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UnknownTowards an explanation for 'unexplained' dizziness in older people.
Not available
S-EPMC11223895 | biostudies-literature
UnknownAn fMRI study of visuo-vestibular interactions following vestibular neuritis.
Not available
S-EPMC6197146 | biostudies-literature
UnknownActivity or connectivity? A randomized controlled feasibility study evaluating neurofeedback training in Huntington's disease.
Not available
S-EPMC7425518 | biostudies-literature
UnknownDe novo variants in CNOT3 cause a variable neurodevelopmental disorder.
Not available
S-EPMC6871531 | biostudies-literature
UnknownClinical and molecular consequences of disease-associated de novo mutations in SATB2.
Not available
S-EPMC5548934 | biostudies-literature
UnknownCTCF variants in 39 individuals with a variable neurodevelopmental disorder broaden the mutational and clinical spectrum.
Not available
S-EPMC6892744 | biostudies-literature
UnknownUse of genome sequencing to hunt for cryptic second-hit variants: analysis of 31 cases recruited to the 100 000 Genomes Project.
Not available
S-EPMC10715503 | biostudies-literature
UnknownPublic health utility of cause of death data: applying empirical algorithms to improve data quality.
Not available
S-EPMC8170729 | biostudies-literature
UnknownEvidence for 28 genetic disorders discovered by combining healthcare and research data.
Not available
S-EPMC7116826 | biostudies-literature
UnknownGenomic Diagnosis of Rare Pediatric Disease in the United Kingdom and Ireland.
Not available
S-EPMC7614484 | biostudies-literature
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