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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 2500 to 2550 of 3776 << Previous Next >>

Clinicopath Conf
Acquired Demyelinating Neuropathy, ? CIDP, ? Motor Neuropathy with Multifocal Conduction Blocks, Cas, 41-1EJM 329:1182-1190,1993., 1993

Hallervorden-Spatz Disease with Bilat Invol of Globus Pallidus & Substantia Nigra:MR Demonstra
J Comput Assist Tomogr 17:961-963, Porter-Grenn,L.,et al, 1993

Cabergoline in Parkinson's Disease:Long-Term Follow-up
Neurol 43:2587-2590, Lera,G.,et al, 1993

Brain Imaging in Late-Onset CM2 Gangliosidosis
Neurol 43:2055-2058, Streifler,J.Y.,et al, 1993

Competent Pts with Adv States of Perm Paralysis Have the Right to Forgo Life-Sustaining Therapy
Neurol 43:224-225, Bernat,J.L.,et al, 1993

A Novel Antineuronal Antibody in Stiff-Man Syndrome
Neurol 43:114-120, Darnell,R.B.,et al, 1993

Autoantibodies to a 128-kd Synaptic Protein in Three Women with the Stiff-Man Syndrome & Breast Cancer
NEJM 328:546-551, Folli,F.,et al, 1993

Movement Disorders with Cerebral Toxoplasmosis and AIDS
Movement Disorders 8:107-112, Nath,A.,et al, 1993

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

Clinicopath Conf
Cysticercosis Involving Basal Cisterns of Brain, Case 8-1993, NEJM 328:566-573993., , 1993

Oral Megadose Methylprednisolone Therapy in a Pt with Chronic Progressive MS
Neurol 43:230, Gucuyener,K.,et al, 1993

Rapidly Progressive Aphasic Dementia and Motor Neuron Disease
Ann Neurol 33:200-207, Caselli,R.J.,et al, 1993

Signal Loss in the Motor Cortex on Magnetic Resonance Images in Amyotrophic Lateral Sclerosis
Ann Neurol 33:218-222, Ishikawa,K.,et al, 1993

Amyotrophic Lateral Sclerosis:Hyperintensity of the Corticospinal Tracts on MR of Spinal Cord
AJR 160:604-606, Friedman,D.P.&Tartaglino,L.M., 1993

Cell Culture Evidence for Neuronal Degeneration in ALS to Glutamate AMPA/Kainate Receptors
Lancet 341:265-268, Couratier,P.,et al, 1993

Motor Neuron Diseases and Amyotrophic Lateral Sclerosis:GM1 Antibodies and Paraproteinemia
Neurol 43:418-420, Sanders,K.A.,et al, 1993

Acute Renal Failure Resulting from Intravenous Immunoglobulin Therapy
Arch Neurol 50:137-139, 1351993., Tan,E.,et al, 1993

Neurological Involvement in Wegener's Granulomatosis:An Analysis of 324 Consecutive Pts at the Mayo Clin
Neurol 33:4-9, Nishino,H.,et al, 1993

Intramedullary Spinal Sarcoidosis:Clinical and Magnetic Resonance Imaging Characteristics
Neurol 43:333-337, Junger,s.S.,et al, 1993

Complications of Intracranial Pressure Monitoring in Fulminant Hepatic Failure
Lancet 341:157-158, Blei,A.T.,et al, 1993

Coxiella (Q fever) -Associated Myelopathy
Neurol 43:338-342, Hwang,Y.M.,et al, 1993

Rasmussen's Chronic Encephalitis in Adults
Arch Neurol 50:269-274, McLachlan,R.S.,et al, 1993

Reduction in Incidence of Optic Nerve Disease with Annual Ivermectin to Control Onchocerciasis
Lancet 341:130-134, 153-1541993., Abiose,A.,et al, 1993

Diag of Occult Muscular Dystrophy:"Chance"Finding of Elevated Serum Aminotransferase Act
J Pediatr 122:254-256, Morse,R.P.&Rosman,N.P., 1993

