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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
amyotrophic lateral sclerosis
anemia
ankle edema
anti GQ1b IgG antibody
anticholinergic drugs
apraxia of eye movements
areflexia
artane
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
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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
degenerative diseases of CNS
delay in diagnosis
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depression
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developmental retardation
dexterity, impaired
diabetes insipidus
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diurnal variation
DNA probes
donut sign
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dopamine
drooling
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drug induced neurologic disorders
dural sinus thrombosis
dysarthria
dysarthria-clumsy hand syndrome
dysdiadochokinesia
dyskinesia
dyskinesia, causes of
dyskinesia, drug induced
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dystonia, classification
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dystonia, symptomatic
dystonia, treatment of
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edema, pedal
efficacy
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encephalitis
encephalitis, autoimmune
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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
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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
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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
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lithium
liver function enzymes
lymphoma
masked facies
mastoiditis
memory, impairment of
meningismus
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meningitis, carcinomatous
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MRI
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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
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muscular dystrophy, Duchenne
muscular dystrophy, facioscapulohumeral
muscular dystrophy, limb-girdle
myasthenia gravis
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myelitis, transverse
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myelitis, transverse, prognosis
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myelopathy, chronic progressive
myoclonic jerks
myoclonus
myoglobinuria
myopathy
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myopathy, thyroid disease causing
myositis
myotonia dystrophica
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neck pain
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next-generation sequencing
NMDA antagonists
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numb clumsy hands syndrome
nystagmus
nystagmus, monocular
obsessive-compulsive disorder
ocular motility, disorders of
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 1400 to 1450 of 2609 << Previous Next >>

Relapse in Guillain-Barre Syndrome after Treatment with Human Immune Globulin
Neurol 43:872-875, 8571993., Inrani,D.N.,et al, 1993

Human Immune Globulin Infusion in Guillain-Barre Syndrome:Worsening During & After Treatment
Neurol 43:1034-1036, 8571993., Castro,L.H.M.&Ropper,A.H., 1993

Serologic Evidence of Previous Campylobacter Jejuni Infection in Patients with the Guillain-Barre Syndrome
Ann Int Med 118:947-953, Mishu,B.,et al, 1993

Fulminant Rhabdomyolysis in a Patient with Dermatomyositis
Neurol 43:844-845, Caccamo,D.V.,et al, 1993

Drug Therapy of Idiopathic Inflammatory Myopathies:Response to Prednisone Azathioprine, & Methotrexate
Am J Med 94:379-387, Joffe,M.M.,et al, 1993

The Treatment of Inclusion Body Myositis:A Retrospective Review & Random, Prospective Trial of Immunosupp Therapy
Medicine 72:225-235, Leff,R.L.,et al, 1993

Treatment of Inclusion-Body Myositis with High-Dose Intravenous Immunoglobulin
Neurol 43:876-879, Soueidan,S.A.&Dalakas,M.C., 1993

Inclusion Body Myositis Presenting Solely as Dysphagia
Neurol 43:1241-1243, Riminton,D.S.,et al, 1993

Spasmodic Torticollis Occurring During Alcohol Withdrawal
Neurol 43:623-624, DeKeyser,J., 1993

Cerebellar Infarction, Clinical and Anatomic Observations in 66 Cases
Stroke 24:76-83, Kase,C.S.,et al, 1993

Magnetic Resonance Imaging in Hereditary and Idiopathic Ataxia
Neurol 43:318-325, Wullner,U.,et al, 1993

Sudden Bilateral Hearing Impairment in Vertebrobasilar Occlusive Disease
Stroke 24:132-137, Huang,M.,et al, 1993

Callosal Atrophy with Reduced Cortical Oxygen Metabolism in Carotid Artery Disease
Stroke 24:88-93, Yamauchi,H.,et al, 1993

Icepick-like Pains
Lance, J. W. In, The Headaches, Raven Press, NY, Ch 91, p 609, , 1993

The Pathogenesis of Superficial Siderosis of the Central Nervous System
Ann Neurol 34:646-653, 635-6361993., Koeppen,A.H.,et al, 1993

The Motor Disorder of Multiple System Atrophy
JNNP 56:1239-1242, Quinn,N.P.&Marsden,C.D., 1993

Intensive Management and Treatment of Severe Guillain-Barre Syndrome
Crit Care Med 21:433-446, Hund,E.F.,et al, 1993

Serum anti-GQ1b IgG antibody is Associated with Ophthalmoplegia in Miller Fisher Syndrome and Guillain-Barre Syndrome: Clinical and Immunohistochemical Studies
Neurol 43:1911-1917, Chiba, A.,et al, 1993

Angelman Syndrome: Clinical Profile
J Child Neurol 7:270-280, Zori,R.T.,et al, 1992

Treatment of Hemifacial Spasm with Botulinum Toxin
Muscle & Nerve 15:1045-1049992., Yoshimura,D.M.,et al, 1992

