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abscess, intracerebral
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Adies pupil
adolescent medicine
advances in neurology
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algorithm
alpha-fetoprotein
altered states of consciousness
alternating hemiplegia
alternating hemiplegia of childhood
AMPA receptor antibodies
amyloidosis
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anti GQ1b IgG antibody
anticholinergic drugs
apraxia of eye movements
areflexia
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arthralgia
arthrogryposis multiplex
ascites
ataxia
ataxia telangiectasia
ataxia, cerebellar
ataxia, truncal
ataxic-dystonia syndromes
athetosis
athetosis, causes of
atlanto-axial subluxation
ATP1A3 gene
attention deficit disorder with hyperactivity
autoantibodies
autoimmune basal ganglia encephalitis
autoimmune disease
autonomic dysfunction
autonomic neuropathy
Babinski sign
basal ganglia, calcification of
basal ganglia, lesion of
basal ganglia, lesion, bilateral
behavioral disorder
benign essential tremor
biopterin deficiency
bladder dysfunction
blepharospasm
botulinum toxin
bradykinesia
brain atrophy
brainstem, atrophy
brainstem, lesion of
burning skin
calcification, intracranial
camptocormia
carbamazepine
carcinoembryonic antigen
carcinoma
carotid artery disease
carotid artery occlusion, neck
carotid artery stenosis
CAT scan
CAT scan, abnormal
CAT scan, emission
CAT scan, emission, abnormal
CAT scan, isodense lesion with acute hemorrhage
cataracts
catecholamine
cavernous sinus, syndrome
central nervous system, infection of
cerebellar ataxia, children
cerebellar ataxia, hereditary
cerebellar atrophy, primary
cerebellar atrophy, secondary
cerebellar degeneration
cerebellar lesion
cerebellum
cerebral cortical atrophy
cerebral hypoperfusion
cerebral ischemia
cerebral palsy
cerebral palsy, associated problems with
cerebral vasculature, calcification
cerebral venous thrombosis
cerebrospinal fluid
cerebrospinal fluid, abnormal
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, gold sol.curve of
cerebrospinal fluid, xanthochromia of
cerebrovascular accident
cerebrovascular accident, infancy and childhood
ceruloplasmin, serum
cervical spine
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chelation therapy
children
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chorea, causes of
choreoathetosis
choreoathetosis, paroxysmal
chromosomal abnormality
chromosome 11
chromosome 14
chromosome 9
cisternogram, radionuclide
Clinical Pathologic Conference(C.P.C.)
coccidioidomycosis
cognition
cogwheel rigidty
complications
compression fracture
contractures, joint
cornea, opacity of
cranial nerve palsies
cranial neuropathy
cranial neuropathy, multiple
deferiprone
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delay in diagnosis
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depression
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developmental retardation
dexterity, impaired
diabetes insipidus
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differential diagnosis
diphenhydramine
diplopia
diurnal variation
DNA probes
donut sign
dopa responsive dystonia
dopamine
drooling
drop attacks
drug induced neurologic disorders
dural sinus thrombosis
dysarthria
dysarthria-clumsy hand syndrome
dysdiadochokinesia
dyskinesia
dyskinesia, causes of
dyskinesia, drug induced
dysphagia
dysphonia
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dystonia musculorum deformens
dystonia musculorum deformens, carrier
dystonia, axial
dystonia, cervical
dystonia, children
dystonia, classification
dystonia, etiology of
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dystonia, symptomatic
dystonia, treatment of
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edema, pedal
efficacy
empyema, epidural
empyema, subdural
encephalitis
encephalitis, autoimmune
encephalitis, brainstem
encephalitis, focal
encephalitis, paraneoplastic
encephalopathy
encephalopathy, progressive
endarterectomy, carotid
enzyme, defect
episodic neurologic deficits
equinovarus
esophageal varices
exome sequencing
eye movement, disorders of
facial expression abnormality
facial movement disorder
facial nerve palsy
Fahr disease
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fatigue
fine motor function, impaired
foot deformity
frontal lobe, pathologic signs of
fungal infection, CNS
gait disorder
galactorrhea
gamma amino butyric acid
gamma amino butyric acid receptor antibody
gammaglobulin therapy, intravenous
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gene mutation
genetic counselling
genetic linkage
genetic neurologic disorders
genetic testing
gests antagoniste
Gilles de la Tourette syndrome
globus pallidus
globus pallidus, stimulation
GLUT1 deficiency syndrome
glutamic acid decarboxylase, antibody
granuloma, pulmonary
grasp reflex
growth retardation
Guillain Barre syndrome
hands, fisted
head nodding
headache, positional
hearing loss
heparin, subcutaneous
hepatic encephalopathy
hepatic encephalopathy, treatment of
hepatic failure
hepatolenticular degeneration(Wilson's disease)
hepatolenticular degeneration(Wilson's disease), presymptomatic
Hodgkin's disease
homovanillic acid
hospitalization
Huntington's chorea
hydrocephalus
hydrocephalus, normal pressure
hyperreflexia
hypertonia
hypoalbuminemia
hypocalcemia
hypoglycorrhachia
hypoparathyroidism
hypoparathyroidism, idiopathic
hyporeflexia
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hypotonia
