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acetylcholine receptor antibody
acoustic nerve
acute intermittant porphyria
Adies pupil
adrenergic blocker
adult polyglucosan body disease
adverse drug reaction
agitation
akathisia
alcoholism
allodynia
alopecia
alpha adrenergic blocker
aluminum
Alzheimer's disease
amphiphysin antibodies
amyloidosis
amyotrophic lateral sclerosis
anatomy of
anisocoria
anorexia
antibodies to voltage-gated calcium channels
antiganglioside antibodies
antineurofascin antibodies
antitoxin
areflexia
arm weakness
ataxia
ataxia, cerebellar
ataxia, progressive
atypical
autoantibodies
autoimmune autonomic ganglionopathy
autoimmune disease
autonomic cardiovascular reflexes
autonomic dysfunction
autonomic dysfunction, acute
autonomic dysfunction, evaluation of
autonomic nervous system
autonomic neuropathy
autosomal dominant leukodystrophy
axonal degeneration
Babinski sign
bladder dysfunction
bone scanning
botulinum toxin
botulism
botulism antitoxin
botulism immune globulin
botulism, infant
bradycardia
bradykinesia
brain atrophy
bulbar palsy
bulbar palsy, acute
burning paresthesia
cachexia
calf atrophy
campylobacter infection
carcinoma
carcinoma of lung
CAT scan
CAT scan, abnormal
CAT scan, chest
CAT scan, emission, abnormal
cataracts
cerebellar degeneration
cerebellar lesion
cerebellar vermis
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, oligoclonal IgG in
chest pain
chewing movements
children
chorea
cingulate island sign
Clinical Pathologic Conference(C.P.C.)
coat-hanger pain
cognition
cogwheel rigidty
coinfection
collapsin response mediator protein 5 IgG
complications
confabulation
confusion
constipation
contactin associated protein like 1 antibodies
contactin associated protein like 2 antibodies
corpus callosum
corpus callosum, lesion of
cranial nerve palsies
cranial neuropathy
cranial neuropathy, multiple
cry, abnormal
cry, weak
crying
cyanosis
cyst, arachnoid, infant
deep tendon reflexes
degenerative diseases of CNS
delay in diagnosis
dementia
dementia, familial
dementia, rapidly progressive
dementia, subcortical
depression
dermatomyositis
diabetes mellitus
diabetes mellitus, chemical
dialysis
dialysis dementia
dialysis disequilibrium syndrome
differential diagnosis
diplopia
disorientation
distal muscle atrophy
distal muscle weakness
dizziness
dysarthria
dysdiadochokinesia
dysmetria
dysphagia
dyspnea
edema, pedal
electroencephalogram, abnormalities of
electromyogram
electromyogram, incremental response
encephalitis, autoimmune
encephalitis, brainstem
encephalitis, paraneoplastic
encephalomyelitis
encephalopathy
ephedrine
epidemiology of neurology
erectile dysfunction
exercise
exercise-related muscle strength increase
exome sequencing
extrapyramidal movement disorder, progressive
facial asymmetry
facial weakness
facial weakness, bilateral
falling
familial
fasciculation
fatal familial insomnia
fatigue
feeding disorder
fibrillations
Fisher's syndrome
flaccid paralysis
fludrocortisone
food poisoning
food-borne infection
gait disorder
gait, spastic
gammaglobulin therapy, intravenous
gammaglobulin therapy, intravenous, refractory
ganglionitis
gastroparesis
gene mutation
genetic neurologic disorders
genetic testing
glaucoma
glucose tolerance test, abnormal
glycogen storage disease
guanethidine
Guillain Barre syndrome
Guillain Barre syndrome, axonal form
