TCTR20220121007尚未招募不适用
nderstanding the genetic architecture of amyotrophic lateral sclerosis in Thais
Research Administration Section, Faculty of Medicine, Chiang Mai University0 个研究点目标入组 15 人开始时间: 2022年1月21日最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 尚未招募
- 发起方
- 入组人数
- 15
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
- 20 Years 至 N/A (No limit)(—)
- 性别
- All
入选标准
- •Amyotrophic lateral sclerosis patients in category of possible, probable and definite ALS at any stage of disease defined by El Escorial criteria.
排除标准
- •Other types of motor neuron disease or other causes of weakness
研究者
相似试验
已完成
不适用
Molecular pathway analysis of Amyotrophic Lateral Sclerosis by genome-wide expression profiling of human blood and skin fibroblasts.Amyotrophic Lateral Sclerosis (ALS)10029317motor neuron diseaseNL-OMON31437niversitair Medisch Centrum Utrecht2,000
招募中
不适用
Identification of the new biomarkers of amyotrophic lateral sclerosisAmyotrophic lateral sclerosisJPRN-UMIN000013111agoya University Graduate school of Medicine60
招募中
不适用
Elucidating the genetic pathomechanism underlying rare and hereditary kidney diseasesChronic kidney diseaseDRKS00008910Institut für HumangenetikUniklinik Köln3,000
已完成
不适用
Muscle internal mechanics in individuals with generalized joint hypermobility (GJH): a comparison of patients with Hypermobility Spectrum Disorder/ Ehlers-Danlos Syndromes vs dancers vs healthy non-hypermobile control subjects Muscle mechanics in hypermobilityhealthy volunteersQ79.6Ehlers-Danlos syndromeDRKS00027889DLR - Institut für Luft- Und RaumfahrtAbteilung für für Muskel- und Knochenstoffwechsel48
已完成
不适用
Research on the pathogenesis of autosomal dominant polycystic kidney diseaseAutosomal dominant polycystic kidney diseaseJPRN-UMIN000019614Otsuka Pharmaceutical Co., Ltd.255
