Zobrazeno 1 - 10
of 482
pro vyhledávání: '"Hyperammonaemia"'
Ureaplasma urealyticum infection following organ transplantation: a case report and narrative review
Autor:
Hongru Zhang, Liping Yang
Publikováno v:
Renal Failure, Vol 46, Iss 2 (2024)
Objective One case of Ureaplasma urealyticum (UU) infection after kidney transplantation was reported, and relevant literature was collected to provide a scientific reference basis for clinical diagnosis and treatment.Methods A case of UU infection a
Externí odkaz:
https://doaj.org/article/13bbebc1fa474b1897787abb59bfbbac
Autor:
Mildrid Yeo, Preeya Rehsi, Megan Dorman, Stephanie Grunewald, Julien Baruteau, Anupam Chakrapani, Emma Footitt, Helen Prunty, Melanie McSweeney
Publikováno v:
JIMD Reports, Vol 64, Iss 5, Pp 317-326 (2023)
Abstract In urea cycle disorders (UCDs) ammonia scavenger drugs, usually sodium‐based, have been the mainstay of treatment. Increasingly, glycerol phenylbutyrate (GPB, Ravicti®) is being used but scant real‐world data exist regarding clinical ou
Externí odkaz:
https://doaj.org/article/cb4630541705478ab681b28299176d20
Publikováno v:
JIMD Reports, Vol 63, Iss 6, Pp 536-539 (2022)
Abstract Carbonic anhydrase VA deficiency is a recently described inherited cause of paediatric hyperammonaemia. Most published cases describe patients with only one episode of hyperammonaemia whilst others report patients who had up to three metabol
Externí odkaz:
https://doaj.org/article/65028c6e89254908abc0799bf889c2d9
Akademický článek
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Akademický článek
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Publikováno v:
Case Reports in Gastroenterology, Vol 16, Iss 2, Pp 313-319 (2022)
Hepatic encephalopathy (HE) is a frequent and debilitating complication of liver disease and is oftentimes associated with hyperammonaemia. However, hyperammonaemia may occur in underlying conditions other than acute or chronic liver failure and clin
Externí odkaz:
https://doaj.org/article/500a7b4519b94e3599587187816ab45e
Autor:
Nandaki Keshavan, Michelle Wood, Lucy M. Alderson, Mario Cortina‐Borja, Rachel Skeath, Mel McSweeney, Marjorie Dixon, Maureen A. Cleary, Emma Footitt, Spyros Batzios
Publikováno v:
JIMD Reports, Vol 63, Iss 2, Pp 123-130 (2022)
Abstract Arginase deficiency is a rare autosomal recessive urea cycle disorder (UCD) caused by mutations in the ARG1 gene encoding arginase that catalyses the hydrolysis of arginine to ornithine and urea. Patients have hyperargininaemia and progressi
Externí odkaz:
https://doaj.org/article/3a5fd91f81d1406a9b90d2ee80e7491a
Autor:
Mildrid Yeo, Preeya Rehsi, Megan Dorman, Stephanie Grunewald, Julien Baruteau, Anupam Chakrapani, Emma Footitt, Helen Prunty, Melanie McSweeney
Publikováno v:
JIMD Reports, Vol 63, Iss 2, Pp 137-145 (2022)
Abstract Long‐term management of urea cycle disorders (UCDs) often involves unlicensed oral sodium benzoate (NaBz) which has a high volume and unpleasant taste. A more palatable treatment is licenced and available (glycerol phenylbutyrate [GPB], Ra
Externí odkaz:
https://doaj.org/article/15e4a12d942640829b4d39a2b6c7adb6
Autor:
Patrick A. Walsh
Publikováno v:
Frontiers in Physiology, Vol 13 (2022)
Hitherto, the rabbit has long been known to have a very poor tolerance to non—volatile acid. In this study, we tested the hypothesis that acid resilience in the acidotic rabbit can be increased by enhancing the plasma availability of a naturally oc
Externí odkaz:
https://doaj.org/article/4cd176b876124bfcbb5922a77084ebdb
Autor:
Anna Hadjihambi, Cristina Cudalbu, Katarzyna Pierzchala, Dunja Simicic, Chris Donnelly, Christos Konstantinou, Nathan Davies, Abeba Habtesion, Alexander V. Gourine, Rajiv Jalan, Patrick S. Hosford
Publikováno v:
JHEP Reports, Vol 4, Iss 8, Pp 100509- (2022)
Background & Aims: Increased plasma ammonia concentration and consequent disruption of brain energy metabolism could underpin the pathogenesis of hepatic encephalopathy (HE). Brain energy homeostasis relies on effective maintenance of brain oxygenati
Externí odkaz:
https://doaj.org/article/61b571bae53140f4bb2037e851d603c1