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accommodation
accomodation, abnormal
addiction, heroin
addiction, heroin-neurologic complications with
advances in neurology
adverse drug reaction
affect, flat
agitation
akinesia
akinesia of eyelid function
akinetic mute
alemtuzumab
alien hand syndrome
alpha-synuclein
Alzheimer's disease
amantadine
amphotericin B
angiography, cerebral
anti IgLON5
anticholinergic drugs
antihistamines
aphasia
aphasia, progressive, primary
apraxia
apraxia of eye movements
apraxia of eyelid opening
arm swing, reduced
Asians
aspiration
ataxia
ataxia, progressive
ataxic gait
atypical
autoantibodies
autoimmune disease
autonomic dysfunction
axonal spheroid
Babinski sign
basal ganglia
basal ganglia, degeneration
basal ganglia, lesion of
basal ganglia, lesion, bilateral
behavioral disorder
biologic markers
biopterin deficiency
blepharospasm
blinking
blinking, reduced
bradykinesia
bradykinesia, facial
bradyphrenia
brain atrophy
brainstem, deformity of
brainstem, dysfunction
brainstem, lesion of
bulbar dysfunction
cachexia
camptocormia
carbamazepine
carbidopa
CAT scan, abnormal
CAT scan, angiography
CAT scan, angiography, false negative
CAT scan, emission
CAT scan, emission, abnormal
CAT scan, venography
catatonia
caudate nucleus, lesion of, bilateral
cerebellar atrophy, primary
cerebellar lesion
cerebellum
cerebral cortex
cerebral cortical atrophy
cerebral infarction
cerebral palsy
cerebrovascular accident
ceruloplasmin, serum
Charcot's sign
chasing the dragon
children
chorea
choreoathetosis
cirrhosis
Clinical Pathologic Conference(C.P.C.)
coagulopathy
cognition
cogwheel rigidty
coma
complications
confusion
contractures, joint
convergence
convergence, impaired
cortical-basal ganglionic degeneration
cyanide poison
deep gray nuclei
degenerative diseases of CNS
delay in diagnosis
dementia
dementia, presenile
dementia, rapidly progressive
dementia, thalamic
depression
developmental milestones, loss of
diabetes dialysis basal ganglia syndrome
diabetes mellitus
diabetes mellitus, neurologic manifestations of
diagnostic criteria
dialysis
differential diagnosis
disability, neurological
distal muscle atrophy
dopa responsive dystonia
dopamine agonist
driving
drooling
drug abuse
drug abuse, inhalation
drug abuse, neurologic complications of
dural arteriovenous malformation
dysarthria
dysdiadochokinesia
dyskinesia
dyskinesia, buccal lingual facial
dyskinesia, facial
dysmetria
dysphagia
dyspraxia
dystonia
dystonia musculorum deformens
dystonia, face
dystonia, focal
dystonia, treatment of
efficacy
electroencephalogram, abnormalities of
encephalitis
encephalitis, autoimmune
encephalitis, episodic
encephalitis, viral
encephalopathy
enolase
enzyme inhibition
executive dysfunction
extrapyramidal movement disorder, progressive
eye movement, disorders of
eyelid opening, difficulty with
facial appearance, abnormal
facial expression abnormality
falling
false negative
familial
fatigue
fetal tissue
fever
fine motor function, impaired
fistula, arterio-venous, dural
fracture, long bone
frontal behavioral spatial syndrome
frontal lobe, anatomy and physiology
gait disorder
gait, festinating
gaze palsy
gaze palsy, supranuclear
gaze palsy, vertical
gene
gene mutation
genetic neurologic disorders
glabellar sign
globus pallidus, lesion of
glutamate dehydrogenase deficiency
granular osmiphilic material
grimacing
gyrus, abnormal
Hallervorden Spatz disease
handwriting
headache
hearing loss
hemiparesis
hemorrhage, putamenal
hemorrhage, thalamic
hepatolenticular degeneration(Wilson's disease)
heralding manifestation
herpes virus infection
hip fracture
HLA
human immunodeficiency virus type 1
human immunodeficiency virus type 1, acute infection
Huntington's chorea
hydrocephalus
hyperreflexia
hypersomnia
hypometric saccades
hypophonia
iatrogenic neurologic disorders
imbalance
imbalance, postural
immunotherapy
inclusion bodies
inclusion bodies, eosinophilic cytoplasmic
inclusion bodies, intranuclear
infection
intellectual deficit
intellectual deterioration
interferon beta 1-a
internal capsule
introverted
iron, brain
Jakob-Creutzfeldt disease
Jakob-Creutzfeldt disease, young adult
jaw jerk, abnormal
Kayser-Fleischer ring
kinesia paradoxica
L-dopa
L-dopa, drug interactions with and side effects of
L-dopa, potentiators of
leg dragging
lenticular nucleus, lesion of
lenticular nucleus, lesion of, bilateral
leucine rich glioma inactivated 1 antibodies
leukemia, neurologic findings assoc.with
leukoencephalopathy
leukoencephalopathy, hereditary diffuse
leukoencephalopathy, toxic
levitation
Lewy body
lid
lid abnormalities
livedo reticularis
logopenia
lumbar puncture, complications of
manganese intoxication
marche a petits pas
masked facies
memory, impairment of
meningitis
metabolic acidosis
metabolic disorder, primary
micrographia
microhemorrhage, intracerebral
midbrain
midbrain, atrophy
midbrain, compression
Mini Mental Status Examination
misdiagnosis
