A family with adult-onset cerebral adrenoleucodystrophy

[1]  H. Moser.  Adrenoleukodystrophy: phenotypic variability and implications for therapy , 1992, Journal of Inherited Metabolic Disease.

[2]  A. Seters,et al.  Adult adrenoleukodystrophy: the clinical spectrum in a large Dutch family , 1992, Journal of Neurology.

[3]  C. Adamsbaum,et al.  A two-year trial of oleic and erucic acids ("Lorenzo's oil") as treatment for adrenomyeloneuropathy. , 1993, The New England journal of medicine.

[4]  Jean Mosser,et al.  Putative X-linked adrenoleukodystrophy gene shares unexpected homology with ABC transporters , 1993, Nature.

[5]  M. Weller,et al.  Very‐late‐onset adrenoleukodystrophy , 1992, Neurology.

[6]  W. E. Clark,et al.  Adrenoneuropathy: characteristic gross findings and association with Hashimoto's thyroiditis and accelerated atherosclerosis. , 1991, Modern Pathology.

[7]  H. Nagara,et al.  Adrenoleukodystrophy: A correlation between saturated very long‐chain fatty acids in mononuclear cells and phenotype , 1991, Annals of neurology.

[8]  E. Bertini,et al.  Experience on therapy of adrenoleukodystrophy and adrenomyeloneuropathy. , 1991, Developmental neuroscience.

[9]  H. Moser,et al.  Clinical aspects of adrenoleukodystrophy and adrenomyeloneuropathy. , 1991, Developmental neuroscience.

[10]  A. Sadeghi‐Nejad,et al.  Adrenomyeloneuropathy presenting as Addison's disease in childhood. , 1990, The New England journal of medicine.

[11]  A. J. Kumar,et al.  The adrenoleukodystrophies. , 1987, Critical reviews in neurobiology.