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Differential
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abducens nerve paralysis
acetazolamide
acute cerebellar ataxia
adverse drug reaction
agitation
alcohol
alcohol, neurologic complications with
alcoholic withdrawal states, DT's, convulsions, etc.
alcoholism
Alexanders disease
Alexanders disease, adult onset
algorithm
alternating hemiplegia
alternating hemiplegia of childhood
amaurosis fugax
aminoacidopathies
aminoacidurias
amyloid angiopathy, cerebral
anemia
aneurysm
aneurysm, vertebral basilar system
angiitis
angiitis, granulomatous of CNS
angiography, cerebral, beaded vessels
angiography, cerebral
angiography, cerebral, negative
angiography, vertebral artery
anorexia
anti IgLON5
anti MAG antibodies
antibodies to voltage-gated calcium channels
anxiety
aphasia
apnea
areflexia
arrhythmia, cardiac
arteritides
arthralgia
astrogliopathy
ataxia
ataxia, cerebellar
ataxia, hereditary
ataxia, paroxysmal
ataxia, progressive
ataxia, truncal
ataxic gait
ATP1A3 gene
atrial fibrillation
autoantibodies
autoimmune disease
autoimmune GFAP astrocytopathy
autonomic dysfunction
axonal injury
B 12 deficiency
B12
Babinski sign
basal ganglia, lesion, bilateral
behavior modification
behavior, combative
behavioral disorder
Behcet's syndrome
benign positional vertigo
benzodiazepine
bladder dysfunction
brain biopsy
brain biopsy, stereotaxic
brainstem, infarction of
brainstem, lesion of
brucellosis
brucellosis, nervous system involvement with
bulbar palsy
calcium antagonist
calcium channel dysfunction
carbamazepine
carcinoma
cardiomyopathy
CAT scan
CAT scan, abnormal
CAT scan, angiography
cataracts
celiac disease, adult
central core disease
cerebellar ataxia, children
cerebellar ataxia, hereditary
cerebellar atrophy, primary
cerebellar degeneration
cerebellar infarction
cerebellar lesion
cerebellar peduncle
cerebellar vermis
cerebral cortex
cerebral embolism
cerebral embolism, cardiac origin
cerebral infarction
cerebrospinal fluid, cytology
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, gammaglobulin of
cerebrospinal fluid, proteincytologic dissociation
cerebrospinal fluid, xanthochromia of
cerebrovascular accident
cerebrovascular accident, young adult
channelopathy
Charcot-Marie-Tooth
chemotherapy, CNS treatment and complications with
children
chills
chloride channel dysfunction
chorea
chromosomal abnormality
chromosome 19
ciguatera poisoning
Clinical Pathologic Conference(C.P.C.)
clubfoot as related to neurologic disease
cognition
collagen vascular disease
coma
coma, episodic
complications
concentration, impaired
confusion
congestive heart failure
conjunctivitis
conversion reaction
cranial nerve palsies
crying
cryopyrin-associated periodic syndrome
deafness
deafness, sudden
deafness, unilateral
deep gray nuclei
degenerative diseases of CNS
delay in diagnosis
delirium
dementia
dementia, rapidly progressive
dementia, subcortical
demyelinating disease
dentate nuclei, lesion of
developmental retardation
dexterity, impaired
diabetes mellitus
diagnostic criteria
diet
differential diagnosis
digital subtraction angiography
dilantin
diplopia
disability, neurological
diurnal variation
diving
dizziness
down-beat nystagmus
down-beat nystagmus, primary position of gaze
drowsiness
drug induced neurologic disorders
drug withdrawal
dysarthria
dysmetria
dysphagia
dyspnea
dyspraxia
dystonia
dystonia, psychogenic
electrocardiogram, abnormal
electroencephalogram
electroencephalogram, abnormalities of
electromyogram
embolism
encephalitis
encephalitis, autoimmune
encephalitis, brainstem
encephalitis, viral
encephalopathy
encephalopathy, acute
episodic disorders
episodic neurologic deficits
episodic unconsciousness
epistaxis
Epstein-Barr virus
exercise
exercise intolerance
exome sequencing
eye movement, disorders of
face, numbness of
facial nerve palsy
facial weakness
faciobrachial dystonic seizure
failure to thrive
falling
familial
familial hemiplegic migraine
familial periodic ataxia
fasciculation
fatal familial insomnia
fatigue
fever
fever, recurrent
fine motor function, impaired
Fisher's syndrome
fistula, perilymphatic
foot deformity
Friedreich's ataxia
frontal bossing
fundus, abnormality of
gait disorder
gait, spastic
gene
gene mutation
genetic neurologic disorders
