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Differential
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accommodation
accomodation, abnormal
achilles tendon, enlarged
acquired immunodeficiency syndrome
acquired immunodeficiency syndrome dementia complex
adverse drug reaction
affect, flat
alexia
algorithm
alien hand syndrome
Alzheimer's disease
amyotrophic lateral sclerosis
ANA
angiography, cerebral, beaded vessels
angiography, cerebral
angiography, cerebral, negative
anomic aphasia
anticholinergic drugs
antiviral agents
aphasia
aphasia, classification of
aphasia, progressive, primary
apraxia
arthralgia
ataxia
ataxia, cerebellar
ataxia, frontal
ataxia, hereditary
ataxia, progressive
ataxic gait
autoimmune disease
Babinski sign
bacterial infection
bacterial infection, CNS
basal ganglia, degeneration
behavior modification
behavioral disorder
Bell's phenomenon
blinking
blinking, reduced
bradykinesia
bradyphrenia
brain atrophy
brain biopsy
brainstem, lesion of
C0ORF72
cachexia
calcium antagonist
camptocormia
carbon monoxide poisoning
CAT scan, abnormal
CAT scan, angiography
CD4 counts
cerebellar atrophy, primary
cerebellar degeneration
cerebellitis
cerebellum, disease of
cerebral cortical atrophy
cerebrospinal fluid, abnormal
cerebrospinal fluid, drainage of
cerebrospinal fluid, elevated protein of
cerebrovascular accident
cerebrovascular accident, young adult
children
chronic lymphocytic inflammation with pontine perivascular enhancement responsive to steroids
Clinical Pathologic Conference(C.P.C.)
cognition
cogwheel rigidty
coma
complications
concentration, impaired
confusion
conjunctivitis
contractures, joint
convergence
convergence, impaired
conversion reaction
corpus callosum
corpus callosum, lesion of
cortical-basal ganglionic degeneration
Coxiella burnetti
crying, pathologic
cryopyrin-associated periodic syndrome
cystatin C mutation
degenerative diseases of CNS
dementia
dementia, familial
dementia, frontal lobe type
dementia, frontotemporal
dementia, presenile
dementia, rapidly progressive
dementia, subcortical
demyelinating disease
depression
developmental retardation
diagnostic criteria
differential diagnosis
digital subtraction angiography
diplopia
disability, neurological
disconnection syndrome
dizziness
dopamine agonist
drug induced neurologic disorders
dysarthria
dysdiadochokinesia
dysmetria
dysphagia
dyspraxia
dystonia
electroencephalogram, abnormalities of
electroencephalogram, triphasic delta waves
electromyogram
encephalitis
encephalitis, brainstem
encephalitis, human immunodeficiency virus type 1
encephalitis, viral
encephalopathy
encephalopathy, delayed
episodic disorders
Erdheim-Chester disease
eye movement, disorders of
falling
familial
fasciculation
fatigue
fever
fever, recurrent
finger nose finger test
Fisher C.M.
foam cells
Friedreich's ataxia
frontal behavioral spatial syndrome
frontal bossing
frontal lobe, atrophy
frontal lobe, behavior with disease of
frontal lobe, pathologic signs of
frontotemporal dementia, behavioral variant
gait disorder
gait, apraxic
gait, festinating
gait, spastic
gaze palsy, vertical
gene
gene mutation
genetic neurologic disorders
genetic testing
glabellar sign
grasp reflex
hallucination
hallucination, visual
handwriting
head circumference
headache
headache, awakened by
headache, awakening with
headache, bifrontal
headache, occipital
headache, recurrent
headache, severe
hearing loss
heel swelling
hemiparesis
highly active antiretroviral therapy
hip flexor weakness
histiocytosis
human immunodeficiency virus type 1
hydrocephalus
hydrocephalus, normal pressure
hydrocephalus, normal pressure, etiology
hyperreflexia
hypersomnia
hypertrophic intracranial pachymeningitis
hypometric saccades
hypomyelination
hypophonia
hyporeflexia
imbalance
imbalance, postural
immune reconstitution inflammatory syndrome
immunosuppression
immunosuppressive agents
impulsivity
inattention
incontinence, fecal
infection
intellectual deficit
intellectual deterioration
intracerebral hemorrhage
irritability
Jakob-Creutzfeldt disease
