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Differential
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abducens nerve paralysis
acoustic nerve
acral sensory symptoms
Addison's disease
Adies pupil
adrenoleukodystrophy
adrenomyeloneuropathy
adult polyglucosan body disease
advances in neurology
adverse drug reaction
alcohol intolerance
alkylating agents
altered states of consciousness
alternating rapid movement
amitriptyline
amyloid
amyloid angiopathy, cerebral
amyloidosis
amyloidosis, oculoleptomeningeal, familial
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, epidemiology of
amyotrophic lateral sclerosis, familial
amyotrophic lateral sclerosis, guamian type of
ankle reflex, absent
anterior interosseous neuropathy
anterior tibial muscle weakness
antimetabolite
areflexia
arm atrophy
arm weakness
arrhythmia, cardiac
arthralgia
arthrogryposis multiplex
arthropathy
arthropathy, neuropathic
arylsulfatase B
asparginase
asymptomatic
ataxia
ataxia, cerebellar
ataxia, hereditary
ataxia, progressive
ataxia, sensory
ataxia, truncal
ataxic gait
atonic bladder
auditory evoked brainstem potentials
autonomic dysfunction
autonomic nervous system
autonomic neuropathy
autonomic neuropathy, idiopathic
Babinski sign
bacterial infection
Bassen-Kornzweig syndrome
benign essential tremor
blacks
bladder dysfunction
blindness
blood dyscrasias, neurologic findings with
brachial neuritis
brachial neuritis, acute
brachial neuritis, bilateral
brachial neuritis, prognosis of
brachial plexus
brachial plexus neuropathy
brachial plexus neuropathy, bilateral
brachial plexus neuropathy, familial
brachial plexus neuropathy, recurrent
burning paresthesia
caloric testing
cardiomyopathy
case studies
CAT scan, abnormal
CAT scan, metrizamide
CAT scan, myelogram with
cataracts
cataracts, congenital
cauda equina
cauda equina, enhancement
cauda equina, lesion of
cavernous sinus
cavernous sinus, lesion of
central core disease
cerebellar ataxia, neuropathy and vestibular areflexia syndrome
cerebellar atrophy, secondary
cerebellar lesion
cerebellum, disease of
cerebro hepato renal syndrome
cerebrospinal fluid, pressure low
cerebrospinal fluid, xanthochromia of
cerebrotendinous xanthomatosis
Charcot-Marie-Tooth
chemotherapy, CNS treatment and complications with
children
cholesterol
cholesterol, HDL
chorea
chromosomal abnormality
chromosome 16
chromosome 17
claudication, intermittent of cauda equina
Clinical Pathologic Conference(C.P.C.)
clubfoot as related to neurologic disease
Cockayne's syndrome
cold temperature
coloboma
compression neuropathy
compression neuropathy, recurrent
cornea, abnormal
cornea, opacity of
corpus callosum, lesion of
cough
cranial nerve enhancement
cranial nerve enlargement
cranial nerves
cranial neuropathy
cranial neuropathy, multiple
deafness
degenerative diseases of CNS
Dejerine-Sottas syndrome
dementia
demyelinating disease
denervation of muscle
dermatomyositis
diabetes mellitus
diarrhea
differential diagnosis
diplegia, brachial
diplopia
diplopia, transient
disability, neurological
dissociated sensory loss
distal muscle atrophy
distal muscle weakness
DNA probes
down-beat nystagmus
drug induced neurologic disorders
dysarthria
dysdiadochokinesia
dysmetria
dysmorphic
dysphagia
dyspraxia
electrocardiogram, abnormal
electroencephalogram, inflammatory disease
electromyogram
electronystagmography
electroretinograph
encephalopathy
entrapment neuropathy
enzyme, muscle disease
epidemiology of neurology
episodic neurologic deficits
erythromelalgia
evoked potentials
eye movement, disorders of
face, numbness of
facial nerve palsy, bilateral
facial pain
facial weakness
facial weakness, bilateral
falling
familial
family planning
fasciculation
Fazio-Londe's disease
fever
fibrillations
fine motor function, impaired
fluorouracil
flush syndrome
foot deformity
foot drop
foot numbness
Friedreich's ataxia
fundus, abnormality of
gadolinium
gait disorder
gene
gene mutation
genetic counselling
genetic diagnosis
genetic diagnosis, prenatal
genetic linkage
genetic neurologic disorders
