PSORIASIS AND PSORIATIC ARTHRITIS RESEARCH REGISTRY

该子项目是利用NIH/NCRR资助的中心赠款提供的资源的许多研究子项目之一。子项目和研究者（PI）可能从另一个NIH来源获得了主要资金，因此可以在其他CRISP条目中表示。所列机构为中心，不一定是研究者所在机构。研究者希望建立一个银屑病和银屑病关节炎患者的登记系统。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顾性数据（标准护理实验室结果和X射线，以及问卷）以及体格检查。将收集一些血液用于储存。每年将进行2-4次会面。患者（>18岁）将在HJD登记，并通过私人医生的连续转诊。计划招收100人。

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.