1. Adrenoleukodystrophy: a clinical and pathological study of 17 cases;Schaumburg, H.H.; Powers, J.H.; Raine, C.S.; Suzuki, K.; Richardson, E.P.;Arch Neurol,1975
2. Adrenomyeloneuropathy: a probable variant of adrenoleukodystrophy;Griffsn, J.W.; Goren, E.; Schaumburg, H.; Engel, W.K.; Loriaux, L.;Neurology,1977
3. Adrenoleukodystrophy: impaired oxidation of very long chain fatty acids in white blood cells, cultured skin fibroblasts and amniocytes;Singh, I.; Moser, A.E.; Moser, H.W.; Kishimoto, Y.;Pediatr Res,1984
4. Peroxisomal lignoceroyl-CoA ligase deficiency in childhood,1988
5. Adrenoleukodystrophy: evidence for X linkage, inactivation, and selection favouring the mutant allele;Migeon, B.R.; Moser, H.W.; Moser, A.B.; Axelman, J.; Sillence, D.; Norum, R.A.,1981