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Differential
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achilles tendon, enlarged
acute ataxia of childhood
acute cerebellar ataxia
agitation
akinetic mute
alcohol intolerance
alcoholism
alternating rapid movement
alternating rapid movement, impaired
ammonia
ANA
anasarca
anemia
angiography, cerebral
ankle edema
anorexia
anti Yo antibody
aphasia
aphonia
areflexia
ascites
ataxia
ataxia telangiectasia
ataxia, acute onset
ataxia, cerebellar
ataxia, progressive
ataxia, sensory
ataxia, truncal
ataxic gait
atypical
autoantibodies
autoimmune encephalopathy
automobile accidents
B 12 deficiency
Babinski sign
bacterial infection
basal ganglia, lesion of
basal ganglia, lesion, bilateral
behavior, combative
behavioral disorder
belligerent
biologic markers
blepharospasm
bradykinesia
brain biopsy
brainstem, atrophy
brainstem, lesion of
CAG repeats
carbon monoxide poisoning
carcinoma
carcinoma of breast
cardiomyopathy
CAT scan
CAT scan, angiography
CAT scan, angiography, false negative
CAT scan, perfusion
CAT scan, venography
cataracts
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
cerebrospinal fluid, oligoclonal IgG in
cerebrovascular accident
cerebrovascular accident, complications with
cerebrovascular accident, location of
cerebrovascular accident, multiple
cerebrovascular accident, silent
ceruloplasmin, serum
choking
chromosomal abnormality
chromosome 17
Clinical Pathologic Conference(C.P.C.)
clonus
cognition
cognition, slowed
coma
complications
confusion
cortical infarction
cough
cranial nerve palsies
cranial neuropathy, multiple
Creutzfeldt-Jakob disease, genetic
crying, pathologic
cystatin C mutation
deep gray nuclei
delay in diagnosis
delirium
delusion
dementia
dementia, familial
dementia, frontal lobe type
dementia, frontotemporal
dementia, presenile
dementia, rapidly progressive
dementia, thalamic
dementia, transmissible
depression
dexterity, impaired
diabetes mellitus
diarrhea
diet
differential diagnosis
difficulty climbing stairs
diplopia
disability, neurological
disorientation
dizziness
down-beat nystagmus
down-beat nystagmus, primary position of gaze
DPPX
DPPX, antibodies, encephalitis
drooling
dural arteriovenous malformation
dysarthria
dysdiadochokinesia
dysgraphia
dysmetria
dysphagia
dystonia
dystonia, face
dystonia, focal
ear, pain in
echolalia
edema, pedal
EDTA(ehtylenediamine tetraacetic acid)
ejection fraction, abnormal
electroencephalogram, abnormalities of
electroencephalogram, periodic complexes
electromyogram
emotional lability
encephalitis
encephalitis, autoimmune
encephalitis, brainstem
encephalomyelitis, postinfectious
encephalopathy
encephalopathy, delayed
encephalopathy, progressive
Epstein-Barr virus
Erdheim-Chester disease
esophageal varices
euphoria
executive dysfunction
eye movement, disorders of
facial expression abnormality
falling
false negative
familial
fatigue
fever
fine motor function, impaired
finger nose finger test
finger numbness
fistula, arterio-venous, dural
foam cells
food-borne infection
Friedreich's ataxia
frontal lobe, atrophy
gait disorder
gammaglobulin therapy, intravenous
gastric partitioning
gaze palsy, horizontal
gene
gene mutation
genetic neurologic disorders
genetic testing
Gerstmann-Straussler-Scheinker disease
grandiosity
hallucination
hand weakness
hands, fisted
handwriting
head nodding
headache
heel swelling
heel-knee-shin test
hemidystonia
hemorrhage, thalamic
hepatic encephalopathy
hepatic failure
hepatolenticular degeneration(Wilson's disease)
hepatolenticular degeneration(Wilson's disease), presymptomatic
heralding manifestation
hiccoughs
hiccoughs, intractable
histiocytosis
hoarseness
hyperammonemic encephalopathy
hyperesthesia
hyperhomocysteinemia
hyperosmolality
hyperreflexia
hypersomnia
hypoalbuminemia
hypometric saccades
hypotonia
iatrogenic neurologic disorders
imbalance
imbalance, postural
immunohistochemistry
impulsivity
inattention
incarceration
incontinence, fecal
incoordination
infection
infectious mononucleosis
infectious mononucleosis, neurologic findings with
inferior olivary nucleus
insomnia
intellectual deficit
intellectual deterioration
Jakob-Creutzfeldt disease