monoamine oxidase inhibitors
mood change
mortality
movement disorder
movement disorder, extrapyramidal
movement disorder, treatment of
MPTP
MRI
MRI, abnormal
MRI, angiography
MRI, angiography, false negative
MRI, CAT scan compared to
MRI, contrast enhanced
MRI, diffusion weighted
MRI, disappearing lesion on
MRI, high signal foci on
MRI, high signal intensity of basal ganglia
MRI, lesion burden
MRI, paramagnetic effect
MRI, punctate pattern
MRI, T1 weighted high signal foci
MRI, venography
MRS
multiple sclerosis
multiple sclerosis, relapsing
multiple sclerosis, treatment of
multiple system atrophy
myoclonic jerks
myoclonus
myorhythmia
nausea and vomiting
neck extension
neuroaxonal leukodystrophy
neurologic disease, diagnoses of
neurologic disease, tempo
neurologic signs
neurologic symptoms
neuron specific enolase
neuronal ceroid-lipofuscinosis
neuronal intranuclear inclusion disease
neuroophthalmology
neuropathology
neuropathology, brain
neuropathy
neurotoxic
non-dominant hemisphere
occupational neurologic disorders
ocular motility, disorders of
ocular myopathy
ocular myopathy, differential diagnosis
old age, neurology of
ophthalmoplegia
orthostatic hypotension
pain, abdominal
pallidotomy
PANK2 mutation
parietal lobe, lesion of
Parkinson disease
Parkinson disease, akinetic form
Parkinson disease, asymmetric onset
Parkinson disease, atypical
Parkinson disease, dementia with
Parkinson disease, diagnosis
Parkinson disease, differential diagnosis of
Parkinson disease, drug induced
Parkinson disease, etiology of
Parkinson disease, freezing phenomena in
Parkinson disease, heterogeneity of
Parkinson disease, juvenile
Parkinson disease, L-dopa nonresponsive
Parkinson disease, nonmotor problems of
Parkinson disease, on-off phenomena in
Parkinson disease, pathogenesis of
Parkinson disease, surgical treatment of
Parkinson disease, treatment of
Parkinson disease, unilateral
Parkinsonism multiple-system atrophy
Parkinsonism syndrome
perseveration
personality change
phenothiazine
placebo effect
pleocytosis of cerebrospinal fluid
polycythemia, secondary
polyneuropathy
postural abnormality
preclinical
prion disease
procyclidine
prognosis
progressive myoclonic epilepsy
progressive neurologic disorder
progressive supranuclear palsy
protein 14-3-3, cerebrospinal fluid
protein 14-3-3, cerebrospinal fluid, false negative
pseudobulbar palsy
psychiatric problems in neurologic disorders
psychological testing
psychological testing, neurologic problems
psychomotor retardation
ptosis
pure akinesia
pyridoxine
rapidly progressing neurologic illness
reading disorder, acquired
reading problem, causes of
real-time quaking-induced conversion
rehabilitation for neurologic disorders
release phenomena
remote effect of cancer on the nervous system
renal failure
reserpine and reserpine like drugs
retinitis pigmentosa
retropulsion
reversible neurologic disorder
review article
rigidity
rigidity, axial
Romberg's sign
saccadic eye movements
saccadic eye movements, abnormal
safety
sagging of the brain
seizure
sensorineural hearing loss
sensory loss
sensory loss, cortical
seroconversion
shunt procedure, lumboperitoneal
shunt procedure, lumboperitoneal-complications of
sinemet
sleep pathology and physiology
slurred speech
spasticity
speech disorder
speech disorder, childhood
speech, soft
spinocerebellar ataxia type 1
spongy degeneration of brain
stare
startle reaction
stem cell transplantation
stereotaxic surgery
stimulation, deep brain
stooped posture
striatum, lesion of
striatum, lesion of, bilateral
suck reflex
suicide
symmetric brain lesions
synucleinopathy
tandem gait, ataxic
tau protein
tauopathy
temporal lobe, lesion
temporal lobe, lesion, bilateral
thalamus, lesion of
thalamus, lesion of-bilateral
thrombocytopenia
toe walking
tonic foot response
tonsillar herniation of cerebellum
toxins, nervous system
treatment of neurologic disorder
treatment, empirical
tremor
tremor, intention
tremor, resting
turning in bed
twins
upgaze, paralysis of
uremia
urinary incontinence
urinary tract infection
venous hypertension
venous ischemia
visual impairment
vitamin E
vitamin E deficiency
vitamin, multiple
voice, abnormality of
walking, difficulty with
weakness
weakness, progressive
weight loss
wheelchair
white matter disease
wide based gait
work loss
workup
writing
Showing articles 50 to 54 of 54 << Previous

Glutamate Dehydrogenase Deficiency in Patients with Olivopontocerebellar Atrophy
Neurol 33:1322-1326, Duvoisin,R.C.,et al, 1983

Drug Therapy of Parkinsonism
NEJM 295:814, Bianchine,J.R., 1976

Progressive Supranuclear Palsy-Case Study
NEJM 293:346, Richardson,E.P., 1975

Corticodentatonigral Degeneration with Neuronal Achromasia
Arch Neurol 18:20-33, Rebeiz,J.J.,et al, 1968

Parkinson's Disease
In Handbk of Clinical Neurology, Vinken, P. J. & Bruyn, G. W. , Ed, North-Holland Publ Co, Amsterdam, 6:173, 1968. Selby, G., 1968



Showing articles 50 to 54 of 54 << Previous