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Differential
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acquired immunodeficiency syndrome
adolescent medicine
adverse drug reaction
akathisia
akinesia of eyelid function
alcohol, neurologic complications with
alcoholism
algorithm
alien hand syndrome
alpha-fetoprotein
alternating hemiplegia
alternating hemiplegia of childhood
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, Parkinson-dementia-complex
ANA
anergy
anoxia
anti IgLON5
antibiotics
anticardiolipin antibodies
anticonvulsants, untoward effects of
antiphospholipid antibody syndrome
aphasia
aphasia, progressive, primary
apraxia
apraxia of eye movements
apraxia of eyelid opening
arbovirus
areflexia
ataxia
ataxia telangiectasia
ataxia, cerebellar
ataxia, hereditary
ataxia, progressive
ataxia, truncal
ataxic gait
ataxin
ataxin-2
athetosis
ATP1A3 gene
atypical
autoantibodies
autoimmune basal ganglia encephalitis
autoimmune cerebellar ataxia
autoimmune disease
autoimmune encephalopathy
autonomic dysfunction
B 12 deficiency
B12
Babinski sign
baclofen
bacterial infection
basal ganglia
basal ganglia, lesion of
basal ganglia, lesion, bilateral
benign essential tremor
bent spine syndrome
bilirubin encephalopathy
biologic markers
biotin
biotin deficiency
biotin deficiency, juvenile form
biotin-responsive basal ganglia disease
blepharospasm
blinking
blinking, reduced
bone marrow transplantation
botulinum toxin
botulinum toxin, complications of
bradykinesia
bradykinesia, facial
bradyphrenia
brain atrophy
brain biopsy
brain damage
brainstem
brainstem, infarction of
brainstem, lesion of
Brueghel's syndrome
cachexia
CAG repeats
camptocormia
carcinoembryonic antigen
carcinoma
carcinoma of breast
cardiomyopathy
carotid artery disease
carotid artery occlusion, neck
carotid artery stenosis
CAT scan
CAT scan, abnormal
CAT scan, chest
CAT scan, muscle
caudate nucleus, atrophy
central nervous system, infection of
cerebellar ataxia, children
cerebellar ataxia, hereditary
cerebellar atrophy, primary
cerebellar atrophy, secondary
cerebellar degeneration
cerebellar lesion
cerebellitis, autoimmune
cerebellum, disease of
cerebral cortex
cerebral hypoperfusion
cerebrospinal fluid
cerebrospinal fluid, abnormal
cerebrospinal fluid, enzymes in
cerebrospinal fluid, gammaglobulin of
cerebrospinal fluid, oligoclonal IgG in
cerebrovascular accident
cerebrovascular accident, multiple
cerebrovascular accident, three territory involvement
Charcot's sign
chewing movements
children
chorea
choreoathetosis
choreoathetosis, paroxysmal
chromosomal abnormality
chromosome 11
chromosome 20
chronic progressive external ophthalmoplegia
cirrhosis
Clinical Pathologic Conference(C.P.C.)
cognition
cogwheel rigidty
collagen vascular disease
concussion
confabulation
confusion
congenital infection, CNS
consanguinity
contractures, joint
controversies in neurology
conversion reaction
corpus callosum, thinning
cortical-basal ganglionic degeneration
cost
cost effectiveness
cranial neuropathy
cranial neuropathy, multiple
creatine phosphokinase(CPK)elevated
Cuba
deep gray nuclei
degenerative diseases of CNS
delay in diagnosis
dementia
dementia, frontotemporal
dementia, presenile
dementia, rapidly progressive
dementia, reversible
dementia, subcortical
dementia, treatment of
Dengue fever
developmental milestones, loss of
developmental retardation
diabetes insipidus
diabetes mellitus
diagnostic criteria
diarrhea
differential diagnosis
diplopia
disorientation
distal muscle atrophy
dopa responsive dystonia
DPPX
DPPX, antibodies, encephalitis
driving
drooling
drug abuse
drug abuse, neurologic complications of
dysarthria
dysdiadochokinesia
dyskinesia
dyskinesia, buccal lingual facial
dysphagia
dystonia
dystonia, cervical
dystonia, children
dystonia, drug induced
dystonia, face
dystonia, focal
dystonia, painful
dystonia, treatment of
electroencephalogram, abnormalities of
electromyogram
encephalitis
encephalitis, autoimmune
encephalitis, episodic
encephalitis, paraneoplastic
encephalitis, viral
encephalomyelitis
encephalopathy
encephalopathy, neonatal
encephalopathy, progressive
endarterectomy, carotid
endemic area
enolase
enzyme, defect
epidemiology of neurology
episodic neurologic deficits
evidence-based research
exercise intolerance
exome sequencing
extralimbic encephalitis
extrapyramidal movement disorder, progressive
eye movement, disorders of
