Adrenoleukodystrophy: A correlation between saturated very long-chain fatty acids in mononuclear cells and phenotype
Author:
Publisher
Wiley
Subject
Clinical Neurology,Neurology
Reference14 articles.
1. Linkage of adrenoleukodystrophy to a polymorphic DNA probe
2. FATTY ACID ABNORMALITY IN ADRENOLEUKODYSTROPHY
3. Brain gangliosides in adrenoleukodystrophy
4. Adrenoleukodystrophy: Impaired oxidation of long chain fatty acids in cultured skin fibroblasts and adrenal cortex
5. Peroxisomal lignoceroyl-CoA ligase deficiency in childhood adrenoleukodystrophy and adrenomyeloneuropathy.
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1. Molecular Biomarkers for Adrenoleukodystrophy: An Unmet Need;Cells;2021-12-06
2. Peroxisomal Disorders;Swaiman's Pediatric Neurology;2012
3. Diagnosis of X-linked adrenoleukodystrophy in blood leukocytes;Clinical Biochemistry;2007-09
4. ABCD1 translation-initiator mutation demonstrates genotype-phenotype correlation for AMN;Neurology;2001-12-11
5. A fluorimetric liquid chromatography for highly sensitive analysis of very long chain fatty acids as naphthoxyethyl derivatives;Chromatographia;2000-03
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