Neuronal intranuclear (hyaline) inclusion disease and fragile X-associated tremor/ataxia syndrome: a morphological and molecular dilemma
Open Access
- 3 July 2017
- journal article
- research article
- Published by Oxford University Press (OUP) in Brain
- Vol. 140 (8), e51
- https://doi.org/10.1093/brain/awx156
Abstract
No abstract availableFunding Information
- European Research Council (RIBOMYLOME_309545)
This publication has 19 references indexed in Scilit:
- Molecular Pathophysiology of Fragile X-Associated Tremor/Ataxia Syndrome and Perspectives for Drug DevelopmentThe Cerebellum, 2016
- A Majority of FXTAS Cases Present with Intranuclear Inclusions Within Purkinje CellsThe Cerebellum, 2016
- Neurocognitive endophenotypes in CGG KI and Fmr1 KO mouse models of Fragile X-Associated disorders: an analysis of the state of the fieldF1000Research, 2013
- Fragile X-associated tremor/ataxia syndrome (FXTAS): pathology and mechanismsActa Neuropathologica, 2013
- Neurodegenerative diseases: Quantitative predictions of protein–RNA interactionsRNA, 2012
- Ubiquilin immunoreactivity in cytoplasmic and nuclear inclusions in synucleinopathies, polyglutamine diseases and intranuclear inclusion body diseaseActa Neuropathologica, 2012
- Fibroblast phenotype in male carriers of FMR1 premutation allelesHuman Molecular Genetics, 2009
- Neuropathology of fragile X-associated tremor/ataxia syndrome (FXTAS)Brain, 2005
- The Fragile-X Premutation: A Maturing PerspectiveAmerican Journal of Human Genetics, 2004
- Adult‐onset neuronal intra nuclear hyaline inclusion diseaseNeurology, 1986