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aciduria
acquired immunodeficiency syndrome
acquired immunodeficiency syndrome-related complex
advances in neurology
adverse drug reaction
agitation
akathisia
akinesia of eyelid function
alcohol
algorithm
alien hand syndrome
Alzheimer's disease
amantadine
anomic aphasia
anterocollis
anti basal ganglia antibodies
anti IgLON5
anticholinergic drugs
aphasia
aphasia, progressive, primary
aphonia
applause sign
apraxia
apraxia of eye movements
apraxia of eyelid opening
apraxia, constructional
arm swing, reduced
astrocytoma
asymptomatic
ataxia
ataxia, progressive
athetosis
athetosis, causes of
attention deficit disorder with hyperactivity
atypical
autoantibodies
autoimmune basal ganglia encephalitis
autoimmune disease
autonomic dysfunction
axillary nerve
Babinski sign
baclofen
basal ganglia
basal ganglia, degeneration
basal ganglia, infarction
basal ganglia, lesion of
basal ganglia, lesion, bilateral
behavioral disorder
benign essential tremor
bent spine syndrome
beta adrenergic blocker
biologic markers
biopterin deficiency
blepharitis
blepharospasm
blinking
blinking, reduced
botulinum toxin
bradykinesia
bradykinesia, facial
brain atrophy
Brueghel's syndrome
bruxism
bulbar palsy
butyrophenone
calcium antagonist
calcium antagonist, side effects of
calculations
camptocormia
carbamazepine
carbon monoxide poisoning
CAT scan
CAT scan, abnormal
CAT scan, emission
CAT scan, emission, abnormal
CAT scan, false negative
CAT scan, muscle
catecholamine
central hypoventilation
central nervous system, infection of
cerebral cortical atrophy
cerebral ischemia
cerebral palsy
cerebrospinal fluid
cerebrospinal fluid, abnormal
cerebrovascular accident
cerebrovascular accident, complications with
ceruloplasmin, serum
Charcot's sign
children
China
chorea
chorea, causes of
choreoathetosis
chromosomal abnormality
chromosome 14
chromosome 19
chromosome 20
chromosome 6
cinnarizine
cirrhosis
Clinical Pathologic Conference(C.P.C.)
clozapine
cognition
cogwheel rigidty
complications
comprehension, impaired
conjugate gaze, forced
consanguinity
contractures, joint
convergence, impaired
conversion reaction
copper metabolism, abnormal
cortical-basal ganglionic degeneration
creatine phosphokinase(CPK)elevated
crying, pathologic
cultured skin fibroblasts
cyanide poison
deep gray nuclei
degenerative diseases of CNS
delay in diagnosis
dementia
depression
developmental milestones, loss of
developmental retardation
dexterity, impaired
diagnostic criteria
differential diagnosis
diplopia
disability, neurological
diurnal variation
dopa responsive dystonia
dopamine
dopamine agonist
dopamine antagonist
downward gaze
drooling
drug induced neurologic disorders
drug withdrawal
dysarthria
dyskinesia
dyskinesia, buccal lingual facial
dyskinesia, causes of
dyskinesia, drug induced
dyslexia
dysmetria
dysphagia
dyspraxia
dystonia
dystonia musculorum deformens
dystonia, axial
dystonia, cervical
dystonia, children
dystonia, classification
dystonia, delayed onset
dystonia, drug induced
dystonia, etiology of
dystonia, evaluation of
dystonia, face
dystonia, focal
dystonia, painful
dystonia, post traumatic
dystonia, psychogenic
dystonia, treatment of
dystonic reaction, acute
DYT1 mutation
efficacy
electromyogram
emotional lability
encephalitis
encephalitis lethargica
encephalitis, autoimmune
encephalitis, brainstem
encephalitis, viral
encephalopathy
encephalopathy, progressive
enzyme, defect
epidemiology of neurology
equinovarus
exercise
exercise-induced neurologic dysfunction
extrapyramidal
extrapyramidal movement disorder, progressive
eye movement, disorders of
facial appearance, abnormal
facial expression abnormality
falling
familial
fine motor function, impaired
flunarizine
fluoxetine
foot deformity
frontal behavioral spatial syndrome
frontal lobe, atrophy
gait disorder
gait, apraxic
galactorrhea
gamma amino butyric acid
gangliosidosis GM1
gaze palsy
gaze palsy, supranuclear
gaze palsy, vertical
gene
gene mutation
genetic counselling
genetic diagnosis, prenatal
genetic neurologic disorders
genetic testing
gests antagoniste
Gilles de la Tourette syndrome
glabellar sign
globus pallidus
globus pallidus, lesion of
globus pallidus, lesion of, bilateral
GLUT1 deficiency syndrome
grasp reflex
grimacing
Hallervorden Spatz disease
Hallervorden Spatz disease, late onset
hallucination, visual
haloperidol
hand weakness
hands, fisted
head injury
head nodding
hearing loss
hemiballismus
hemichorea
hemidystonia
hemifacial spasm
hemiparesis
hepatic encephalopathy
hepatic encephalopathy, treatment of
hepatic failure
hepatolenticular degeneration(Wilson's disease)
hepatosplenomegaly
heralding manifestation
HLA
hoarseness
homovanillic acid
human immunodeficiency virus type 1
Huntington's chorea
hyperreflexia
hyperthermia
hypertonia
hypometric saccades
hypophonia
hyporeflexia
iatrogenic neurologic disorders
ideomotor apraxia
imbalance
imbalance, postural
inattention
inborn errors of metabolism
incontinence, fecal
infusion pump
insomnia
intellectual deficit
intellectual deterioration
intracerebral hemorrhage
iron, brain
Jakob-Creutzfeldt disease
jaw jerk, abnormal
Kayser-Fleischer ring
kyphosis
language disorder in adults
laughing, pathologic
L-dopa
L-dopa, delayed treatment in Parkinsonism
L-dopa, drug interactions with and side effects of
L-dopa, enteral infusion, continuous
leg spasms
leg spasms, painful
Leigh's disease
levitation
Lewy body disease, diffuse
lipid storage disorder of CNS
lithium
liver disease
lobar atrophy
low back pain