genetic testing
genu of corpus callosum
giant axonal neuropathy
Guillain Barre syndrome
hair analysis
Hallervorden Spatz disease
hallucination
hammertoes
hand deformity
hand numbness
hand weakness
headache
hearing loss
heavy metal intoxication
heel-knee-shin test
hemiparesis
hemiparesis, transient
hepatitis C virus
hepatomegaly
hepatosplenomegaly
Hicks disease
high arched feet
human genome
human immunodeficiency virus type 1
hydrocephalus
hyperreflexia
hyperthyroidism
hyponatremia
hyporeflexia
hypotelorism
idiopathic polyneuropathy
imbalance
impotence
inappropriate antidiuretic(A.D.H.)hormone, CNS involvement with
incidence
inclusion bodies
inclusion bodies, eosinophilic cytoplasmic
incoordination
intellectual deficit
internuclear ophthalmoplegia
intracerebral hemorrhage
intracerebral hemorrhage, familial
intrinsic hand muscles, wasting of
Isaacs syndrome
isoniazid
jaw pain
Jewish
Kearns-Sayre syndrome
keratitis
klippel feil syndrome
Korsakoff's psychosis
Kugelberg-Welander syndrome
kyphoscoliosis, neurologic causes of
kyphosis
laminectomy, cervical
laminectomy, lumbar
Laurence-Moon-Bardet-Biedl syndrome
Leber's congenital amaurosis
leg weakness, bilateral
leprosy
leukemia, neurologic findings assoc.with
leukodystrophy
leukoencephalopathy
leukopenia
light-near dissociation, causes of
liver transplantation
lumbosacral plexopathy
lumbosacral plexus
lymphadenopathy
macular degeneration
magnetic stimulation
magnetic stimulation, brain
median neuropathy
meningismus
meningoencephalopathy
mental retardation
methotrexate
methylhydrazine derivatives
midbrain, atrophy
middle cerebellar peduncle, lesion
middle cerebellar peduncle, lesion, bilateral
misdiagnosis
mitochondrial disease
molecular genetics
monoamine oxidase inhibitors
mononeuropathy
mononeuropathy multiplex
mononeuropathy, children
mononeuropathy, recurrent
monoparesis
motor neuron disease
movement disorder
MRI
MRI, abnormal
MRI, brachial plexus
MRI, contrast enhanced
MRI, cranial nerves
MRI, diffusion tensor
MRI, diffusion weighted
MRI, disappearing lesion on
MRI, peripheral nerve
MRI, spinal cord
MRI, spine
mucopolysaccharidoses
multiple system atrophy
muscle atrophy, focal
muscle atrophy, progressive
muscle cramp
muscle diseases, characteristics of
muscle hypertrophy
muscle pain
muscle weakness
muscle weakness, proximal
muscle, metabolic disorders of
muscular dystrophy
muscular dystrophy, Duchenne
muscular dystrophy, facioscapulohumeral
muscular dystrophy, limb-girdle
myasthenia gravis
myasthenia gravis, familial incidence of
myasthenia gravis, nystagmus in
myasthenia gravis, ocular
myasthenia gravis, sensory loss with
myasthenic crisis
myelin protein zero gene
myelogram
myelogram, cervical
myelomalacia
myeloneuropathy
myelopathy
myeloradiculopathy
myokymia
myopathy
myopathy, carcinomatous
myopathy, mitochondrial
myopathy, thyroid disease causing
myopia
myositis
myotonia dystrophica
nausea and vomiting
neck pain
nerve biopsy
nerve biopsy, indication
nerve conduction studies
nerve conduction studies, sensory
nerve growth factor
nerve growth stimulating activity
nerve hypertrophy
nerve root enhancement
nerve root hypertrophy
neuritis, causes of
neuroblastoma
neurofibrillary degeneration
neurofibromatosis 1
neurogenic bladder
neurologic complications of, systemic cancer
neurologic complications of, systemic disease
neurologic disease
neurologic disease, diagnoses of
neuromuscular disease, electrodiagnosis of
neuromyotonia
neuronal ceroid-lipofuscinosis
neuronopathy, sensory
neuropathy
neuropathy, amyloid
neuropathy, ataxic
neuropathy, classification of
neuropathy, demyelinating
neuropathy, diabetic
neuropathy, etiologies of
neuropathy, hereditary peripheral
neuropathy, hypertrophic
neuropathy, motor
neuropathy, onion bulb
neuropathy, peripheral
neuropathy, peripheral, treatment
neuropathy, recurrent
neuropathy, sensory
neuropathy, sensory, hereditary
neuropathy, work up for
neurotoxin
neurotrophin-3
next-generation sequencing
night blindness
nitrogen mustard
numbness, extremity
nystagmus
nystagmus, dissociated
