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【動画】「cough medicine」を説明してみよう (日経BP)

診察室やカンファレンスなどでよく使う医療英語のエッセンスを、今日も楽しく学んでいきましょう。 今日のレッスンも「説明力トレーニング」です。「この薬って何ですか?...

  1. 入学定員減は 医学生の学力低下が背景に?...
  2. 心電図の新たな名著になるかもしれない書籍...
  3. マスクが足りない!医療機関でも深刻な事態...
  4. 新型コロナウイルス対応まっただ中の保健所...

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「"Hernandez DG "[Author]」の検索結果

120件中 1件~20件表示    検索結果をPubMedで見る PubMedで見る

Penetrance of Parkinson's Disease in LRRK2 p.G2019S Carriers Is Modified by a Polygenic Risk Score.

High-resolution inference of genetic relationships among Jewish populations.

Finnish Parkinson's disease study integrating protein-protein interaction network data with exome sequencing analysis.

Genetic modifiers of risk and age at onset in GBA associated Parkinson's disease and Lewy body dementia.

Race-specific alterations in DNA methylation among middle-aged African Americans and Whites with Metabolic Syndrome.

Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies.

Genomewide association study of Parkinson's disease clinical biomarkers in 12 longitudinal patients' cohorts.

Novel age-associated DNA methylation changes and epigenetic age acceleration in middle-aged African Americans and whites.

Blood Leukocyte DNA Methylation Predicts Risk of Future Myocardial Infarction and Coronary Heart Disease.

Genetic risk of Parkinson disease and progression:: An analysis of 13 longitudinal cohorts.

Association of dietary folate and vitamin B-12 intake with genome-wide DNA methylation in blood: a large-scale epigenome-wide association analysis in 5841 individuals.

Parkinson's disease age at onset genome-wide association study: Defining heritability, genetic loci, and α-synuclein mechanisms.

Heritability and genetic variance of dementia with Lewy bodies.

Assessment of APOE in atypical parkinsonism syndromes.

A candidate gene study of risk for dementia in older, post-menopausal women: Results from the Women's Health Initiative Memory Study.

Analysis of repeated leukocyte DNA methylation assessments reveals persistent epigenetic alterations after an incident myocardial infarction.

A paradoxical relationship between family history, onset age, and genetic risk in Parkinson's disease.

A comprehensive screening of copy number variability in dementia with Lewy bodies.

Coding variation in GBA explains the majority of the SYT11-GBA Parkinson's disease GWAS locus.

Frequency of Loss of Function Variants in LRRK2 in Parkinson Disease.

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