Author:
Hediger Nina,Landolt Markus A.,Diez-Fernandez Carmen,Huemer Martina,Häberle Johannes
Funder
Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung (CH)
Subject
Genetics (clinical),Genetics
Reference47 articles.
1. Ah Mew N, Krivitzky L, McCarter R, Batshaw M, Tuchman M, Urea Cycle Disorders Consortium of the Rare Diseases Clinical Research N (2013) Clinical outcomes of neonatal onset proximal versus distal urea cycle disorders do not differ. J Pediatr 162: 324–329.e1.
https://doi.org/10.1016/j.jpeds.2012.06.065
2. Ah Mew N, Simpson KL, Gropman AL, Lanpher BC, Chapman KA, Summar ML (1993) Urea cycle disorders overview. In: Pagon RA, Adam MP, Ardinger HH, Wallace SE, Amemiya A, Bean LJH, Bird TD, Ledbetter N, Mefford HC, Smith RJH, Stephens K (eds) (2017) GeneReviews(R), 2017/22/06. University of Washington, Seattle
3. Alfadhel M, Mutairi FA, Makhseed N, Jasmi FA, Al-Thihli K, Al-Jishi E, AlSayed M, Al-Hassnan ZN, Al-Murshedi F, Häberle J, Ben-Omran T (2016) Guidelines for acute management of hyperammonemia in the Middle East region. Ther Clin Risk Manag 12:479–487.
https://doi.org/10.2147/TCRM.S93144
4. Bachmann C (2003) Outcome and survival of 88 patients with urea cycle disorders: a retrospective evaluation. Eur J Pediatr 162:410–416
5. Batshaw ML (1983) Sodium benzoate and arginine: alternative pathway therapy in inborn errors of urea synthesis. Prog Clin Biol Res 127:69–83
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