Jakob-Creutzfeldt disease, cerebellar variant
Jakob-Creutzfeldt disease, variant
Kayser-Fleischer ring
lactic dehydrogenase(LDH)
lateropulsion
laughing, pathologic
leg swelling
leukoencephalopathy
leukopenia
level of consciousness, decreased
listeria monocytogenes
listeriosis, CNS
liver disease
liver function enzymes
lobar atrophy
logopenia
lumbar puncture, complications of
lymphoma
lymphoma involving CNS
lymphoma, primary of CNS
manganese intoxication
mania
masked facies
medulla oblongata, lesion of
memory, defect of recent
memory, impairment of
meningitis-encephalitis PCR panel
mental status, abnormal
methylmalonic acid, serum
methylmalonic acidemia
micrographia
microhemorrhage, intracerebral
midbrain, atrophy
middle cerebellar peduncle, lesion
misdiagnosis
molecular genetics
mood change
mortality
motor neuron disease
movement disorder
movement disorder, extrapyramidal
MRI
MRI, abnormal
MRI, angiography
MRI, angiography, false negative
MRI, contrast enhanced
MRI, diffusion weighted
MRI, disappearing lesion on
MRI, false negative
MRI, negative
MRI, punctate pattern
MRI, ring sign
MRI, T1 weighted high signal foci
MRI, venography
multiple sclerosis, differential diagnosis of
multiple sclerosis, misdiagnosis
muscle biopsy
mutism
myelinolysis, extrapontine
myelomalacia
myoclonic jerks
myoclonus
myoclonus, stimulus sensitive
nausea and vomiting
neck pain
neoplastic angioendotheliosis
nerve conduction studies
neurologic disease, diagnoses of
neurologic signs
neuronopathy, sensory
neuropathology
neuropathy
neuropathy, sensory
next-generation sequencing
nutritional deficiency
nystagmus
olivary degeneration, hypertrophic
ophthalmoplegia, progressive external
optic atrophy
osmotic demyelination syndrome
otitis, neurologic complications with
palatal myoclonus
paraneoplastic cerebellar degeneration
paranoia
paraphasias
paresthesias
paresthesias, hands
Parkinson disease
Parkinson disease, L-dopa nonresponsive
Parkinsonism syndrome
pathologic reflex
penicillamine
pernicious anemia
personality change
pleocytosis of cerebrospinal fluid
POLG1 gene
polymerase chain reaction
pons, lesion of
positional head-hanging test
post infectious cerebellar ataxia
postinfectious
postural abnormality
pregnancy, neurologic complications in
prion disease
prion protein gene
prisoner
prognosis
progressive ataxia and palatal tremor
progressive neurologic disorder
protein 14-3-3, cerebrospinal fluid
pseudobulbar palsy
psychiatric disorder
psychiatric problems in neurologic disorders
psychomotor retardation
psychosis
psychotic behavior
ptosis
ptosis, bilateral
pull test
pursuit eye movements, abnormal
RAPID CT perfusion maps
rapid onset dystonia parkinsonism
rapidly progressing neurologic illness
reading disorder, acquired
real-time quaking-induced conversion
rehabilitation for neurologic disorders
release phenomena
remote effect of cancer on the nervous system
renal stones
retropulsion
reversible neurologic disorder
review article
rigidity
Romberg's sign
saccadic eye movements, abnormal
seizure
sleep pathology and physiology
slit lamp examination
slurred speech
spasticity
speech disorder
speech disorder, non aphasic
speech, loss of
speech, pressured
speech, slowed
spinocerebellar ataxia
spinocerebellar ataxia type 7
splenomegaly
spongy degeneration of brain
spontaneous remission
square wave jerks
staggering
startle myoclonus
startle reaction
suicide
swallow evaluation
symmetric brain lesions
systemic illness
tandem gait, ataxic
tangential
tau protein
tauopathy
thalamus, lesion of
thalamus, lesion of-bilateral
thrombocytopenia
titubation
tongue, numbness of
treatment of neurologic disorder
tremor
tremor, cerebellar
tremor, intention
trientine dihydrochloride
trinucleotide repeats
upgaze, paralysis of
urinary incontinence
venous hypertension
venous ischemia
vertigo
vestibulopathy
vibratory sensation, abnormal
viral infection
viral infection, CNS
vision, blurred
visual acuity, decreased
vitamin E deficiency
voice, abnormality of
walking frame
walking, difficulty with
weight loss
welder
wheelchair
white matter disease
wide based gait
work loss
workup
writing
zinc
Showing articles 650 to 700 of 754 << Previous Next >>

