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Addison's disease
adrenoleukodystrophy
advances in neurology
adverse drug reaction
Alexanders disease
algorithm
aminoacidurias
amniocentesis
arylsulfatase A
arylsulfatase A pseudodeficiency
asymptomatic
ataxia
ataxia, cerebellar
atidarsagene autotemcel
auditory evoked brainstem potentials
behavioral disorder
bone marrow transplantation
burning feet
Canavan's disease
carcinoma of pancreas
CAT scan
CAT scan, abnormal
CAT scan, demyelinating disease
cerebellar lesion
cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy
cerebral edema, cytotoxic
cerebrospinal fluid, elevated protein of
children
cholelithiasis
chromosomal abnormality
chronic graft versus host disease
Clinical Pathologic Conference(C.P.C.)
cognition
complications
conjunctival biopsy
controversies in neurology
cornea, abnormal
cornea, opacity of
corpus callosum
corpus callosum, lesion of
cortical blindness
cranial nerve enhancement
cultured skin fibroblasts
Cushing's syndrome
deafness
dementia
dementia, childhood
demyelinating disease
depression
developmental milestones, loss of
differential diagnosis
dysmorphic
dystonia
dystonia, focal
efficacy
electroencephalogram, abnormalities of
electromyogram
electron microscopy
encephalitis
encephalopathy
enzyme treatment
enzyme, defect
evoked potentials
Fabry's disease
facial appearance, abnormal
falling
familial
frontal lobe, behavior with disease of
frontal lobe, lesion of
frontal lobe, pathologic signs of
gait disorder
gangliosidosis GM1
gangliosidosis GM2
gangliosidosis, generalized
gene mutation
gene therapy
genetic diagnosis
genetic diagnosis, prenatal
genetic neurologic disorders
genetic screening
Hallervorden Spatz disease
hallucination
hallucination, auditory
hepatolenticular degeneration(Wilson's disease)
hepatosplenomegaly
Hurler's syndrome
hyperadrenalism
hyperparathyroidism
hyperthyroidism
hypoglycemia
hypoparathyroidism
hypothyroidism
imbalance
inborn errors of metabolism
inborn errors of metabolism, screening
intellectual deterioration
internal capsule
Krabbe's disease
leg weakness, bilateral
leukocyte enzyme abnormality
leukodystrophy
leukoencephalopathy
leukoencephalopathy, differential diagnosis
lipid storage disorder of CNS
lysosomal storage disease
memory, impairment of
mental retardation
metabolic disorder, primary
metabolic disorder, primary-screening tests
metachromatic leukodystrophy
metachromatic leukodystrophy, adult onset
metachromatic leukodystrophy, juvenile
metachromatic leukodystrophy, late-infantile
mitochondrial disease
MRI
MRI, abnormal
MRI, contrast enhanced
MRI, diffusion weighted
MRI, gradient-echo
mucopolysaccharidoses
multiple sclerosis
multiple sclerosis, cognitive presenttion
multiple sclerosis, differential diagnosis of
multiple sclerosis, familial
muscular dystrophy, Duchenne
neonatal screening, genetic neurologic disorders
neoplasm, intracranial
nerve biopsy
nerve conduction studies
neuroaxonal dystrophy
neuroendocrinology
neurologic disease, diagnoses of
neuronal ceroid-lipofuscinosis
neuropathology, brain
neuropathy
neuropathy, peripheral
neuropsychiatry
Niemann-Pick disease
ophthalmoplegia, plus syndrome
optic atrophy
pain, abdominal
paraparesis
paraparesis, spastic
Pelizaeus Merzbacher
penicillamine
pernicious anemia
phenylketonuria
phenylketonuria, adult onset
pheochromocytoma
porphyria
prenatal diagnosis by amniocentesis
prevention of neurologic disorders
prognosis
progressive multifocal leucoencephalopathy
progressive neurologic disorder
psychiatric manifestations of brain tumors
psychiatric problems in neurologic disorders
psychological testing
psychosis
psychosis, cause of
pyramidal tract dysfunction
quadriparesis
review article
safety
Sandhoff's disease
Schilder's disease
schizophrenia
screening
seizure
short stature
skin, biopsy
somatosensory evoked potentials
speech disorder
speech disorder, childhood
sphingolipodoses
spongy degeneration of brain
stem cell transplantation
sural nerve
symmetric brain lesions
syphilis, neurologic complications with
systemic lupus erythematosus
Tay-Sachs disease
titubation
treatment of neurologic disorder
tremor
urinary sulfatidase excretion
visual evoked response
white matter disease
white matter disease, periventricular
Showing articles 150 to 151 of 151 << Previous

Myelinoclastic Diffuse & Transitional Sclerosis
Handbook of Clinical Neurol, Ed by Vinken & Bruyn 9:46970., Poser,C., 1970

Neuro CPC of MGH
Acute Necrotizing Hemorrhagic Encephalopathy, NEJM 265:34-401961., , 1961



Showing articles 150 to 151 of 151 << Previous