Guillain Barre syndrome, complications
Guillain Barre syndrome, differential diagnosis of
Guillain Barre syndrome, etiology of
Guillain Barre syndrome, prognosis of
Guillain Barre syndrome, variant forms of
hallucination, auditory
head bobbing
heat intolerance
hemifacial atrophy
hemiparesis
heralding manifestation
hoarseness
honey
Horner's syndrome
hot bath test
H-reflex testing
hyperamylasemia
hyperhidrosis
hyperreflexia
hypertension
hypohidrosis
hypokalemic paralysis
hyponatremia
hypoosmolality of serum
hypophonia
hyporeflexia
hyposmia
hypotension, neurologic causes of
hypotension, systemic
hypothermia
hypotonia
hypotonia, infants
IgG4-related disease
ileus, paralytic
imbalance
imbalance, postural
immunologic disease
immunology and the nervous system
immunotherapy
impotence
inappropriate antidiuretic(A.D.H.)hormone, CNS involvement with
inattention
inclusion bodies
inclusion bodies, eosinophilic cytoplasmic
inclusion bodies, eosinophilic intranuclear
inclusion bodies, intranuclear
infant, evaluation of
insight, loss
insomnia
intellectual deficit
intellectual deterioration
intrinsic hand muscles, wasting of
irritability
irritable baby
Jewish
juvenile distal and segmental muscular atrophy
laughing
laughing, pathologic
L-dopa
leg weakness, bilateral
lethargy
leucine rich glioma inactivated 1 antibodies
leukodystrophy
leukoencephalopathy
life expectancy
lightheaded
light-near dissociation, causes of
limbic encephalitis
livedo reticularis
malignancy screen
malignancy, occult
marche a petits pas
masked facies
memory, defect of recent
memory, impairment of
mental status, abnormal
metabolic disorder, primary
middle cerebellar peduncle, lesion, bilateral
midodrine
mimics
Mini Mental Status Examination
misdiagnosis
monoamine oxidase inhibitors
mononeuritis multiplex
mortality
Morvan's fibrillary chorea
motor neuron disease
movement disorder
movement disorder, extrapyramidal
MRI
MRI, abnormal
MRI, contrast enhanced
MRI, diffusion weighted
MRI, lumbosacral plexus
multiple sclerosis
multiple system atrophy
muscle atrophy, progressive
muscle cramp
muscle pain
muscle strength, testing
muscle twitching
muscle weakness
muscle weakness, proximal
muscle weakness, sudden onset of
myasthenia gravis
myasthenia gravis, paraneoplastic
myasthenic syndrome
myelomalacia
myeloneuropathy
myelopathy
myelopathy, necrotizing
myoclonic jerks
myokymia
nausea and vomiting
neck pain
neck weakness
nephrotic syndrome
nerve biopsy
nerve conduction studies
nerve growth factor
nerve growth stimulating activity
nerve root enhancement
nerve root hypertrophy
neuroblastoma
neurofibromatosis 1
neurogenic bladder
neurologic complications of, systemic disease
neurologic disease, diagnoses of
neurologic disease, multifocal
neurologic signs
neuromuscular blockade
neuromuscular disease, electrodiagnosis of
neuromuscular junction
neuromuscular junction, abnormality of
neuromyotonia
neuronal cell surface antigen
neuronal intranuclear inclusion disease
neuronopathy, sensory
neuropathology
neuropathy
neuropathy, amyloid
neuropathy, autoimmune
neuropathy, hereditary peripheral
neuropathy, painful
neuropathy, paraneoplastic
neuropathy, peripheral
neuropathy, sensory
neuropathy, sensory, hereditary
neuroprotective agents
neurotoxin
next-generation sequencing
NMDA antagonists
node of Ranvier
nodopathy, autoimmune
