Case reportSymptomatic female heterozygotes for adrenoleukodystrophy: A report of two unrelated cases and review of the literature
References (29)
- et al.
Phospholipids in X-linked adrenoleukodystrophy white matter: fatty acid abnormalities before the onset of demyelination
J Neurol Sci
(1992) - et al.
Identification of female carriers of adrenoleukodystrophy
J Pediatr
(1983) - et al.
Adrenoleukodystrophy (X-linked)
- et al.
Adrenoleukodystrophy
Endocrinol Metab Clin North Am
(1991) - et al.
X-linked adrenoleukodystrophy: biochemical diagnosis and enzyme defect
J Inher Metab Dis
(1992) - et al.
Putative X-linked adrenoleukodystrophy gene shares unexpected homology with ABC transporters
Nature
(1993) - et al.
Penetrating the perioxisome
Nature
(1993) - et al.
Adrenoleukodystrophy: phenotypic variability and implications for therapy
J Inher Metab Dis
(1992) Adrenoleukodystrophy (adreno-testiculoleuko-myelo-neuropathic complex)
Clin Neuropathol
(1985)- et al.
Adrenoleukodystrophy — clinical and biochemical diagnosis
Aust N Z J Med
(1983)
Clinical aspects of adrenoleukodystrophy and adrenomyeloneuropathy
Dev Neurosci
(1991)
Adrenoleukodystrophy: survey of 303 cases
The adrenoleukodystrophies
CRC Crit Rev Neurobiol
(1987)
Capillary gas-liquid chromatographic-mass spectrometric measurement of very long chain (C22 to C26) fatty acids in microliter samples of plasma
J Lipid Res
(1985)
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