Jakob-Creutzfeldt disease, cerebellar variant
jaw jerk, abnormal
kinesia paradoxica
lacunar infarction
laughing, pathologic
L-dopa
leg dragging
leg weakness, bilateral
Legionnaires'disease
lethargy
Lewy body
lobar atrophy
lumbar drain
marche a petits pas
masked facies
memory, defect of recent
memory, impairment of
meningitis
meningitis, aseptic
meningitis, neurologic aspects and complications of
mental status, abnormal
micrographia
middle cerebellar peduncle, lesion
miosis
misdiagnosis
motor dysfunction
motor neuron disease
movement disorder
movement disorder, extrapyramidal
movement disorder, psychogenic
MRI
MRI, abnormal
MRI, angiography
MRI, contrast enhanced
MRI, contrast enhanced, high dose
MRI, diffusion weighted
MRI, disappearing lesion on
MRI, high signal intensity of basal ganglia
MRI, negative
MRI, nodular enhancement
multimodal neuroimaging
multiple system atrophy
mutism
myelopathy
myoclonus
nausea and vomiting
neurologic complications of, systemic disease
neurologic disease, diagnoses of
neurologic disease, tempo
neurologic examination
neurologic signs
neurologic symptoms
neuropathology
neuropathy, demyelinating
next-generation sequencing
nystagmus
nystagmus, gaze-evoked
nystagmus, upbeating on upgaze
ocular motility, disorders of
old age, neurology of
opportunistic infection, CNS
optic ataxia
optic atrophy
optic atrophy, bilateral
oscillopsia
paranoia
paraparesis, spastic
Parkinson disease
Parkinson disease, diagnosis
Parkinson disease, freezing phenomena in
Parkinson disease, L-dopa nonresponsive
Parkinson disease, pathogenesis of
Parkinson disease, surgical treatment of
Parkinson disease, treatment of
Parkinsonism syndrome
PAS positive
PAS positive material in the brain
pathologic reflex
patient information and support
Pelizaeus Merzbacher
perivascular enhancement
Persistent postural-perceptual dizziness
personality change
pes cavus
photophobia
pleocytosis of cerebrospinal fluid
pneumonia
polymerase chain reaction
polymerase chain reaction, false negative
pons, lesion of
posterior leukoencephalopathy syndrome
precipitating factors
prion disease
prognosis
progressive multifocal leucoencephalopathy
progressive neurologic disorder
progressive supranuclear palsy
proprioception, abnormal
pseudobulbar palsy
psychiatric problems in neurologic disorders
psychological testing
psychological testing, neurologic problems
psychomotor retardation
pupil
pupil, light reflex, abnormal
Q fever
rash
recurrent
red eye
reflex, cutaneous
release phenomena
respiratory tract infection
retropulsion
reversible cerebral vasoconstrictive syndromes
reversible neurologic disorder
review article
rickettsial organism
rigidity
rooting reflex
seizure
selective serotonin reuptake inhibitors
sensorineural hearing loss
sensory loss
serologic testing
serotonin norepinephrine reuptake inhibitors
short stature
short steps
shunt procedure, ventricular
shunt procedure, ventricular-complications of
sinemet
single photon emission computed tomography
skin, lesions in neurologic disorders
skull bone, thickening
slow virus infection of CNS
slurred speech
smell
snout reflex
somnolence
speech disorder
speech, soft
splenium of corpus callosum
spongy degeneration of brain
stare
startle myoclonus
startle reaction
steroid therapy, CNS treatment and complications with
stooped posture
subarachnoid hemorrhage
subarachnoid hemorrhage, cerebral convexity
subcortical U fibers
suck reflex
suicide
systemic illness
systemic lupus erythematosus
tandem gait, ataxic
tau protein
tauopathy
temporal lobe, atrophy
thrombocytopenia
tongue, fasciculations of
transient neurologic deficit
treatment of neurologic disorder
tremor
tremor, resting
turning in bed
twins
upgaze
upgaze, paralysis of
urinary incontinence
vasculopathy
vasospasm, cerebral
ventriculostomy
vibratory sensation, abnormal
viral infection
viral infection, CNS
visual impairment
voice, abnormality of
walking frame
walking, difficulty with
weakness, generalized
weight loss
wheelchair
white matter disease
wide based gait
writing
Showing articles 550 to 600 of 1411 << Previous Next >>

