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Differential
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abdominal cramps
acid maltase deficiency
acid maltase deficiency, adult
acral sensory symptoms
acute intermittant porphyria
adrenoleukodystrophy
adrenomyeloneuropathy
adult polyglucosan body disease
adult-onset leukodystrophy, with neuroaxonal spheroids
adverse drug reaction
agalsidase alfa
alopecia
alpha glucosidase
alternating rapid movement
aminoacidopathies
aminoacidurias
amniocentesis
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, guamian type of
angina pectoris
angiokeratoma
anhidrosis
anterior horn cell disease
anterior tibial muscle weakness
anti GQ1b IgG antibody
anticonvulsants
anticonvulsants, selection of
antiviral agents
apraxia
areflexia
arm swing, reduced
Arnold Chiari malformation
arthropathy
arthropathy, neuropathic
arylsulfatase A
aspartate aminotransferase
aspiration
asymptomatic
ataxia
ataxia telangiectasia
ataxia, cerebellar
ataxia, progressive
ataxia, sensory
athetosis
atidarsagene autotemcel
attention deficit disorder with hyperactivity
attention span
atypical
autoantibodies
autonomic dysfunction
axonal degeneration
axonal spheroid
axonal transection
Babinski sign
basal ganglia
basal ganglia, calcification of
basal ganglia, lesion of
basal ganglia, lesion, bilateral
basilar impression
Bassen-Kornzweig syndrome
behavioral disorder
bladder dysfunction
blindness
blindness, transient
blood dyscrasias, neurologic findings with
bone marrow biopsy
bone marrow transplantation
bradykinesia
brain atrophy
brain biopsy
brain biopsy, complications of
brain biopsy, false negative
brain biopsy, indication
brainstem, infarction of
bulbar palsy
burning feet
burning feet, differential diagnosis of
burning hands
burning paresthesia
calcification, intracranial
calcifications, intracranial, punctate
carcinoma
cardiomyopathy
CAT scan
CAT scan, abnormal
CAT scan, false negative
cataplexy
cataracts
cerebellar ataxia, children
cerebellar ataxia, children, differential diagnosis of
cerebellar atrophy, primary
cerebellar degeneration
cerebellar infarction
cerebellar lesion
cerebellum, disease of
cerebral cortical atrophy
cerebral ischemia
cerebral vasculature, calcification
cerebro hepato renal syndrome
cerebrospinal fluid, gammaglobulin of
cerebrospinal fluid, proteincytologic dissociation
cerebrotendinous xanthomatosis
cerebrovascular accident
cerebrovascular accident, cryptogenic
cerebrovascular accident, familial occurrence
cerebrovascular accident, non atherosclerotic cause of
cerebrovascular accident, young adult
cerebrovascular disease
cerebrovascular disease, cardiovascular disease with
chemotherapy, CNS treatment and complications with
cherry red spot
cherry red spot-myoclonus syndrome
children
chorea
choreoathetosis
chromosomal abnormality
chronic graft versus host disease
Clinical Pathologic Conference(C.P.C.)
coagulopathy
Cockayne's syndrome
cognition
cogwheel rigidty
complications
compression fracture
congestive heart failure
conjunctival biopsy
consanguinity
contractures, joint
conversion reaction
conversion reaction, children
cornea, abnormal
cornea, opacification in infancy-causes of
cornea, opacity of
corneal dystrophy
corpus callosum
corpus callosum, hypoplastic
corpus callosum, lesion of
corpus callosum, thinning
cranial nerves, toxins effecting
cranial neuropathy, multiple
creatine phosphokinase(CPK)elevated
creatinine, elevated
cry, abnormal
cultured skin fibroblasts
cystinosis
deep gray nuclei
degenerative diseases of CNS
delay in diagnosis
dementia
dementia, childhood
dementia, diagnostic evaluation of
dementia, familial
dementia, frontal lobe type
dementia, presenile
dental pulp biopsy
dentatorubral-pallidoluysian atrophy
depression
developmental disability
developmental milestones, loss of
developmental retardation
diagnostic criteria
diarrhea
differential diagnosis
difficulty going down stairs
diplopia
disability, neurological
distal muscle weakness
DNA probes
drooling
dropped head syndrome
drug induced neurologic disorders
dysarthria
dysdiadochokinesia
dysmetria
dysmorphic
dysostosis multiplex
dysphagia
dystonia
dystonia, face
dystonia, focal
dystonic lipidosis
echocardiogram
efficacy
electroencephalogram
electroencephalogram, abnormalities of
electromyogram
electron microscopy
electronystagmography
electroretinograph
encephalitis, brainstem
encephalopathy
enzyme treatment
enzyme, defect
episodic disorders
episodic neurologic deficits
exercise intolerance
exome sequencing
eye movement, disorders of
Fabry's disease
facial appearance, abnormal
falling
familial
Farber's disease
fatigue
fever
