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abscess, intracerebral
abscess, intracerebral, multiple
achilles tendon, enlarged
acute ataxia of childhood
acute cerebellar ataxia
adolescent medicine
adult-onset leukodystrophy, with neuroaxonal spheroids
advances in neurology
adverse drug reaction
affect, flat
agitation
akathisia
alcohol intolerance
alpha-synuclein
alternating hemiplegia
alternating hemiplegia of childhood
alternating rapid movement
alternating rapid movement, impaired
Alzheimer's disease, misdiagnosis
amphetamines
amyotrophic lateral sclerosis
anemia
angiography, cerebral
animal exposure
ankle edema
anorexia
anosmia
anti IgLON5
anti Tr antibodies
anti Yo antibody
antidepressant
aphasia
aphonia
apnea
areflexia
ascites
ataxia
ataxia telangiectasia
ataxia, acute onset
ataxia, cerebellar
ataxia, progressive
ataxia, sensory
ataxia, truncal
ataxic gait
ATP1A3 gene
atypical
autoantibodies
autoimmune cerebellar ataxia
autoimmune disease
autoimmune encephalopathy
automatic behavior
automobile accidents
autonomic dysfunction
axonal spheroid
B 12 deficiency
B12
Babinski sign
basal ganglia, lesion of
basal ganglia, lesion, bilateral
behavioral disorder
Benedikt's syndrome
biologic markers
bovine spongiform encephalopathy
bradykinesia
bradyphrenia
brain atrophy
brain biopsy
brainstem, atrophy
brainstem, lesion of
brainstem, syndrome
bulbar palsy
burning paresthesia
C0ORF72
CAG repeats
carbon monoxide poisoning
carcinoma
carcinoma of breast
CAT scan, abnormal
CAT scan, angiography
CAT scan, angiography, false negative
CAT scan, emission, abnormal
CAT scan, venography
catalepsy
cataplexy
cataracts
cauda equina, enhancement
caudate nucleus, lesion of, bilateral
central nervous system, infection of
cerebellar ataxia, autosomal recessive
cerebellar ataxia, hereditary
cerebellar ataxia, neuropathy and vestibular areflexia syndrome
cerebellar atrophy, primary
cerebellar atrophy, secondary
cerebellar cognitive affective syndrome
cerebellar degeneration
cerebellar lesion
cerebellitis
cerebellitis, autoimmune
cerebellum, disease of
cerebral cortex
cerebral cortical atrophy
cerebral edema
cerebrospinal fluid, abnormal
cerebrospinal fluid, oligoclonal IgG in
cerebrospinal fluid, protein of
cerebrovascular accident, mimics
ceruloplasmin, serum
chewing movements
children
chills
choking
chorea
choreoathetosis
chromosomal abnormality
cingulate island sign
Claude's syndrome
Clinical Pathologic Conference(C.P.C.)
clonus
cognition
cognition, slowed
cogwheel rigidty
coma
coma, episodic
complications
confabulation
confusion
constipation
controversies in neurology
conversion reaction
corpus callosum, lesion of
cough
cranial nerve enhancement
cranial neuropathy
cranial neuropathy, multiple
Creutzfeldt-Jakob disease, genetic
crying, pathologic
cystatin C mutation
deep gray nuclei
degenerative diseases of CNS
delay in diagnosis
delusion
dementia
dementia, age at onset
dementia, familial
dementia, frontal lobe type
dementia, frontotemporal
dementia, presenile
dementia, rapidly progressive
dementia, reversible
dementia, thalamic
dementia, transmissible
dementia, treatment of
depression
developmental retardation
diabetes mellitus
diagnostic criteria
diarrhea
diet
differential diagnosis
difficulty climbing stairs
diplopia
disability, neurological
dizziness
dopa responsive dystonia
down-beat nystagmus
DPPX
DPPX, antibodies, encephalitis
driving
drooling
drowsiness
dural arteriovenous malformation
dysarthria
dysdiadochokinesia
dyskinesia
dysmetria
dysphagia
dystonia
dystonia, face
dystonia, focal
ear, pain in
edema, pedal
efficacy
electroencephalogram, periodic complexes
electromyogram
encephalitis
encephalitis, acanthamoeba
encephalitis, amebic
encephalitis, autoimmune
encephalomyelitis, postinfectious
encephalopathy
encephalopathy, delayed
encephalopathy, progressive
enolase
epidemiology of neurology
episodic disorders
episodic neurologic deficits
episodic unconsciousness
Epstein-Barr virus
Erdheim-Chester disease
escherichia coli
esophageal varices
executive dysfunction
exercise intolerance
eye movement, disorders of
facial expression abnormality
faciobrachial dystonic seizure
falling
false negative
familial
fasciculation
fatal familial insomnia
fatigue
fever
fine motor function, impaired
finger nose finger test
finger numbness
fingerprint bodies
Fisher C.M.
