About: General (medium-chain) acyl-CoA dehydrogenase deficiency (non-ketotic dicarboxylic aciduria): quantitative urinary excretion pattern of 23 biologically significant organic acids in three cases

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About: General (medium-chain) acyl-CoA dehydrogenase deficiency (non-ketotic dicarboxylic aciduria): quantitative urinary excretion pattern of 23 biologically significant organic acids in three cases Goto Sponge NotDistinct Permalink

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scientific article published on 01 August 1983

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в серпні 1983 (uk) im August 1983 veröffentlichter wissenschaftlicher Artikel (de) artículu científicu espublizáu n'agostu de 1983 (ast) scientific article published on 01 August 1983 (en)
publication date	wds:Q71032475-F3712F7E-D836-4895-BA9C-D58C3129AB55
publication date	1983-08-01 00:00:00Z (xsd:dateTime)
author name string	wds:Q71032475-852AB383-1B99-4FA2-9370-C0E795B4E35A wds:Q71032475-92311E01-3DC2-450B-A993-7C5A38C6B341 wds:Q71032475-973D22F4-7C47-4F03-972B-E5CEE1BEDA5F wds:Q71032475-B0F7C0D0-9081-4CED-BCE0-DF3032CDE4B7 wds:Q71032475-B3373BA2-1169-4A42-B25B-8DF78B8104CE wds:Q71032475-E0178ED7-4F92-4CEB-83FE-CF2C6D3515BB wds:Q71032475-E4AB3DE6-558B-4E7D-8DD7-13C186C06962
author name string	N Gregersen P B Mortensen M David K Rasmussen S Kølvraa P Divry N Hobolth
rdfs:label	General (medium-chain) acyl-CoA dehydrogenase deficiency (non-ketotic dicarboxylic aciduria): quantitative urinary excretion pattern of 23 biologically significant organic acids in three cases (en) General (medium-chain) acyl-CoA dehydrogenase deficiency (non-ketotic dicarboxylic aciduria): quantitative urinary excretion pattern of 23 biologically significant organic acids in three cases (nl)
skos:prefLabel	General (medium-chain) acyl-CoA dehydrogenase deficiency (non-ketotic dicarboxylic aciduria): quantitative urinary excretion pattern of 23 biologically significant organic acids in three cases (en) General (medium-chain) acyl-CoA dehydrogenase deficiency (non-ketotic dicarboxylic aciduria): quantitative urinary excretion pattern of 23 biologically significant organic acids in three cases (nl)
name	General (medium-chain) acyl-CoA dehydrogenase deficiency (non-ketotic dicarboxylic aciduria): quantitative urinary excretion pattern of 23 biologically significant organic acids in three cases (en) General (medium-chain) acyl-CoA dehydrogenase deficiency (non-ketotic dicarboxylic aciduria): quantitative urinary excretion pattern of 23 biologically significant organic acids in three cases (nl)
title	wds:Q71032475-6FA26659-BA90-49EA-901B-B179BC3E8AE1
title	General (medium-chain) acyl-CoA dehydrogenase deficiency (non-ketotic dicarboxylic aciduria): quantitative urinary excretion pattern of 23 biologically significant organic acids in three cases (en)
page(s)	wds:Q71032475-4B8E393B-ED57-4B13-A183-DA0B65CD0260
page(s)	181-191
instance of	wds:Q71032475-EE2E222F-AEA6-4B35-979E-8E377F63504C
instance of	scholarly article
main subject	wds:Q71032475-44E56782-544B-4954-A09E-2B0AD8B5379F wds:Q71032475-F85D76D6-F1EF-4938-B39C-B2C6F729130C
main subject	medium chain acyl-CoA dehydrogenase deficiency ketosis
PubMed ID	wds:Q71032475-E91EFACE-11B1-465F-B078-FC3060ABD61E
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/6616873
PubMed ID	6616873
published in	wds:Q71032475-951BCC51-BB38-4F62-BC6D-16DF40A1A333
published in	Clinica Chimica Acta
issue	wds:Q71032475-D9C6D413-2206-4CFE-9D2F-99E400C11C72
volume	wds:Q71032475-D994CEAB-EF26-4B91-9FBB-DD302B140A74
issue	2
volume	132
DOI	wds:Q71032475-90595AA7-8BC4-49E8-AD9A-092B2EDFA186
DOI	http://dx.doi.org/10.1016/0009-8981(83)90246-2
DOI	10.1016/0009-8981(83)90246-2
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q71032475
