Liver involvement in urea cycle disorders: a review of the literature
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://link.springer.com/article/10.1007/s10545-017-0088-5/fulltext.html
Reference157 articles.
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2. Aronson PL, Mistry RD (2011) Ornithine transcarbamylase deficiency presenting as hepatitis. Pediatr Emerg Care 27:527–529. https://doi.org/10.1097/PEC.0b013e31821d86c1
3. Atiq M, Holt AF, Safdar K et al (2008) Adult onset urea cycle disorder in a patient with presumed hepatic encephalopathy. J Clin Gastroenterol 42:213–214. https://doi.org/10.1097/01.mcg.0000225628.84168.25
4. Badizadegan K, Perez-Atayde AR (1997) Focal glycogenosis of the liver in disorders of ureagenesis: its occurrence and diagnostic significance. Hepatol Baltim Md 26:365–373. https://doi.org/10.1002/hep.510260217
5. Batshaw ML, Tuchman M, Summar M et al (2014) A longitudinal study of urea cycle disorders. Mol Genet Metab 113:127–130. https://doi.org/10.1016/j.ymgme.2014.08.001
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