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NCT01611467
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, Metabolic Diseases, +5 more
- Locations
-
- Covance Research Unit, Inc Madison, Wisconsin, United States
NCT02939144
- Conditions
- Apparent Mineralocorticoid Excess, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, +5 more
- Locations
-
- The Royal Wolverhampton NHS Trust Wolverhampton, West Midlands, United Kingdom
NCT00759525
- Conditions
- Apparent Mineralocorticoid Excess (AME), Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, +5 more
- Locations
-
- Brigham and Women's Hospital Boston, Massachusetts, United States
NCT00474942
- Conditions
- Apparent Mineralocorticoid Excess Syndrome, Cardiovascular Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, +10 more
- Locations
-
- Mount Sinai School of Medicine New York, United States
- University of Texas Southwestern Medical Center Dallas, Texas, United States
- University of Sao Paulo São Paulo, Brazil
- University of Lyon Lyon, France
Active, Not Recruiting
Early Check: Expanded Screening in Newborns
NCT03655223
- Conditions
- 17 Alpha-Hydroxylase Deficiency, 3-Hydroxy-3-Methylglutaric Aciduria, 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency, +456 more
- Locations
-
- RTI International Research Triangle Park, North Carolina, United States