Pregnancy in a healthy woman with untreated citrullinemia
Author:
Publisher
Wiley
Subject
Genetics(clinical)
Reference40 articles.
1. Hyperammonemia in Women with a Mutation at the Ornithine Carbamoyltransferase Locus
2. Molecular genetic research into carbamoyl-phosphate synthase I: Molecular defects and linkage markers
3. Determination of Phenylalanine Hydroxylase Activity in Patients with Phenylketonuria and Hyperphenylalaninemia
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1. The management and clinical outcomes of pregnancies in women with urea cycle disorders: A review of the literature and results of an international survey;Journal of Inherited Metabolic Disease;2023-12-09
2. Hyperammonemia in a pregnant woman with citrullinemia type I: a case report and literature review;BMC Pregnancy and Childbirth;2022-12-19
3. Citrullinemia in a newborn: a case report;Russian Journal of Child Neurology;2022-12-17
4. Gene Therapy in Combination with Nitrogen Scavenger Pretreatment Corrects Biochemical and Behavioral Abnormalities of Infant Citrullinemia Type 1 Mice;International Journal of Molecular Sciences;2022-11-29
5. Nutrition Management of Maternal Metabolic Disorders;Nutrition Management of Inherited Metabolic Diseases;2022
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