Disease: Fragile X-associated tremor/ataxia syndrome
- <em>Drosophila melanogaster</em> as a Model to Study Fragile X-Associated Disorders
- <em>FMR1</em> Disorders
- A Case of Fragile-X-Associated Tremor/Ataxia Syndrome Without Tremor
- A Longitudinal Study of Executive Function in Daily Life in Male Fragile X Premutation Carriers and Association with FXTAS Conversion
- A postmortem MRI study of cerebrovascular disease and iron content at end-stage of fragile X-associated tremor/ataxia syndrome
- A Postmortem MRI Study of Cerebrovascular Disease and Iron Content at End-Stage of Fragile X-Associated Tremor/Ataxia Syndrome
- AAGGG repeat expansions trigger RFC1-independent synaptic dysregulation in human CANVAS Neurons
- Advances on the Mechanisms and Therapeutic Strategies in Non-coding CGG Repeat Expansion Diseases
- An Update on the Adult-Onset Hereditary Cerebellar Ataxias: Novel Genetic Causes and New Diagnostic Approaches
- Apolipoproteine and KLOTHO Gene Variants Do Not Affect the Penetrance of Fragile X-Associated Tremor/Ataxia Syndrome
- Atypical vocal quality in women with the FMR1 premutation: an indicator of impaired sensorimotor control
- Between Order and Chaos: Understanding the Mechanism and Pathology of RAN Translation
- Blood Proteome Profiling Reveals Biomarkers and Pathway Alterations in Fragile X PM at Risk for Developing FXTAS
- Brain Metabolomics in Fragile X-Associated Tremor/Ataxia Syndrome (FXTAS)
- Case Series: Vestibular Migraines in Fragile X Premutation Carriers
- Clinical implications of somatic allele expansion in female FMR1 premutation carriers
- Digital gait markers to potentially distinguish fragile X-associated tremor/ataxia syndrome, Parkinson's disease, and essential tremor
- Dissecting the roles of EIF4G homologs reveals DAP5 as a modifier of CGG repeat-associated toxicity in a Drosophila model of FXTAS
- Editorial: Genotype-phenotype correlations in neurodegenerative diseases: From clinical features to neuroimaging signatures
- Enlarged perivascular spaces and their association with motor, cognition, MRI markers and cerebrovascular risk factors in male fragile X premutation carriers
- Evaluation of AQP4 functional variants and its association with fragile X-associated tremor/ataxia syndrome
- Exploration of SUMO2/3 Expression Levels and Autophagy Process in Fragile X-Associated Tremor/Ataxia Syndrome: Addressing Study Limitations and Insights for Future Research
- FMR1 Carriers Report Executive Function Changes Prior to Fragile X-Associated Tremor/Ataxia Syndrome: A Longitudinal Study
- Fragile X Syndrome and FMR1 premutation: results from a survey on associated conditions and treatment priorities in Italy
- Fragile X-Associated Neuropsychiatric Disorders (FXAND) in Young Fragile X Premutation Carriers
- Fragile X-associated tremor/ataxia syndrome treated with multitarget deep brain stimulation
- FXTAS Neuropathology Includes Widespread Reactive Astrogliosis and White Matter Specific Astrocyte Degeneration
- Glial dysregulation in the human brain in fragile X-associated tremor/ataxia syndrome
- I<sup>123</sup>-FP-CIT (DaTSCAN) SPECT beyond the Most Common Causes of Parkinsonism: A Systematic Review
- Insight and Recommendations for Fragile X-Premutation-Associated Conditions from the Fifth International Conference on <em>FMR1</em> Premutation
- Managing tremor in fragile X-associated tremor/ataxia syndrome with botulinum neurotoxin: report of a success
- Mimics or Multiplicity: 2 Cases of Rare Neurological Conditions Discovered Following Presentation with Richardson's Syndrome Phenotype
- Mitochondrial dysfunction in brain tissues and Extracellular Vesicles Fragile X-associated tremor/ataxia syndrome
- Mitochondrial dysfunction in Fragile X syndrome and Fragile X-associated tremor/ataxia syndrome: prospect use of antioxidants and mitochondrial nutrients
- Mouse models of fragile X-related disorders
- Neurodegeneration of White and Gray Matter in the Hippocampus with FXTAS
- Open-Label Sulforaphane Trial in FMR1 Premutation Carriers with Fragile-X-Associated Tremor and Ataxia Syndrome (FXTAS)
- Potential Prodromal Digital Postural Sway Markers for Fragile X-Associated Tremor/Ataxia Syndrome (FXTAS) Detected via Dual-Tasking and Sensory Manipulation
- Prevalence and Characterization of <em>NOTCH2NLC</em> GGC Repeat Expansions in Koreans: From a Hospital Cohort Analysis to a Population-Wide Study
- Psychiatric Manifestations in Early to Middle Stages of Fragile X-Associated Tremor-Ataxia Syndrome (FXTAS)
- Recent advances in CGG repeat diseases and a proposal of fragile X-associated tremor/ataxia syndrome, neuronal intranuclear inclusion disease, and oculophryngodistal myopathy (FNOP) spectrum disorder
- Reversible encephalitis-like episodes in fragile X-associated tremor/ataxia syndrome: a case report
- Ribosomal quality control factors inhibit repeat-associated non-AUG translation from GC-rich repeats
- Ribosomal quality control factors inhibit repeat-associated non-AUG translation from GC-rich repeats
- RNA structure promotes liquid-to-solid phase transition of short RNAs in neuronal dysfunction
- Role of fragile X messenger ribonucleoprotein 1 in the pathophysiology of brain disorders: a glia perspective
- Sensorimotor and inhibitory control in aging <em>FMR1</em> premutation carriers
- Structure and Alternative Splicing of the Antisense FMR1 (ASFMR1) Gene
- The Frequency of Intermediate Alleles in Patients with Cerebellar Phenotypes
- The neuropathological mechanism on guanine-rich repeat expansion diseases
- Trehalose consumption ameliorates pathogenesis in an inducible mouse model of the Fragile X-associated tremor/ataxia syndrome
- Ultra-high-field 7-Tesla magnetic resonance imaging in fragile X tremor/ataxia syndrome (FXTAS)
- Unmethylated Mosaic Full Mutation Males without Fragile X Syndrome
- White matter astrocyte degeneration in FXTAS
- Widening the Phenotype of Fragile-X Tremor Ataxia Syndrome in Females: Spasmodic Dysphonia in Two Patients