fistula, arterio-venous, dural
fluency
foam cells
foot numbness
Friedreich's ataxia
frontal lobe, anatomy and physiology
frontal lobe, atrophy
frontotemporal dementia, behavioral variant
gait disorder
gait, festinating
gamma amino butyric acid
gammaglobulin therapy, intravenous
gaze palsy, horizontal
gene
gene mutation
genetic counselling
genetic neurologic disorders
genetic testing
genu of corpus callosum
granular osmiphilic material
growth hormone
gyrus, abnormal
hallucination
hallucination, hypnagogic
hallucination, visual
hand weakness
hands, fisted
handwriting
head nodding
headache
hearing loss
heel swelling
heel-knee-shin test
hemidystonia
hemimyoclonic jerks
hemiparesis
hemorrhage, thalamic
hepatic encephalopathy
hepatic failure
hepatolenticular degeneration(Wilson's disease)
hepatolenticular degeneration(Wilson's disease), presymptomatic
heralding manifestation
herniation syndromes, intracranial
histiocytosis
HLA
hoarseness
hyperesthesia
hyperosmolality
hyperreflexia
hypersomnia
hypersomnia, idiopathic
hypoalbuminemia
hypocretin
hypoglycemia
hypometric saccades
hyponatremia
hypophonia
hyposmia
hypothalamus
hypotonia
iatrogenic neurologic disorders
imbalance
imbalance, postural
immunocompetent
immunohistochemistry
immunologic disease
immunomodulation
immunosuppression
immunotherapy
impulsivity
inattention
inclusion bodies
inclusion bodies, eosinophilic cytoplasmic
inclusion bodies, intranuclear
incontinence, fecal
incoordination
infectious mononucleosis
infectious mononucleosis, neurologic findings with
inferior olivary nucleus
insight, loss
insomnia
intellectual deficit
intellectual deterioration
intracranial hypertension, benign
intracranial pressure, increased
Jakob-Creutzfeldt disease
Jakob-Creutzfeldt disease, cerebellar variant
Jakob-Creutzfeldt disease, variant
Jakob-Creutzfeldt disease, young adult
Kayser-Fleischer ring
lactic acidemia
lateropulsion
laughing, pathologic
L-dopa
leg weakness, bilateral
lesions too numerous to count
leucine rich glioma inactivated 1 antibodies
leukocytosis
leukodystrophy
leukoencephalopathy
leukoencephalopathy, adult onset, sporadic
leukopenia
Lewy body
Lewy body disease, diffuse
limbic encephalitis
liver disease
liver function enzymes
lobar atrophy
logopenia
lumbar puncture, complications of
lymphoma
lymphoma involving CNS
lymphoma, primary of CNS
masked facies
MELAS syndrome
memory, defect of recent
memory, impairment of
meningeal enhancement
meningitis
meningitis, acinetobacter calcoaceticus var.antitratus
meningitis, carcinomatous
meningoencephalitis
meningoencephalitis, amoebic
mental status, abnormal
microcephaly
microhemorrhage, intracerebral
midbrain
midbrain, atrophy
midbrain, infarction of
midbrain, lesion of
middle cerebellar peduncle, lesion
migraine
mild cognitive impairment
mimics
misdiagnosis
mitochondrial disease
mitochondrial encephalomyopathy
modafinil
molecular genetics
monoclonal antibodies
mood change
mortality
motor neuron disease
motor neuron disease, misdiagnosis
movement disorder
movement disorder, extrapyramidal
movement disorder, hyperkinetic
MRI
MRI, abnormal
MRI, angiography
MRI, angiography, false negative
MRI, contrast enhanced
MRI, diffusion weighted
MRI, disappearing lesion on
MRI, false negative
MRI, fast
MRI, negative
MRI, perfusion
MRI, punctate pattern
MRI, venography
multiple sclerosis
multiple sclerosis, differential diagnosis of
multiple sclerosis, misdiagnosis
multiple sleep latency test
multiple system atrophy
muscle biopsy
muscle weakness, proximal
mutism
myasthenia gravis
myelinolysis, extrapontine
myelomalacia
myoclonic jerks
myoclonus
myoclonus, epilepsy
myopathy
myopathy, mitochondrial
myxedema, neurologic manifestations of
narcolepsy
nausea and vomiting
negative
nerve conduction studies
nerve root biopsy
neuroaxonal dystrophy
neuroaxonal leukodystrophy
neuroleptic
neuroleptic sensitivity
neurologic complications of, systemic disease
neurologic disease, diagnoses of
neurologic examination, focal
neurologic signs
neuron specific enolase
neuronal ceroid-lipofuscinosis
neuronal intranuclear inclusion disease
neuronal loss
neuronopathy, sensory
neuropathology
neuropathology, brain
neuropathy
neuropathy, sensory
next-generation sequencing
night sweats
Nothnagel's syndrome
numbness, generalized
nutritional deficiency
nystagmus
nystagmus, monocular