iatrogenic neurologic disorders
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immunodeficiency
immunosuppression
immunotherapy
inborn errors of metabolism
inclusion bodies, intranuclear
intellectual deficit
intellectual deterioration
intracranial hypertension, benign
intracranial pressure, increased
iron, brain
jugular foramen syndrome
Kayser-Fleischer ring
klippel feil syndrome
L-dopa
leg spasms
leg spasms, painful
leg weakness, bilateral
leucine rich glioma inactivated 1 antibodies
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leukopenia
Lhermitte's sign
limbic encephalitis
lithium
liver function enzymes
lymphoma
masked facies
mastoiditis
memory, impairment of
meningismus
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meningitis, carcinomatous
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mental retardation
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mimics
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MRI
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MRI, paramagnetic effect
MRI, spinal cord
MRI, spinal cord, increased intramedullary cord signal
MRI, spine
multiple sclerosis
multiple system atrophy
Munchausen syndrome
muscle diseases, characteristics of
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muscle weakness, proximal
muscle, metabolic disorders of
muscular dystrophy
muscular dystrophy, Duchenne
muscular dystrophy, facioscapulohumeral
muscular dystrophy, limb-girdle
myasthenia gravis
myasthenic crisis
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myelitis, transverse
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myelitis, transverse, prognosis
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myelopathy, chronic progressive
myoclonic jerks
myoclonus
myoglobinuria
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myositis
myotonia dystrophica
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NMDA antagonists
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numb clumsy hands syndrome
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ophelia syndrome
ophthalmoplegia
optic atrophy
optic neuropathy
osteomyelitis
osteomyelitis, skull
otitis, neurologic complications with
pain
pallidotomy
PANK2 mutation
paraparesis
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Parkinson disease, differential diagnosis of
Parkinson disease, dystonia with
Parkinson disease, juvenile
Parkinsonism syndrome
paroxysmal dystonic choreoathetosis
paroxysmal hemiplegia
paroxysmal neurologic deficits
parsidol
pathology
pediatric autoimmune neuropsychiatric disorders associated with streptococcal infection
penicillamine
personality change
phenylketonuria
pigmentary retinopathy
plasmapheresis
pleocytosis of cerebrospinal fluid
pneumoencephalogram(PEG)
poison, neurologic problems with
poliomyelitis
polymyositis
polyneuropathy
pons, lesion of
porphyria
postural abnormality
potassium channel antibodies
practice guidelines
precipitating factors
pregnancy, neurologic complications in
primary familial brain calcification
PRKN gene
progeria
prognosis
progressive neurologic disorder
prolactin, elevated
pseudohypoparathyroidism
psychiatric disorder
psychiatric problems in neurologic disorders
psychological testing, neurologic problems
psychosis
pupil, abnormality in neurologic disorders
pupil, tonic
quadriparesis
quality of life
radiation hypersensitivity
radiculopathy
rapid onset dystonia parkinsonism
rapidly progressing neurologic illness
recurrent
Red flags
renal stones
respiratory failure
retinopathy
reversible neurologic disorder
review article
RFLPs
rigidity
Riley-Day syndrome
risk factors
rituximab
safety
sarcoidosis
scoliosis
screening
sedimentation rate, elevated
seizure
sensorineural hearing loss
sensory level
sensory tricks
serologic testing
serologic testing, false negative
seronegative
sexual dysfunction in neurologic disease
shaking
short stature
sicca syndrome
sinemet
sinusitis
Sjogren's syndrome
Sjogren's syndrome, neurologic manifestations of
skin, lesions in neurologic disorders
sleep pathology and physiology
slit lamp examination
spastic dysphonia
speech disorder
speech disorder, childhood
speech disorder, non aphasic
spinal cord
spinal cord, lesion of
spinal muscular atrophy
spinocerebellar ataxia
spinocerebellar ataxia type 28
spinocerebellar degeneration
splenomegaly
startle reaction
status epilepticus
stereotaxic surgery
steroid
steroid therapy, CNS treatment and complications with
stiff man syndrome
stimulation, deep brain
stimulation, deep brain, bilateral
striatal encephalitis
striopallidodentate calcifications, familial idiopathic
substantia nigra
symmetric brain lesions
tardive dyskinesia
tardive dystonia
telangiectases
tetrahydrobiopterin
thalamus, lesion of-bilateral
thrombocytopenia
thrombophlebitis
thrombophlebitis, prophylaxis
toe walking
tonic foot response
tonic spasms
torticollis
transient ischemic attack
transient ischemic attack, limb shaking
transient neurologic deficit
trauma
treatment of neurologic disorder
tremor
tremor, postural
trientine dihydrochloride
trigeminal neuralgia
tripping
tyrosine hydroxylase deficiency
unconsciousness
unconsciousness, transient
urinary incontinence
urinary retention
urinary urgency
valium
vasospasm, cerebral
visual loss
walking
walking frame
walking, difficulty with
Werdnig-Hoffman disease
wheelchair
white matter disease
Wolfram syndrome
workup
wrist drop
writers cramp
xerophthalmia
xerostomia
zinc
Showing articles 1250 to 1300 of 2609 << Previous Next >>