genetic testing
GFAP gene
GFAP-IgG
gliadin antibodies
globus pallidus, lesion of, bilateral
glutamic acid decarboxylase, antibody
gluten sensitivity
gluten-free diet
Guillain Barre syndrome
gynecomastia
hallucination
hallucination, visual
hammertoes
head circumference
head injury
head lag
head turning
head turning, neurologic complications with
headache
headache, bifrontal
headache, episodic
headache, occipital
headache, recurrent
headache, severe
hearing loss
heart block
hemianopia, homonymous
hemimyoclonic jerks
hemiparesis
hemiplegia
hemosiderosis of CNS, superficial
hepatomegaly
hepatosplenomegaly
herpes virus
hoarseness
hyperhidrosis
hyperreflexia
hypersegmented polys
hypersomnia
hypertension
hyperthermia
hyperthyroidism
hypertrophic intracranial pachymeningitis
hypoglycorrhachia
hypokalemia
hypokalemic periodic paralysis
hyponatremia
hypophonia
hypotension, systemic
hypotonia
hypotonia, infants
iatrogenic neurologic disorders
imbalance
imbalance, postural
immunomodulation
immunotherapy
inattention
inborn errors of metabolism
inclusion bodies, eosinophilic intranuclear
inclusion bodies, intranuclear
incoordination
infection
infectious mononucleosis
infectious mononucleosis, neurologic findings with
insomnia
intellectual deficit
intellectual deterioration
intracerebral hemorrhage
intracerebral hemorrhage, recurrent
intracerebral hemorrhage, young adult
irritability
kyphoscoliosis, neurologic causes of
lactic acidemia
lacunar infarction, differential diagnosis of
lateropulsion
leg numbness
leg weakness, bilateral
Leigh's disease
leptospirosis
lethargy
leucine rich glioma inactivated 1 antibodies
leukemia
leukodystrophy
leukoencephalopathy
lightheaded
limbic encephalitis
lorazepam
lysosomal storage disease
macrocephaly
malignant hyperpyrexia
maple syrup urine disease
mastoiditis
memory, defect of recent
memory, impairment of
Meniere's disease
meningeal enhancement
meningitis
meningitis, aseptic
meningitis, bacterial
meningitis, carcinomatous
meningitis, fungal
meningitis, Mollaret's
meningitis, recurrent
meningitis, TB
meningoencephalitis
meningoencephalomyelitis
mental status, abnormal
metabolic acidosis
metabolic disorder, primary
methotrexate
microcephaly
microhemorrhage, intracerebral
middle cerebellar peduncle
middle cerebellar peduncle, lesion
middle cerebellar peduncle, lesion, bilateral
migraine
migraine, hemiplegic
mimics
misdiagnosis
mitochondrial disease
molecular genetics
mononeuropathy
mononeuropathy multiplex
monoparesis
mortality
motor dysfunction
motor neuron disease
motor neuron disease, misdiagnosis
movement disorder
movement disorder, hyperkinetic
movement disorder, psychogenic
MRI
MRI pattern
MRI, abnormal
MRI, angiography
MRI, contrast enhanced
MRI, curvilinear peppering enhancement
MRI, diffusion weighted
MRI, disappearing lesion on
MRI, FLAIR
MRI, negative
MRI, nodular enhancement
multimodal neuroimaging
multiple sclerosis
multiple sclerosis, pain in
multiple sclerosis, paroxysmal symptoms in
muscle atrophy, progressive
muscle biopsy
muscle cramp
muscle pain
muscle weakness
muscular dystrophy
muscular dystrophy, Becker
muscular dystrophy, cardiovascular changes with
muscular dystrophy, Duchenne
myasthenic syndrome
myelitis
myelopathy
myoclonic jerks
myoclonus
myokymia
myopathy
myotonia
myotonia congenita
myotonia dystrophica
nasal septum, perforation of
nausea and vomiting
negative
neoplasm, primary of CNS
neurologic complications of, systemic disease
neurologic disease
neurologic disease, diagnoses of
neurologic evaluation
neurologic examination, focal
neurologic signs
neurologic symptoms
neurologic symptoms, unexplained
neurologic testing
neuromyotonia
neuronal intranuclear inclusion disease
neuroophthalmology
neuropathology
neuropathology, brain
neuropathy
neuropathy, amyloid
neuropathy, ataxic
neuropathy, hereditary peripheral
neuropathy, hypertrophic
neuropathy, onion bulb
neuropathy, peripheral
neuropathy, recurrent
neuropathy, sensory
neuropathy, vasculitic, systemic
neurotoxic
neurotoxicity, acute
night blindness
night sweats
NOTCH2NLC
nystagmus
nystagmus, gaze-paretic
nystagmus, hereditary
nystagmus, intermittent
nystagmus, monocular
nystagmus, periodic
nystagmus, vertical
ophthalmoplegia
ophthalmoplegia, recurrent
optic ataxia
optic atrophy
