Not applicableStudy completedNCT06850519What this trial is testingGenetic Risk Factors of the Sneddon SyndromeWho this might be right forSneddon Syndrome Karl Landsteiner University of Health Sciences 40
Not applicableLooking for participantsNCT06935578What this trial is testingRAre, But Not aLone: a Large Italian Network to Empower the Impervious diaGNostic Pathway of Rare cerEbrovascular Diseases (ALIGNED)Who this might be right forCADASILCADASIL (Diagnosis)Moya Moya Disease+5 more Fondazione I.R.C.C.S. Istituto Neurologico Carlo Besta 500
Not applicableLooking for participantsNCT06092346What this trial is testingA Natural History Study Seeks to Understand the Clinical, Genomic, Pharmacological, Laboratory, and Dietary Determinates of Pyrimidine and Purine Metabolism DisordersWho this might be right forAMPD3, OMIM*102772, AMP Deaminase DeficiencyAK1, OMIM *103000, Adenylate Kinase DeficiencyAMPD1, OMIM *102770, Myopathy Due to Myoadenylate Deaminase Deficiency+25 more National Human Genome Research Institute (NHGRI)
Not applicableUnknownNCT01952275What this trial is testingObservational Study of the Genetic Architecture of Neutrophil-Mediated Inflammatory Skin DiseasesWho this might be right forOther Specified Inflammatory Disorders of Skin or Subcutaneous TissuePyoderma GangrenosumErosive Pustular Dermatosis of the Scalp+25 more University of Zurich 600