Idiopathic Intracranial Hypertension:Report of Seven Cases
Am J Med 93:391-395, Jain,N.&Rosner,F., 1992

The Sit-up Test:An Alternative Clinical Test for Evaluating Pediatric Torticollis
Pediatrics 90:612-615, Caputo,A.R.,et al, 1992

Botulinum Toxin, Useful in Adult Onset Focal Dystonias
BMJ 305:1169-1170, Lees,A.J., 1992

Hemifacial Spasm:Evaluation of Magnetic Resonance Imaging & Magnetic Resonance Tomographic Angiography
Ann Neurol 32:502-506, Adler,C.H.,et al, 1992

Pseudotumor Cerebri in a Boy with Systemic Lupus Erythematosus
Am J Dis Child 146:1417-1419, Vachvanichsanong,P.,et al, 1992

Neuropsychiatric Systemic Lupus Erythematosus in Elderly People:A Case Series
JNNP 55:1157-1161, Dennis,M.S.,et al, 1992

Neurologic Manifestations of Progressive Systemic Sclerosis
Arch Neurol 49:1292-1295, Averbuch-Heller,L.,et al, 1992

Coma Assoc with Bursts of Abnor Movements & Cognitive Disturb:Acute Encephalopathy of Obscure Origin
J Pediatr 121:845-851, Sebire,G.,et al, 1992

Clinicopath Conf
PEOMS Syndrome, Case 39-1992, NEJM 327:1014-1021992., , 1992

Risks and Benefits of Shunting in Carotid Endarterectomy
Stroke 23:1583-1587, Halsey,J.H., 1992

Detection of Intracranial Emboli in Patients with Symptomatic Extracranial Carotid Artery Disease
Stroke 23:1652-1654, Siebler,M.,et al, 1992

Isolated Granulomatous Angiitis of the Spinal Cord
Ann Neurol 32:580-582, Caccamo,D.V.&Garcia,J.H., 1992

MRI of Intracranial Neurovascular Compression
J Comput Assist Tomogr 16:503-505, Furuya,Y.,et al, 1992

Acute Toxic Reaction to Carbamazepine:Clinical Effects and Serum Concentrations
J Pediatr 121:295-299, Tibballs,J., 1992

Delayed Cyanide Induced Dystonia
JNNP 55:198-199, Valenzuela,R.,et al, 1992

Neurolymphomatosis:A Clinicopathologic Syndrome Re-emerges
Neurol 42:1136-1141, Diaz-Arrastia,R.,et al, 1992

Cerebellar and Cerebral Abnormalities in Rett Syndrome:A Quantitative MR Analysis
AJR 159:177-183, Murakami,J.W.,et al, 1992

Cerebellar Symptoms as Presenting Manifest of Bilirubin Encephal in Children with Crigler-Najjar Type I Disease
Pediatrics 89:768-770, Labrune,P.H.,et al, 1992

Subacute Idiopathic Demyelinating Polyradiculoneuropathy
Arch Neurol 49:612-616, Hughes,R.,et al, 1992

Early Guillain-Barre Syndrome without Inflammation
Arch Neurol 49:979-981, Ropper,A.H.&Adelman,L., 1992

Pure Sensory Guillain-Barre Syndrome
JNNP 55:411-415, Miralles,F.,et al, 1992

Plasma Exchange In Guillain-Barre Syndrome:One-Year Follow-up
French Coop Group on Plasma Exchange in Guillain-Barre Syndrome, Ann Neurol 32:94-971992., , 1992

A Randomized Trial Comparins Intravenous Immune Globulin and Plasma Exchange in Guillain-Barre Syndrome
NEJM 326:1123-1129, VanDerMeche,F.G.A.,et al, 1992

The Guillain-Barre Syndrome
NEJM 326:1130-1136, Ropper,A.H., 1992

Generalized Myositis in Behcet Disease:TReatment with Cyclosporine
Ann Int Med 116:651-653, Lingenfelser,T.,et al, 1992

Controlled Trial of Plasma Exchange and Leukapheresis in Polymyositis and Dermatomyositis
NEJM 326:1380-1384, Miller,F.W.,et al, 1992

Familial Inclusion Body Myositis:Evidence for Autosomal Dominant Inheritance
Neurol 42:897-902, Nevile,H.E.,et al, 1992

Pravastatin-Associated Inflammatory Myopathy
NEJM 327:649-650, Schalke,B.B.,et al, 1992

Wilson's Disease:The Problem of Delayed Diagnosis
JNNP 55:692-696, Walshe,J.M.&Yealland,M., 1992

Dysphagia After Botulinum Toxin Injections for Spasmodic Torticolli:Clinical and Radiologic Findings
Neurol 42:1307-1310, Comella,C.L.,et al, 1992



Showing articles 1400 to 1450 of 2609 << Previous Next >>