manganese intoxication
masked facies
medical-legal aspects of neurology
memory, defect of recent
memory, impairment of
meningitis
mental status, abnormal
metabolic disorder, primary
metoclopramide
midbrain
midbrain, atrophy
mimics
misdiagnosis
mitochondrial disease
molecular genetics
monoamines
mortality
movement disorder
movement disorder, delayed onset
movement disorder, drug induced
movement disorder, extrapyramidal
movement disorder, psychogenic
movement disorder, treatment of
MRI
MRI, abnormal
MRI, CAT scan compared to
MRI, diffusion weighted
MRI, eye of tiger sign
MRI, gradient-echo
MRI, high signal foci on
MRI, high signal intensity of basal ganglia
MRI, mouse ears
MRI, negative
MRI, paramagnetic effect
MRI, susceptibility weighted
MRI, T1 weighted high signal foci
multiple sclerosis
multiple system atrophy
muscle biopsy
muscle spasm, face
muscle weakness
muscular dystrophy
mutism
myasthenia gravis
myoclonic jerks
myoclonus
myoclonus, segmental
myopathy
myopathy, metabolic
mysoline
neck flexion
neoplasm, intracranial
neoplasm, primary intracerebral
neoplasm, primary of CNS
neurochemistry
neurodegeneration with brain iron accumulation
neuroleptic
neuroleptic malignant syndrome
neuroleptic, atypical
neurologic complications
neurologic complications of, surgery
neurologic disease
neurologic disease, diagnoses of
neurologic disease, diagnoses of, clinical bedside
neurologic disease, tempo
neurologic signs
neurologic symptoms
neuroophthalmology
neuropathology
neurotomy
neurotoxin
neurotransmitter
next-generation sequencing
Niemann-Pick disease
nonsteroidal anti-inflammatory drug
norepinephrine
obsessive-compulsive disorder
ocular motility, disorders of
ocular myopathy
ocular myopathy, differential diagnosis
oculogyric crisis
old age, neurology of
opened mouth
ophthalmoplegia
optokinetic nystagmus, abnormal
pain
palilalia
PANK2 mutation
paraparesis
paraplegia, in flexion
parasomnia
paraspinal muscle
paraspinal muscle weakness
parkin gene
Parkinson disease
Parkinson disease, atypical
Parkinson disease, axial symptoms
Parkinson disease, differential diagnosis of
Parkinson disease, drug induced
Parkinson disease, dystonia with
Parkinson disease, familial
Parkinson disease, fluctuations in
Parkinson disease, freezing phenomena in
Parkinson disease, juvenile
Parkinson disease, L-dopa nonresponsive
Parkinson disease, mode of onset
Parkinson disease, on-off phenomena in
Parkinson disease, postencephalitic
Parkinson disease, prognosis of
Parkinson disease, progression
Parkinson disease, psychogenic
Parkinson disease, rapid onset
Parkinson disease, surgical treatment of
Parkinson disease, treatment of
Parkinson disease, tremor, absence of
Parkinson disease, unilateral
Parkinson disease, young onset
Parkinsonism syndrome
paroxysmal nonkinesigenic dyskinesia
pathologic reflex
patient information and support
penguin silhouette sign
penicillamine
personality change
phenothiazine
phenothiazine, dyskinesia associated with
phenylketonuria
Pick's disease
pigmentary retinopathy
pleocytosis of cerebrospinal fluid
POLG1 gene
polycythemia, secondary
pons, lesion of
postural abnormality
procyclidine
prognosis
progressive neurologic disorder
progressive supranuclear palsy
prolactin, elevated
propranolol
pseudobulbar palsy
psychiatric disorder
psychiatric problems in neurologic disorders
psychomotor retardation
psychosis
ptosis
pull test
putamen, lesion of
putamen, lesion of, bilateral
quadriplegia
rapid onset dystonia parkinsonism
rapidly progressing neurologic illness
reading problem, causes of
Red flags
reflex sympathetic dystrophy
release phenomena
renal failure
repetition, impaired
respirations in CNS disease
restless leg syndrome
retinal degeneration
retinitis pigmentosa
retinopathy
retrocollis
retropulsion
Rett's syndrome
reversible neurologic disorder
review article
rhabdomyolysis
rigidity
rigidity, axial
Riley-Day syndrome
running
saccadic eye movements, abnormal
salivation, excessive
scoliosis
seizure
selective serotonin reuptake inhibitors
sensorineural hearing loss
sensory loss
sensory loss, cortical
sensory tricks
sequencing difficulty
short stature
sinemet
single photon emission computed tomography
sleep apnea, obstructive
sleep pathology and physiology
slit lamp examination
somnolence
spastic dysphonia
speech disorder
speech disorder, childhood
speech, loss of
splenomegaly
stare
stimulation, deep brain
stimulation, thalamic
stooped posture
striatal encephalitis
subarachnoid hemorrhage
substantia nigra
suck reflex
swallow evaluation
symmetric brain lesions
tardive dyskinesia
tardive dyskinesia, treatment of
tardive dystonia
tasikinesia
tau protein
tauopathy
tetrabenazine
tetrahydrobiopterin
thalamic tumors
thalamus, lesion of
thalamus, lesion of-bilateral
tic
toe walking
tonic foot response
tonic spasms
torticollis
torticollis, post traumatic
toxoplasmosis, CNS
trauma
treatment failure
treatment of neurologic disorder
tremor
tremor, intention
tremor, jaw
tremor, leg
tremor, post traumatic
tremor, postural
tremor, psychogenic
tremor, treatment of
tremor, voice
tripping
tyrosine hydroxylase deficiency
upgaze
upgaze, paralysis of
urinary incontinence
vasospasm, cerebral
viral infection
viral infection, CNS
vision, blurred
visual symptoms
visuospatial disturbance
vocal cord paralysis
walking
walking frame
walking, difficulty with
weakness, progressive
wheelchair
Whipple's disease
wide based gait
workup
writers cramp
xerophthalmia
X-linked dystonia-parkinsonism syndrome
Showing articles 0 to 50 of 1659 Next >>

