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aciduria
adverse drug reaction
akinetic mute
algorithm
alien hand syndrome
altered states of consciousness
Alzheimer's disease
amnesia
AMPA receptor antibodies
amygdala
amyotrophic lateral sclerosis, misdiagnosis
anemia
anemia, iron deficiency
angiitis, isolated of CNS
anti HMGCR antibody
antibodies to myelin oligodendrocyte glycoprotein
anticholinergic drugs
antimicrosomal antibodies
antithyroid antibodies
aphasia
aphasia, progressive, primary
aphonia
apraxia
ataxia
ataxic gait
atypical
autoantibodies
autoimmune basal ganglia encephalitis
autoimmune disease
autoimmune encephalopathy
autoimmune GFAP astrocytopathy
autonomic cardiovascular reflexes
autonomic dysfunction
axonal degeneration
axonal injury
B 12 deficiency
Babinski sign
basal ganglia
basal ganglia, infarction
basal ganglia, lesion of
basal ganglia, lesion, bilateral
behavioral disorder
biopterin deficiency
biotin
biotin deficiency
biotin deficiency, juvenile form
biotin-responsive basal ganglia disease
blepharospasm
blinking, reduced
botulinum toxin
brachium pontis
bradykinesia
brain atrophy
brain biopsy
brainstem, lesion of
burst suppression pattern, electroencephalogram
cachexia
camptocormia
carbamazepine
carcinoma
carcinoma of lung
CAT scan
CAT scan, abnormal
CAT scan, chest
CAT scan, emission
CAT scan, emission, abnormal
celiac disease, adult
central nervous system, infection of
cerebellar lesion
cerebellum
cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy
cerebral cortex
cerebral cortical atrophy
cerebral infarction, subcortical
cerebral palsy
cerebrospinal fluid, abnormal
cerebrospinal fluid, elevated protein of
cerebrovascular accident
cerebrovascular accident, mimics
cerebrovascular disease
children
chondroitin sulfate C
chromosomal abnormality
chromosome 14
chromosome 19
chronic lymphocytic inflammation with pontine perivascular enhancement responsive to steroids
Clinical Pathologic Conference(C.P.C.)
clinical trials
clonus
cognition
cogwheel rigidty
coma
complications
compulsivity
confusion
contractures, joint
coronavirus
cortical-basal ganglionic degeneration
COVID-19
creatine phosphokinase(CPK)elevated
deep gray nuclei
degenerative diseases of CNS
delay in diagnosis
delusion
dementia
dementia, differential diagnosis of
dementia, rapidly progressive
dementia, reversible
dementia, screening for
dementia, subcortical
dementia, treatment of
depression
developmental milestones, loss of
diagnostic criteria
differential diagnosis
diplopia
disorientation
diurnal variation
dizziness
dopa responsive dystonia
dopamine
drug induced neurologic disorders
dysarthria
dyskinesia
dysmetria
dysphagia
dystonia
dystonia musculorum deformens
dystonia, axial
dystonia, cervical
dystonia, children
dystonia, classification
dystonia, etiology of
dystonia, evaluation of
dystonia, face
dystonia, focal
dystonia, painful
dystonia, treatment of
DYT1 mutation
edema, periorbital
efficacy
electrical stimulation
electroencephalogram
electroencephalogram, abnormalities of
electroencephalogram, focal delta activity
electroencephalogram, triphasic delta waves
electromyogram
electron microscopy
emotional lability
encephalitis
encephalitis, autoimmune
encephalitis, brainstem
encephalitis, paraneoplastic
encephalitis, viral
encephalopathy
encephalopathy, Hashimoto's
encephalopathy, metabolic
encephalopathy, progressive
enzyme, defect
epilepsia partialis continua
equinovarus
evidence-based research
extralimbic encephalitis
extraocular muscle enlargement
extraocular muscle lesion
extrapyramidal movement disorder, progressive
eye movement, disorders of
eye, pain in
failed medical management
falling
familial
fever
fluctuate
foot deformity
frontal behavioral spatial syndrome
gadolinium
gait disorder
galactorrhea
gammaglobulin therapy, intravenous
gastrointestinal disease, neurologic complications
gaze palsy
gaze palsy, supranuclear
gaze palsy, vertical
gene
gene mutation
genetic counselling
genetic neurologic disorders
genetic testing
gests antagoniste
GFAP-IgG
glabellar sign
GLUT1 deficiency syndrome
glutamic acid decarboxylase, antibody
gluten-free diet
granulomatosis with polyangiitis
gyrus, abnormal
hallucination
hand weakness
hands, fisted
head injury
head nodding
headache
hemidystonia
hemiparesis
hepatolenticular degeneration(Wilson's disease)
heralding manifestation
herpes simplex encephalitis
hippocampus
hippocampus, hyperintense
Hodgkin's disease
Hodgkin's disease, neurologic involvement with
hummingbird sign
hyperreflexia
hypertension
hyperthyroidism
hypertonia
hyponatremia
hypophonia
hyporeflexia
hypothyroidism
iatrogenic neurologic disorders
imbalance
imbalance, postural
immunohistochemistry
immunologic disease
immunosuppressive agents
immunotherapy
inappropriate antidiuretic(A.D.H.)hormone
inborn errors of metabolism
inclusion bodies
inclusion bodies, eosinophilic cytoplasmic
insular cortex
intellectual deterioration
intestinal biopsy
iron, serum, low
Jakob-Creutzfeldt disease
L-dopa
leg spasms
leg spasms, painful
leg weakness, bilateral
lethargy
leukoencephalopathy
level of consciousness, decreased
level of consciousness, fluctuating
Lewy body
Lewy body disease, diffuse
limbic encephalitis
limbic system
liver function enzymes
malabsorption
malabsorption syndrome
malignancy screen
marche a petits pas
masked facies
mediastinum, mass of
memory, defect of recent
memory, impairment of
meningeal enhancement
meningitis
meningoencephalitis
meningoencephalomyelitis
mental status, abnormal
mesial temporal lobe
methotrexate
microangiopathy, brain
midbrain
midbrain, atrophy
mimics
Mini Mental Status Examination
misdiagnosis
molecular genetics
movement disorder
