Impact of enteral arginine supplementation on lysine metabolism in humans: A proof‐of‐concept for lysine‐related inborn errors of metabolism-Reference-Cited by-同舟云学术

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Impact of enteral arginine supplementation on lysine metabolism in humans: A proof‐of‐concept for lysine‐related inborn errors of metabolism

Published:2020-03-30 Issue:5 Volume:43 Page:952-959
ISSN:0141-8955
Container-title:Journal of Inherited Metabolic Disease
language:en
Short-container-title:Jrnl of Inher Metab Disea

Author:

Schmidt Zoe¹,Murthy Gayathri¹,Ennis Madeleine¹,Stockler‐Ipsiroglu Sylvia¹²³,Elango Rajavel¹⁴^ORCID

Affiliation:

1. BC Children's Hospital Research Institute BC Children's Hospital Vancouver British Columbia Canada

2. Division of Biochemical Genetics BC Children's Hospital Vancouver British Columbia Canada

3. Department of Pediatrics University of British Columbia Vancouver British Columbia Canada

4. School of Population and Public Health University of British Columbia Vancouver British Columbia Canada

Funder

B.C. Children's Hospital Foundation

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/jimd.12233

Reference26 articles.

1. Nutritional Consequences of Interspecies Differences in Arginine and Lysine Metabolism

2. Lysine α-ketoglutarate reductase, but not saccharopine dehydrogenase, is subject to substrate inhibition in pig liver

3. Proposed recommendations for diagnosing and managing individuals with glutaric aciduria type I: second revision

4. Lysine restricted diet for pyridoxine-dependent epilepsy: First evidence and future trials

5. Safety, efficacy and physiological actions of a lysine-free, arginine-rich formula to treat glutaryl-CoA dehydrogenase deficiency: Focus on cerebral amino acid influx

Cited by 15 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. L-arginine: its role in human physiology, in some diseases and mainly in viral multiplication as a narrative literature review;Future Journal of Pharmaceutical Sciences;2024-08-08

2. Assessment of urinary 6‐oxo‐pipecolic acid as a biomarker for ALDH7A1 deficiency;Journal of Inherited Metabolic Disease;2024-07-22

3. Highly sensitive l -lysine molecularly imprinted two-dimensional photonic crystal hydrogel sensor;Journal of Macromolecular Science, Part A;2024-05-10

4. Dietary management for pyridoxine‐dependent epilepsy due to α‐aminoadipic semialdehyde dehydrogenase deficiency, a follow‐on from the international consortium guidelines;JIMD Reports;2024-04-03

5. Tolerable Upper Intake Level for Individual Amino Acids in Humans: A Narrative Review of Recent Clinical Studies;Advances in Nutrition;2023-07

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