is cites work of	Biosynthesis, degradation and pharmacological importance of the fatty acid amides Molecular cloning of cDNAs encoding rat and human medium-chain acyl-CoA dehydrogenase and assignment of the gene to human chromosome 1 Construction of an Acid-Tolerant Rhizobium leguminosarum Biovar Trifolii Strain with Enhanced Capacity for Nitrogen Fixation. Medium-chain acyl-CoA dehydrogenase deficiency: molecular aspects Neonatal onset of medium-chain acyl-CoA dehydrogenase deficiency in two siblings. The use of phenylpropionic acid as a loading test for medium-chain acyl-CoA dehydrogenase deficiency The microsomal dicarboxylyl-CoA synthetase Medium-chain and long-chain acyl CoA dehydrogenase deficiency: clinical, pathologic and ultrastructural differentiation from Reye's syndrome. The inborn errors of mitochondrial fatty acid oxidation Fatty acid oxidation disorders as primary cause of sudden and unexpected death in infants and young children: an investigation performed on cultured fibroblasts from 79 children who died aged between 0-4 years Implication of a peroxisomal enzyme in the catabolism of glutaryl-CoA. Octanoic acidemia and octanoylcarnitine excretion with dicarboxylic aciduria due to defective oxidation of medium-chain fatty acids Radiation metabolomics. 1. Identification of minimally invasive urine biomarkers for gamma-radiation exposure in mice Molecular genetic characterization and urinary excretion pattern of metabolites in two families with MCAD deficiency due to compound heterozygosity with a 13 base pair insertion in one allele Symptoms and signs in organic acidurias Fatty acyl-CoA dehydrogenase deficiency: enzyme measurement and studies on alternative metabolism Gas chromatography--mass spectrometry (GC--MS) diagnosis of two cases of medium chain acyl-CoA dehydrogenase deficiency {Omega}-oxidation of {alpha}-chlorinated fatty acids: identification of {alpha}-chlorinated dicarboxylic acids. Metabolic profiling with gas chromatography-mass spectrometry and its application to clinical medicine Molecular characterization of medium-chain acyl-CoA dehydrogenase (MCAD) deficiency: identification of a lys329 to glu mutation in the MCAD gene, and expression of inactive mutant enzyme protein in E. coli A new patient with dicarboxylic aciduria suggestive of medium-chain Acyl-CoA dehydrogenase deficiency presenting as Reye's syndrome. Synthesis, purification, and characterization of dicarboxylylmono-coenzyme A esters Products and intermediates of the beta-oxidation of [U-14C]hexadecanedionoyl-mono-CoA by rat liver peroxisomes and mitochondria Synthesis, characterisation and high-performance liquid chromatography of C6C16 dicarboxylyl-mono-coenzyme A and -mono-carnitine esters Role of 3-Hydroxy Fatty Acid-Induced Hepatic Lipotoxicity in Acute Fatty Liver of Pregnancy. Compartmentation of dicarboxylic acid beta-oxidation in rat liver: importance of peroxisomes in the metabolism of dicarboxylic acids Generalised dicarboxylic aciduria: a common finding in neonates Novel glycine conjugates in medium-chain acyl-CoA dehydrogenase deficiency Riboflavin-responsive ethylmalonic-adipic aciduria Inherited disorders of straight chain fatty acid oxidation Analysis of abnormal urinary metabolites in the newborn period in medium-chain acyl-CoA dehydrogenase deficiency Azelaic and pimelic acids: metabolic intermediates or artefacts? Fatty acids and Reye's syndrome
is cites work of	wds:Q37229038-577CB032-32D8-4962-9B98-79B7B2191641 wds:Q41521678-5F121829-1FA7-42AF-A423-E53ABD765B91 wds:Q47546227-85261294-E04C-429E-91EE-5D306E308E28 wds:Q42228864-F395FC30-6C6E-47BD-8048-8AC42B71782B wds:Q70499021-9ACA6919-C5E9-4CC8-B5F7-80EA123265D4 wds:Q28290744-DB404EC9-904B-4ADA-8AD1-7B7DD69B6F26 wds:Q36744400-3E623951-653B-4A57-8E86-935EAF76109D wds:Q37155833-0CC43A67-F7A8-4415-AE2C-7D32D02F1BF9 wds:Q69256470-C68A3D18-E883-4475-B93E-CF08D8C398D2 wds:Q41990916-8207E991-2781-48C4-8026-16C1049DDAA7 wds:Q70510092-4D0815BD-5C34-4D73-8A2E-E62B3FC81A44 wds:Q28298666-4292A1CB-FD46-4A0D-8C9B-866D157B2005 wds:Q24316978-2E645A21-B7BC-448E-9A04-A10ED822A293 wds:Q28332118-9B5E5B2A-3815-4A2A-B51B-E886F9FA8BA5 wds:Q35705892-203FFB8B-A360-45BA-B341-66717E06D613 wds:Q42828857-2BFBAF49-5354-4237-9B08-E0FF2116B0B8

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