movement disorder, drug induced
movement disorder, extrapyramidal
movement disorder, treatment of
MRI
MRI pattern
MRI, abnormal
MRI, contrast enhanced
MRI, contrast enhanced, curvilinear pattern
MRI, contrast enhanced, high dose
MRI, curvilinear peppering enhancement
MRI, diffusion weighted
MRI, disappearing lesion on
MRI, FLAIR
MRI, linear enhancement
MRI, mass effect on
MRI, negative
MRI, nodular enhancement
MRI, orbit
MRI, punctate pattern
MRI, serial
MRI, spinal cord
MRS
multiple sclerosis
multiple sclerosis, treatment of
multiple system atrophy
muscle biopsy
muscle biopsy, extraocular
muscle pain
muscle spasm
muscle weakness
myelitis
myelitis, autoimmune
myelitis, longitudinal
myelopathy
myoclonus
myopathy
myopathy, drug-induced
myopathy, necrotizing
myopathy, necrotizing, autoimmune
myopathy, steroid responsive
myopathy, toxic
myositis
myositis, ocular
necrotizing vasculitis
neuroaxonal degeneration
neurochemistry
neurologic complications of, systemic disease
neurologic disease, diagnoses of
neurologic disease, tempo
neurologic examination, focal
neurologic signs
neurologic symptoms
neuromuscular disease, electrodiagnosis of
neuromyelitis optica spectrum disorder
neuropathology
neuropathology, brain
neuropsychiatry
neurotomy
new onset refractory status epilepticus
next-generation sequencing
NMDA antagonists
nystagmus, gaze-evoked
nystagmus, upbeating on upgaze
obsessive-compulsive disorder
ophelia syndrome
optic neuropathy
orbit, biopsy
orbit, inflammation in
orbit, lesions of
orbital apex
orthostatic hypotension
oscillopsia
pain
pallidotomy
panic attacks
papillitis
paraparesis
Parkinson disease
Parkinson disease, akinetic form
Parkinson disease, arteriosclerotic
Parkinson disease, asymmetric onset
Parkinson disease, benign tremulous
Parkinson disease, dementia with
Parkinson disease, diagnosis
Parkinson disease, differential diagnosis of
Parkinson disease, duration
Parkinson disease, dystonia with
Parkinson disease, early symptoms
Parkinson disease, fluctuations in
Parkinson disease, heterogeneity of
Parkinson disease, intractable
Parkinson disease, juvenile
Parkinson disease, L-dopa nonresponsive
Parkinson disease, misdiagnosis
Parkinson disease, nonmotor problems of
Parkinson disease, on-off phenomena in
Parkinson disease, prognosis of
Parkinson disease, rapid onset
Parkinson disease, rapid progression
Parkinson disease, surgical treatment of
Parkinson disease, treatment of
Parkinson disease, tremor, absence of
Parkinson disease, unilateral
Parkinson disease, young onset
Parkinsonism multiple-system atrophy
Parkinsonism syndrome
paroxysmal neurologic disorder
perivascular enhancement
perivascular inflammation
personality change
pleocytosis of cerebrospinal fluid
pons, atrophy
pons, lesion of
pontocerebellar atrophy
postural abnormality
practice guidelines
prion disease
prognosis
progressive encephalomyelitis with rigidity syndrome
progressive neurologic disorder
progressive supranuclear palsy
prolactin, elevated
proptosis
proptosis, unilateral
pseudobulbar palsy
psychiatric disorder
psychiatric problems in neurologic disorders
psychosis
psychotic behavior
ptosis
ptosis, unilateral
pull test
pyramidal tract dysfunction
rapid onset dystonia parkinsonism
rapidly progressing neurologic illness
recurrent
Red flags
release phenomena
remote effect of cancer on the nervous system
responsive cortical stimulation
reversible neurologic disorder
review article
rigidity
risk factors
risk-benefit assessment
rituximab
Romberg's sign
saccadic eye movements, abnormal
safety
salivary gland enlargement
sarcoidosis, CNS
Saudi Arabia
scoliosis
scotoma
seizure
seizure, children
seizure, drug resistance
seizure, focal
seizure, intractable
seizure, intractable, treatment of
seizure, medication failure
seizure, surgical treatment of
seizure, treatment of
sensory tricks
serologic testing
seronegative
severe acute respiratory syndrome
short stature
sialadenitis
sinemet
skin, biopsy
small vessel disease
snout reflex
spasticity
speech disorder
speech disorder, childhood
spinal cord, lesion of
splenium of corpus callosum
stare
statin therapy
statin therapy, discontinuation
status epilepticus
status epilepticus, recurrent
stereotaxic surgery
steroid
steroid responsive encephalitis
steroid responsive encephalopathy
steroid therapy, CNS treatment and complications with
stimulation, deep brain
striatal encephalitis
striatum, lesion of
striatum, lesion of, bilateral
strokelike episodes
stuporous
substantia nigra
supratentorial lymphocytic inflam parenchy perivasc enhanc responsive to steroids
swallow evaluation
symmetric brain lesions
synucleinopathy
syphilis, neurologic complications with
systemic illness
tandem gait, ataxic
tardive dystonia
tau protein
tauopathy
temporal lobe
temporal lobe, lesion
temporal lobe, lesion, bilateral
tetrahydrobiopterin
thalamotomy
thalamus, focused ultrasound ablation
thyroglobulin antibodies
thyroid peroxidase antibodies
thyroid stimulating immunoglobulins
thyroiditis
thyrotropin
toe walking
tonic foot response
torticollis
toxic encephalopathy
transglutaminase antibodies
transient neurologic deficit
treatment of neurologic disorder
tremor
tremor, intention
tremor, postural
tremor, surgical treatment of
tremor, treatment of
tripping
tumor necrosis factor
tyrosine hydroxylase deficiency
ultrasonography
urinary incontinence
urinary retention
vasculitides
viral infection
viral infection, CNS
visual field defect
visual loss
vitamin D deficiency
vitamin deficiency
walking
walking frame
walking, difficulty with
weakness
weakness, proximal
weight loss
West Nile fever
wheelchair
white matter disease
wide based gait
workup
Showing articles 50 to 89 of 89 << Previous

