Sign Up to like & get recommendations! 0
Published in 2020 at "Movement Disorders Clinical Practice"
DOI: 10.1002/mdc3.12942
Abstract: Fragile X–associated tremor/ataxia syndrome (FXTAS) is a late‐onset neurodegenerative disorder associated with premutation alleles (55–200 CGG repeats) of the fragile X mental retardation 1 (FMR1) gene. FXTAS is characterized by the presence of ubiquitin‐positive inclusions… read more here.
Sign Up to like & get recommendations! 1
Published in 2020 at "Movement Disorders Clinical Practice"
DOI: 10.1002/mdc3.13084
Abstract: Fragile X–associated tremor and ataxia syndrome (FXTAS) is a late‐onset neurodegenerative disorder linked to the FMR1 premutation. read more here.
Sign Up to like & get recommendations! 0
Published in 2018 at "Journal of Neurology"
DOI: 10.1007/s00415-018-8823-x
Abstract: BackgroundIn uncommon tremor disorders, clinical efficacy and optimal anatomical targets for deep brain stimulation (DBS) remain inadequately studied and insufficiently quantified.MethodsWe performed a systematic review of PubMed.gov and ClinicalTrials.gov. Relevant articles were identified using the… read more here.
Sign Up to like & get recommendations! 0
Published in 2018 at "Brain Imaging and Behavior"
DOI: 10.1007/s11682-018-9928-7
Abstract: Fragile X-associated tremor ataxia syndrome is an inherited neurodegenerative disorder caused by premutation expansions (55–200 CGG repeats) of the FMR1 gene. There is accumulating evidence to suggest that early cognitive and brain imaging signs may… read more here.
Sign Up to like & get recommendations! 1
Published in 2022 at "Molecular neurobiology"
DOI: 10.1007/s12035-021-02697-z
Abstract: Expansion of CGG trinucleotide repeats in 5' untranslated region of the FMR1 gene is the causative mutation of neurological diseases such as fragile X syndrome (FXS), fragile X-associated tremor/ataxia syndrome (FXTAS), and ovarian disorder such… read more here.
Sign Up to like & get recommendations! 0
Published in 2017 at "Neurotherapeutics"
DOI: 10.1007/s13311-017-0569-0
Abstract: Fragile X-associated tremor/ataxia syndrome (FXTAS) is a progressive neurodegenerative disorder that affects approximately 45% of male and 16% of female carriers of a fragile X mental retardation 1 (FMR1) gene premutation over the age of… read more here.
Sign Up to like & get recommendations! 0
Published in 2020 at "Neurobiology of Disease"
DOI: 10.1016/j.nbd.2020.105013
Abstract: Fragile X associated tremor/ataxia syndrome (FXTAS) is a late-onset neurodegenerative disorder caused by expansion of CGG repeats in the 5' UTR of the fragile X mental retardation 1 (FMR1) gene. Using the well-established FXTAS Drosophila… read more here.
Sign Up to like & get recommendations! 0
Published in 2021 at "Neurobiology of Disease"
DOI: 10.1016/j.nbd.2021.105427
Abstract: CGG expansions between 55 and 200 in the 5'-untranslated region of the fragile-X mental retardation gene (FMR1) increase the risk of developing the late-onset debilitating neuromuscular disease Fragile X-Associated Tremor/Ataxia Syndrome (FXTAS). While the science… read more here.
Sign Up to like & get recommendations! 0
Published in 2020 at "Scientific Reports"
DOI: 10.1038/s41598-020-67946-y
Abstract: Fragile X associated tremor/ataxia syndrome (FXTAS) is a late adult-onset neurodegenerative disorder that affects movement and cognition in male and female carriers of a premutation allele of 55–200 CGG repeats in the Fragile X mental… read more here.
Sign Up to like & get recommendations! 1
Published in 2022 at "Proceedings of the National Academy of Sciences of the United States of America"
DOI: 10.1073/pnas.2118124119
Abstract: Significance Expansion of 55-200 CGG repeats in the 5′ untranslated region of FMR1 predisposes carriers to fragile X–associated tremor/ataxia syndrome (FXTAS), a late-onset neurodegenerative disorder. FXTAS demonstrates incomplete penetrance, which strongly suggests the presence of… read more here.