, Ataxia, and Rigidity in a Large Family With TATA Box-Binding Protein Mutation

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3. Early Neurodegeneration in R6/2 Mice Carrying the Huntington’s Disease Mutation with a Super-Expanded CAG Repeat, Despite Normal Lifespan;Journal of Huntington's Disease;2018-02-24

4. Is There Convincing Evidence that Intermediate Repeats in the HTT Gene Cause Huntington’s Disease?;Journal of Huntington's Disease;2015-07-01

5. Pathological Nerve Cell Alterations in Huntington’s Disease (HD) and Their Possible Role for the Demise of Nerve Cells;The Neuropathology of Huntington’s Disease: Classical Findings, Recent Developments and Correlation to Functional Neuroanatomy;2015