Practice Parameter: Diagnosis and Prognosis of New Onset Parkinson Disease (An Evidence-Based Review)
Neurol 66:968-975, Suchowersky,O.,et al, 2006

Dopa-responsive Dystonic Camptocormia
Neurol 66:1779, Van Gerpen,J.A., 2006

Clinicopath Conf, Dopamine-Responsive-Dystonia Caused by a Mutation in the GCH1 Gene
NEJM 355:831-839, Case 26-2006, 2006

Dystonia
NEJM 355:818-829, Tarsy,D. &Simon,D.K., 2006

MR Findings in Hashimoto Encephalopathy
AJNR 25:807-808, Song,Y.M.,et al, 2004

Clinicopath Conf, Multiple-System Atrophy
NEJM 351:912-921, Case 27-2004, 2004

An Organic Cause of Neuropsychiatric Illness in Adolescence
Lancet 361:572, Taylor,S.E.,et al, 2003

Hashimoto Encephalopathy
Arch Neurol 60:164-171, Chong,J.Y.,et al, 2003

Amnesic Syndrome with Bilateal Mesial Temporal Lobe Involvement in Hashimoto's Encephalopathy
Neurol 54:737-739, McCabe,D.J.H.,et al, 2000

Hashimoto's Encephalitis as a Differential Diagnosis of Creutzfeldt-Jakob Disease
JNNP 66:172-176, Seipelt,M.,et al, 1999

Diagnostic Criteria for Parkinson Disease
Arch Neurol 56:33-39, Gelb,D.J.,et al, 1999

Clinical Correlates of Vascular Parkinsonism
Arch Neurol 56:98-102, Winikates,J.&Jancovic,J., 1999

