Fifteen years of urea cycle disorders brain research: Looking back, looking forward
Urea cycle disorders (UCD) are inherited diseases resulting from deficiency in one of six
enzymes or two carriers that are required to remove ammonia from the body. UCD may be …
enzymes or two carriers that are required to remove ammonia from the body. UCD may be …
Seizure Characteristics and EEG Features in Intoxication Type and Energy Deficiency Neurometabolic Disorders in the Pediatric Intensive Care Unit: Single-Center …
Background Acute metabolic crises in inborn errors of metabolism (such as urea cycle
disorders, organic acidemia, maple syrup urine disease, and mitochondrial disorders) are …
disorders, organic acidemia, maple syrup urine disease, and mitochondrial disorders) are …
Unraveling the Link: Seizure Characteristics and Ammonia Levels in Urea Cycle Disorder During Hyperammonemic Crises
M Chanvanichtrakool, JM Schreiber, WL Chen… - Pediatric Neurology, 2024 - Elsevier
Background This retrospective clinical study performed at a single clinical center aimed to
identify the prevalence of seizures in individuals with urea cycle disorders (UCDs) with and …
identify the prevalence of seizures in individuals with urea cycle disorders (UCDs) with and …