Mutism after Closed Head Injury
Arch Neurol 40:601-606, Levin,H.S.,et al, 1983

Unrecognized Chronic Lithium Neurotoxic Reactions
JAMA 250:2029-2030, Lewis,D.A., 1983

Recognising & Preventing Duchenne Muscular Dystrophy
BMJ 287:1083-1084, Firth,M.A.,et al, 1983

Motor Aphasia Unaccompanied by Faciobrachial Weakness
Neurol 33:519-521, Masdeu,J.C.,et al, 1983

Blepharospasm & Orofacial-Cervical Dystonia:Clinical & Pharmacological Findings in 100 Patients
Ann Neurol 13:402-411, Jankovic,J.,et al, 1983

Juvenile Progressive Bulbar Palsy
Arch Neurol 40:351-353, Albers,J.W.,et al, 1983

Supranuclear Gaze Palsy in Familial Creutzfeldt-Jakob Disease
Arch Neurol 40:618-622, Bertoni,J.M.,et al, 1983

Dialysis Encephalopathy, Clinical, Electroencephalographic & Interventional Aspects
Medicine 62:129-141, O'Hare,J.A., 1983

Delayed Neurologic Sequelae in Carbon Monoxide Intoxication
Arch Neurol 40:433-435, Choi,I.I.S., 1983

Clin. Path. Conference
Multiple-System Atrophy with Parkinsonism, Case 28-13, NEJM 308:1406-1414983., , 1983

Global Aphasia Without Hemiparesis:A Sign of Embolic Encephalopathy
Neurol 32:403-406, VanHorn,G.,et al, 1982

Localization in Transcortical Sensory Aphasia
Arch Neurol 39:475-478, Kertesz,A.,et al, 1982

Spinocerebellar Degeneration Secondary to Chronic Intestinal Malabsorption:A Vitamin E Deficiency Syndrome
Ann Neurol 12:419-424, Harding,A.E.,et al, 1982

"Tip-of-the-tongue"Phenomenon in Parkinson Disease
Neurol 32:567-570, Matison,R.,et al, 1982

The Child Who is Slow to Talk
BMJ 285:671-672, Robinson,R.J., 1982

Aphasia With Nonhemorrhagic Lesions in the Basal Ganglia & Internal Capsule
Arch Neurol 39:15-20, Damasio,A.R.,et al, 1982

Narcolepsy-Cataplexy
Arch Neurol 39:164-168, Kales,A.,et al, 1982

Pronounced Cerebellar Features in Legionnaires'Disease
BMJ 283:276, Maskill,M.R., 1981

Primary Lateral Sclerosis
Arch Neurol 38:630-633, Beal,M.F.,et al, 1981

Speech Disorders of Parkinsonism:A Review
JNNP 44:751-758, Critchley,E.M.R., 1981