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

Long-Term Follow-Up of Levodopa Responsiveness in Generalized Dystonia
Arch Neurol 55:1320-1323, Dewey,R.B.,et al, 1998

Natural History & Survival of 14 Pts with Corticobasal Degeneration Confirmed as Postmortem Exam
JNNP 64:184-189, Wenning,G.K.,et al, 1998

Steroid-Responsive Myopathy with Deficient Chondroitin Sulfate C in Skeletal Muscle Conn Tissue
Neurol 50:526-529, Al-Lozi,M.T.,et al, 1998

Dopa-Responsive Dystonia, Some Pieces of the Puzzle are Still Missing
Neurol 50:853-855, Nygaard,T.G.&Wooten,G.F., 1998

Comparison of Extrapyramidal Features in 31 Path Cases of Diffuse Lewy Body Disease & 34 Cases of Parkinson's
Neurol 48:376-380, Louis,E.D.,et al, 1997

Reversible MRI Findings in a Patient with Hashimoto's Encephalopathy
Neurol 49:246-247, Bohnen,N.I.L.J.,et al, 1997

Posteroventral Medial Pallidotomy in Levodopa-Unresponsive Parkinsonism
Arch Neurol 54:1026-1029, Krauss,J.K.,et al, 1997

A Woman with a Relapsing Psychosis Who Got Better with Prednisone
Lancet 347:1288, Cohen,L.,et al, 1996

Some Specific Clinical Features Differentiate Multiple System Atrophy (Striatonigral Variety) from Parkinson's Disease
Arch Neurol 52:294-298, Colosimo,C.,et al, 1995

Electroencephalographic Findings in Hashimoto's Encephalopathy
Neurol 45:977-981, Henchey,R.,et al, 1995

Dopamine, Dystonia, and the Deficient Co-Factor
Lancet 345:1130, Williams,A.C., 1995

Multiple System Atrophy presenting as Parkinsonism:Clinical Features and Diagnostic Criteria
JNNP 59:144-151, Albanese,A.,et al, 1995

Early Differential Diagnosis of Parkinson's Disease with F-flurodeoxyglucose and Positron Emission Tomography
Neurol 45:1995-2004, Eidelberg,D.,et al, 1995

Dopa-Responsive Dystonia:Pathological and Biochemical Observations in a Case
Ann Neurol 35:396-402, 3811994., Rajput,A.H.,et al, 1994

A Clinicopathologic Study of 100 Cases of Parkinson's Disease
Arch Neurol 50:140-148, Hughes,A.J.,et al, 1993

Comparison of Striatal 18F-dopa Uptake in Adult-Onset Dystonia-Parkinsonism, Parkinson's & Dopa-Responsive Dystonia
Neurol 43:1563-1568, Turjanski,N.,et al, 1993

Levodopa-Nonresponsive Lewy Body Parkinsonism:Clinicopathologic Study of Two Cases
Neurol 42:1323-1327, Mark,M.H.,et al, 1992

Stereotactic Ventrolateralis Thalamotomy for Refractory Tremor in Post-Levodopa Era Parkinson's Dis
J Neurosurg 75:723-730, Fox,M.W.,et al, 1991

Hashimoto's Encephalopathy:A Steroid-Responsive Disorder Associated with High Anti-Thyroid Antibody Titers-Report of 5 Cases
Neurol 41:228-233, Shaw,P.J.,et al, 1991

Dopa-Responsive Dystonia:Long-Term Treatment Response and Prognosis
Neurol 41:174-181, Nygaard,T.G.,et al, 1991

Dopa-responsive Dystonia:[18F]Dopa Positron Emission Tomography
Ann Neurol 30:24-30, Sawle,G.V.,et al, 1991

Stereotaxic Thalamotomy-Experiences from the Levodopa Era
JNNP 53:427-430, Wester,K.&Hauglie-Hanssen,E., 1990

Dopa-Responsive Dystonia:The Spectrum of Clinical Manifestations in a Large North American Family
Neurol 40:66-69, Nygaard,T.G.,et al, 1990

Dopa Responsive Dystonia:A Treatable Condition Misdiagnosed as Cerebral Palsy
BMJ 298:1019-1020, Boyd,K.&Patterson,V., 1989

Diffuse Lewy Body Disease:Clinical Features in 15 Cases
JNNP 52:709-717, Byrne,E.J., 1989

Hereditary Dystonia-Parkinsonism Syndrome of Juvenile Onset
Neurol 36:1424-1428, Nygaard,T.C.&Duvoisin,R.C., 1986

An 81-Year-Old Man with Imbalance and Memory Impairment
, Golbe,L.I.,et al,



Showing articles 50 to 89 of 89 << Previous