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Differential
(Click to cross reference)
adolescent medicine
alien hand syndrome
alpha-fetoprotein
anti IgLON5
anticholinergic drugs
aphasia
aphasia, progressive, primary
aphonia
applause sign
apraxia
apraxia of eye movements
arm swing, reduced
ataxia
ataxia telangiectasia
ataxia, cerebellar
ataxia, progressive
ataxia, truncal
ataxic-dystonia syndromes
athetosis
autoantibodies
Babinski sign
basal ganglia, degeneration
biologic markers
biopterin deficiency
blepharospasm
bradykinesia
bruxism
bulbar palsy
carbamazepine
carcinoembryonic antigen
carcinoma
central hypoventilation
cerebellar ataxia, children
cerebellar ataxia, hereditary
cerebellar degeneration
cerebral cortical atrophy
cerebral palsy
cerebral palsy, associated problems with
children
chorea
choreoathetosis
chromosomal abnormality
chromosome 11
chromosome 14
chromosome 20
Clinical Pathologic Conference(C.P.C.)
cognition
cogwheel rigidty
comorbidities
conjugate gaze, forced
conversion reaction
cortical-basal ganglionic degeneration
crying, pathologic
degenerative diseases of CNS
delay in diagnosis
dementia
dexterity, impaired
diabetes mellitus
diagnostic criteria
differential diagnosis
diplopia
diurnal variation
dopa responsive dystonia
downward gaze
drooling
dysarthria
dysarthria-clumsy hand syndrome
dyskinesia
dysmetria
dysphagia
dyspraxia
dystonia
dystonia musculorum deformens
dystonia, cervical
dystonia, face
dystonia, focal
dystonia, treatment of
emotional lability
enzyme, defect
equinovarus
exercise
exercise-induced neurologic dysfunction
exome sequencing
eye movement, disorders of
falling
familial
fine motor function, impaired
foot deformity
frontal behavioral spatial syndrome
gait disorder
gait, apraxic
gangliosidosis GM1
gaze palsy
gaze palsy, supranuclear
gaze palsy, vertical
gene
gene mutation
genetic counselling
genetic diagnosis, prenatal
genetic linkage
genetic neurologic disorders
genetic testing
glabellar sign
globus pallidus, lesion of
globus pallidus, lesion of, bilateral
grasp reflex
grimacing
growth retardation
Hallervorden Spatz disease
Hallervorden Spatz disease, late onset
hand weakness
hands, fisted
hemidystonia
hemifacial spasm
hepatolenticular degeneration(Wilson's disease)
HLA
hoarseness
hyperreflexia
hypometric saccades
hypophonia
hypotonia
ideomotor apraxia
imbalance
imbalance, postural
immunodeficiency
immunosuppression
inattention
inclusion bodies, intranuclear
incontinence, fecal
insomnia
intellectual deficit
intellectual deterioration
iron, brain
Jakob-Creutzfeldt disease
Kayser-Fleischer ring
laughing, pathologic
L-dopa
leg weakness, bilateral
leukemia
liver disease
lymphoma
masked facies
memory, defect of recent
memory, impairment of
meningitis
mental retardation
midbrain
midbrain, atrophy
mimics
misdiagnosis
molecular genetics
mortality
movement disorder
movement disorder, extrapyramidal
movement disorder, psychogenic
movement disorder, treatment of
MRI
MRI, abnormal
MRI, diffusion weighted
MRI, eye of tiger sign
MRI, mouse ears
MRI, negative
MRI, paramagnetic effect
MRI, spine
multiple system atrophy
muscle spasm, face
myelopathy
myelopathy, chronic progressive
myoclonic jerks
myoclonus
neurocutaneous disease
neuroendocrinology
neurologic disease, diagnoses of
neurologic disease, diagnoses of, clinical bedside
neurologic disease, tempo
neurologic evaluation
neurologic examination
neurologic signs
neurologic symptoms
neuronal intranuclear inclusion disease
neuroophthalmology
neuropathology
neuropathy
numb clumsy hands syndrome
nystagmus
ocular motility, disorders of
opened mouth
palilalia
PANK2 mutation
paraparesis
parasomnia
Parkinson disease
Parkinson disease, axial symptoms
Parkinson disease, differential diagnosis of
Parkinson disease, dystonia with
Parkinson disease, juvenile
Parkinson disease, L-dopa nonresponsive
Parkinson disease, treatment of
Parkinson disease, tremor, absence of
Parkinsonism syndrome
pathology
penguin silhouette sign
personality change
pigmentary retinopathy
pitfalls
postural abnormality
PRKN gene
procyclidine
progeria
prognosis
progressive neurologic disorder
progressive supranuclear palsy
pseudobulbar palsy
psychiatric disorder
psychiatric problems in neurologic disorders
psychomotor retardation
psychosis
pull test
radiation hypersensitivity
rapid onset dystonia parkinsonism
rapidly progressing neurologic illness
Red flags
release phenomena
respirations in CNS disease
retinopathy
retrocollis
Rett's syndrome
reversible neurologic disorder
review article
rigidity
rigidity, axial
risk factors
running
saccadic eye movements, abnormal
salivation, excessive
sensory loss, cortical
sequencing difficulty
short stature
sinemet
single photon emission computed tomography
skin, lesions in neurologic disorders
sleep apnea, obstructive
sleep pathology and physiology
slit lamp examination
speech disorder
spinal cord
spinal cord, lesion of
spinal muscular atrophy
spinocerebellar ataxia
spinocerebellar ataxia type 28
spinocerebellar degeneration
stare
suck reflex
swallow evaluation
tau protein
tauopathy
telangiectases
tetrahydrobiopterin
toe walking
tonic foot response
treatment of neurologic disorder
tremor
tremor, intention
tremor, jaw
tremor, postural
tripping
upgaze
upgaze, paralysis of
urinary incontinence
vision, blurred
visual symptoms
vocal cord paralysis
walking
walking frame
walking, difficulty with
wheelchair
wide based gait
Showing articles 400 to 450 of 8316 << Previous Next >>

