NMR spectroscopic studies on the late onset form of 3-methylglutaconic aciduria type I and other defects in leucine metabolism-Reference-Cited by-同舟云学术

NMR spectroscopic studies on the late onset form of 3-methylglutaconic aciduria type I and other defects in leucine metabolism

Published:2006 Issue:2 Volume:19 Page:271-278
ISSN:0952-3480
Container-title:NMR in Biomedicine
language:en
Short-container-title:NMR Biomed.

Author:

Engelke Udo F. H.,Kremer Berry,Kluijtmans Leo A. J.,van der Graaf Marinette,Morava Eva,Loupatty Ference J.,Wanders Ronald J. A.,Moskau Detlef,Loss Sandra,van den Bergh Erik,Wevers Ron A.

Publisher

Wiley

Subject

Spectroscopy,Radiology, Nuclear Medicine and imaging,Molecular Medicine

Reference23 articles.

1. Use of proton nuclear magnetic resonance spectroscopy in detection and study of organic acidurias.

2. 750 MHz 1H NMR spectroscopy characterisation of the complex metabolic pattern of urine from patients with inborn errors of metabolism: 2-hydroxyglutaric aciduria and maple syrup urine disease

3. Possibilities of selective screening for inborn errors of metabolism using high-resolution 1H-FT-NMR spectrometry

4. Standardized method for high-resolution 1H-NMR of cerebrospinal fluid

5. 3-Hydroxy-3-methylglutaryl-CoA lyase deficiency studied using 2-dimensional proton nuclear magnetic resonance spectroscopy

Cited by 51 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. Asymptomatic 3-methylglutaconic aciduria type 1 detected by high C5-OH on newborn screening;Molecular Genetics and Metabolism Reports;2024-03

2. 3-Methylglutarylcarnitine: A biomarker of mitochondrial dysfunction;Clinica Chimica Acta;2023-11

3. 3‐Methylglutaconyl‐CoA hydratase deficiency: When ascertainment bias confounds a biochemical diagnosis;JIMD Reports;2022-09-14

4. 3-Methylglutaconic Aciduria Type I;Neurology Genetics;2022-09-07

5. Diversion of Acetyl CoA to 3-Methylglutaconic Acid Caused by Discrete Inborn Errors of Metabolism;Metabolites;2022-04-21