Pilot Study For Hypothermia Treatment In Hyperammonemic Encephalopathy In Neonates And Very Young Infants
Condition(s):Urea Cycle Disorders; Organic AcidemiasLast Updated:June 1, 2015Completed
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Condition(s):Urea Cycle Disorders; Organic AcidemiasLast Updated:June 1, 2015Completed
Condition(s):Hepatic Encephalopathy; Urea Cycle DisordersLast Updated:January 16, 2017Completed
Condition(s):Argininosuccinic Aciduria; Argininosuccinate Lyase Deficiency; Urea Cycle DisordersLast Updated:January 18, 2020Completed
Condition(s):Urea Cycle Disorder; Crigler-Najjar Syndrome; Acute on Chronic Liver FailureLast Updated:February 14, 2024Enrolling by invitation
Condition(s):Ornithine Transcarbamylase Deficiency; Ornithine Transcarbamylase Deficiency Disease; Ornithine Carbamoyltransferase Deficiency (Disorder); Urea Cycle Disorders, InbornLast Updated:February 13, 2024Not yet recruiting
Condition(s):Inborn Errors of Metabolism; Propionic Aciduria; Methylmalonic Aciduria; Urea Cycle DisorderLast Updated:March 1, 2024Completed
Condition(s):Amino Acid Metabolism, Inborn ErrorsLast Updated:June 24, 2005Completed
Condition(s):Urea Cycle Disorders, Inborn; Inborn Errors of Metabolism; Propionic Acidemia; Methylmalonic Acidemia; Carbamyl Phosphate Synthetase DeficiencyLast Updated:May 29, 2014Withdrawn
Condition(s):Inborn Errors of Metabolism; Urea Cycle Disorder; Maple Syrup Urine Disease; Phenylketonurias; Methylmalonicacidemia; OTC Deficiency; Aminoacidopathy; Patient Reported Outcome MeasurementsLast Updated:November 4, 2020Completed
Condition(s):Urea Cycle Disorder; Organic Acidemia; Maple Syrup Urine Disease; Glutaric Acidemia I; Fatty Acid Oxidation Disorder; Hypoxic-Ischemic EncephalopathyLast Updated:February 7, 2024Recruiting
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