facial appearance, abnormal
facial expression abnormality
facial movement disorder
facial nerve palsy
falling
false negative
familial
fasciculation
fatal familial insomnia
fever
fluctuate
fluorescent treponema antibody absorption/false positive
Fragile-X associated tremor/ataxia-syndrome
fragile-X syndrome
frontal behavioral spatial syndrome
frontal lobe, anatomy and physiology
gait disorder
galactorrhea
gamma amino butyric acid receptor antibody
gammaglobulin therapy, intravenous
gaze palsy
gaze palsy, supranuclear
gaze palsy, vertical
gene
gene mutation
genetic counselling
genetic linkage
genetic neurologic disorders
genetic testing
glabellar sign
globus pallidus
globus pallidus, lesion of
globus pallidus, lesion of, bilateral
glutamic acid decarboxylase, antibody
granulomatous disease
growth retardation
Guillain Barre syndrome
gyrus, abnormal
Hallervorden Spatz disease
Hallervorden Spatz disease, late onset
hallucination
hallucination, visual
hammertoes
head injury
headache
hearing loss
hemifacial spasm
hemiparesis
hepatic failure
hepatolenticular degeneration, non-Wilsonian
hepatomegaly
hepatosplenomegaly
heralding manifestation
hippocampus
hippocampus, hyperintense
Horner's syndrome
human immunodeficiency virus type 1
Huntington's chorea
Huntington's disease, children
hydrocephalus
hyperammonemic encephalopathy
hyperbilirubinemia
hyperbilirubinemia, CNS abnormality after
hypercalcemia
hyperesthesia
hyperreflexia
hypersomnia
hypertonia
hypocomplementemia
hypophonia
hyporeflexia
hyposmia
hypothalamus, disturbance of
hypothyroidism
hypotonia
hypoxia
hypoxic encephalopathy
imbalance
imbalance, postural
immunocompetent
immunodeficiency
immunomodulation
immunosuppression
immunotherapy
inattention
inborn errors of metabolism
incidence
inclusion bodies
inclusion bodies, eosinophilic cytoplasmic
inclusion bodies, eosinophilic intranuclear
inclusion bodies, intranuclear
infection
insight, loss
insomnia
intellectual deficit
intellectual deterioration
internal capsule
intracranial hypertension, benign
intravenous
iron, brain
Isaacs syndrome
Jakob-Creutzfeldt disease
jaundice
jaw jerk, abnormal
kernicterus
ketoacidosis
kyphosis
Latvia
L-dopa
leg spasms
leg spasms, painful
lenticular nucleus, lesion of, bilateral
leukemia
leukoencephalopathy
Lewy body
Lewy body disease, diffuse
lid abnormalities
limbic encephalitis
liver disease
lordosis
low back pain
lymphadenopathy, hilar
lymphoma
maculopathy
manganese intoxication
marche a petits pas
masked facies
mediastinum, mass of
memory, defect of recent
memory, impairment of
meningitis
meningitis, aseptic
meningitis, carcinomatous
mental retardation
mental status, abnormal
metabolic acidosis
metabolic disorder, primary
methcathinone
methylmalonic acidemia
microcephaly
midbrain, atrophy
middle cerebellar peduncle, lesion
middle cerebellar peduncle, lesion, bilateral
migraine
mimics
Mini Mental Status Examination
misdiagnosis
mitochondrial disease
mitochondrial disease, pathogenesis
molecular genetics
mononeuropathy
mortality
movement disorder
movement disorder, drug induced
movement disorder, extrapyramidal
movement disorder, hyperkinetic
movement disorder, paroxysmal
MRI
MRI, abnormal
MRI, diffusion weighted
MRI, disappearing lesion on
MRI, eye of tiger sign
MRI, false negative
MRI, gradient-echo
MRI, high signal intensity of basal ganglia
MRI, negative
MRI, paramagnetic effect
MRI, susceptibility weighted
MRI, T1 weighted high signal foci
MRS
multiple sclerosis
multiple system atrophy
muscle biopsy
muscle cramp
muscle spasm
muscle stiffness
muscle weakness
muscular dystrophy
myasthenia gravis
myelitis
myelopathy
myelopathy, hepatic
myoclonic jerks
myoclonus
myoclonus, cortical
myoclonus, epilepsy
myoclonus, segmental
myopathy
myopathy, metabolic
myositis
nausea and vomiting
neck weakness
neurocutaneous disease
neurodegeneration with brain iron accumulation
neuroendocrinology
neurologic complications of, systemic disease
neurologic consultation
neurologic disease
neurologic disease, diagnoses of
neurologic disease, multifocal
neurologic disease, tempo
neurologic signs
neuron specific enolase
neuronal intranuclear inclusion disease
neuronopathy
neuronopathy, sensory
neuroophthalmology
neuropathology
neuropathology, brain
neuropathy
neuropathy, peripheral
neurotoxic
neurotoxin
next-generation sequencing
NOTCH2NLC
nutritional deficiency
nystagmus
nystagmus, gaze-evoked
nystagmus, monocular