nonresponsive
NOTCH2NLC
ocular dysmetria
onconeural antibodies
ophthalmoplegia
ophthalmoplegia, acute
ophthalmoplegia, bilateral, acute
ophthalmoplegia, total
opsoclonus-myoclonus syndrome
optic neuropathy
oral contraceptives
orthostatic hypotension
orthostatic hypotension, idiopathic
orthostatic hypotension, treatment of
osteoporosis
pain
pain, abdominal
pain, leg
palate, paralysis
pancreatitis
paralysis
paralysis, acute areflexic
paraneoplastic cerebellar degeneration
paresthesias
Parkinson disease
Parkinson disease, atypical
Parkinson disease, differential diagnosis of
Parkinson disease, familial
Parkinson disease, L-dopa nonresponsive
Parkinsonism multiple-system atrophy
Parkinsonism syndrome
paroxysmal neurologic deficits
peripheral nerve, lesion of
pheochromocytoma
physical therapy
plasmapheresis
pleocytosis of cerebrospinal fluid
polyglucosan body
polyglucosan body disease
polymerase chain reaction
polyneuropathy
polyneuropathy, uremic
porphyria
posterior leukoencephalopathy syndrome
postural abnormality
posturography
prevention of neurologic disorders
prion disease
prognosis
progressive hemifacial atrophy
progressive neurologic disorder
progressive supranuclear palsy
pruritus
pseudobulbar palsy
psychiatric problems in neurologic disorders
psychological testing
psychosis
psychosis, acute
psychotic behavior
ptosis
ptosis, bilateral
pulmonary embolism
pupil, abnormality in neurologic disorders
pupil, dilated and fixed, bilateral
pupil, dilated, bilateral
pupil, light reflex, abnormal
pupil, oval
pupil, tonic
pure autonomic failure
pyramidal tract
pyramidal tract dysfunction
quadriparesis
quadriplegia
radiculopathy
Red flags
reflex sympathetic dystrophy
reflex sympathetic dystrophy, children
remote effect of cancer on the nervous system
renal failure
renal transplantation
renal tubular acidosis
repetitive nerve stimulation
respirator
respiratory failure
retinopathy
review article
rigidity
Riley-Day syndrome
risk factors
Romberg's sign
salivation, excessive
schizophrenia
scleroderma
scleroderma, neurologic involvement with
screening
seizure
sensory ganglia
serum lipase, elevated
shoulder, pain in
Shy-Drager syndrome
sicca syndrome
single-fiber electromyography
Sjogren's syndrome
skin, biopsy
skin, temperature difference
sleep pathology and physiology
SNCA duplication
spasticity
spinal cord, lesion of
stare
steroid
steroid therapy, CNS treatment and complications with
subcortical U fibers
suck, poor
sweating
sweating, abnormality of
sympathetic block
sympathetic nervous system
sympathomimetic drugs
syncope
synucleinopathy
systemic illness
tachycardia
tandem gait, ataxic
tensilon test, false positive
thalamus, lesion of-bilateral
thermography
thymoma
tongue, impaired movements of
tongue, weakness
trauma
treatment of neurologic disorder
tremor
trinucleotide repeats
uremia
uremic encephalopathy
urinary frequency
urinary incontinence
urinary retention
urine osmolality, elevated
vasopressin
viral infection
vision, blurred
visual loss
vocal cord paralysis
walking, difficulty with
Watson-Schwartz reaction
weakness
weakness, acute
weakness, generalized
weakness, infant
weakness, progressive
weakness, proximal
weight loss
wheelchair
white hair
white matter disease
wide based gait
workup
xerophthalmia
xerostomia
Showing articles 3000 to 3050 of 3776 << Previous Next >>

