Chronic liver disease and impaired hepatic glycogen metabolism in argininosuccinate lyase deficiency-Reference-Cited by-同舟云学术

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Chronic liver disease and impaired hepatic glycogen metabolism in argininosuccinate lyase deficiency

Published:2020-02-27 Issue:4 Volume:5 Page:
ISSN:2379-3708
Container-title:JCI Insight
language:en
Short-container-title:

Author:

Burrage Lindsay C.,Madan Simran,Li Xiaohui,Ali Saima,Mohammad Mahmoud,Stroup Bridget M.^ORCID,Jiang Ming-Ming,Cela Racel,Bertin Terry,Jin Zixue,Dai Jian,Guffey Danielle^ORCID,Finegold Milton,Nagamani Sandesh,Minard Charles G.^ORCID,Marini Juan,Masand Prakash,Schady Deborah,Shneider Benjamin L.,Leung Daniel H.,Bali Deeksha,Lee Brendan^ORCID

Funder

National Institutes of Health

National Urea Cycle Disorders Foundation

Burroughs Wellcome Fund

Howard Hughes Medical Institute

Genzyme

Cancer Prevention and Research Institute of Texas

Publisher

American Society for Clinical Investigation

Subject

General Medicine

Link

https://insight.jci.org/articles/view/132342/files/pdf

Reference56 articles.

1. Argininosuccinase deficiency in fibroblasts cultured from patients with argininosuccinic aciduria

2. Requirement of argininosuccinate lyase for systemic nitric oxide production

3. Nitric-Oxide Supplementation for Treatment of Long-Term Complications in Argininosuccinic Aciduria

4. Expanding the phenotype in argininosuccinic aciduria: need for new therapies

5. Systemic hypertension in two patients with ASL deficiency: A result of nitric oxide deficiency?

Cited by 11 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Retrospective analysis of arginase 1 deficiency progression in adults over 5 years at a single metabolic centre;JIMD Reports;2024-09-10

2. mRNA therapy corrects defective glutathione metabolism and restores ureagenesis in preclinical argininosuccinic aciduria;Science Translational Medicine;2024-01-10

3. The incidence of movement disorder increases with age and contrasts with subtle and limited neuroimaging abnormalities in argininosuccinic aciduria;Journal of Inherited Metabolic Disease;2023-12-04

4. Health-related quality of life in a systematically assessed cohort of children and adults with urea cycle disorders;Molecular Genetics and Metabolism;2023-11

5. Early allograft dysfunction in a pediatric liver allograft with an occult pathogenic mutation in the urea cycle;American Journal of Transplantation;2023-05

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