optic atrophy, bilateral
oscillopsia
otitis, neurologic complications with
pain
pain, abdominal
pain, leg
pain, testicular
palatal myoclonus
palinopsia
papilledema
papillitis
paralysis
paralysis, acute areflexic
paramyotonia congenita
paraparesis
paraparesis, spastic
paraplegia
paresthesias
paresthesias, feet
Parkinson disease, dystonia with
Parkinsonism syndrome
paroxysmal hemiplegia
paroxysmal neurologic deficits
paroxysmal tonic upgaze
pathologic reflex
patient information and support
periarteritis nodosa
periodic paralysis
periodic paralysis, thyrotoxic
peripheral blood smear
perivascular enhancement
perivascular inflammation
pernicious anemia
peroxisomal disease
Persistent postural-perceptual dizziness
personality disorder
pes cavus
phytanic acid
pleocytosis of cerebrospinal fluid
polymerase chain reaction
polyneuropathy
polyneuropathy, chronic relapsing
pons, lesion of
posterior leukoencephalopathy syndrome
potassium
potassium channel antibodies
potassium channel dysfunction
precipitating factors
pregnancy, neurologic complications in
prevention of neurologic disorders
primary episodic ataxia
prion disease
prognosis
progressive neurologic disorder
propofol
psychiatric disorder
psychiatric problems in neurologic disorders
psychomotor retardation
psychosis
psychosis, acute
pulmonary infiltrates
pyramidal tract
pyramidal tract dysfunction
pyruvate dehydrogenase deficiency
pyruvate metabolism, abnormality of
quadriplegia, transient
rapid onset dystonia parkinsonism
rapidly progressing neurologic illness
rash
recurrent
red eye
Red flags
Refsum's disease
REM sleep behavior disorder
remote effect of cancer on the nervous system
respiratory tract infection
retinal artery occlusion
retinal detachment
retinitis pigmentosa
retinopathy
reversible cerebral vasoconstrictive syndromes
reversible neurologic disorder
review article
rheumatoid arthritis
rheumatoid arthritis factor(R.A.factor)
rhinorrhea
Romberg's sign
sarcoidosis
scoliosis
scotoma
screening
scuba diving
sedimentation rate, elevated
seizure
seizure, differential diagnosis of
seizure, withdrawal
selective serotonin reuptake inhibitors
sensorineural hearing loss
sensory loss
serologic testing
serotonin norepinephrine reuptake inhibitors
short stature
sinusitis
skin, biopsy
skin, lesions in neurologic disorders
skull bone, thickening
sleep pathology and physiology
slurred speech
sneeze
sodium channel dysfunction
spinocerebellar ataxia
spinocerebellar ataxia type 6
spinocerebellar degeneration
spongy degeneration of brain
status epilepticus
steroid responsive encephalopathy
steroid therapy, CNS treatment and complications with
stress, emotional
strokelike episodes
subarachnoid hemorrhage, cerebral convexity
subcortical U fibers
suck, poor
sudden death
superior cerebellar artery infarction
superior cerebellar artery syndrome
superior cerebellar peduncle
supratentorial lymphocytic inflam parenchy perivasc enhanc responsive to steroids
swimming
symmetric brain lesions
tachycardia
tandem gait, ataxic
temporal lobe, lesion
temporal lobe, lesion, bilateral
term infant
testicular biopsy
thalamus, lesion of
third nerve palsy
thyrotoxicosis
tinnitus
tonic spasms
toxic encephalopathy
transient ischemic attack
transient neurologic deficit
treatment of neurologic disorder
tremor
tremor, postural
tremor, psychogenic
trigeminal neuralgia
trigeminal neuropathy
trigeminal neuropathy, sensory
trinucleotide repeats
unconsciousness
unconsciousness, episodic
unconsciousness, transient
upgaze
upgaze, sustained
urea-cycle enzymopathies
uremia
urinary frequency
urinary incontinence
uveitis
vaccination, neurologic complications with
valium
valsalva maneuver
vasculopathy
vasospasm, cerebral
vertebral artery
vertebral artery disease
vertebral artery occlusion
vertebral artery stenosis
vertebral-basilar insufficiency
vertigo
vertigo, episodic
vertigo, treatment of
violent behavior
viral infection
viral infection, CNS
Virchow-Robin spaces, dilated
vision, blurred
visual field defect
visual fields, constricted
vitamin E deficiency
vocalizations
Vogt-Koyanagi-Harada syndrome
walking, difficulty with
weakness
weakness, acute
weakness, episodic
weakness, generalized
weight loss
white matter disease
wide based gait
workup
Showing articles 1300 to 1350 of 2314 << Previous Next >>

