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About 2,310 results

ALLMedicine Hyperammonemia Center

Research & Reviews  1,125 results

Successful Management of Noncirrhotic Hyperammonemia Syndrome after Kidney Transplantat...
https://doi.org/10.1111/tid.13332
Transplant Infectious Disease : an Official Journal of the Transplantation Society; Cheema F, Kutzler HL et. al.

May 19th, 2020 - Noncirrhotic hyperammonemia (NCH) is a rare but often fatal complication of solid organ transplantation. We present a case wherein an infectious cause of NCH was suspected following kidney transplantation (KT) and the patient was promptly started ...

Hyperammonemia syndrome due to Ureaplasma urealyticum in a kidney transplant recipient:...
https://doi.org/10.1111/tid.13328
Transplant Infectious Disease : an Official Journal of the Transplantation Society; Higgins AB, Farmakiotis D et. al.

May 15th, 2020 - Ureaplasma species (spp.) are common colonizers of the urogenital tract but may cause systemic infection in immunocompromised patients. They release significant amounts of ammonia via urea hydrolysis and have been recently implicated in the pathog...

Split AAV-Mediated Gene Therapy Restores Ureagenesis in a Murine Model of Carbamoyl Pho...
https://doi.org/10.1016/j.ymthe.2020.04.011
Molecular Therapy : the Journal of the American Society of Gene Therapy; Nitzahn M, Allegri G et. al.

May 3rd, 2020 - The urea cycle enzyme carbamoyl phosphate synthetase 1 (CPS1) catalyzes the initial step of the urea cycle; bi-allelic mutations typically present with hyperammonemia, vomiting, ataxia, lethargy progressing into coma, and death due to brain edema ...

Mitochondrial carbonic anhydrase VA deficiency in three Indian infants manifesting earl...
https://doi.org/10.1016/j.braindev.2020.04.007
Brain & Development; Konanki R, Akella RRD et. al.

May 3rd, 2020 - Hyperammonemia and hyperlactatemia in neonates and young children with non-specific biochemical markers poses a diagnostic challenge. An accurate diagnosis is essential for effective management. We present three infants from unrelated families, on...

Carbamazepine Toxicity Workup
https://emedicine.medscape.com/article/813654-workup

Apr 28th, 2020 - Laboratory Studies The workup in a patient with suspected carbamazepine poisoning should include appropriate comprehensive serum and urine drug screening, plus analysis of the following: Alcohol level, if alcohol toxicity is suspected. Serum elect...

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Drugs  15 results see all →

Clinicaltrials.gov  1,155 results

Successful Management of Noncirrhotic Hyperammonemia Syndrome after Kidney Transplantat...
https://doi.org/10.1111/tid.13332
Transplant Infectious Disease : an Official Journal of the Transplantation Society; Cheema F, Kutzler HL et. al.

May 19th, 2020 - Noncirrhotic hyperammonemia (NCH) is a rare but often fatal complication of solid organ transplantation. We present a case wherein an infectious cause of NCH was suspected following kidney transplantation (KT) and the patient was promptly started ...

Hyperammonemia syndrome due to Ureaplasma urealyticum in a kidney transplant recipient:...
https://doi.org/10.1111/tid.13328
Transplant Infectious Disease : an Official Journal of the Transplantation Society; Higgins AB, Farmakiotis D et. al.

May 15th, 2020 - Ureaplasma species (spp.) are common colonizers of the urogenital tract but may cause systemic infection in immunocompromised patients. They release significant amounts of ammonia via urea hydrolysis and have been recently implicated in the pathog...

Split AAV-Mediated Gene Therapy Restores Ureagenesis in a Murine Model of Carbamoyl Pho...
https://doi.org/10.1016/j.ymthe.2020.04.011
Molecular Therapy : the Journal of the American Society of Gene Therapy; Nitzahn M, Allegri G et. al.

May 3rd, 2020 - The urea cycle enzyme carbamoyl phosphate synthetase 1 (CPS1) catalyzes the initial step of the urea cycle; bi-allelic mutations typically present with hyperammonemia, vomiting, ataxia, lethargy progressing into coma, and death due to brain edema ...

Mitochondrial carbonic anhydrase VA deficiency in three Indian infants manifesting earl...
https://doi.org/10.1016/j.braindev.2020.04.007
Brain & Development; Konanki R, Akella RRD et. al.

May 3rd, 2020 - Hyperammonemia and hyperlactatemia in neonates and young children with non-specific biochemical markers poses a diagnostic challenge. An accurate diagnosis is essential for effective management. We present three infants from unrelated families, on...

Carbamazepine Toxicity Workup
https://emedicine.medscape.com/article/813654-workup

Apr 28th, 2020 - Laboratory Studies The workup in a patient with suspected carbamazepine poisoning should include appropriate comprehensive serum and urine drug screening, plus analysis of the following: Alcohol level, if alcohol toxicity is suspected. Serum elect...

see more →

News  15 results

Winners all
https://www.mdedge.com/chestphysician/article/184478/society-news/winners-all/page/0/1?channel=28399

Dec 3rd, 2018 - Case Report Slide Winners Ze Ying Tan: All that wheezes is not asthma Jason Lam: Pulmonary mucor mycetoma Adam Young: Nonresolving pneumonia and cyclic fevers in an immunocompetent patient Ritu Modi: Histopathological misdiagnosis of pulmonary coc.

Hyperammonemia May Signal the Presence of Generalized Convulsive Seizures
https://www.mdedge.com/neurology/epilepsyresourcecenter/article/111997/hyperammonemia-may-signal-presence

Aug 26th, 2016 - Elevated blood ammonia levels may help differentiate epileptic generalized convulsive seizures (GCS) from other events, suggests a recent report in Epilepsia. When Rawan Albadareen and associates measured blood ammonia levels in 78 patients with G.

Case Studies in Toxicology: A Common Procedure, an Uncommon Complication
https://www.mdedge.com/emergencymedicine/article/88055/toxicology/case-studies-toxicology-common-procedure-uncommon/page/0/1

Oct 1st, 2014 - Glycine Glycine 1. 5% is the most common irrigant solution used; as such, it produces the highest incidence of TURP syndrome.

More on hyperammonemia
https://www.mdedge.com/psychiatry/article/64325/more-hyperammonemia

May 1st, 2011 - The authors of the “The mysterious foreign accent” (Cases that Test Your Skills, Current Psychiatry, March 2011, p. 57-63) left us hanging by tantalizing us with an axis III diagnosis of asymptomatic hyperammonemia.

FDA Approves Carglumic Acid Therapy for Rare Genetic Disorder
https://www.medscape.com/viewarticle/718847

Mar 18th, 2010 - March 19, 2010 — The US Food and Drug Administration (FDA) has approved carglumic acid dispersible tablets (Carbaglu, Orphan Europe, a Recordati company) for treatment of a rare genetic disoder N-acetylglutamate synthase deficiency, which causes h...

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