Amino Acids Profiling for the Diagnosis of Metabolic Disorders-Reference-Cited by-同舟云学术

Amino Acids Profiling for the Diagnosis of Metabolic Disorders

Published:2020-04-29 Issue: Volume: Page:
ISSN:
Container-title:Biochemical Testing - Clinical Correlation and Diagnosis
language:
Short-container-title:

Author:

Sandlers Yana

Publisher

IntechOpen

Link

http://www.intechopen.com/download/pdf/66048

Reference51 articles.

1. Sandlers Y. The future perspective: Metabolomics in laboratory medicine for inborn errors of metabolism. Translational Research. 2017. DOI: 10.1016/j.trsl.2017.06.005

2. National Institutes of Health Consensus Development Panel. National Institutes of Health Consensus Development Conference Statement: Phenylketonuria: Screening and management, October 16-18, 2000. Pediatrics. 2001;108:972-982. Available from: http://www.ncbi.nlm.nih.gov/pubmed/11581453 [Accessed: 20 November 2018]

3. Levy HL, Ghavami M. Maternal phenylketonuria: A metabolic teratogen. Teratology. 1996;53:176-184. DOI: 10.1002/(SICI)1096-9926(199603)53:3<176::AID-TERA5>3.0.CO;2-2

4. Longo N. Disorders of biopterin metabolism. Journal of Inherited Metabolic Disease. 2009;32:333-342. DOI: 10.1007/s10545-009-1067-2

5. De Braekeleer M, Larochelle J. Genetic epidemiology of hereditary tyrosinemia in Quebec and in Saguenay-Lac-St-Jean. American Journal of Human Genetics. 1990;47:302-307. Available from: http://www.ncbi.nlm.nih.gov/pubmed/2378355 [Accessed: 20 November 2018]

Cited by 5 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. Whole exome sequencing in energy deficiency inborn errors of metabolism: A systematic review;Molecular Genetics and Metabolism Reports;2024-09

2. L-proline determination by molecularly imprinted nanoparticles: A potential nanoscale tool for the diagnosis of metabolic disorders;Journal of Chromatography A;2024-08

3. Plasma Metabolomic Profiling Reveals Four Possibly Disrupted Mechanisms in Systemic Sclerosis;Biomedicines;2022-03-04

4. Defining Blood Plasma and Serum Metabolome by GC-MS;Metabolites;2021-12-24

5. Molecular and biochemical investigations of inborn errors of metabolism-altered redox homeostasis in branched-chain amino acid disorders, organic acidurias, and homocystinuria;Free Radical Research;2021-01-27