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Differential
(Click to cross reference)
acute disseminated encephalomyelitis
akinetic mute
amnestic syndrome
amniocentesis
anatomy of
aqueduct of Sylvius, stenosis
aqueductal stenosis
ataxia, hereditary
Babinski sign
basal ganglia, lesion of
basal ganglia, lesion, bilateral
blindness
calcarine artery
CAT scan
CAT scan, abnormal
cerebral venous infarction
cerebral venous thrombosis
cerebrovascular accident
cherry red spot
children
chromosomal abnormality
Clinical Pathologic Conference(C.P.C.)
craniopharyngioma
deep gray nuclei
dementia
dementia, thalamic
developmental milestones, loss of
developmental retardation
differential diagnosis
drooling
dropped head syndrome
encephalitis
encephalitis, viral
encephalopathy
encephalopathy, neonatal
enzyme, defect
Fabry's disease
fundus, abnormality of
gangliosidosis GM2
genetic counselling
genetic diagnosis, prenatal
genetic neurologic disorders
genetic screening
glioma
hemangioma, cerebral
hemianopia, homonymous
hexosaminidase-A
hexosaminidase-A and B
Huntington's chorea
hypersomnia
hypomyelination
hypotonia
hypoxic encephalopathy
intracranial hypertension, benign
Jewish
Krabbe's disease
lacunar infarction
lenticular nucleus, lesion of, bilateral
leukocyte enzyme abnormality
leukodystrophy
level of consciousness, decreased
lipid storage disorder of CNS
lysosomal storage disease
metabolic disorder, primary-screening tests
metachromatic leukodystrophy
molecular genetics
MRI
MRI, abnormal
MRI, CAT scan compared to
MRI, diffusion weighted
MRI, hypointense signal foci on
multiple sclerosis
muscle spasm
muscular dystrophy
muscular dystrophy, Duchenne
myelinolysis, extrapontine
neurofibromatosis 1
neuropathology
optic atrophy
optic glioma
optic neuritis
optic neuritis, bilateral
papilledema
pediatric neurology
pituitary, adenoma
pons, lesion of
pontine glioma
prenatal diagnosis by amniocentesis
prevention of neurologic disorders
psychomotor retardation
retrobulbar neuritis
review article
rigidity
Sandhoff's disease
Schilder's disease
screening
seizure
skin, biopsy
spasticity
spinocerebellar degeneration
startle reaction
subacute sclerosing panencephalitis(S.S.P.E.)Dawson's disease
symmetric brain lesions
Tay-Sachs disease
thalamic tumors
thalamic tumors, bilateral
thalamus
thalamus, infarction of
thalamus, infarction, bilateral
thalamus, lesion of
thalamus, lesion of-bilateral
thiamine deficiency
tone, muscle, increased
top of the basilar syndrome
vision, failure of in childhood
visual acuity, decreased
Wernicke's encephalopathy
white matter disease
Showing articles 0 to 15 of 15

Clinicopathologic Conference, Tay-Sacks Disease (GM2, Gangliosidosis)
NEJM 370:1830-1841, Case 14-2014, 2014

Inherited Metabolic Diseases of the Nervous System, Tay Sachs Disease
Adams & Victors Principles of Neurology, Chp 37, pg 957, Ropper, A.H.,et al, 2014

Differential Diagnosis of Bilateral Thalamic Lesions
Clin Neuroradiol 17:3-22, Linn,J.,et al, 2007

MR Findings in Tay-Sachs Disease
J Comput Assist Tomogr 20:551-555, Mugikura,S.,et al, 1996

The Prevention of Neurogenetic Disease
Arch Neurol 52:356-362, 3451995., Rosenberg,R.N.&Iannaccone,S.T., 1995

Tay-Sachs Disease-Carrier Screening, Prenatal Diagnosis, and the Molecular Era
JAMA 270:2307-2315, Kaback,M.,et al, 1993

Screening for Carriers of Tay-Sachs Disease Among Ashkenazi Jews
NEJM 323:6-12, Triggs-Raine,B.L.,et al, 1990

Amaurotic Family Idiocy
Am J Dis Child 142:53-56, Abt,I.A., 1988

Screening for Inherited Metabolic Diseases in Adults with Neurological Disease
Lancet 1:1101, Wierzbicki,A.S.,et al, 1988

The Cherry-Red Spot in Tay-Sachs & Other Storage Diseases
Ann Neurol 17:356-360, Kivlin,J.D.,et al, 1985

Spinocerebellar Degeneration:Hexosaminidase A & B Deficiency in Two Adult Sisters
Neurol 29:380-384, Oonk,J.G.W.,et al, 1979

Prenatal Genetic Diagnosis in 3000 Amniocenteses
NEJM 300:157-163, Golbus,M.S.,et al, 1979

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 0 to 15 of 15