Von Recklinghausen Neurofibromatosis
NEJM 305:1617-1627, Riccardi,V.M., 1981

Metastasis to the Base of the Skull:Clinical Findings in 43 Patients
Neurol 31:530-537, Greenberg,H.S.,et al, 1981

Paroxysmal Symptoms as the First Manifestations of Multiple Sclerosis
JNNP 43:296-304, Twomey,J.A.,et al, 1980

Adult Celiac Disease Presenting as Cerebellar Syndrome
Neurol 30:245-249 1980., Finelli,P.F.,et al, 1980

The Aphasia Syndrome of Stroke in the Left Anterior Cerebral Artery Territory
Arch Neurol 37:97-l00, Alexander,M.P.,et al, 1980

Acquired Aphasia with Convulsive Disorder:Course & Prognosis
Neurol 30:524-529, Mantovani,J.F.,et al, 1980

Human Cerebellar Hypoplasia, A Syndrome of Diverse Causes
Arch Neurol 37:300-305, Sarnatt,H.B.,et al, 1980

Juvenile Metachromatic Leukodystrophy
Arch Neurol 37:42-46, Haltia,T.,et al, 1980

Ocular Myasthenia:Diagnosis & Therapy
In Neuro-Ophthalmology, Vol X ed. by J. Glaser. CV Mosby Co, St. Louis, Daroff,R., 1980

Sydenham Chorea:An Update
Neurol 30:331-334, Nausieda,P.A.,et al, 1980

Aphasia After Left Hemispheric Intracerebral Hemorrhage
Neurol 30:1193-1202, Alexander,M.P.,et al, 1980

Children's Language Disorders:Recent Research Advances
Ann Neurol 7:497-507, Ludlow,C.L., 1980

Narcolepsy:Regional Cerebral Blood Flow During Sleep & Wakefulness
Neurol 29:61-67, Sakai,F.,et al, 1979

Tapia's Syndrome
Arch Neurol 36:257-260, Schoenberg,B.S.,et al, 1979

Language Deficits After Apparent Clinical Recovery from Childhood Aphasia
Ann Neurol 6:405-409, Woods,B.,et al, 1979

Aphemia with Hemiplegic Migraine
Neurol 29:1317-1318, Jenkyn,L.R., 1979

Fusiform Basilar Artery Aneurysm in a Child
Neurol 29:1045-1049, Read,D.,et al, 1979

Dysarthria-Clumsy Hand Syndrome Produced by Capsular Infarct
Ann Neurol 6:263-265, Spertell,R.B.,et al, 1979

Familial Periodic Ataxia
Arch Neurol 36:568-569, Donat,J.R.,et al, 1979

Aphasia Rehabilitation
Arch Neurol 36:187, Benson,D.F., 1979

Aphasia, The Sole Manifestation of Focal Status Epilepticus
Neurol 29:745-748, Hamilton,N.G.,et al, 1979

Self-Limited Granulomatous Angiitis of the Cerebellum
Ann Neurol 5:490-492, Beresford,H.R.,et al, 1979

Hereditary Paroxysmal Ataxia:Response to Acetazolamide
Neurol 28:1259-1264, Griggs,R.C.,et al, 1978

Aphasia Following Infarction of the Left Supplementary Motor Area
Neurol 28:1220-1223, Masdeu,J.C.,et al, 1978

Identification of Speech Lateralization by Intracarotid Injection of Methohexital
Ann Neurol 4:86, Willmore,L.J.,et al, 1978

Changing Patterns of Childhood Aphasia
Ann Neurol 3:273, Woods,B.T.,et al, 1978

Speech Arrest in a Dextral with a Right MesialFfrontal Astrocytoma
Arch Neurol 35:252, Caplan,L.R.,et al, 1978

Diagnosis of Treatable Wilson's Disease
NEJM 298:1347, Cartwright,G.E., 1978

Dominant Spinopontine Atrophy
Arch Neurol 35:156, Pogacar,S.,et al, 1978

Clinical Aspects of Spasmodic Dysphonia
JNNP 41:361, Aminoff,M.J.,et al, 1978



Showing articles 650 to 700 of 754 << Previous Next >>