DRKS00008910招募中不适用
Elucidating the genetic pathomechanism underlying rare and hereditary kidney diseases
Institut für HumangenetikUniklinik Köln0 个研究点目标入组 3,000 人开始时间: 2016年6月16日最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 发起方
- 入组人数
- 3,000
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
- 18 Years 至 one（—）
- 性别
- All
入选标准
- •Suspected rare or inherited kidney disease
排除标准
- 未提供
研究者
相似试验
招募中
不适用
Investigation of the genetic basis of unexplained monogenic diseasesMonogenic, rare diseasesDRKS00034194Institut für Humangenetik und Genommedizin der Uniklinik RWTH Aachen3,000
已完成
不适用
A study to improve our understanding of the genetic causes of swelling in babies before birthFetal oedema/hydrops with a focus on lymphatic related hydropsPregnancy and ChildbirthConditions involving the integument and temperature regulation of fetus and newbornISRCTN22076461St George’s University Hospitals NHS Foundation Trust60
已完成
不适用
Identification of the genetic pathways involved in patients overreacting to radiotherapyNL-OMON35606MAASTRO clinic6
招募中
不适用
Investigation of the underlying pathomechanisms found in defects of the neurotransmitter, Pterine -, phenyl alanine, and 5-Methyltetrahydrofolate metabolism in induced pluripotent stem cells (iPSC) and derivativesDRKS00010150niversitätsklinikum Heidelberg50
尚未招募
不适用
Molecular, genetic and neuroimaging mechanisms of relapse recovery in multiple sclerosis: exploring the role of brain-derived neurotrophic factorG35Multiple sclerosisDRKS00031011Klinik für Neurologie, Universitätsklinikum Frankfurt200