fine motor function, impaired
fingerprint bodies
Fisher's syndrome
foam cells
fracture, pathologic
Friedreich's ataxia
frontal lobe, anatomy and physiology
frontal lobe, lesion of
fucosidosis
fundus, abnormality of
gait disorder
gait, spastic
galactosidase
gangliosides
gangliosidosis GM1
gangliosidosis GM2
gangliosidosis, generalized
gargoylism
Gaucher's disease
gaze palsy
gaze palsy, supranuclear
gaze palsy, vertical
gene
gene mutation
gene therapy
genetic counselling
genetic diagnosis
genetic diagnosis, prenatal
genetic linkage
genetic neurologic disorders
genetic screening
genetic testing
genu of corpus callosum
give-way weakness
globus pallidus
globus pallidus, lesion of
globus pallidus, lesion of, bilateral
glucocerebrosidase
glycogen storage disease
glycoprotein
GM1 ganglioside
GM1 ganglioside antibodies
granular osmiphilic material
growth retardation
Guillain Barre syndrome
Guillain Barre syndrome, ophthalmoplegia in
Hallervorden Spatz disease
hand pain
handwriting
head injury
headache
hearing loss
heat intolerance
heavy metal intoxication
hemiparesis
hemiplegia
hemisensory loss
hemorrhagic diathesis
hepatic failure
hepatitis
hepatolenticular degeneration(Wilson's disease)
hepatomegaly
hepatosplenomegaly
heralding manifestation
herpes virus infection
hexosaminidase-A
hexosaminidase-A and B
high arched feet
histochemistry
Hoover's sign
Hurler's syndrome
hydrocephalus
hyperreflexia
hypertonia
hypohidrosis
hypomyelination
hypotension, systemic
hypotonia
hypotonia, infants
iatrogenic neurologic disorders
imbalance
immunofluorescence
immunosuppression
inattention
inborn errors of metabolism
inborn errors of metabolism, screening
inclusion bodies
inclusion bodies, eosinophilic cytoplasmic
inclusion bodies, intracytopasmic
incoordination
infection, recurrent
intellectual deficit
intellectual deterioration
intelligence quotient
internuclear ophthalmoplegia
internuclear ophthalmoplegia, bilateral
intrathecal chemotherapy
intrathecal medication
intrinsic hand muscles, wasting of
introverted
iridoplegia
Jakob-Creutzfeldt disease
jaundice
Jewish
Kearns-Sayre syndrome
klippel feil syndrome
Krabbe's disease
kyphoscoliosis, neurologic causes of
lactic acidemia
Lafora's disease
laughing
laughing, pathologic
Laurence-Moon-Bardet-Biedl syndrome
lead poisoning
learning disability, in children
Leigh's disease
leprosy
leukocyte enzyme abnormality
leukocyte peroxidase
leukodystrophy
leukoencephalopathy
leukoencephalopathy, adult onset, sporadic
leukoencephalopathy, differential diagnosis
leukoencephalopathy, hereditary diffuse
Lewy body disease, diffuse
life expectancy
limb-girdle weakness
lipid storage disorder of CNS
liver disease
lymphadenopathy
lymphocyte fingerprint profiles
lysosomal storage disease
lysosomes, abnoral
macrocephaly
macular degeneration
marche a petits pas
Marinesco-Sjogren syndrome
megalencephaly
memory, defect of recent
memory, impairment of
meningitis, chronic
mental retardation
MERRF syndrome
metabolic disorder, primary
metabolic disorder, primary-screening tests
metachromatic leukodystrophy
metachromatic leukodystrophy, adult onset
metachromatic leukodystrophy, juvenile
metachromatic leukodystrophy, late-infantile
methotrexate
microangiopathy, brain
microcephaly
mimics
misdiagnosis
mitral valve prolapse
molecular genetics
mongolism
monoclonal antibodies
mortality
motor neuron disease
movement disorder
movement disorder, extrapyramidal
MRI
MRI, abnormal
MRI, black holes on
MRI, demyelinating disease
MRI, diffusion weighted
MRI, high signal foci on
MRI, hypointense signal foci on
MRI, magnetization transfer sequence
MRI, serial
MRI, spinal cord
MRS
mucopolysaccharidoses
multiple sclerosis
multiple sclerosis, differential diagnosis of
multiple sclerosis, disability status scale
multiple sclerosis, misdiagnosis
muscle biopsy
muscle spasm
muscle wasting, diffuse
muscle weakness
muscle weakness, proximal
muscular dystrophy, Duchenne
myelomalacia
myeloneuropathy
myelopathy
myocardial infarction
myoclonic jerks
myoclonus
myoclonus, epilepsy
myopathy
myopathy, mitochondrial
myopathy, vacuolar
myopia
N-acetyl-L-aspartic acid
negative
neonatal screening, genetic neurologic disorders
neoplasm, primary of CNS
nerve biopsy
neuraminidase deficiency
neuroaxonal dystrophy
neuroaxonal dystrophy, infantile
neuroaxonal dystrophy, juvenile
neuroaxonal leukodystrophy
neurofibrillary degeneration
neurogenic bladder
neuroichthyosis
neurolipidosis IV
neurologic complications of, systemic cancer
neurologic complications of, systemic disease
neurologic disease
neurologic disease, diagnoses of
neurologic examination
neurologic symptoms
neurologic testing
