cysteine and Adrenoleukodystrophy

cysteine has been researched along with Adrenoleukodystrophy in 2 studies

Research

Studies (2)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	2 (100.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Ferdinandusse, S; Mayatepek, E; Meissner, T; Wanders, RJ	1
Berger, J; Korosec, T; Molzer, B; Unterrainer, G	1

Other Studies

2 other study(ies) available for cysteine and Adrenoleukodystrophy

Article	Year
Analysis of cysteinyl leukotrienes and their metabolites in bile of patients with peroxisomal or mitochondrial beta-oxidation defects. Clinica chimica acta; international journal of clinical chemistry, 2004, Volume: 345, Issue:1-2 Topics: Acyl-CoA Dehydrogenases; Adrenoleukodystrophy; Bile; Biotransformation; Chromatography, High Pressure Liquid; Cysteine; Gas Chromatography-Mass Spectrometry; Humans; Leukotrienes; Mitochondria, Liver; Oxidation-Reduction; Peroxisomes; Zellweger Syndrome	2004
A de novo adrenoleukodystrophy gene (ABCD1) mutation S636I without detectable ABCD1 protein and a R104C mutation with normal amounts of protein from an Austrian patient collective. Human mutation, 2000, Volume: 16, Issue:6 Topics: Adrenal Insufficiency; Adrenoleukodystrophy; Adult; Amino Acid Substitution; Arginine; ATP Binding Cassette Transporter, Subfamily D; ATP Binding Cassette Transporter, Subfamily D, Member 1; ATP-Binding Cassette Transporters; Cysteine; Humans; Isoleucine; Mutation, Missense; Proteins; Serine	2000

Article

Year

Analysis of cysteinyl leukotrienes and their metabolites in bile of patients with peroxisomal or mitochondrial beta-oxidation defects.

Clinica chimica acta; international journal of clinical chemistry, 2004, Volume: 345, Issue:1-2

Topics: Acyl-CoA Dehydrogenases; Adrenoleukodystrophy; Bile; Biotransformation; Chromatography, High Pressure Liquid; Cysteine; Gas Chromatography-Mass Spectrometry; Humans; Leukotrienes; Mitochondria, Liver; Oxidation-Reduction; Peroxisomes; Zellweger Syndrome

2004

A de novo adrenoleukodystrophy gene (ABCD1) mutation S636I without detectable ABCD1 protein and a R104C mutation with normal amounts of protein from an Austrian patient collective.

Human mutation, 2000, Volume: 16, Issue:6

Topics: Adrenal Insufficiency; Adrenoleukodystrophy; Adult; Amino Acid Substitution; Arginine; ATP Binding Cassette Transporter, Subfamily D; ATP Binding Cassette Transporter, Subfamily D, Member 1; ATP-Binding Cassette Transporters; Cysteine; Humans; Isoleucine; Mutation, Missense; Proteins; Serine

2000