Published in Case Rep Crit Care on April 10, 2016
Hyperammonemia: What Urea-lly Need to Know: Case Report of Severe Noncirrhotic Hyperammonemic Encephalopathy and Review of the Literature. Case Rep Med (2016) 0.76
Late presentation of fatal hyperammonemic encephalopathy after Roux-en-Y gastric bypass. Proc (Bayl Univ Med Cent) (2017) 0.75
Disorders of carnitine transport and the carnitine cycle. Am J Med Genet C Semin Med Genet (2006) 2.33
Mutations and polymorphisms in the human ornithine transcarbamylase (OTC) gene. Hum Mutat (2006) 1.61
New genetic defects in mitochondrial fatty acid oxidation and carnitine deficiency. Adv Pediatr (1987) 1.43
Hyperammonemia in the ICU. Chest (2007) 1.29
Serum and CSF glutamine levels in valproate-related hyperammonemic encephalopathy. Epilepsia (2002) 1.26
The pathophysiologic basis of hepatic encephalopathy: central role for ammonia and inflammation. Cell Mol Life Sci (2005) 1.25
Hyperammonemic encephalopathy caused by carnitine deficiency. J Gen Intern Med (2007) 1.17
Current concepts in the pathogenesis of urea cycle disorders. Mol Genet Metab (2010) 1.14
Hyperammonemia encephalopathy: an important cause of neurological deterioration following chemotherapy. Leuk Lymphoma (2007) 1.10
Ornithine transcarbamylase deficiency in females: an often overlooked cause of treatable encephalopathy. J Child Neurol (1995) 1.07
Urea-splitting urinary tract infection contributing to hyperammonemic encephalopathy. Nat Clin Pract Urol (2007) 1.04
Adult nonhepatic hyperammonemia: a case report and differential diagnosis. Am J Med (2010) 1.04
Severe hyperammonaemia in adults not explained by liver disease. Ann Clin Biochem (2012) 1.01
Hyperammonemic coma due to parenteral nutrition in a woman with heterozygous ornithine transcarbamylase deficiency. Gastroenterology (1995) 1.00
Zn(II)-induced cooperativity of Escherichia coli ornithine transcarbamoylase. Proc Natl Acad Sci U S A (1982) 0.96
Neonatal hyperammonemia caused by a defect of carnitine-acylcarnitine translocase. J Pediatr (1995) 0.91
Ornithine transcarbamylase deficiency presenting as encephalopathy during adulthood following bariatric surgery. Arch Neurol (2007) 0.90
Hyperammonemic encephalopathy due to essential amino acid hyperalimentation. Arch Intern Med (1984) 0.89
Hyperammonemic encephalopathy complicating bariatric surgery: a case study and review of the literature. Surg Obes Relat Dis (2013) 0.87
Effects of zinc on hepatic ornithine transcarbamylase (OTC) activity. J Trace Elem Electrolytes Health Dis (1993) 0.87
Hyperammonemic syndrome after Roux-en-Y gastric bypass. Obesity (Silver Spring) (2015) 0.86
Minimal hepatic encephalopathy: time to recognise and treat. Trop Gastroenterol (2008) 0.83
Late-onset ornithine transcarbamylase deficiency: treatment and outcome of hyperammonemic crisis. Pediatrics (2014) 0.81
Reasons and operative outcomes after reversal of gastric bypass and jejunoileal bypass. Obes Surg (2012) 0.78
Clinical neurogenetics: neurologic presentations of metabolic disorders. Neurol Clin (2013) 0.77