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小児がん患者 拠点病院への集約 十分に進まず (NHK)

子どもが亡くなる病気で最も多い小児がんについて、国は、適切な医療や支援を受けられるようにしようと、全国15か所にある拠点病院への患者の集約を進めていますが、国立...

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「"Cheung SW "[Author]」の検索結果

457件中 1件~20件表示    検索結果をPubMedで見る PubMedで見る

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.

Human caudate nucleus subdivisions in tinnitus modulation.

Role of corneal biomechanical properties in predicting of speed of myopic progression in children wearing orthokeratology lenses or single-vision spectacles.

Correction: A new microdeletion syndrome involving TBC1D24, ATP6V0C, and PDPK1 causes epilepsy, microcephaly, and developmental delay.

Cortical networks for speech motor control in unilateral vocal fold paralysis.

Phenotypic association of 15q11.2 CNVs of the region of breakpoints 1-2 (BP1-BP2) in a large cohort of samples referred for genetic diagnosis.

Functional and Structural Brain Plasticity in Adult Onset Single-Sided Deafness.

Vocal motor control and central auditory impairments in unilateral vocal fold paralysis.

BAFopathies' DNA methylation epi-signatures demonstrate diagnostic utility and functional continuum of Coffin-Siris and Nicolaides-Baraitser syndromes.

Pre-treatment observation of axial elongation for evidence-based selection of children in Hong Kong for myopia control.

A new microdeletion syndrome involving TBC1D24, ATP6V0C, and PDPK1 causes epilepsy, microcephaly, and developmental delay.

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