nystagmus, primary position of gaze
old age, neurology of
olivary degeneration, hypertrophic
ophthalmoplegia
ophthalmoplegia, progressive external
opportunistic infection
opportunistic infection, CNS
optic atrophy
orthostatic hypotension
osmotic demyelination syndrome
otitis, neurologic complications with
palatal myoclonus
paraneoplastic cerebellar degeneration
parasitic infection
parasitic infection, CNS
paresthesias
paresthesias, hands
parietal lobe, atrophy
Parkinson disease
Parkinson disease, dementia with
Parkinson disease, dystonia with
Parkinson disease, juvenile
Parkinson disease, L-dopa nonresponsive
Parkinson disease, nonmotor problems of
Parkinson disease, presymptomatic detection
Parkinsonism syndrome
paroxysmal hemiplegia
paroxysmal neurologic deficits
PAS positive
PAS positive material in the brain
pathologic reflex
penicillamine
perseveration
personality change
pituitary, hormones of
pleocytosis of cerebrospinal fluid
pleocytosis of cerebrospinal fluid, neutrophilic
POLG1 gene
polymerase chain reaction
polyneuropathy, chronic inflammatory demyelinating
polysomnogram
pons, lesion of
positional head-hanging test
post infectious cerebellar ataxia
posterior cortical atrophy
postinfectious
postural abnormality
potassium channel antibodies
practice guidelines
precipitating factors
pregnancy, neurologic complications in
prion disease
PRKN gene
prognosis
progressive ataxia and palatal tremor
progressive neurologic disorder
protein 14-3-3, cerebrospinal fluid
protein 14-3-3, cerebrospinal fluid, false negative
proteinuria
protozoan infection
pseudobulbar palsy
psychiatric disorder
psychiatric problems in neurologic disorders
psychomotor retardation
psychosis
psychosis, acute
ptosis
ptosis, bilateral
pull test
pupil, dilated and fixed, bilateral
pursuit eye movements, abnormal
rapid onset dystonia parkinsonism
rapidly fatal neurologic illness
rapidly progressing neurologic illness
reading disorder, acquired
real-time quaking-induced conversion
recurrent
regional cerebral blood flow
rehabilitation for neurologic disorders
release phenomena
REM sleep
REM sleep behavior disorder
remote effect of cancer on the nervous system
renal failure
renal stones
retropulsion
review article
RFC1 gene
rigidity
ritalin
rituximab
Romberg's sign
saccadic eye movements, abnormal
safety
salivation, excessive
sarcoidosis
schizophrenia
seizure
seizure, psychomotor-temporal lobe
selective serotonin reuptake inhibitors
sensorineural hearing loss
sensory loss, leg
sexual intercourse
short stature
sinemet
single photon emission computed tomography
sleep
sleep apnea
sleep offset paralysis
sleep onset paralysis
sleep paralysis
sleep pathology and physiology
slit lamp examination
slurred speech
smell
snoring
somnolence
spasticity
speech disorder
speech disorder, non aphasic
spinocerebellar ataxia
spinocerebellar ataxia type 7
splenomegaly
spongy degeneration of brain
spontaneous remission
square wave jerks
staggering
startle myoclonus
startle reaction
status epilepticus
stimulant drugs
storage disease of CNS
strokelike episodes
stuttering
suicide
swallow evaluation
sweating
symmetric brain lesions
synucleinopathy
systemic illness
tandem gait, ataxic
tau protein
tauopathy
temporal lobe, atrophy
temporal lobe, lesion
temporal lobe, lesion, bilateral
thalamus, lesion of
thalamus, lesion of-bilateral
third nerve palsy
third nerve palsy, bilateral
thrombocytopenia
titubation
tongue, fasciculations of
tonic foot response
treatment of neurologic disorder
tremor
tremor, cerebellar
tremor, intention
tremor, postural
trientine dihydrochloride
trinucleotide repeats
uncal herniation
unconsciousness
unconsciousness, episodic
unconsciousness, transient
undiagnosed
upgaze, paralysis of
urinary incontinence
vegetarianism
venous hypertension
venous ischemia
vertigo
vestibular areflexia
vestibulopathy
vibratory sensation, abnormal
viral infection
viral infection, CNS
vision, blurred
visual acuity, decreased
visuospatial disturbance
vitamin deficiency
vitamin E deficiency
vitiligo
vocalizations
voice, abnormality of
walking frame
walking, difficulty with
walking, difficulty with in dark
weakness
weakness, generalized
weakness, progressive
weight gain
weight loss
wheelchair
white matter disease
wide based gait
work loss
workup
zinc
Showing articles 700 to 750 of 1850 << Previous Next >>

