JPRN-UMIN000019614已完成未知
Research on the pathogenesis of autosomal dominant polycystic kidney disease - ADPKD-Hokkaido-1
适应症
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 入组人数
- 255
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Observational
入排标准
- 年龄范围
- 20years-old 至 ot applicable（—）
- 性别
- All
入选标准
- 未提供
排除标准
- •Patients who meet the following criterion if blood and/or urine samples will be collected: - Patients who, in the opinion of the investigator, are inappropriate for the study
研究者
相似试验
已完成
不适用
Molecular epidemiologie of autosomal dominant polycystic kidney (ADPKD)Q61.2Polycystic kidney, autosomal dominantautosomal dominant polycystic kidney diseaseDRKS00000064niversitätsklinikum Freiburg2,000
已完成
不适用
Molecular and therapeutic apploaches of autosomal recessive familial Alzheimer's disease using APPE693dlta-iPS cells.Familial Alzheimer's disease(APP E693delta).JPRN-UMIN000017836Kawasaki Medical School1
已完成
不适用
Study of the genetic causes of disorders of the aorta, arteries and cardiac valvesaortic dilatationheart valve malformation100822061000751010002363NL-OMON39758niversitair Medisch Centrum Sint Radboud500
尚未招募
不适用
Study on genetic factors in the pathogenesis of Inflammatory Bowel Disease: Gathering a matched control populatioCrohns disease1001796910003816Ulcerative ColitisNL-OMON30241Academisch Medisch Centrum3,000
招募中
不适用
Clinical and molecular genetic aspects of idiopathic epilepsiesseizures1002929910039911epilepsyNL-OMON35523Epilepsiecentrum Kempenhaeghe300