Page 1 of Clinical Trials for "Amino Acid Metabolism, Inborn Errors", 132 Total Matches
- 1Active, not recruitingLast Updated: February 15, 2012Condition(s): Argininosuccinic Aciduria; Amino Acid Metabolism, Inborn Errors; Urea Cycle Disorders
- 2RecruitingLast Updated: June 23, 2005Condition(s): Amino Acid Metabolism, Inborn Errors
- 3RecruitingLast Updated: February 8, 2012Condition(s): Brain Diseases, Metabolic, Inborn; Amino Acid Metabolism, Inborn Errors; Urea Cycle Disorders
- 4CompletedLast Updated: June 23, 2005Condition(s): Amino Acid Metabolism, Inborn Errors
- 5SuspendedLast Updated: October 31, 2011Condition(s): Amino Acid Metabolism, Inborn Errors
- 6Active, not recruitingLast Updated: January 24, 2012Condition(s): Inherited Metabolic Disorder of Nervous System; Amino Acid Metabolism, Inherited Disorders
- 7Not yet recruitingLast Updated: May 11, 2012Condition(s): Propionic Acidemia (PA); Methylmalonic Acidemia (MMA)
- 8Not yet recruitingLast Updated: July 14, 2011Condition(s): Aromatic Amino Acid Decarboxylase Deficiency
- 9RecruitingLast Updated: February 7, 2011Condition(s): Malonic Aciduria; Methylmalonic Acidemia
- 10CompletedLast Updated: August 27, 2009Condition(s): Succinic Semialdehyde; Dehydrogenase Deficiency; Diseases
- 11CompletedLast Updated: October 20, 2010Condition(s): Succinic Semialdehyde Dehydrogenase Deficiency; SSADH Deficiency
- 12RecruitingLast Updated: March 20, 2012Condition(s): Amino Acid Metabolism; Inborn Errors
- 13RecruitingLast Updated: December 6, 2011Condition(s): Urea Cycle Disorders, Inborn; Inborn Errors of Metabolism; Propionic Acidemia; Methylmalonic Acidemia; Carbamyl Phosphate Synthetase Deficiency
- 14Not yet recruitingLast Updated: May 14, 2012Condition(s): Propionic Acidemia (PA); Methylmalonic Acidemia (MMA); Late-onset CPS1 Deficiency (CPSD); Late-onset Ornithine Transcarbamylase Deficiency (OTCD)
- 15CompletedLast Updated: April 12, 2006Condition(s): Phenylketonuria
- 16CompletedLast Updated: June 24, 2010Condition(s): Pompe Disease (Late-onset); Glycogen Storage Disease Type II (GSD-II); Acid Maltase Deficiency Disease; Glycogenosis 2
- 17Active, not recruitingLast Updated: April 19, 2007Condition(s): Phenylketonuria; Galactosemia; Inborn Errors of Metabolism
- 18RecruitingLast Updated: February 20, 2012Condition(s): Hyperhomocysteinemia
- 19CompletedLast Updated: July 14, 2009Condition(s): Urea Cycle Disorders
- 20RecruitingLast Updated: March 10, 2009Condition(s): Phenylketonuria
Clinical Trials content is provided directly by the U.S. National Institutes of Health via ClinicalTrials.gov and is not reviewed separately by ClinicalTrialsFeeds.org. Every page of specific clinical trials information contains a unique identifier which can be used to find further details directly from the National Institutes of Health.
The URL of this page is: http://clinicaltrialsfeeds.org/clinical-trials/results/?cond=%22Amino+Acid+Metabolism%2C+Inborn+Errors%22