Dilated Stomach and Weak Muscles
Lancet 356:1898, Rigby,S.P.,et al, 2000

Predictive Testing for Huntington's Disease: the Calm After the Storm
Lancet 356:1944-1945, Hayden,M.R., 2000

Motor and Cognitive Improvements in Patients with Huntington's Disease after Neurol Trasnplantation
Lancet 356:1975-1979,1945, Bachoud-Levi,A.,et al, 2000

A Five-Year Study of the Incidence of Dyskinesia in Patients With Early Parkinson's Disease who were Treated with Ropinirole or Levodopa
NEJM 342:1484-1491, Rascol,O.,et al, 2000

Presence of Diarrhea and Absence of Tendon Xanthomas in Patients With Cerebrotendinous Xanthomatosis
Arch Neurol 57:520-524, Verrips,A.,et al, 2000

Progressive Dementia and Gait Disorder in a 78 Year Old Woman
JNNP 68:526-531, Tagliati,M.,et al, 2000

Clinical Utility of Surface EMG: Report of the Therapeutics and Technology Assessment Subcommittee of the American Academy of Neurology
Neurol 55:171-177, Pullman,S.L. et al, 2000

Optic Neuritis in Multiple Sclerosis: An Update
The Neurologist 6:205-213, Chan,J.W., 2000

Inborn Errors of Metabolism as a Cause of Neurological Disease in Adults: An Approach to Investigation
JNNP 69: 5-12, Gray,R.G.F. et al, 2000

Family History and DNA Analysis in Patients With Suspected Huntington's Disease
JNNP 69:54-59, Siesling,S. et al, 2000

C1/C2 Rotary Subluxation Due to Spasmodic Torticollis
JNNP 69:135-136, Dalvie,S. et al, 2000

A Case of Lithium-Induced Asterixis
J Am Geriatr Society 48:457, Stewart,J.T. & Williams, L.S., 2000

Relation Between Cholinesterase Inhibitor and Pisa Syndrome
Lancet 355:2222, Kwak,Y.T. et al, 2000

Dynamic CT Perfusion Imaging of Acute Stroke
AJNR 21:1441-1449, Mayer,T.E. et al, 2000

14-3-3 Testing in Diagnosing Creutzfeldt-Jakob Disease
Neurol 55:514-516, Lemstra,A.W. et al, 2000

Treatable Dropped Head Syndrome in Hypothyroidism
Neurol 55:896-897, Askmark,H. et al, 2000

Misleading Results With the 14-3-3 Assay for the Diagnosis of Creutzfeldt-Jakob Disease
Neurol 55:1396-1397, Chapman,T.,et al, 2000

Diagnostic Accuracy of Dementia with Lewy Bodies
ArchNeurol 57:347-351, Hohl,U.,et al, 2000

Rotational Vertebral Artery Occlusion Syndrome with Vertigo Due to "Labyrinthine Excitation"
Neurol 54:1376-1379, Strupp,M.,et al, 2000

Clinicopath Conf,Cerebral Amyloid Angiogpathy and Giant-Cell Inflammatory Reaction to Beta 4-Amyloid and Vasculitis, Case 10-2000
NEJM 342:957-965, , 2000

Progression of Parkinsonian Signs in Alzheimer's Disease
Neurol 54:1284-1289, Wilson,R.S.,et al, 2000

