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Differential
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acoustic neurinoma
acoustic neurinoma, bilateral
acquired immunodeficiency syndrome
adrenoleukodystrophy
advances in neurology
adverse drug reaction
Alexanders disease
algorithm
Alzheimer's disease
Alzheimer's disease, familial
amniocentesis
amyloid angiopathy, cerebral
amyloid angiopathy, hereditary cystatin C
attention deficit disorder with hyperactivity
audiogram
auditory evoked brainstem potentials
basal ganglia, degeneration
basal ganglia, lesion of
Bassen-Kornzweig syndrome
brain biopsy
brainstem, lesion of
bulbar palsy, progressive
calcification, intracranial
CAT scan, emission
CAT scan, emission, abnormal
cataracts
cerebellar lesion
cerebro hepato renal syndrome
cerebrovascular accident
cerebrovascular accident, familial occurrence
cerebrovascular accident, young adult
Charcot-Marie-Tooth
children
chromosomal abnormality
chromosome 17
chromosome 22
chromosome 9
Cockayne's syndrome
cost effectiveness
creatine phosphokinase(CPK)elevated
cryptococcal meningitis
cytomegalovirus infection
dentate nuclei
dentate nuclei, lesion of
DNA probes
drug induced neurologic disorders
dystonia
dystonia musculorum deformens
dystrophin
ear, abnormal
electronystagmography
electroretinograph
encephalitis
encephalitis, focal
encephalitis, Rasmussen's
encephalitis, viral
enzyme, muscle disease
ependymoma
face, elongated
facial appearance, abnormal
familial
fasciculation
fragile-X syndrome
fundus, abnormality of
gadolinium
gene
gene mutation
genetic counselling
genetic diagnosis, prenatal
genetic linkage
genetic neurologic disorders
genetic screening
genetic testing
gynecomastia
Hallervorden Spatz disease
hearing loss
hemiparesis
hepatolenticular degeneration(Wilson's disease)
Huntington's chorea
Huntington's chorea, genetic counselling
Huntington's chorea, late onset
Huntington's chorea, presymptomatic detection of
Huntington's disease, children
hyperactivity
imbalance
immunohistochemistry
immunoperoxidase staining
in situ hybridization
inclusion bodies, intracytopasmic
intracerebral hemorrhage
intracerebral hemorrhage, familial
intracerebral hemorrhage, young adult
joint hypermobility
Kearns-Sayre syndrome
Kugelberg-Welander syndrome
Laurence-Moon-Bardet-Biedl syndrome
leukodystrophy
leukoencephalopathy
macular degeneration
manic-depressive
meningioma
meningitis
meningitis, recurrent
meningitis, relapse
mental retardation
mental retardation, familial
misdiagnosis
molecular genetics
mongolism
motor neuron disease
MRI
MRI, abnormal
MRI, contrast enhanced
mucopolysaccharidoses
muscle biopsy
muscular dystrophy
muscular dystrophy, Becker
muscular dystrophy, differential diagnosis of
muscular dystrophy, Duchenne
muscular dystrophy, Duchenne, carrier
muscular dystrophy, Duchenne, neonatal screening
muscular dystrophy, Duchenne, presymptomatic detection
muscular dystrophy, female occurrence of
muscular dystrophy, limb-girdle
myopathy, mitochondrial
myopia
myotonia dystrophica
neonatal screening, genetic neurologic disorders
neoplasm, intracranial
neoplasm, intracranial, multiple
neoplasm, primary of CNS
neoplasm, primary of CNS-multiple
nerve growth factor
neurofibromatosis 1
neurofibromatosis 2
neurofibromatosis 2, presymptomatic
neurologic disease
neurologic disease, diagnoses of
neuronal ceroid-lipofuscinosis
neuropathology
neuropathy
neuropathy, amyloid
neuropathy, hereditary peripheral
neuropathy, peripheral
neurotransmitter
night blindness
optic atrophy
optic nerve
optic neuropathy
patient information and support
peptides, brain
peroxisomal disease
pigmentary retinopathy
polymerase chain reaction
polyneuropathy, familial
posterior fossa, lesion of
pregnancy, neurologic complications in
prenatal diagnosis by amniocentesis
prognosis
progressive multifocal leucoencephalopathy
progressive spinal muscular atrophy
psychological testing
psychological testing, neurologic problems
recombinant DNA
recurrent
refractive errors
Refsum's disease
retinal degeneration
retinal lesion
retinitis pigmentosa
retinopathy
review article
RFLPs
Rosenthal fibers
seizure
seizure, focal
seizure, intractable, treatment of
sensorineural hearing loss
simian crease
somatostatin
Southern immunoblot test
spinal muscular atrophy
spinocerebellar degeneration
tapetoretinal degeneration
testicular enlargement
tinnitus
treatment of neurologic disorder
Usher's syndrome
viral infection
viral infection, CNS
visual field defect
visual loss
visuospatial disturbance
Von Hippel Lindau
Von Hippel Lindau, carrier
Von Hippel Lindau, screening protocol for
Western immunoblot test
white matter disease
Wood's light
X-linked bulbospinal neuronopathy
X-linked neuropathy
Showing articles 900 to 902 of 902 << Previous

Case Records of MGH-NEJM 286:1047
1972 Progressive Multifocal Leukoencephalopathy., , 1972

MR Mismatch Is Useful for Patient Selection for Thrombolysis: No
Stroke 40:2908-2909,2910, Sch�bitz,W.R.,

Clinical Study of Nine Patients with ReNU Syndrome
, Okamoto,N.,et al,



Showing articles 900 to 902 of 902 << Previous