ocular motility, disorders of
ocular myopathy
ocular myopathy, differential diagnosis
oculomasticatory myorhythmia
old age, neurology of
ophthalmoplegia
ophthalmoplegia, progressive external
optic atrophy
optic neuritis
orthostatic hypotension
palilalia
PANK2 mutation
papilledema
paraparesis, spastic
parasomnia
paraspinal muscle
paraspinal muscle weakness
parenteral alimentation
Parkinson disease
Parkinson disease, arteriosclerotic
Parkinson disease, atypical
Parkinson disease, dementia with
Parkinson disease, diagnosis
Parkinson disease, differential diagnosis of
Parkinson disease, drug induced
Parkinson disease, dystonia with
Parkinson disease, juvenile
Parkinson disease, L-dopa nonresponsive
Parkinson disease, misdiagnosis
Parkinsonism multiple-system atrophy
Parkinsonism syndrome
Parkinsonism, freezing phenomena in
paroxysmal hemiplegia
paroxysmal neurologic deficits
PAS positive
PAS positive material in the brain
pathology
pericarditis
peripheral nerve, lesion of
personality change
pigmentary retinopathy
pituitary, lesion of
pleocytosis of cerebrospinal fluid
POLG1 gene
polymerase chain reaction
polyneuropathy
portal caval shunt
posterior inferior cerebellar artery syndrome
postural abnormality
precipitating factors
preclinical
premature infant
prevention of neurologic disorders
prion disease
PRKN gene
progeria
prognosis
progressive multifocal leucoencephalopathy
progressive neurologic disorder
progressive supranuclear palsy
prolactin, elevated
protein 14-3-3, cerebrospinal fluid
protein 14-3-3, cerebrospinal fluid, false negative
proteinopathy
pseudobulbar palsy
psychiatric disorder
psychiatric problems in neurologic disorders
psychomotor retardation
psychosis
ptosis
putamen, lesion of, bilateral
pyramidal tract
pyramidal tract dysfunction
radiation hypersensitivity
rapid onset dystonia parkinsonism
rapidly progressing neurologic illness
reading disorder, acquired
reading problem, causes of
recurrent
remote effect of cancer on the nervous system
renal stones
retinitis pigmentosa
retinopathy
retropulsion
review article
rigidity
rigidity, axial
Romberg's sign
rubella encephalitis, progressive
rubella syndrome
rubella virus
Russia
saccadic eye movements
saccadic eye movements, abnormal
sarcoidosis
sarcoidosis, CNS
Saudi Arabia
scoliosis
screening
sea-blue histiocytes
seizure
sensorineural hearing loss
serologic testing
serologic testing of cerebrospinal fluid
shaking
sinemet
skin, biopsy
skin, lesions in neurologic disorders
skull x-ray
skull x-ray, abnormal
sleep pathology and physiology
slow virus infection of CNS
spastic dysphonia
spasticity
speech disorder
speech disorder, childhood
spinal cord, lesion of
spinal muscular atrophy
spinocerebellar ataxia
spinocerebellar ataxia type 2
splenomegaly
spongy degeneration of brain
standing difficulty
stare
startle reaction
status epilepticus
status epilepticus, intractable
steroid therapy, CNS treatment and complications with
stiff legs
stiff limb syndrome
stiff man syndrome
stimulant drugs
stooped posture
striatum, lesion of
striatum, lesion of, bilateral
stridor
strokelike episodes
subacute sclerosing panencephalitis(S.S.P.E.)Dawson's disease
subarachnoid hemorrhage
substantia nigra
subthalamic nucleus
symmetric brain lesions
synucleinopathy
systemic illness
systemic lupus erythematosus
systemic lupus erythematosus, neurologic complications with
tandem gait, ataxic
tau protein
tauopathy
telangiectases
teleconsulting
telemedicine
teleneurology
telestroke
temporal lobe, lesion
temporal lobe, lesion, bilateral
term infant
thalamus, lesion of
thalamus, lesion of-bilateral
Three territory sign
thrombophlebitis
thymoma
tinnitus
titubation
tonic foot response
torticollis
transient ischemic attack
transient ischemic attack, limb shaking
transient neurologic deficit
travel history
treatment of neurologic disorder
tremor
tremor, intention
tremor, postural
tremor, writing
trigeminal neuropathy
trinucleotide repeats
tyrosine hydroxylase deficiency
unconsciousness
unconsciousness, transient
uveitis
valium
vegetarianism
viral infection
viral infection, CNS
virus, slow
visual evoked response
visual impairment
vitamin deficiency
walking frame
walking, difficulty with
weakness
weakness, generalized
weakness, progressive
web sites
weight loss
wheelchair
Whipple's disease
white matter disease
wide based gait
workup
writing
Showing articles 600 to 650 of 17967 << Previous Next >>

