• Atypical metachromatic leukodystrophy? Problems with the biochemical diagnosis
• Brain galactolipid content in a patient with pseudoarylsulfatase A deficiency and coincidental diffuse disseminated sclerosis, and in patients with metachromatic, adreno-, and other leukodystrophies
• Diagnosis of arylsulfatase A deficiency in intact cultured cells using a fluorescent derivative of cerebroside sulfate
• Diagnosis of pseudo-arylsulfatase A deficiency with electrophoretic techniques
• Marked clinical difference between two sibs affected with juvenile metachromatic leukodystrophy
• Metachromatic leukodystrophy and pseudoarylsulfatase A deficiency in a Danish family
• Pseudoarylsulfatase A deficiency in a psychiatrically disturbed adolescent
• Pseudoarylsulfatase-A deficiency in the neurologically impaired patient
• Screening patients referred to a metabolic clinic for lysosomal storage disorders