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 Baby Detect : Genomic Newborn Screening NCT05687474 Conditions 3-Hydroxy 3-Methyl Glutaric Aciduria, 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency, 3-Hydroxy-3-Methylglutaryl-CoA Synthase 2 Deficiency, +368 more Locations CRMN, Hôpital La Citadelle — Liège, Wallonia, Belgium View Trial Details
Completed Neurobiology of a Mutation in Glycine Metabolism in Psychotic Disorders NCT01720316 Conditions Amino Acid Metabolism, Inborn Errors, Bipolar Disorder, Bipolar and Related Disorders, +16 more Locations McLean Hospital — Belmont, Massachusetts, United States View Trial Details
Completed Acute Glycine Pharmacodynamic Study NCT01610011 Conditions Amino Acid Metabolism, Inborn Errors, Brain Diseases, Brain Diseases, Metabolic, +13 more Locations McLean Imaging Center, McLean Hospital — Belmont, Massachusetts, United States View Trial Details
