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「"Cheung SW "[Author]」の検索結果

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Tinnitus Neuroimaging.

Orthokeratology with increased compression factor (OKIC): study design and preliminary results.

Parental somatic mosaicism for CNV deletions - A need for more sensitive and precise detection methods in clinical diagnostics settings.

Smell and taste symptom-based predictive model for COVID-19 diagnosis.

Global resting-state functional connectivity of neural oscillations in tinnitus with and without hearing loss.

Higher-Order Aberrations and Axial Elongation in Myopic Children Treated With Orthokeratology.

Corticostriatal functional connectivity of bothersome tinnitus in single-sided deafness.

Cross-modal plasticity in adult single-sided deafness revealed by alpha band resting-state functional connectivity.

Refractive and corneal responses of young myopic children to short-term orthokeratology treatment with different compression factors.

Genome Sequencing Explores Complexity of Chromosomal Abnormalities in Recurrent Miscarriage.

Phase I trial of caudate deep brain stimulation for treatment-resistant tinnitus.

Xq22 deletions and correlation with distinct neurological disease traits in females: further evidence for a contiguous gene syndrome.

Low-pass genome sequencing versus chromosomal microarray analysis: implementation in prenatal diagnosis.

Weekly Changes in Axial Length and Choroidal Thickness in Children During and Following Orthokeratology Treatment With Different Compression Factors.

The influence of orthokeratology compression factor on ocular higher-order aberrations.

Residual Tumor Volume and Location Predict Progression After Primary Subtotal Resection of Sporadic Vestibular Schwannomas: A Retrospective Volumetric Study.

Repeatability of choroidal thickness measurements with Spectralis OCT images.

Copy number variant and runs of homozygosity detection by microarrays enabled more precise molecular diagnoses in 11,020 clinical exome cases.

Cortical-Basal Ganglia-Cerebellar Networks in Unilateral Vocal Fold Paralysis: A Pilot Study.

Interchromosomal template-switching as a novel molecular mechanism for imprinting perturbations associated with Temple syndrome.

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