A Young Woman With Hypertonia, Severe Scoliosis, and Encephalopathy
JAMA Neurol 81:83-84, Hua,L.,et al, 2024

A 6-Year-Old Girl with Progressive Toe Walking
Neurol 98:e769-e773, Libdeh, A.A. & Ibrahim, A., 2022

Neurodegeneration with Brain Iron Accumulation
AIAN 22:267-276, Batla, A. & Gaddipati, C., 2019

MR Imaging of the Brain in Neurologic Wilson Disease
AJNR 40:178-183, Yu, X.-E.,et al, 2019

Thalamic Deep Brain Stimulation for Tremor in Parkinson Disease, Essential Tremor, and Dystonia
Neurol 89:1416-1423, Cury, R.G.,et al, 2017

Clinical Manifestations of the anti-IgLON5 Disease
Neurol 88:1736-1743,1688, Gaig, C.,et al, 2017

A Demure Teenager and Her Dystonic Foot
Neurol 89:e71-e75, Cullinane, P.W.,et al, 2017

Clinical, Genetic, and Radiological Features of Extrapyramidal Movement Disorders in Mitochondrial Disease
JAMA Neurol 73:668-674, Martikainen, M.H.,et al, 2016

Facial Grimacing and Sensorineural Hearing Loss in a Woman with Cirrhosis of the Liver
Neurol 87:e239, Sgobbi de Souza, P.V.,et al, 2016

Dystonia in Children and Adolescents: A Systematic Review and a New Diagnostic Algorithm
JNNP 86:774-781, Van Egmond, M.E.,et al, 2015

