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Differential
(Click to cross reference)
arylsulfatase A
arylsulfatase A pseudodeficiency
metachromatic leukodystrophy
metachromatic leukodystrophy, adult onset
MRI
MRI, abnormal
Showing articles 0 to 10 of 10

Clinical Symptoms of Adult Metachromatic Leukodystrophy and Arylsulfatase A Pseudodeficiency
Arch Neurol 52:408-413, Hageman,A.T.M.,et al, 1995

A 23-Year-Old Woman Presenting with Cognitive Impairment and Gait Disturbance
Neurol 99:997-1003, Chaity,D.K.,et al, 2022

Inherited Metabolic Diseases of the Nervous System, Metachromatic Leukodystrophy
Adams & Victors Principles of Neurology, Chp 37, pg 971, Ropper, A.H.,et al, 2014

Clinicopathological Conference Metachromatic Leukodystrophy (juvenile type)
Case 7-1984, NEJM 310:445-4551984., , 1984

Clinicopathological Conference
Maroteaux-Lamy Syndrome, Case 44-1983, NEJM 309:1109-1117983., , 1983

Juvenile Metachromatic Leukodystrophy
Arch Neurol 37:42-46, Haltia,T.,et al, 1980

Compressive Myelopathy in Maroteaux-Lamy Syndrome:Clinical & Pathological Findings
Ann Neurol 8:336-340, Young,R.,et al, 1980

Multiple Molecular Forms of Arylsulfatase in Different Forms of Metachromatic Leukodystrophy (MLD)
Neurol 29:16-20, Farrell,D.F.,et al, 1979

Deficiency of Arylsulfatase B in 2 Brothers Aged 40 & 38 Years (Maroteaux-Lamy Syndrome, Type B)
Ann Neurol 6:315-325, Pilz,H.,et al, 1979

Monozygotic Twins With Presumed Metachromatic Leukodystrophy
Arch Neurol 35:689-691, Hashimoto,T.,et al, 1978



Showing articles 0 to 10 of 10