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Differential
(Click to cross reference)
arylsulfatase A
arylsulfatase A pseudodeficiency
arylsulfatase B
ataxia
atlanto-axial subluxation
auditory evoked brainstem potentials
CAT scan, abnormal
cerebrospinal fluid, elevated protein of
children
Clinical Pathologic Conference(C.P.C.)
cognition
complications
compression neuropathy
cornea, opacity of
cultured skin fibroblasts
deafness
dementia
dementia, childhood
differential diagnosis
dissociated sensory loss
dysmorphic
dyspraxia
dystonia
dystonia, focal
electroencephalogram, abnormalities of
electromyogram
electron microscopy
enzyme, defect
evoked potentials
falling
frontal lobe, pathologic signs of
gait disorder
gene mutation
genetic neurologic disorders
hydrocephalus
intellectual deterioration
leukodystrophy
lysosomal storage disease
memory, impairment of
mental retardation
metachromatic leukodystrophy
metachromatic leukodystrophy, adult onset
metachromatic leukodystrophy, juvenile
MRI
MRI, abnormal
mucopolysaccharidoses
myelopathy
nerve biopsy
nerve conduction studies
neurologic disease, diagnoses of
neuropathology, brain
neuropathy
neuropathy, peripheral
optic atrophy
papilledema
pregnancy, neurologic complications in
progressive neurologic disorder
psychiatric problems in neurologic disorders
quadriparesis
quadriplegia
radiculopathy
seizure
short stature
speech disorder
speech disorder, childhood
spinal cord, compression of
stem cell transplantation
sural nerve
titubation
tongue, enlarged
treatment of neurologic disorder
tremor
urinary sulfatidase excretion
white matter disease
Showing articles 0 to 10 of 10

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

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

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