nystagmus, gaze-evoked
nystagmus, monocular
optic atrophy
optic atrophy, hereditary
optic nerve
optic neuropathy
orthostatic hypotension
orthostatic hypotension, idiopathic
pain
pain, arm
pain, foot
pain, severe
pain, wrist
papilledema
paralysis
paralysis, recurrent
paraparesis
paraparesis, familial spastic
paraparesis, spastic
paresthesias
paresthesias, feet
paresthesias, lower extremity
patient information and support
peroneal muscle atrophy, causes of
peroneal nerve
peroneal nerve, lesion of
peroxisomal disease
pes cavus
pheochromocytoma
phytanic acid
pigmentary retinopathy
pleocytosis of cerebrospinal fluid
poison, mercury
poison, neurologic problems with
POLG1 gene
poliomyelitis
polyglucosan body
polyglucosan body disease
polymerase chain reaction
polymyositis
polyneuropathy
polyneuropathy, chronic idiopathic
polyneuropathy, chronic inflammatory demyelinating
polyneuropathy, chronic relapsing
polyneuropathy, familial
porphyria
positional head-hanging test
positive sharp waves
post polio syndrome
precipitating factors
pregnancy, neurologic complications in
procarbazine
prognosis
progressive neurologic disorder
proptosis
proximal muscle atrophy
pseudointernuclear ophthalmoplegia
psychological testing
psychosis
ptosis
ptosis, bilateral
puerperium
pulmonary function tests
pupil
pupil, abnormality in neurologic disorders
pupil, dilated and fixed, bilateral
pupil, scalloped
pyramidal
pyramidal tract dysfunction
quadriparesis
quadriplegia, transient
quality of life
radial nerve, palsy of
radiculopathy
reading disorder, acquired
recombinant DNA
recruitment
recruitment, reduced
recurrent
refractive errors
Refsum's disease
respiratory failure
retinal degeneration
retinal lesion
retinitis pigmentosa
retinopathy
reversible neurologic disorder
review article
RFC1 gene
RFLPs
Riley-Day syndrome
risk factors
Romberg's sign
root lesion, nerve
Roussy Levy syndrome
saccadic eye movements, abnormal
sarcoidosis
scoliosis
seizure
sensorineural hearing loss
sensory ganglia
sensory ganglia, abnormal
sensory loss
sensory loss, leg
sensory loss, truncal
sensory nerve action potentials
sensory polyneuropathy
short stature
shoulder, numbness
shoulder, pain in
Shy-Drager syndrome
skin, lesions in neurologic disorders
somatosensory evoked potentials
spasticity
speech disorder
speech disorder, non aphasic
spinal cord, compression of
spinal muscular atrophy
spinal stenosis
spinal stenosis, familial
spinocerebellar ataxia
spinocerebellar degeneration
splenium of corpus callosum
splenomegaly
spontaneous muscle activity
spontaneous remission
steppage gait
steroid therapy, CNS treatment and complications with
stiff man syndrome
strokelike episodes
subdural hematoma
sudden death
suprascapular neuropathy
symmetric brain lesions
syncope
tandem gait, ataxic
Tangier's disease
tapetoretinal degeneration
tauopathy
tensilon test
thalamus, lesion of
thalamus, lesion of-bilateral
thrombocytopenia
thyrotoxicosis
tinnitus
toe walking
tomaculous neuropathy
tongue, enlarged
torticollis
transient neurologic deficit
trauma
treatment of neurologic disorder
tremor
tricresylphosphate
trigeminal nerve
trigeminal nerve, hypertrophy
trigeminal neuralgia
trinucleotide repeats
ulnar neuropathy
ultrasonography, nerve
urinary incontinence
Usher's syndrome
vestibular areflexia
vestibular function, tests of
vestibulopathy
vibratory sensation, abnormal
vinblastine
vincristine neurotoxicity
viral infection
vision, failure of in childhood
visual acuity, decreased
visual evoked response
visual field defect
visual fields, constricted
visual impairment
visual loss
visual loss, congenital
vitreous opacities
vocal cord paralysis
voice, abnormality of
walking frame
walking, difficulty with
walking, difficulty with in dark
weakness
weakness, generalized
weakness, progressive
weakness, proximal
weight loss
Werdnig-Hoffman disease
wheelchair
white matter disease
wide based gait
winging of scapula
wrist drop
X-linked neuropathy
x-ray, spine
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Showing articles 600 to 650 of 5288 << Previous Next >>