Portal-Systemic Myelopathy after Portacaval Shunt Surgery
Arch Int Med 145:1921-1922, Lebovics,E.,et al, 1985

Munchausen's Syndrome Simulating Torsion Dystonia
NEJM 312:1437-1439, Batshaw,M.L.,et al, 1985

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

Cerebellar Infarction in the Superior Cerebellar Artery Distribution
Neurol 35:705-711, Kase,C.S.,et al, 1985

Subcortical Arteriosclerotic Encephalopathy, (Binswanger's Disease)
Arch Neurol 42:951-959, Kinkel,W.R.,et al, 1985

Lacunar Syndrome Due to Intracerebral Hemorrhage
Stroke 16:454-459, Mori,E.,et al, 1985

Blepharospasm, Meige Syndrome, & Hemifacial Spasm:Treatment with Botulinum Toxin
Neurol 35:1499-1500, Mauriello,J.A., 1985

Paraneoplastic Cerebellar Disease, Remission with Excision of the Primary Tumor
Arch Neurol 42:1208-1210, Kearsley,J.H.,et al, 1985

Chediak-Higashi Syndrome
Arch Neurol 41:1001-1002, Pettit,R.E.,et al, 1984

Clinicopathological Conference Metachromatic Leukodystrophy (juvenile type)
Case 7-1984, NEJM 310:445-4551984., , 1984

Ataxic-Hemiparesis, Localization & Clinical Features
Stroke 15:363-365, Huang,C.Y.,et al, 1984

Neuro-ophthalmic Abnormalities in Tourette's Syndrome:Functional & Anatomic Implications
Neurol 34:359-361, Frankel,M.,et al, 1984

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

Spasmodic Dysphonia
Lancet 2:1192, Gowers,W.R.,et al, 1984

Ataxia-Telangiectasia:A Multisystem Hereditary Disease with Immunodeficiency
Ann Int Med 99:367-379, Waldmann,T.A.,et al, 1983

Glutamate Dehydrogenase Deficiency in Patients with Olivopontocerebellar Atrophy
Neurol 33:1322-1326, Duvoisin,R.C.,et al, 1983

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

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

Focal Dystonia & Lacunar Infarction of the Basal Ganglia
Jr. , Arch Neurol 40:61-62983., Russo,L.S., 1983

