Diagnosis of X-linked adrenoleukodystrophy in blood leukocytes
Author:
Publisher
Elsevier BV
Subject
Clinical Biochemistry,General Medicine
Reference21 articles.
1. X-linked adrenoleukodystrophy;Moser,2001
2. X linked adrenoleukodystrophy: clinical presentation, diagnosis, and therapy;van Geel;J. Neurol. Neurosurg. Psychiatry,1997
3. Cerebral X-linked adrenoleukodystrophy: the international hematopoietic cell transplantation experience from 1982 to 1999;Peters;Blood,2004
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1. The genetic landscape of X-linked adrenoleukodystrophy: inheritance, mutations, modifier genes, and diagnosis;The Application of Clinical Genetics;2015-05
2. Abcd2 Is a Strong Modifier of the Metabolic Impairments in Peritoneal Macrophages of Abcd1-Deficient Mice;PLoS ONE;2014-09-25
3. X-linked adrenoleukodystrophy: very long-chain fatty acid metabolism is severely impaired in monocytes but not in lymphocytes;Human Molecular Genetics;2013-12-20
4. Impaired Very Long-chain Acyl-CoA β-Oxidation in Human X-linked Adrenoleukodystrophy Fibroblasts Is a Direct Consequence of ABCD1 Transporter Dysfunction;Journal of Biological Chemistry;2013-06
5. X-linked Adrenoleukodystrophy;Colloquium Series on The Genetic Basis of Human Disease;2013-03-25
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