Hereditary Adult-Onset Alexander's Disease with Palatal Myoclonus, Spastic Paraparesis and Cerebellar Ataxia
Neurol 45:2266-2271, Schwankhaus,J.D.,et al, 1995

Neurodegeneration and Diabetes:UK Nationwide Study of Wolfram (DIDMOAD) Syndrome
Lancet 1458-1463, Barrett,T.G.,et al, 1995

Cerebral Venography and Manometry in Idiopathic Intracranial Hypertension
Neurol 45:2224-2228, King,J.O.,et al, 1995

Delayed Dystonia with Striatal CT Lucencies Induced by a Mycotoxin (3-Nitropropionic Acid)
Neurol 45:2178-2183, He,F.,et al, 1995

Campylobacter Jejuni Infection and Guillain-Barre Syndrome
NEJM 333:1374-1379, 14151995., Rees,J.H.,et al, 1995

Inclusion Body Myositis and Myopathies
Ann Neurol 38:705-713, Griggs,R.C.,et al, 1995

Apolipoprotein E E4 in Inclusion Body Myositis
Ann Neurol 38:957-959, Garlepp,M.J.,et al, 1995

Adult-Onset Spinocerebellar Dysfunction Caused by a Mutation in the Gene for the a-Tocopherol-Transfer Protein
NEJM 333:1313-1318, 13511995., Gotoda,T.,et al, 1995

Dissection of the Internal Carotid Artery After Chiropractic Manipulation of the Neck
Neurol 45:2284-2286, Peters,M.,et al, 1995

Chronic Hypertrophic Cranial Pachymeningitis Associated with HTLV-I Infection
JNNP 59:435-437, Kawano,Y.&Kira,J., 1995

Thrombolytic Therapy in Acute Occlusion of the Intracranial Internal Carotid Artery Bifurcation
AJNR 16:1977-1986, 19941995., Jansen,O.,et al, 1995

Delayed Onset of Fatal Basilar Thrombotic Embolus After Whiplash Injury
Stroke 26:2194-2196, Viktrup,L.,et al, 1995

CT & MRI of Intracavernous Carotid Art Aneurysm with Occlusion of Cervical Internal Carotid Art
J Comput Assist Tomogr 19:1006-1007, Holemans,J.A.&Cox,T.C., 1995

Paroxysmal Dyskinesias:Clinical Features and Classification
Ann Neurol 38:571-579, Demirkiran,M.&Jankovic,J., 1995

Eye Movement Abnormalities in Systemic Lupus Erythematosus
Arch Neurol 52:1145-1149, Keane,J.R., 1995

Clinicopath Conf
Granulomatous Angiitis of CNS, Case 33-1995, NEJM 333:1135-1143995., , 1995

Vertebral Artery Injury after Acute Cervical Spine Trauma:MR Angiography & Assess of Clin Consequences
AJR 164:443-447, 4481995., Friedman,E.,et al, 1995

Stroke Patterns in Unilateral Atherothrombotic Occlusion of the Internal Carotid Artery
Stroke 26:422-425, Mounier-Vehier,F.,et al, 1995

Guidelines for Carotid Endarterectomy
Stroke 26:188-201, Moore,W.S.,et al, 1995

Progressive Cerebral Occlusive Disease after Radiation Therapy
Stroke 26:131-136, Bitzer,M.&Topka,H., 1995

Neurologic Aspects of Inflammatory Bowel Disease
Neurol 45:416-421, Lossos,A.,et al, 1995

Involuntary Movement Disorders Associated with Felbamate
Neurol 45:185-187, Kerrick,J.M.,et al, 1995