Glutamic Acid Decarboxylase Autoantibodies and Neurological Disorders
Neurol Sci 23:145-151, Vianello,M.,et al, 2002

Reversible Metronidazole-Induced Lesions of the Cerebellar Dentate Nuclei
NEJM 346:68-69, Woodruff,B.K.,et al, 2002

Spinocerebellar Ataxia Type 10 is Rare in Populations Other Than Mexicans
Neurol 58:983-984, Matsuura,T.,et al, 2002

Clinicopath Conf, Primary Lymphoma of CNS
NEJM 346:1009-1015, Case 10-2002, 2002

Friedreich Ataxia
Arch Neurol 59:743-747, Lynch,D.R.,et al, 2002

Gluten Sensitivity as a Neurological Illness
JNNP 72:560-563, Hadjivassiliou,M.,et al, 2002

Spontaneous Intracranial Hypotension Causing Reversible Frontotemporal Dementia
Neurol 58:1285-1287, Hong,M.,et al, 2002

Opsoclonus-myoclonus Syndrome Following Epstein-Barr Virus Infection
Neurol 58:1131-1132, Verma,A. &Brozman,B., 2002

Acquired Sexual Parphilia in Patients with Multiple Sclerosis
Arch Neurol 59:1006-1010, Frohman,E.M.,et al, 2002

Utility of Clinical Criteria in Differentiating Frontotemporal Lobar Degeneration (FTLD) From AD
Neurol 58:1608-1615, Rosen,H.J.,et al, 2002

Nanging
Lancet 360:384, Ng, J. &Frith, R., 2002

Clinical Features and ATTCT Repeat Expansion in Spinocerebellar Ataxia Type 10
Arch Neurol 59:1285-1290, Grewal,R.P.,et al, 2002

Neurological Presentation of Fabry's Disease in a 52 Year Old Man
JNNP 73:340-342, Mohanraj,R.,et al, 2002

Clinicopath Conf., Sarcordosis with Hilar and Cervical Lymphadenopathy
NEJM 347:1350-1357, Case 33-2002, 2002

Clinicopath Conf., Acute Disseminated Encephalomyelitis
NEJM 347:1433-1440, Case 34-2002, 2002

Abnormality of Gait as a Predictor of Non-Alzheimer's Dementia
NEJM 347:1761-1768, Verghese,J.,et al, 2002

Legionella Infection
emedicine.com, Mobeen,R., 2002

Fragile X Premutation Carriers: Characteristic MR Imaging Findings of Adult Male Patients with Progressive Cerebellar and Cognitive Dysfunction.
AJNR 23:1757-1766, Brunberg,J.A.,et al, 2002

Brainstem Gliomas in Adults: Prognostic Factors and Classification
Brain 124:2528-2539, Guillamo,J.-S.,et al, 2001

Effects of Bilateral Subthalamic Nucleus Stimulation on Parkinsonian Gait
Neurol 57:144-146, Stolze,H.,et al, 2001

Neurology of Ciguatera
JNNP 70:4-8, Pearn,J., 2001

Clinicopath Conf, Lymphocytic Meningitis and Lymphocytic Encephalomyelitis, Sensory Neuronopathy, Gangliositis, Small-Cell Carcinoma of Lung
NEJM 345:1758-1765, Case 38-2001, 2001