neuronal ceroid-lipofuscinosis
neuroophthalmology
neuropathic pain scale
neuropathology
neuropathology, brain
neuropathy
neuropathy, ataxic
neuropathy, demyelinating
neuropathy, diabetic
neuropathy, hereditary peripheral
neuropathy, medication induced
neuropathy, painful
neuropathy, peripheral
neuropathy, peripheral, treatment
neuropathy, small-fiber
neuropathy, small-fiber, painful sensory
neuropathy, toxic
neurosis
neurotoxin
next-generation sequencing
Niemann-Pick disease
night blindness
nystagmus
nystagmus, dissociated
one and a half syndrome
ophthalmoplegia
ophthalmoplegia, acute
ophthalmoplegia, bilateral, acute
ophthalmoplegia, plus syndrome
ophthalmoplegia, progressive external
ophthalmoplegia, total
optic atrophy
optic nerve
optic neuropathy
optokinetic nystagmus, abnormal
osteopetrosis
overlap syndrome
pain
pain, hysterical
pain, neuropathic
papillitis
paraparesis, familial spastic
paraplegia
paraproteinemia
Parkinson disease, postencephalitic
Parkinsonism syndrome
paroxysmal neurologic deficits
PAS positive
PAS positive material in the brain
patient in waiting
pediatric neurology
peroxisomal disease
personality change
pes cavus
photophobia
pigmentary retinopathy
polyglucosan body
polyglucosan body disease
polymerase chain reaction
polyneuropathy
polyneuropathy, chronic inflammatory demyelinating
polyneuropathy, chronic relapsing
polyneuropathy, uremic
Pompe's disease of glycogen storage
post herpetic neuralgia
posterior column disease
precipitating factors
preclinical
prenatal diagnosis by amniocentesis
prevention of neurologic disorders
prognosis
progressive myoclonic epilepsy
progressive neurologic disorder
proteinuria
pseudobulbar palsy
psychiatric disorder
psychiatric problems in neurologic disorders
psychological testing
psychological testing, children
psychomotor retardation
psychosis
psychotropic drugs
pupil, abnormality in neurologic disorders
putamen, lesion of
putamen, lesion of, bilateral
pyramidal tract
quadriparesis
quadriplegia
radiculopathy
rectal biopsy
refractive errors
Refsum's disease
remote effect of cancer on the nervous system
renal failure
respiratory failure
respiratory tract infection
retina, abnormal
retinal degeneration
retinal lesion
retinitis pigmentosa
retinopathy
retropulsion
review article
rigidity
safety
Salla disease
Sandhoff's disease
schizophrenia
scoliosis, neurologic association with
screening
sea-blue histiocytes
seizure
seizure, children
seizure, hysterical
seizure, laughing as manifestation
seizure, paradoxical
seizure, treatment of
sensorineural hearing loss
sensory loss
sensory loss, psychogenic
sensory testing
sensory testing, split midline on
serologic testing
short stature
sick sinus syndrome
skin, biopsy
skin, lesions in neurologic disorders
skull x-ray, abnormal
slit lamp examination
slurred speech
small vessel disease
spasticity
speech, delayed development of
sphingomyelin
spinal cord
spinal cord, compression of
spinal cord, injury of
spinal cord, injury, management of
spinal cord, lesion of
spine, injury of
spinocerebellar degeneration
splenomegaly
startle reaction
stem cell transplantation
storage disease of CNS
strabismus
stuttering
subacute sclerosing panencephalitis(S.S.P.E.)Dawson's disease
subdural hematoma
systemic illness
tandem gait, ataxic
tapetoretinal degeneration
Tay-Sachs disease
thalamus, lesion of
thalamus, lesion of-bilateral
thallium poisoning
thrombocytopenia
toe walking
tone, muscle, increased
tongue, enlarged
transcutaneous electrical nerve stimulation
treatment of neurologic disorder
tremor
tremor, intention
tricyclic antidepressant
tripping
tuberous sclerosis
Unverricht-Lundborg disease
urea-cycle enzymopathies
urinary incontinence
urinary sulfatidase excretion
urine test for metabolic disorders
Usher's syndrome
vasculitides
vasculopathy
ventricular enlargement
vertebral-basilar insufficiency
vertigo
vestibulopathy
vibratory sensation, abnormal
viral infection, CNS
vision, failure of in childhood
visual acuity, decreased
visual evoked response
visual field defect
visual fields, constricted
visual impairment
visual loss
visual loss, progressive
visual loss, slow
visual loss, transient
vitamin deficiency
vitamin E deficiency
Von Hippel Lindau
walking, delayed
walking, difficulty with
Wallerian degeneration
weakness
weakness, progressive
weakness, proximal
Werdnig-Hoffman disease
West disease
wheelchair
white matter disease
wide based gait
writing
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Clinical Manifestations and Diagnosis of Nocardiosis
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Showing articles 500 to 550 of 7779 << Previous Next >>