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Differential
(Click to cross reference)
adrenoleukodystrophy
basal ganglia, lesion of
bone marrow transplantation
CAT scan
CAT scan, abnormal
cherry red spot
chronic graft versus host disease
conjunctival biopsy
cornea, abnormal
cornea, opacity of
cultured skin fibroblasts
dysarthria
dysmorphic
dystonia
electron microscopy
encephalopathy
enzyme treatment
enzyme, defect
facial appearance, abnormal
gait disorder
gangliosidosis GM1
gangliosidosis GM2
gangliosidosis, generalized
genetic counselling
genetic diagnosis
genetic diagnosis, prenatal
genetic neurologic disorders
grimacing
hepatosplenomegaly
hypotonia
inborn errors of metabolism
Krabbe's disease
lipid storage disorder of CNS
lysosomal storage disease
macrocephaly
mental retardation
metachromatic leukodystrophy
molecular genetics
mortality
MRI
MRI, abnormal
mucopolysaccharidoses
neuroaxonal dystrophy
neurologic disease, diagnoses of
neuronal ceroid-lipofuscinosis
Niemann-Pick disease
ophthalmoplegia, plus syndrome
Parkinsonism syndrome
prenatal diagnosis by amniocentesis
rectal biopsy
review article
rigidity
seizure
short stature
skin, biopsy
speech disorder
stem cell transplantation
thalamus, lesion of
thalamus, lesion of-bilateral
treatment of neurologic disorder
urine test for metabolic disorders
Showing articles 50 to 53 of 53 << Previous

Adult-onset GM2 Gangliosidosis
Neurol 28:1117-1123, O'Neill,B.,et al, 1978

Chronic Hexosaminidase A & B Deficiency
et al. , Ann Neurol 2:156977., Goldie,W.D., 1977

Tay-Sachs Disease-The Use of Tears for the Detection of Heterozygotes
NEJM 289:1072, Carmody,P.,et al, 1973

Failure of Vision in Childhood
Proc Royal Soc Medicine, pp 494-500., , 1850



Showing articles 50 to 53 of 53 << Previous