Spinocerebellar Ataxia Type 2 Presenting as Familial Levodopa-Responsive Parkinsonism
Ann Neurol 50:812-815, Shan,D.,et al, 2001

Recessive Ataxia With Ocular Apraxia
Arch Neurol 58:201-205,173, Barbot,C.,et al, 2001

Cerebellar Ataxia With Anti-Glutamic Acid Decarboxylase Antibodies
Arch Neurol 58:225-230, Honorat,J.,et al, 2001

SCA-12: Tremor with Cerebellar and Cortical Atrophy is Associated with a CAG Repeat Expansion
Neruol 56:299-303,287, O'Hearn,E.,et al, 2001

Headache and CNS White Matter Abnormalities Associated with Gluten Sensitivity
Neurol 56:385-388, Hadjivassiliou,M.,et al, 2001

Genetic Testing in Spinocerebellar Ataxias
Arch Neurol 58:191-195, Tan,E. &Ashizawa,T., 2001

Confusion After Antibiotics
Lancet 357:1410, Gavazzi,C.,et al, 2001

Gluten Sensitivity in Sporadic and Hereditary Cerebellar Ataxia
Ann Neurol 49:540-543, Bushara,K.O.,et al, 2001

Clinical and Neuroradiologic Features of Acute Disseminated Encephalomyelitis in Children
Neurol 56:1308-1312,1257, Hynson,J.L.,et al, 2001

Monoataxia of Upper Extremity in Motor Cortical Infarction
Neurol 56:1418-1419, Noda,K.,et al, 2001

Bilateral Abducens Nerve Paresis Associated with Anti-GQ1b IgG Antibody
Am J Ophthalmol 131:816-818, Sato, K. and Yoshikawa, H., 2001

Ataxia Associated with Hashimotos Disease: Progressive Non-Familial Adult Onset Cerebellar Degeneration with Autoimmune Thyroiditis
JNNP 71:81-87, Selim, M. and Drachman, D.A., 2001

Clinicopath Conf., Pick's Disease, Case 11-2000
NEJM 342:1110-1117, , 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

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

Rhombencephalitis Caused by West Nile Fever Virus
Neurol 55:153, Nichter,C.A. et al, 2000

Evolution of Sporadic Olivopontocerebellar Atrophy Into Multiple System Atrophy
Neurol 55:527-532, Gilman,S. et al, 2000

Abnormal White Matter Signal in Ataxia Telangiectasia
AJNR 21:1483-1485, Ciemins,J.J. & Horowitz,A.L., 2000

Spinocerebellar Ataxia Type 8
Neurol 55:649-657, Day,J.W. et al, 2000

Linkage of Familial Amyotrophic Lateral Sclerosis with Frontotemporal Dementia to Chromosome 9q21-q22
JAMA 284:1664-1669, Hosler,B.A.,et al, 2000

The Clinical Spectrum of Anti-GAD Antibody-Positive Patients with Stiff-Person Syndrome
Neurol 55:1531-1535, Dalakas,M.C.,et al, 2000

Increased Levels of Plasma Malondialdehyde in Friedreich Ataxia
Neurol 55:1752-1753,1600, Emond,M.,et al, 2000

Paraneoplastic Cerebellar Ataxia Due to Autoantibodies Against a Glutamate Receptor
NEJM 342:21-27, Smitt,P.S.,et al, 2000

Very Late-Onset Friedreich Ataxia Despite Large GAA Triplet Repeat Expansions
Arch Neurol 57:246-251, Bidichandani,S.I.,et al, 2000

A Six-Year-Old Girl with Tick paralysis
NEJM 342:90-94, Felz,M.W.,et al, 2000

The Value of Pelvic Thrusting in the Diagnosis of Seizures and Pseudoseizures
Neurol 54:227-229, Geyer,J.D.,et al, 2000

Nitrous Oxide Anesthesia-Associated Myelopathy
ArchNeurol 57:380-382, Marie,R.,et al, 2000



Showing articles 550 to 600 of 1411 << Previous Next >>