Clinical, Neuropath & Genetic Studies of Large Spinocerebellar Ataxia Type 1 (SCA1) Kindred: (CAG) n Early Premonitory Signs & Symp
Neurol 45:24-30, Genis,D.,et al, 1995

Autosomal Dominant Cerebellar Phenotypes:The Genotype has Settled the Issue
Neurol 45:1-5, Rosenberg,R.N., 1995

Increased Incidence of Aortic Aneurysm and Dissection in Giant Cell (Temporal) Arteritis
Ann Int Med 122:502-507, Evans,J.M.,et al, 1995

Cranial MRI in Ataxia-Telangiectasia
Neuroradiology 37:77-82, Sardanelli,F.,et al, 1995

Dysphagia Caused by an Anterior Cervical Osteophyte:Case Report
Neuroradiology 37:58-59, Kodama,M.,et al, 1995

Clinicopath Conf
Progressive Multifocal Leukoencephalopathy & Systemic Lupus Erythematosus, Case 20-1995, NEJM 332:17, 3-17995., 1995

Clinicopath Conf
Qunidine-Induced Thrombocytopenia, Cerebral Hemorrhage, Case 15-1995, NEJM 332:1363-137095., , 1995

Cerebral Venous Thrombosis in Adults:A Study of 40 Cases From Saudi Arabia
Stroke 26:1193-1195, Daif,A.,et al, 1995

Common Carotid Artery Occlusion:Evaluation with Duplex Sonography
AJNR 16:1099-1105, Chang,Y.J.,et al, 1995

Plaque Ulceration & Lumen Thrombus are Main Sources of Cerebral Microemboli in High-Grade Int Carotid Art Steno
Stroke 26:1231-1233, Sitzer,M.,et al, 1995

Ischemic Stroke as First Manifestation of Essential Thrombocythemia, Report of Six Cases
Stroke 26:1463-1466, Arboix,A.,et al, 1995

C-5 Radiculopathy as a Manifestation of Giant Cell Arteritis
Neurol 45:1222-1224, Rivest,D.,et al, 1995

Prevalence and Outcome of Symptomatic Carotid Lesions in Young Adults
BMJ 310:1363-1366, Carolei,A.,et al, 1995

Ultrasound Findings in Carotid Artery Dissection:Analysis of 43 Patients
Neurol 45:691-698, Sturzenegger,M.,et al, 1995

Massive Infarcts Involving the Territory of the Anterior Choroidal Artery and Cardioembolism
Stroke 26:609-613, Levy,R.,et al, 1995

Levorotatory Form of 5-Hydroxytryptophan in Friedreich's Ataxia
Arch Neurol 52:456-460, Trouillas,P.,et al, 1995

Double-Blind Study with Levorotatory form of Hydroxytryptophan in Pts with Degen Cerebellar Dis
Arch Neurol 52:451-455, 4401995., Wessel,K.,et al, 1995

Kayser-Fleischer Ring:Hepatolenticular Degeneration (Wilson's Disease)
Neurol 45:1261-1262, Finelli,P.F., 1995

Hematologic Manifestations of AIDS
In Hematology-Basic Principles & Practice, Churchill Liningstone, NY Ch 155, p2171., Hoxie,J.A., 1995

Erdheim-Chester Disease and Slowly Progressive Cerebellar Dysfunction
JNNP 58:238-240, Fukazawa,T.,et al, 1995

Machado Joseph Disease Maps to Same Region of Chromosome 14 as Spinocerebellar Ataxia Type 3 Locus
J Med Genet 32:25-31, Twist,E.C.,et al, 1995

Idiopathic CD4+T-Cell Lymphocytopenia and Subacute Inflammatory Demyelinating Polyradiculoneuropathy
Neurol 45:196-197, Ferrer,X.,et al, 1995

Invasive Aspergilloma of the Frontal Base Causing Internal Carotid Artery Occlusion
Surg Neurol 44:483-488, Satoh,H.,et al, 1995

Primary Angiitis of the Central Nervous System:Report of Two Cases and Review of the Literature
Neurosurg 36:173-179, Ozawa,T.,et al, 1995

Intensive Care of Acute Guillain-Barre Syndrome
Can J Neurol Sci 21:S23-S27, Ropper.,A.H., 1994

Pain in the Guillain-Barre Syndrome: A Clinical Review
Pain 59:159-164, Pentland,B. &Donald,S.M., 1994

Autonomic Involvement in Guillain-Barre Syndrome:A Review
Muscle & Nerve 17:1145-1155994., Zochodne,D.W., 1994

Experience in the Diagnosis of Headaches That Start in Elderly People
JNNP 57:1255-1257, Pascual,J.&Berciano,J., 1994



Showing articles 1250 to 1300 of 2609 << Previous Next >>