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Your search for Hypoammonemia AND humans[mesh] AND review[publication type] retrieved no results
Hyperammonemia in review: pathophysiology, diagnosis, and treatment.
Auron A, Brophy PD. Auron A, et al. Pediatr Nephrol. 2012 Feb;27(2):207-22. doi: 10.1007/s00467-011-1838-5. Epub 2011 Mar 23. Pediatr Nephrol. 2012. PMID: 21431427 Review.
A variety of environmental causes and medications may also lead to ammonia toxicity. Hyperammonemia refers to a clinical condition associated with elevated ammonia levels manifested by a variety of symptoms and signs, including significant central nervous system (CNS) abno …
A variety of environmental causes and medications may also lead to ammonia toxicity. Hyperammonemia refers to a clinical condition as …
Hyperammonemia in Inherited Metabolic Diseases.
Ribas GS, Lopes FF, Deon M, Vargas CR. Ribas GS, et al. Cell Mol Neurobiol. 2022 Nov;42(8):2593-2610. doi: 10.1007/s10571-021-01156-6. Epub 2021 Oct 19. Cell Mol Neurobiol. 2022. PMID: 34665389 Review.
Therefore, hyperammonemic patients present potentially life-threatening neuropsychiatric symptoms, whose severity is related with the hyperammonemia magnitude and duration, as well as the brain maturation stage. Inherited metabolic diseases caused by enzymatic defects that …
Therefore, hyperammonemic patients present potentially life-threatening neuropsychiatric symptoms, whose severity is related with the hyp
The Role of RRT in Hyperammonemic Patients.
Gupta S, Fenves AZ, Hootkins R. Gupta S, et al. Clin J Am Soc Nephrol. 2016 Oct 7;11(10):1872-1878. doi: 10.2215/CJN.01320216. Epub 2016 May 19. Clin J Am Soc Nephrol. 2016. PMID: 27197910 Free PMC article. Review.
Hyperammonemia is an important cause of cerebral edema in both adults with liver failure and children with inborn errors of metabolism. ...We review the available literature on the use of continuous venovenous hemofiltration, peritoneal dialysis, and hemodialysis in neonat
Hyperammonemia is an important cause of cerebral edema in both adults with liver failure and children with inborn errors of metabolis
Suggested guidelines for the diagnosis and management of urea cycle disorders: First revision.
Häberle J, Burlina A, Chakrapani A, Dixon M, Karall D, Lindner M, Mandel H, Martinelli D, Pintos-Morell G, Santer R, Skouma A, Servais A, Tal G, Rubio V, Huemer M, Dionisi-Vici C. Häberle J, et al. J Inherit Metab Dis. 2019 Nov;42(6):1192-1230. doi: 10.1002/jimd.12100. Epub 2019 May 15. J Inherit Metab Dis. 2019. PMID: 30982989 Review.
In 2012, we published guidelines summarizing and evaluating late 2011 evidence for diagnosis and therapy of urea cycle disorders (UCDs). With 1:35 000 estimated incidence, UCDs cause hyperammonemia of neonatal (~50%) or late onset that can lead to intellectual disability o …
In 2012, we published guidelines summarizing and evaluating late 2011 evidence for diagnosis and therapy of urea cycle disorders (UCDs). Wit …
Carnitine Inborn Errors of Metabolism.
Almannai M, Alfadhel M, El-Hattab AW. Almannai M, et al. Molecules. 2019 Sep 6;24(18):3251. doi: 10.3390/molecules24183251. Molecules. 2019. PMID: 31500110 Free PMC article. Review.
Sarcopenia and Frailty in Cirrhosis: Assessment and Management.
Bunchorntavakul C. Bunchorntavakul C. Med Clin North Am. 2023 May;107(3):589-604. doi: 10.1016/j.mcna.2022.12.007. Epub 2023 Feb 20. Med Clin North Am. 2023. PMID: 37001955 Review.
The complex pathogenesis of sarcopenia in cirrhosis is mainly determined by hyperammonemia and malnutrition. Sarcopenia/frailty screening and reevaluation should be undertaken in all cirrhotic patients. ...
The complex pathogenesis of sarcopenia in cirrhosis is mainly determined by hyperammonemia and malnutrition. Sarcopenia/frailty scree …
Pathophysiology of hepatic encephalopathy and future treatment options.
González-Regueiro JA, Higuera-de la Tijera MF, Moreno-Alcántar R, Torre A. González-Regueiro JA, et al. Rev Gastroenterol Mex (Engl Ed). 2019 Apr-Jun;84(2):195-203. doi: 10.1016/j.rgmx.2019.02.004. Epub 2019 Apr 20. Rev Gastroenterol Mex (Engl Ed). 2019. PMID: 31014748 Free article. Review. English, Spanish.
Hepatic Encephalopathy.
Wijdicks EF. Wijdicks EF. N Engl J Med. 2016 Oct 27;375(17):1660-1670. doi: 10.1056/NEJMra1600561. N Engl J Med. 2016. PMID: 27783916 Review. No abstract available.
Clinical practice: the management of hyperammonemia.
Häberle J. Häberle J. Eur J Pediatr. 2011 Jan;170(1):21-34. doi: 10.1007/s00431-010-1369-2. Epub 2010 Dec 17. Eur J Pediatr. 2011. PMID: 21165747 Free article. Review.
Hyperammonemia is a life-threatening condition which can affect patients at any age. ...The hepatic urea cycle is the main pathway to detoxify ammonia; it can be defective due to an inherited enzyme deficiency or secondary to accumulated toxic metabolites or substrate depl
Hyperammonemia is a life-threatening condition which can affect patients at any age. ...The hepatic urea cycle is the main pathway to
Current approaches to hepatic encephalopathy.
Vidal-Cevallos P, Chávez-Tapia NC, Uribe M. Vidal-Cevallos P, et al. Ann Hepatol. 2022 Nov-Dec;27(6):100757. doi: 10.1016/j.aohep.2022.100757. Epub 2022 Sep 14. Ann Hepatol. 2022. PMID: 36115576 Free article. Review.
While the pathophysiology of HE is not entirely understood, three critical factors have been identified: hyperammonaemia, systemic inflammation and oxidative stress by glutaminase gene alterations. ...
While the pathophysiology of HE is not entirely understood, three critical factors have been identified: hyperammonaemia, systemic in …
691 results