Recruiting Rare Disease Patient Registry & Natural History Study - Coordination of Rare Diseases at Sanford NCT01793168 Conditions 1p36 Deletion Syndrome, 3-Methylglutaconic Aciduria, Type V, 4p Deletion Syndrome, Non-Wolf-Hirschhorn Syndrome, +698 more Locations Sanford Health — Sioux Falls, South Dakota, United States Online Patient Enrollment System — Sydney, Australia View Trial Details
Completed Pegzilarginase in Subjects <24 Months Old With Arginase 1 Deficiency NCT06582524 Conditions Amino Acid Metabolism, Inborn Errors, Arginase 1 Deficiency, Brain Diseases, +11 more Locations Univ. Klinik für Kinder- und Jugendheilkunde Medizinische Universität — Graz, Austria Unidade de Doenças Metabólicas Pediatria, Hospital Santa Maria — Lisbon, Portugal Bradford Royal Infirmary Duckworth Lane — Bradford, United Kingdom View Trial Details
