“Genetic”的搜索结果，显示 431-440 项，共有 6561 项

1. 神经科- 临床试验- 妙佑医疗国际

   ... genetic difference can be found in different patient groups. Electrophysiological Biomarkers for Parkinson's Disease. Scottsdale/Phoenix, Ariz. This study ...

2. 放射科- 临床试验- 妙佑医疗国际

   The Parkinson Progression Marker Initiative (PPMI) is a study to assess progression of clinical features, digital outcomes, and imaging, biologic and genetic ...

3. Spinal tumor

   Genetic conditions such as neurofibromatosis type 2 (NF2) and Von Hippel-Lindau disease, which can lead to tumors in the spine or brain. Most people with ...

4. 放射科- 临床试验- 妙佑医疗国际

   The purpose of this study is to determine endothelial gene expression from guidewire biopsy during clinically indicated endovascular procedures. The genetic ...

5. 神经科- 临床试验- 妙佑医疗国际

   The purpose of this study is to create a repository for cerebellar ataxia and nucleotide repeat diseases in order to fully investigate the genetic and ...

6. 神经科- 临床试验- 妙佑医疗国际

   ... genetic markers of Parkinson's disease (PD) progression in study ... The purpose of this study is to create a repository for cerebellar ataxia and nucleotide ...

7. Clinical Trials - 临床试验- 妙佑医疗国际儿童中心

   Monogenic Kidney Stone - Genetic Testing. Rochester, Minn. 90 genes related to Monogenic Stone Disease will be determined via DNA analysis by the Mayo Rare ...

8. 骨科外科- 临床试验- 妙佑医疗国际

   The purpose of this study is to determine unique genetic profile of patients requiring MUA following bilateral pTKA via genetic sequencing, to determine ...

9. 房颤会在家族中遗传吗？ - 妙佑医疗国际

   Ragab AAY, et al. The genetic puzzle of familial atrial fibrillation. Frontiers in Cardiovascular Medicine. 2020; doi:10.3389/fcvm.2020.00014. January CT ...

10. 心血管医学- 临床试验- 妙佑医疗国际

    1. To identify the genetic causes of bicuspid aortic valve disease and its associated thoracic aortic disease. 2. To identify potential pathways to predict the ...