Spontaneous and Reflex Movements in Brain Death
Neurol 54:221-223, Saposnik,G.,et al, 2000

Congenital Muscular Dystrophy with Rigid Spine Syndrome:A Clinical, Pathological, Radiological, and Genetic Study
Ann Neurol 47:152-161, 143, Flanigan,K.M.,et al, 2000

Myoclonus Secondary to Albuterol (Salbutamol) instillation
Neurol 54:2022-2023, Micheli,F.,et al, 2000

Progressive Multifocal Leukoencephalopathy Presenting with an Isolated Focal Movement Disorder
Movement Disorder 15:1006-1009, Stockhammer,G.,et al, 2000

A 5-Month, Randomized, Placebo-controlled Trial of Galantamine in AD
Neurol 54:2269-2276, Tariot,P.N.,et al, 2000

Galantamine in AD
Neurol 54:2261-2268, Raskind,M.A.,et al, 2000

Niemann-Pick Disease Type C: Two Cases and an Update
Movement Disorders 15:1199-1203, Uc,E.Y.,et al, 2000

Lymphomatosis Cerebri Presenting as a Rapidly Progressive Dementia: Clinical, Neuroimaging and Pathologic Findings
Dement Geriatr Cogn Disord 10:152-157, Bakshi,R.,et al, 1999

Seizures and Creutzfeldt-Jakob Disease
NCMJ 60:108-109, Cokgor,I.,et al, 1999

Restless Legs Syndrome Improved By Pramipecole, A Double-Blind Randomized Trial
Neurol 52:938-943, Montplaisir,J.,et al, 1999

Parkinsonism after Taking Ecstasy
NEJM 340:1443, Mintzer,S.,et al, 1999

Oculogyric Crisis as an Initial Manifestation of Wilson's Disease
Neurol 52:714-715, Lee,M.S.,et al, 1999

Lamotrigine-Induced Tourettism
Neurol 52:1191-1194, Lombroso,C.T., 1999

Rapidly Progressive Dementia
Lancet 353:1150, Bornke,C.,et al, 1999

Clinicopath Conf:Burkitt-Like B-Cell Lymphoma, Nocardiosis
NEJM 340:1188-1196, Case 11-1999, 1999

Clinicopath Conf:Lymphoplasmocytic Lymphoma with Motor Neuronopathy,Waldenstrom's Macroglobulinemia
NEJM 340:1661-1669, , 1999

Familial Paroxysmal Dystonic Choreoathetosis,Clinical Findings in a Large Japanese Family and Genetic Linkage to 2q
Arch Neurol 56:721-726, Matsuo,H.,et al, 1999

Molecular Basis of the Neurodegenerative Disorders
NEJM 340:1970-1980, Martin,J.B., 1999

Focal, Steroid Responsive Myositis Causing Dropped Head Syndrome
Muscle & Nerve 22:769-771, Biran,I.,et al, 1999

Prognostic Factors of Guillain-Barre Syndrome After Intravenous Immunoglobulin or Plasma Exchange?
Neurol 53:598-604, Visser,L.H.,et al, 1999

Amyloid Myopathy:An Underdiagnosed Entity
Ann Neurol 43:719-728, Spuler,S.,et al, 1999

Adult-Onset Nemaline Myopathy:Another Cause of Dropped Head
Muscle & Nerve 22:1146-1150, Lomen-Hoerth,C.,et al, 1999

Neuro-Ophthalmic Manifestations of Diabetes
Ophthalmology 106:1047-1048, Sadun,A.A., 1999

Rapid-Onset Dystonia-Parkinsonism:Linkage to Chromosome 19q13
Ann Neurol 46:176-182, Kramer,P.L.,et al, 1999

Adult-Onset "Infant" Botulism:An Unusual Cause of Weakness in the Intensive Care Unit
Neurol 53:891, Li,L.Y.J.,et al, 1999

A Randomized Trial of Risperidone,Placebo,and Haloperidol for Behavioral Symptoms of Dementia
Neurol 53:946-955,899, DeDeyn,P.P.,et al, 1999

Acute Dystonia Induced by Drug Treatment
BMJ 319:623-626, vanHarten,P.N.,et al, 1999

Clinicopath Conf, Creutzfeldt-Jakob Disease,Case 28-1999
NEJM 341:901-908, , 1999

Weak at the Knees
Lancet 354:1696, Webster,G.&Beynon,H., 1999



Showing articles 700 to 750 of 1850 << Previous Next >>