Pages that link to "Q36927093"

The following pages link to Size bias of fragile X premutation alleles in late-onset movement disorders. (Q36927093):

Displaying 46 items.

• Advances in the treatment of fragile X syndrome (Q24632814) (← links)
• Mapping of an origin of DNA replication in the promoter of fragile X gene FMR1 (Q24683661) (← links)
• RNA-mediated neurodegeneration in fragile X-associated tremor/ataxia syndrome (Q26992035) (← links)
• Molecular Correlates and Recent Advancements in the Diagnosis and Screening of FMR1-Related Disorders (Q28077980) (← links)
• A review of fragile X premutation disorders: expanding the psychiatric perspective (Q33440958) (← links)
• Fragile X-associated tremor/ataxia syndrome: clinical phenotype, diagnosis, and treatment (Q33477846) (← links)
• Evidence for RNA-mediated toxicity in the fragile X-associated tremor/ataxia syndrome (Q33649463) (← links)
• Lifetime prevalence of mood and anxiety disorders in fragile X premutation carriers (Q33684243) (← links)
• FMR1 CGG allele size and prevalence ascertained through newborn screening in the United States (Q33781086) (← links)
• The primary cognitive deficit among males with fragile X-associated tremor/ataxia syndrome (FXTAS) is a dysexecutive syndrome. (Q33901895) (← links)
• Small CGG repeat expansion alleles of FMR1 gene are associated with parkinsonism (Q33924503) (← links)
• Molecular Mechanisms of Fragile X Syndrome: A Twenty-Year Perspective (Q34226308) (← links)
• The fragile X-associated tremor ataxia syndrome (FXTAS) in Indonesia (Q34262287) (← links)
• Relationships between age and epi-genotype of the FMR1 exon 1/intron 1 boundary are consistent with non-random X-chromosome inactivation in FM individuals, with the selection for the unmethylated state being most significant between birth and pubert (Q34544358) (← links)
• FMR1 CGG repeat length predicts motor dysfunction in premutation carriers. (Q34721602) (← links)
• CGG-repeat length threshold for FMR1 RNA pathogenesis in a cellular model for FXTAS (Q34955465) (← links)
• The FMR1 gene and fragile X-associated tremor/ataxia syndrome (Q35061671) (← links)
• Microsatellite repeat instability and neurological disease (Q35064141) (← links)
• The fragile x mental retardation syndrome 20 years after the FMR1 gene discovery: an expanding universe of knowledge (Q35170163) (← links)
• Clinical utility gene card for: fragile X mental retardation syndrome, fragile X-associated tremor/ataxia syndrome and fragile X-associated primary ovarian insufficiency (Q35230078) (← links)
• Capturing the fragile X premutation phenotypes: a collaborative effort across multiple cohorts (Q35809701) (← links)
• Molecular basis of genetic neuropsychiatric disorders (Q36846974) (← links)
• Detection of early FXTAS motor symptoms using the CATSYS computerised neuromotor test battery (Q36966647) (← links)
• CGG-repeat length and neuropathological and molecular correlates in a mouse model for fragile X-associated tremor/ataxia syndrome. (Q37021134) (← links)
• The fragile X continuum: new advances and perspectives (Q37150380) (← links)
• Screening for expanded alleles of the FMR1 gene in blood spots from newborn males in a Spanish population (Q37261871) (← links)
• Towards a Better Molecular Diagnosis of FMR1-Related Disorders-A Multiyear Experience from a Reference Lab. (Q37296765) (← links)
• The fragile X prevalence paradox (Q37310009) (← links)
• RNA-mediated pathogenesis in fragile X-associated disorders (Q37399680) (← links)
• The fragile x-associated tremor and ataxia syndrome (FXTAS) (Q37806971) (← links)
• Human Inducible Pluripotent Stem Cells and Autism Spectrum Disorder: Emerging Technologies (Q38596601) (← links)
• Fragile X-Associated Tremor/Ataxia Syndrome (FXTAS) Motor Dysfunction Modeled in Mice (Q38851924) (← links)
• A genetic study of the FMR1 gene in a Sardinian multiple sclerosis population (Q40715457) (← links)
• Clinical significance of tri-nucleotide repeats in Fragile X testing: a clarification of American College of Medical Genetics guidelines (Q42751272) (← links)
• Fragile X-associated tremor/ataxia syndrome--an older face of the fragile X gene (Q43517185) (← links)
• FMR1 premutation carrier frequency in patients undergoing routine population-based carrier screening: insights into the prevalence of fragile X syndrome, fragile X-associated tremor/ataxia syndrome, and fragile X-associated primary ovarian insuffici (Q44165815) (← links)
• Recommendations from multi-disciplinary focus groups on cascade testing and genetic counseling for fragile X-associated disorders (Q46702599) (← links)
• MRI and SPECT of midbrain and striatal degeneration in fragile X-associated tremor/ataxia syndrome (Q46849839) (← links)
• Genetics of tremor (Q50073947) (← links)
• Fragile-X syndrome and fragile X-associated tremor/ataxia syndrome: two faces of FMR1. (Q50277634) (← links)
• Women who carry a fragile X premutation are biologically older than noncarriers as measured by telomere length. (Q53799975) (← links)
• Fragiles X-assoziiertes Tremor-/Ataxie-Syndrom (Q56971626) (← links)
• Static and dynamic postural control deficits in aging fragile X mental retardation 1 (FMR1) gene premutation carriers (Q61446016) (← links)
• [Fragile X premutation presenting as postural tremor and ataxia (FXTAS syndrome)] (Q79938871) (← links)
• Fragile X syndrome carrier screening in pregnant women in Chinese Han population (Q90999236) (← links)
• Prevalence of fragile X-associated tremor/ataxia syndrome: A survey of essential tremor patients with cerebellar signs or extrapyramidal signs (Q92491945) (← links)