Isolated Painless Manual Incoordination in 57 Musicians
JNNP 50:291-295, Newmark,J.&Hochberg,F.H., 1987

Classification of Parkinsonism
in Handbook of Parkinson's Disease, Marcel Dekker, Inc, New York, Ch 3, p 61., Koller,W.C., 1987

Carbamazepine Side Effects in Children and Adults
Pellock. J. M. , Epilepsia 28:S64-S707., , 1987

Creutzfeldt-Jakob Disease:Clinical Analysis of a Consecutive Series of 230 Neuropathologically Verified Cases
Ann Neurol 20:597-602, Brown,P.,et al, 1986

Oculomasticatory Myorhythmia:A Unique Movement Disorder Occurring in Whipple's Disease
Ann Neurol 20:677-683, Schwartz,M.A.,et al, 1986

Infantile Bilateral Striatal Necrosis, Clinicopathological Classification
Arch Neurol 43:677-680, Mito,T.,et al, 1986

Painful Tonic Spasms Caused by Putaminal Infarction
Stroke 17:1319-1321, Merchut,M.P.,et al, 1986

Metoclopramide-Induced Parkinsonism in Hemodialysis Patients
Arch Int Med 146:2070-2071, Sirota,R.A.,et al, 1986

Tardive Dyskinesia Associated with High-Dose Intravenous Metoclopramide
NEJM 315:518-519, Breitbart,W., 1986

Locus Ceruleus Lesions & Eosinophilic Inclusions in MPTP-Treated Monkeys
Ann Neurol 20:449-455, Forno,L.S.,et al, 1986

Cocaine & Tourette's Syndrome
NEJM 315:398, Mesulam,M.M., 1986

Parkinsonism, Tardive Dyskinesia, Akathisia, & Depression Induced by Flunarizine
Lancet 1:1303-1304, Chouza,C.,et al, 1986

Clinicopath. Conference
Pick's Disease of Brain, with Frontal Lobar Atrophy, Degen of Basal Ganglia, Case 16-1986, NEJM 314:, 101-,1986., 1986

The Clinical Features & Natural History of the Steele-Richardson-Olszewski Syndrome (Prog Supranuclear Palsy)
Neurol 36:1005-1006, Maher,E.R.,et al, 1986

The Neuroleptic Malignant Syndrome:Agent and Host Interaction
Acta Psychiatr Scand 73:337-347, Shaley,A.&Munitz,H., 1986

Segmental Myoclonus Clinical and Pharmacologic Study
Arch Neurol 43:1025-1031, Jankovic,J.&Pardo,R., 1986

Acid Maltase Deficiency
Engel, A. G. in Engel and Banker, Myology, McGraw-Hill Co, New York, Ch 55, p. 1629-1651, , 1986

Reversible Parkinsonism Related to Meperidine
NEJM 312:509, Lieberman,A.N.,et al, 1985

Tetrabenazine Induces Acute Dystonic Reactions
Ann Neurol 17:200-202, Burke,R.E.,et al, 1985

Acute Exacerbation of Parkinson's Disease with Sulindac
Ann Neurol 17:104-105, Sandyk,R.,et al, 1985

