A case of adult onset type II citrullinemia with portal-systemic shunt
Author:
Publisher
Elsevier BV
Subject
Clinical Neurology,Neurology
Reference17 articles.
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2. The gene mutated in adult-onset type II citrullinaemia encodes a putative mitochondrial carrier protein;Kobayashi;Nat Genet,1999
3. Feasibility of auxiliary partial orthotopic liver transplantation from living donors for patients with adult-onset type II citrullinemia;Yazaki;Liver Transpl,2004
4. Adult-onset type II citrullinemia and idiopathic neonatal hepatitis caused by citrin deficiency: involvement of the aspartate glutamate carrier for urea synthesis and maintenance of the urea cycle;Saheki;Mol Genet Metab,2004
5. Reduced carbohydrate intake in citrin-deficient subjects;Saheki;J Inherit Metab Dis,2008
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2. Management of late onset urea cycle disorders—a remaining challenge for the intensivist?;Annals of Intensive Care;2021-01-06
3. Successful treatment of adult-onset type II citrullinemia with a low-carbohydrate diet and l-arginine after DNA analysis produced a definitive diagnosis;Clinical Journal of Gastroenterology;2020-01-02
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5. Liver transplantation using grafts with rare metabolic disorders;Digestive and Liver Disease;2015-04
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