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

Sensory Ataxia, A Residual Disability of Guillain-Barre Syndrome
Arch Neurol 40:86-89, Sobue,G.,et al, 1983

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

Blepharospasm Associated with Brainstem Lesions
Neurol 33:1237-1240, Jankovic,J.,et al, 1983

Treatment of Hyperkinetic Movement Disorders with Tetrabenazine:A Double-blind Crossover Study
Ann Neurol 11:41-47, Jankovic,J., 1982

Capsular Ataxic Hemiparesis
Arch Neurol 39:585-586, Ichikawa,K.,et al, 1982

Hydrocephalus as a Cause of Disturbances of Gait in the Elderly
Neurol 32:1358-1363, Fisher,C.M., 1982

Neurologic Complications of Hyperthyroidism
Arch Neurol 38:669-670, Bulens,C., 1981

Meige Syndrome (blepharospasm-oromandibular Dystonia) after Long-term Neuroleptic Therapy
Neurol 31:1555-1556, Weiner,W.J.,et al, 1981

Computed Tomography in Ataxia-Telangiectasia
J Comput Assist Tomogr 5:660-661, Assencio-Ferreira,V.J.,et al, 1981

Epstein-Barr-virus-carrying Lymphoma in a Patient with Ataxia-telangiectasia
BMJ 282:425-427, Saemundsen,A.K.,et al, 1981

Ataxic Hemiparesis with Trigeminal Weakness
Neurol 31:635-636, Sakai,T.,et al, 1981

Homolateral Ataxia & Crural Paresis:Case Report
Neurol 30:1013-1015, Perman,G.P.,et al, 1980

Nervous System Toxicity of Chemo Agents
Young, DF, in Vinken PJ, Bruyn GW, Handbook of Clin Neurol, North-Holland Publ Co, Amster, Vol 39, 1, 80, p 104, 1980

Hysterical Gaits
In the Neurologic Examination, Ed. Russell N. DeJong, 4th Edition, Harper & Row, Publ, Hagerstown, p, 426, 1979

Meige's Disease, A Clinical Form of Facial Convulsion, Bilateral & Medial
Arch Neurol 36:635-637, Tolosa,E.S.,et al, 1979

Meige Disease:Striatal Dopaminergic Preponderance
Neurol 29:1126-1130, Tolosa,E.S.,et al, 1979

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

Helper & Suppressor T-Lymphocyte Leukemia In Ataxia Telangiectasia
NEJM 300:700-704, Saxon,A.,et al, 1979

Neurologic Disturbances in Pagets Disease of Bone:Response to Calcitonin
Neurol 29:448-457, Chen,J.R.,et al, 1979

Hydrocephalic Dementia in Pagets Disease of the Skull:Treatment by Ventriculoatrial Shunt
Neurol 29:513-516, Goldhammer,Y.,et al, 1979

A Case of Schwartz-Jampel Syndrome with Unusual Muscle Biopsy Findings
Ann Neurol 3:93, Fariello,R.,et al, 1978

Ataxia Telangiectasia
Arch Neurol 35:553-554, Teplitz,R.L., 1978

Eye Movements in Ataxia-telangiectasia
Neurol 28:1099-1104, Baloh,R.W.,et al, 1978

Ataxic Hemiparesis
Arch Neurol 35:126, Fisher,C.M., 1978

Extreme Insulin Resistance in Ataxia Telangiectasia
NEJM 298:1164, Bar,R.S.,et al, 1978

Aggravation of Tardive Dyskinesia by Phenytoin
NEJM 298:457, DeVeaugh-Geiss,J., 1978

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

Reversible Corticospinal Tract Disease Due to Hyperthyrodisim
Arch Neurol 34:647, Garcia,C.A.,et al, 1977

Effects of Learning on Visceral Functions-Biofeedback
NEJM 296:1274, Miller,N.E.,et al, 1977

A Syndrome of Early Recognition of Occult Hydrocephalus & Cerebral Atrophy
Quart J Med 183:365, Botez,M.I.,et al, 1977



Showing articles 400 to 450 of 8316 << Previous Next >>