A 56-year-old Man with Cognitive Impairment and Difficulty Tying his Necktie
Neurol 85:e116-e122, Baker, J.M.,et al, 2015

Deep-Brain Stimulation - Entering the Era of Human Neural-Network Modulation
NEJM 371:1369-1373, Okun, M.S., 2014

Withdrawing Amantadine in Dyskinetic Patients with Parkinson Disease
Neurol 82:300-307, Ory-Magne, F.,et al, 2014

Viral Infections of the Nervous System, Chronic Meningitis, and Prior Diseases, Encephalitis Lethargica (non Economo Disease, sleeping sickness)
Adams & Victors Principles of Neurology, Chp 33, pg 768, Ropper, A.H.,et al, 2014

Disorders of the Nervous System Caused by Drugs, Toxins, and Chemical Agents, Antipsychosis Drugs
Adams & Victors Principles of Neurology Chp 43, pg 1208, Ropper, A.H.,et al, 2014

Degenerative Diseases of the Nervous System, Progressive Supranuclear Palsy
Adams & Victors Principles of Neurology, Chp 39, pg 1096, Ropper, A.H.,et al, 2014

Facial Bradykinesia
JNNP 84:681-685, Bologna, M.,et al, 2013

Parkin Disease
JAMA Neurol 70:571-579, Doherty, K.,et al, 2013

Criteria for the Diagnosis of Corticobasal Degeneration
Neurol 80:496-503, Armstrong, M.J.,et al, 2013

Dopa-Responsive Dystonia Revisited
Arch Neurol 69:1558-1562, Tadic, V.,et al, 2012

Deep Brain Stimulation
JAMA 305:732, Pluta,R.,et al, 2011

Rapidly Progressive Corticobasal Degeneration Syndrome
Case Rep Neurol 3:185-190, Herrero Valverde, A.,et al, 2011

Clinicopath Conf, Rapid-Onset-Dystonia-Parkinsonism Due to a Mutation in the ATP1A3 Gene
NEJM 362:2213-2219, Case 17-2010, 2010

A 75-Year-Old Woman with Progressive Right-Hand Tremor and Inability to Use Her Right Side
Neurol 73:1399-1405, Kertesz,A.,et al, 2009

Progressive Supranuclear Palsy: A Current Review
The Neurologist 14:79-88, Lubarsky,M. &Juncos,J.L., 2008

Wilson Disease: Description of 282 Patients Evaluated Over 3 Decades
Medicine 86:112-121, Taly,A.B., et al, 2007

Deep Brain Stimulation
Neurologist 13:237-252, Kem,DS. &Kumar,R., 2007

Dopamine-Responsive Dystonia
eMedicine (Apr), Nikhar,N.K., 2006

Familial Dopa-Responsive Cervical Dystonia
Neurol 66:599-601, Schneider,S.A.,et al, 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

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

Parkinsons Disease with Camptocormia
JNNP 77:1223-1228,1205, Bloch,F.,et al, 2006

Camptocormia
Neurol 65:355-359, Azher,S.N. &Jankovic,J., 2005

Ophthalmologic Features of Parkinson's Disease
Neurol 62:177-180, Biousse,V.,et al, 2004

Post-Stroke Movement Disorders; Report of 56 Patients
JNNP 75:1568-1574, Alarcon,F.,et al, 2004

Genetic, Clinical, and Radiographic Delineation of Hallervorden-Spatz Syndrome
NEJM 348:33-40, Hayflick,S.J.,et al, 2003

Therapies for Movement Disorders
Arch Neurol 59:699-702, Goetz,C.G &Hinson,V.K., 2002

HIV-Related Movement Disorders, Epidemiology, Pathogenesis and Management
CNS Drugs 16:663-668, Cardoso,F., 2002

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

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

Delayed Movement Disorders After Carbon Monoxide Poisoning
Eur Neurol 42:141-144, Choi,I.S. &Cheon,H.Y., 1999

Clinical Presentation and Pharmacological Therapy in Corticobasal Degeneration
Arch Neurol 55:957-961, Kompoliti,K.,et al, 1998

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

Accuracy of the Clinical Diagnosis of Corticobasal Degeneration:A clinicopathologic Study
Neurol 48:119-125, Litvan,I.,et al, 1997

Low-Dose Clozapine Improves Dyskinesias in Parkinson's Disease
Neurol 48:658-662, Durif,F.,et al, 1997

Bent Spine Syndrome
JNNP 60:51-54, Serratrice,G.,et al, 1996



Showing articles 0 to 50 of 1659 Next >>