Positron Emission Tomography in a Patient with Progressive Multifocal Leukoencephalopathy
Neurol 38:1864-1867, Kiyosawa,M.,et al, 1988

The Molecular Genetic Revolution, Its Impact on Clinical Neurology
Arch Neurol 45:1366-1376, Payne,C.S.&Roses,A.D., 1988

MR Imaging of the Brain in Myelopathy Associated with Human T-Cell Lymphotropic Virus Type I
J Comput Assist Tomogr 12:750-754, Hara,Y.,et al, 1988

Plasmapheresis in Treatment of Human T-Lymphotropic Virus Type-I Associated Myelopathy
Lancet 2:1109-1113, Matsuo,H.,et al, 1988

Elevated Serum Antibody Titers to Epstein-Barr Virus in HTLV-I Associated Myelopathy (HAM)
Neurol 38:1650-1653, Itoyama,Y.,et al, 1988

Medullary Lesion Revealed by MRI in a Case of MS with Respiratory Arrest
Neuroradiology 30:574-576, Mochizuki,A.,et al, 1988

Correlation of Neuropsychological and MRI Findings in Chronic/Progressive Multiple Sclerosis
Neurol 38:1826-1829, Franklin,G.M.,et al, 1988

Isolated Central Respiratory Failure Due to Syringomyelia and Arnold-Chiari Malformation
BMJ 297:1448-1449, Bullock,R.,et al, 1988

Risk Factors for Falls Among Elderly Persons Living in the Community
NEJM 319:1701-1707, Tinetti,M.E.,et al, 1988

Pulmonary Function and Dysfunction in Multiple Sclerosis
Arch Neurol 45:1245-1249, Smeltzer,S.C.,et al, 1988

Risk Factors for Progressive Supranuclear Palsy
Neurol 38:1546-1552, Davis,P.H.,et al, 1988

Progressive Language Impairment without Dementia:A Case with Isolated Category Specific Semantic Defect
JNNP 51:1201-1207, Basso,A.,et al, 1988

Clinicopath Conf
Progressive Multifocal Leukoencephalopathy, Chronic Lymphocytic Leukemia, Case Record 45-1988, NEJM, 19:8-1280,1988., 1988

Pelagic Paralysis
Lancet 1:161-164, Mills,A.R.&Passmore,R., 1988

CT & MRI in Maple Syrup Urine Disease
Neurol 38:486-488, Uziel,G.,et al, 1988

Role of Contrast Enhancement in Cerebral CT of Carbon Monoxide Poisoning
J Comput Assist Tomogr 12:341-343, Zeiss,J.&Brinker,R., 1988

Asterixis Mimicking Drop Attacks in Chronic Renal Failure
Neurol 38:663, Massey,E.W.,et al, 1988

Autoantibodies to Glutamic Acid Decarboxylase in Pt with Stiff-Man Syndr, Epilepsy & Type I Diabetes Mellitus
NEJM 318:1012-1020, Solimena,M.,et al, 1988

Stiff-Man Syndrome, An Autoimmune Disease
NEJM 318:1060-1062, Layzer,R.B., 1988

Human Immunodeficiency Virus-Associated Myopathy:Analysis of 11 Pts
Ann Neurol 24:79-84, Simpson,D.M.&Bender,A.N., 1988

Acquired Immunodeficiency Syndrome, Magnetic Resonance Patterns of Brain Involvement with Pathologic Correlation
Arch Neurol 45:731-736, Jarvik,J.G.,et al, 1988

Detection of HTLV-I DNA & Antigen in Spinal Fluid & Blood of Pts with Chronic Progressive Myelopathy
NEJM 318:1141-1147, 11951988., Bhagavati,S.,et al, 1988

Amyotrophic Lateral Sclerosis, Recent Advances in Pathogenesis & Therapeutic Trials
Arch Neurol 45:189-202, Mitsumoto,H.,et al, 1988

The Natural History of Motoneuron Loss in Amyotrophic Lateral Sclerosis
Neurol 38:409-413, Munsat,T.L.,et al, 1988

Use of Composite Scores (Megascores) to Measure Deficit in Amyotrophic Lateral Sclerosis
Neurol 38:405-408, Andres,P.L.,et al, 1988

Malignant Monophasic Multiple Sclerosis or"Marburg's Disease"
Neurol 38:1153-1155, Mendez,M.F.&Pogacar,S., 1988