Paraneoplastic Cerebellar Degeneration
Arch Int Med 157:1258-1262, Bolla,L.&Palmer,R.M., 1997

Serum Autoantibodies in Childhood Opsoclonus-Myoclonus Syndrome:Analysis of Antigenic Targets in Neural Tissues
J Pediatr 130:878-884, 8851997., Connolly,A.M.,et al, 1997

Postprandial Transient Visual Loss
Ophthalmology 104:397-401, Levin,L.A.&Mootha,V.V., 1997

Severe but Transient Parkinsonism after Tetanus Vaccination
JNNP 63:258, Reijneveld,J.C.,et al, 1997

New Variant Creutzfeldt-Jakob Disease:Neurological Features and Diagnostic Tests
Lancet 350:903-907, Zeidler,M.,et al, 1997

The Expansion of the CAG Repeat in Ataxin-2 is a Frequent Cause of Autosomal Dominant Spinocerebellar Ataxia
Neurol 49:1009-1013, Lorenzetti,D.,et al, 1997

Spinocerebellar Ataxia Type 6, Molecular & Clin Features of 35 Japanese Pts (1 Homozygous for CAG Repeat Expan)
Neurol 49:1238-1243, 11961997., Matsumura,R.,et al, 1997

Clinical and Molecular Features of Spinocerebellar Ataxia Type 6
Neurol 49:1243-1246, 11961997., Stevanin,G.,et al, 1997

Bradycardia and Asystole Induced by Partial Seizures:A Case Report and Literature Review
Neurol 48:1712-1714, Devinsky,O.,et al, 1997

A 36-Year-Old Woman Recuperating From a Stroke
JAMA 277:1970-1976, Alexander,M., 1997

Ischemic Stroke After Acute Myocardial Infarction
Stroke 28:762-767, Mooe,T.,et al, 1997

Pure or Predominant Sensory Stroke Due to Brain Stem Lesion
Stroke 28:1761-1764, Kim,J.S.&Bae,Y.H., 1997

Clinical Characteristics & Mgt of Acute Stroke in Pts with Atrial Fib Admitted to US Univ Hosp
Neurol 48:1598-1604, Albers,G.W.,et al, 1997

Does Paroxysmal Atrial Fibrillation Confer a Paroxysmal Thromboembolic Risk
Lancet 349:1565-1566, Lip,G.Y.H., 1997

Risk for Clinical Thromboembolism Assoc with Conversion to Sinus Rhythm in Pts with Atrial Fib Lasting<48 Hrs
Ann Int Med 126:615-620, Weigner,J.M.,et al, 1997

Embolic Brain Infarction in Nonrheumatic Atrial Fibrillation
Neurol 48:1593-1597, Yamanouchi,H.,et al, 1997

Primary Care Physician-Reported Secondary and Tertiary Stroke Prevention Practices
Stroke 28:746-751, Goldstein,L.B.,et al, 1997

Stroke Recurrence:Predictors, Severity, and Prognosis, The Copenhagen Stroke Study
Neurol 48:891-895, Jorgensen,H.S.,et al, 1997

Management of Anticoagulation Before and AFter Elective Surgery
NEJM 336:1506-1511, Kearon,C.&Hirsh,J., 1997

Clinicopath Conf
Progressive Supranuclear Palsy, Case 26, 1997, NEJM 337:549-55697., , 1997

Phenotypic Variability in Friedreich Ataxia:Role of the Associated GAA Triplet Repeat Expansion
Ann Neurol 41:675-682, Montermini,L.,et al, 1997

Frataxin Gene of Friedreich's Ataxia is Targeted to Mitochondria
Ann Neurol 42:265-269, Priller,J.,et al, 1997

Three Hundred Sixty-Degree Rotation of the Posterior Semicircular Canal for Trtm of Benign Positional Vertigo
Neurol 49:729-733, Lempert,T.,et al, 1997

Balance in the Healthy Elderly
Arch Neurol 54:976-981, Camicioli,R.,et al, 1997

Pain After Thalamic Stroke:Right Diencephalic Predominance and Clinical Features in 180 Patients
Neurol 48:1196-1199, Nasreddine,Z.S.&Saver,J.L., 1997