Experience with Screening Newborns for Duchenne Muscular Dystrophy in Wales
BMJ 306:357-360, 3491993., Bradley,D.M.,et al, 1993

Duchenne Dystrophy:Randomized, Controlled Trial of Prednisone (18 months) & Azathioprine (12 months)
Neurol 43:520-527, Griggs,R.C.,et al, 1993

Cyclosporine Increases Muscular Force Generation in Duchenne Muscular Dystrophy
Neurol 43:527-532, Sharma,K.R.,et al, 1993

Progressive Multifocal Leucoencephalopathy
Brit J Hosp Med 50:187-192, Sweeney,B.J.,et al, 1993

Hemorrhagic Necrosis and Vascular Injury in Carbon Monoxide Poisoning:MR Demonstration
AJNR 14:168-170, Silverman,C.S.,et al, 1993

Occurrence of MS-Like Illness in Women Who Have a Leber's Hereditary Optic Neuropathy Mitochondrial DNA Mutation
Brain 115:979-989, Harding,A.E.,et al, 1992

Efficacy of Cytarabine in Progressive Multifocal Leucoencephalopathy in AIDS
Lancet 339:306, Nicoli,F.,et al, 1992

Progressive Multifocal Leukoencephalopathy in HIV-1-Infected Children
AIDS 6:837-841, Berger,J.R.,et al, 1992

PML:More Neurological Bad News for AIDS Patients
Lancet 340:943-944, , 1992

Mosaic Express of Dystrophin in Carriers of Becker's Muscular Dyst & X-Linked Synd of Myalgia & Cramps
NEJM 327:1100, Minetti,C.&Bonilla,E., 1992

Upper Gastrointestinal Tract Motility in Children with Progressive Muscular Dystrophy
J Pediatr 121:720-724, Staiano,A.,et al, 1992

Chronic Encephalitis (Rasmussen's Syndrome) and Ipsilateral Uveitis
Ann Neurol 32:826-829, Harvey,A.S.,et al, 1992

Brief Report:Autosomal Dominant Familial Hypoparathyroidism, Sensorineural Deafness, and Renal Dysplasia
NEJM 327:1069-1074, Bilous,R.W.,et al, 1992

Familial Creutzfeldt-Jakob Disease (Codon 200 Mutation) with Supranuclear Palsy
Bertoni. J. M. , et al, JAMA 268:2413-2415., , 1992

Serum Antibodies to L-Type Calcium Channels in Patients with Amyotrophic Lateral Sclerosis
NEJM 327:1721-1728, 17521992., Smith,R.G.,et al, 1992

Travel and Ciguatera Fish Poisoning
Arch Int Med 152:2049-2053, Lange,W.R.,et al, 1992

Sumatriptan for Migraine
The Medical Letter, 34:91-931992., , 1992

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

Familial Adult-Onset Muscular Dystrophy with Leukoencephalopathy
Ann Neurol 32:577-580, vanEngelen,B.G.M.,et al, 1992

MRI and SPECT in Amyotrophic Lateral Sclerosis, Demonstr of Upper Motor Neurone Invol by Neuroimaging
Neuroradiology 34:389-393, Udaka,F.,et al, 1992

Facioscapulohumeral Dystrophy, In Skeletal Muscle Pathology
Churchhill Livingstone, NY, p285, 30392., Mastaglia,F.L.&Walton,J., 1992

Lidocaine Unmasks Silent Demyelinative Lesions in Multiple Sclerosis
Neurol 42:2088-2093, Sakurai,M.,et al, 1992

Multiple Sclerosis with Very Late Onset
Neurol 42:1907-1910, Hooge,J.P.&Redekop,W.K., 1992

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

Human T Lymphotropic Virus Type I-Assoc Myelopathy, A Rpt of 10 Pts Born in US
Arch Neurol 49:1113-1118, Sheremata,W.A.,et al, 1992

Chronic Myelopathy Associated with Human T-Lymphotropic Virus Type I (HTLV-I)
Ann Int Med 117:933-946, Gessain,A.&Gout,O., 1992



Showing articles 2500 to 2550 of 3776 << Previous Next >>