Prevalence and Natural History of Progressive Supranuclear Palsy
Neurol 38:1031-1034, Golbe,L.I.,et al, 1988

Cerebral Hypometabolism in Progressive Supranuclear Palsy Studied with Positron Emission Tomography
Ann Neurol 24:399-406, Foster,N.L.,et al, 1988

The Minor Symptoms of Increased Intracranial Pressure:101 Pts with Benign Intracranial Hypertension
Neurol 38:1461-1464, Round,R.&Keane,J.R., 1988

Acute Paralysis from Inhaled Barium Carbonate
Arch Neurol 45:579-580, Shankle,R.&Keane,J.R., 1988

MR Imaging of Intrachiasmatic Hemorrhage
J Comput Assist Tomogr 12:535-536, Moffit,B.,et al, 1988

Chronic Unilateral Optic Neuropathy:A Magnetic Resonance Study
Ann Neurol 24:3-11, Eidelberg,D.,et al, 1988

Neurological Basis of Respiratory Complications in Achondroplasia
Ann Neurol 24:89-93, Nelson,F.W.,et al, 1988

Magnetic Resonance Imaging in the Assessment of Medullary Compression in Achondroplasia
Am J Dis Child 142:989-992, Thomas,I.T.,et al, 1988

Diagnostic Criteria for Rett Syndrome
The Rett Syndrome Diagnostic Criteria Work Group, Ann Neurol 23:425-4281988., , 1988

Rett Syndrome:Natural History and Management
Pediatrics 82:1-10, Moeschler,J.B.,et al, 1988

Right-Sided Brain Lesions in Infants Following Extracorporeal Membrane Oxygenation
Pediatrics 82:155-161, Schumacher,R.E.,et al, 1988

Neurologic and Cognitive Deficits in Children with Cystinosis
J Pediatr 112:912-914, Trauner,D.A.,et al, 1988

Clinical Predictors of Electrophysiologic Findings in Pts with Syncope of Unknown Origin
Arch Int Med 148:1922-1928, Denes,P.,et al, 1988

Minor Anomalies in Offspring of Epileptic Mothers
J Pediatr 112:521-529, 579-5811988., Gaily,E.,et al, 1988

Limb Pain in Migraine & Cluster Headache
JNNP 51:1022-1031, Guiloff,R.J.&Fruns,M., 1988

Prolonged Survival & Partial Recovery in AIDS-Associated Progressive Multifocal Leukoencephalopathy
Neurol 38:1060-1065, Berger,J.R.&Mucke,L., 1988

A Prospective Study of Acute Idiopathic Neuropathy, I, Clinical Features & Their Prognostic Value
JNNP 51:605-612, Winer,J.B.,et al, 1988

Progressive Multifocal Leukoencephalopathy after Cardiac Transplantation
Neurol 38:995-996, Hall,W.A.,et al, 1988

Fatal Adult Respiratory Distress Syndrome in a Patient with Lyme Disease
JAMA 259:2737-2739, Kirsch,M.,et al, 1988

Early-Onset Benign Autosomal Dominant Limb-Girdle with Contractures (Bethlem Myopathy)
Neurol 38:573-580, Mohire,M.D.,et al, 1988

Gene Studies in Newborn Males with Duchenne Muscular Dystrophy Detected by Neonatal Screening
Lancet 2:425-427, Greenberg,C.R.,et al, 1988

Effect of Chronic Treatment with the Calcium Antagonist Diltiazem in Duchenne Muscular Dystrophy
Neurol 38:609-613, Bertorini,T.E.,et al, 1988

Characterization of Dystrophin in Muscle-Biopsy Spec from Pts with Duchenne's or Becker's Muscular Dystrophy
NEJM 318:1363-1368, 13921988., Hoffman,E.P.,et al, 1988

Dystrophin
Editorial, Lancet 2:429-4301988., , 1988



Showing articles 3000 to 3050 of 3776 << Previous Next >>