PSORIASIS AND PSORIATIC ARTHRITIS RESEARCH REGISTRY

这个子项目是利用由NIH/NCRR资助的中心拨款提供的资源的许多研究子项目之一。子项目和调查员(PI)可能从另一个NIH来源获得了主要资金，因此可能会出现在其他CRISE条目中。列出的机构是针对中心的，而不一定是针对调查员的机构。研究人员希望建立牛皮癣和牛皮癣关节炎患者的登记。参与者将被要求签署知情同意书，这将允许收集前瞻性和回溯性的数据(护理标准实验室结果和X光，以及问卷)和体检。一些血液将被收集起来储存。相遇将每年进行2-4次。患者(&gt；18岁)将在HJD登记，并由私人医生以连续方式转介。计划招收100名学生。

This subproject is one of many research subprojects utilizing the resources provided by a Center grant funded by NIH/NCRR. The subproject and investigator (PI) may have received primary funding from another NIH source, and thus could be represented in other CRISP entries. The institution listed is for the Center, which is not necessarily the institution for the investigator. The investigators wish to establish a registry of patients with psoriasis and psoriatic arthritis. Participants will be asked to sign informed consent, which will allow the collection of data (standard of care lab results and X-rays, as well as a questionnaire) both prospective and retrospective in nature and a physical exam. Some blood will be collected for storage. Encounters will be made 2-4 times a year. Patients (>18 years of age) will be enrolled at HJD and by referral from private doctors in serial fashion. Enrollment of 100 is planned.