Literature DB >> 6243418

Amino acid acylation: a mechanism of nitrogen excretion in inborn errors of urea synthesis.

S Brusilow, J Tinker, M L Batshaw.   

Abstract

Treatment of a patient deficient in carbamyl phosphate synthetase with benzoate or phenylacetic acid resulted in an increase in urinary nitrogen, which could be accounted for by the respective amino acid acylation product, hippurate or phenylacetylgultamine. Benzoate treatment of four hyperammonemic comatose patients led to clinical improvement and a return of plasma ammonium levels toward normal.

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Year:  1980        PMID: 6243418     DOI: 10.1126/science.6243418

Source DB:  PubMed          Journal:  Science        ISSN: 0036-8075            Impact factor:   47.728


  30 in total

Review 1.  Ornithine carbamoyl transferase deficiency: findings, models and problems.

Authors:  C Bachmann
Journal:  J Inherit Metab Dis       Date:  1992       Impact factor: 4.982

2.  One Year Experience of Pheburane(®) (Sodium Phenylbutyrate) Treatment in a Patient with Argininosuccinate Lyase Deficiency.

Authors:  Sema Kalkan Uçar; Burcu Ozbaran; Yasemin Atik Altinok; Melis Kose; Ebru Canda; Mehtap Kagnici; Mahmut Coker
Journal:  JIMD Rep       Date:  2015-02-10

3.  In vivo nitrogen metabolism in ornithine transcarbamylase deficiency.

Authors:  M Yudkoff; Y Daikhin; I Nissim; A Jawad; J Wilson; M Batshaw
Journal:  J Clin Invest       Date:  1996-11-01       Impact factor: 14.808

Review 4.  Current state of knowledge of hepatic encephalopathy (part I): newer treatment strategies for hyperammonemia in liver failure.

Authors:  Rune Gangsoy Kristiansen
Journal:  Metab Brain Dis       Date:  2016-09-21       Impact factor: 3.584

Review 5.  Intellectual and developmental disabilities research centers: Fifty years of scientific accomplishments.

Authors:  Steven U Walkley; Leonard Abbeduto; Mark L Batshaw; Anita Bhattacharyya; Susan Y Bookheimer; Bradley T Christian; John N Constantino; Jean de Vellis; Daniel A Doherty; David L Nelson; Joseph Piven; Annapurna Poduri; Scott L Pomeroy; Rodney C Samaco; Huda Y Zoghbi; Michael J Guralnick
Journal:  Ann Neurol       Date:  2019-07-27       Impact factor: 10.422

6.  A defect of the urea cycle--a case report.

Authors:  E R Naughten; M P Flavin; N G O'Brien
Journal:  Ir J Med Sci       Date:  1984-12       Impact factor: 1.568

7.  Organic acidaemia and Hyperammonaemia: review.

Authors:  M Walser; P M Stewart
Journal:  J Inherit Metab Dis       Date:  1981       Impact factor: 4.982

8.  Ammonia control in children ages 2 months through 5 years with urea cycle disorders: comparison of sodium phenylbutyrate and glycerol phenylbutyrate.

Authors:  Wendy Smith; George A Diaz; Uta Lichter-Konecki; Susan A Berry; Cary O Harding; Shawn E McCandless; Cindy LeMons; Joe Mauney; Klara Dickinson; Dion F Coakley; Tristen Moors; Masoud Mokhtarani; Bruce F Scharschmidt; Brendan Lee
Journal:  J Pediatr       Date:  2013-01-13       Impact factor: 4.406

9.  Treatment of hyperargininaemia due to arginase deficiency with a chemically defined diet.

Authors:  S D Cederbaum; S J Moedjono; K N Shaw; M Carter; E Naylor; M Walzer
Journal:  J Inherit Metab Dis       Date:  1982       Impact factor: 4.982

10.  In vivo measurement of ureagenesis with stable isotopes.

Authors:  M Yudkoff; Y Daikhin; X Ye; J M Wilson; M L Batshaw
Journal:  J Inherit Metab Dis       Date:  1998       Impact factor: 4.982

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