Transient Neurological Attacks in the General Population
Stroke 28:768-773, Bots,M.L.,et al, 1997

Bilat Periventricular Nodular Heterotopia with Mental Retard & Syndactyly in Boys:New X-Linked MR Synd
Neurol 49:1042-1047, Dobyns,W.B.,et al, 1997

Multiple-System Atrophy is Genet Distinct from Ident Inherited Causes of Spinocerebellar Degen
Neurol 49:1598-1604, Brandmann,O.,et al, 1997

Cerebral & Cerebellar Atrophy on Serial MRI in an Initially Symptom Free Subject at Risk of Familial Prion Disease
BMJ 315:856-857, Fox,N.C.,et al, 1997

Cerebral Manifestation of Erdheim-Chester Disease:Clinical and Radiologic Findings
Neurol 49:1702-1705, Bohlega,S.,et al, 1997

Ocular Findings in Ramsay Hunt Syndrome
J Neuro-Ophthalmol 17:199-201, Mansour,A.M.&Bailey,B.J., 1997

Friedreich's Ataxia GAA Repeat Expansion in Pts with Recessive or sporadic Ataxia
Neurol 49:1004-1009, Geschwind,D.H.,et al, 1997

Broadened Friedreich's Ataxia Phenotype after Gene Cloning, Minimal GAA Expan Causes Late Spastic Ataxia
Neurol 49:1617-1620, Ragno,M.,et al, 1997

Atrophy of Cerebellum & Brainstem in Dentatorubral Pallidoluysian Atrophy, CAG Repeat Size on MRI Findings
Neurol 49:1605-1612, Koide,R.,et al, 1997

Rapid Spongiform Degeneration of the Cerebrum and Cerebellum in Creutzfeldt-Jakob Encephalitis:Serial MR Findings
AJNR 18:583-586, Tzeng,B-C.,et al, 1997

Adult-Onset Neimann-Pick Type C Disease, Clinical, Biochemical and Genetic Study
Arch Neurol 54:1536-1541, Lossos,A.,et al, 1997

CSF Antigliadin Antibodies and the Ramsay Hunt Syndrome
Neurol 49:1131-1133, Chinnery,P.F.,et al, 1997

Atrial Fibrillation and Stroke, Mortality & Causes of Death AFter the First Acute Ischemic Stroke
Stroke 28:311-315, Kasrisalo,M.M.,et al, 1997

Atrial Fibrillation and Dementia in a Population-Based Study, The Rotterdam Study
Stroke 28:316-321, Ott,A.,et al, 1997

Thromboembolism Prophylaxis in Chronic Atrial Fibrillation:Practice Patterns in Community & Tertiary-Care Hosp
Stroke 28:72-76, Munschauer,F.E.,et al, 1997

Accuracy of the Clinical Diagnosis of Corticobasal Degeneration:A clinicopathologic Study
Neurol 48:119-125, Litvan,I.,et al, 1997

Is There a Gulf War Syndrome? Searching for Syndromes by Factor Analysis of Symptoms
JAMA 227:215-222, 2591997., Haley,R.W.,et al, 1997

Self-Reported Exposure to Neurotoxic Chemical Combinations in the Gulf War:A Cross-Sectional Epidemiologic Study
JAMA 227:231-237, 2591997., Haley,R.W.&Kurt,T.L., 1997

Machado-Joseph Disease in 4 Chinese Pedigrees:Molecular Analysis of 15 Pts
Neurol 48:482-485, Zhou,Y.X.,et al, 1997

Familial Idiopathic Brain Calcification with Autosomal Dominant Inheritance
Neurol 48:645-649, Kobari,M.,et al, 1997

CIDP:Clinical Features & Responses to Trtm in 67 Consecutive Pts with/without a Monoclonal Gammopathy
Neurol 48:321-328, Gorson,K.G.,et al, 1997

Autoantibodies to Glutamic Acid Decarboxylase in Three Patients With Cerebellar Ataxia, Late-Onset Insulin-Dependent Diabetes Mellitus, and Polyendocrine Autoimmunity
Neurol 49:1026-1030, Saiz,A.,et al, 1997

Mycoplasma Pneumoniae Infection Associated with an Acute Brainstem Syndrome
Acta Neurol Scand 93:203-206, OBrien, P.M.,et al, 1996

An Emotional 13-Year Old Girl
Lancet 348:1000, Kanabar,D.J.,et al, 1996

Acute Demyelinating Polyneuropathy with Arsenic Ingestion
Muscle & Nerve 19:1611-1613996., Greenberg,S.A., 1996



Showing articles 1300 to 1350 of 2314 << Previous Next >>