Extrapyramidal Reactions with Metoclopramide
BMJ 291:930-932, Bateman,D.N.,et al, 1985

Wernicke's Encephalopathy
NEJM 312:1035-1039, Reuler,J.B.,et al, 1985

Limb Shaking-A Carotid TIA
Stroke 16:444-448, Baquis,G.D.,et al, 1985

Repetitive Involuntary Movement Associated with Episodic Cerebral Ischemia
Ann Neurol 18:244-250, Yanagihara,T.,et al, 1985

Atypical Presentation of Progressive Supranuclear Palsy
Ann Neurol 17:334-343, Davis,P.H.,et al, 1985

The Clinical Syndrome of Striatal Dopamine Deficiency, Parkinsonism Induced by MPTP
NEJM 312:1418-1421, Burns,R.S.,et al, 1985

Permanent Human Parkinsonism Due to 1-Methyl-4-Phenyl-1, 2, 3, 6-Tetrahydropyridine (MPTP) :Seven Cases
Neurol 35:949-956, Ballard,P.A.,et al, 1985

Heterogeneity in Dementia of the Alzheimer Type:Evidence of Subgroups
Neurol 35:453-461, Mayeux,R.,et al, 1985

Inflammatory Myopathies
Ann Neurol 17:215-227, 317-3231985., Mastaglia,F.L.,et al, 1985

Creutzfeldt-Jakob Disease of Long Duration:Clinicopathological Characteristics
Ann Neurol 16:295-304, Brown,P.,et al, 1984

Nystagmus in Motor Neuron Disease:Clinicopathological Study of Two Cases
Ann Neurol 16:71-77, Kushner,M.J.,et al, 1984

Extrapyramidal Signs in Alzheimer's Disease
Neurol 34:1114-1116, Molsa,P.K.,et al, 1984

Unusual Spontaneous Movements in Brain-Dead Patients
Neurol 34:1089-1092, Ropper,A.H., 1984

Metoclopramide & Tardive Dyskinesia in the Elderly
BMJ 289:397-398, Orme,M.L., 1984

Phenobarbital-Induced Dyskinesia in a Neurologically Impaired Child
Neurol 34:1600-1601, Wiznitzer,M.,et al, 1984

Tardive Dyskinesia:Current Clinical Issues
Neurol 34:1348-1353, Burke,R.E., 1984

Involvement of Upper-Airway Muscles in Extrapyramidal Disorders
NEJM 311:438-442, Vincken,W.G.,et al, 1984

Drug-Induced Parkinsonism in the Elderly
Lancet 2:1082-1083, Stephen,P.J.,et al, 1984

Chronic Parkinsonism Secondary to Intranasal Administration of a Product of Meperidine-Analogue Synthesis
NEJM 310:325, Wright,J.M.,et al, 1984

Hyperammonemia in Asterixis Induced by Carbamazepine:Two Case Reports
Acta Neurologica Scand 69:186-189, Ambrosetto,G.,et al, 1984

Myoclonus Induced by Metoclopramide Therapy
Arch Int Med 143:2201-2202, Hyser,C.G.,et al, 1983

Persisting Neurologic Sequelae of Lithium Carbonate Therapy
Arch Neurol 40:747-751, MacDonaldson,I.,et al, 1983

Meperidine-Associated Myoclonus & Seizures in Long-Term Hemodialysis Patients
Ann Neurol 14:593, Hochman,M.S., 1983

Clinicopathological Conference
Case 49-1983, Creutzfeldt-Jakob, NEJM 309:1440-1449983., , 1983

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

Progressive Supranuclear Palsy:Clinical Features & Response to Treatment in 16 Patients
Ann Neurol 13:273-278, Jackson,J.A.,et al, 1983

Nuclear Magnetic Resonance Imaging in Movement Disorders
Ann Neurol 13:690-691, Lukes,S.A.,et al, 1983

Parkinson's Disease in a Chemist Working with l-Methyl-4-Phenyl-1, 2, 5, 6-Tetrahydropyridine
NEJM 309:310, Langston,J.W.,et al, 1983

Parkinsonism Secondary to Neurosyphillis. A Case Report.
S Afr Med J 63:665-666, Sandy,R., 1983

Sudden Onset of Involuntary Movement Disorders with Arteriovenous Malformations of the Basal Ganglia
The Mount Sinai J Med 49:438-442, Diamond,M.S.,et al, 1982



Showing articles 600 to 650 of 17967 << Previous Next >>