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Differential
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abducens nerve paralysis
abortion, spontaneous
advances in neurology
adverse drug reaction
ageusia
algorithm
alpha-fetoprotein
Alzheimer's disease
amaurosis fugax
amaurosis fugax, unilateral vs.bilateral
amyloid angiopathy, cerebral
amyotrophic lateral sclerosis
anemia
aneurysm
aneurysm, multiple intracranial
anosmia
anticardiolipin antibodies
anticoagulant, treatment
antiphospholipid antibodies
antiphospholipid antibody syndrome
apraxia of eye movements
Argyll Robertson pupil
arteritides
arthralgia
arthritis
aspirin
ataxia
ataxia telangiectasia
ataxia, cerebellar
ataxia, truncal
atrial myxoma
autoantibodies
autoimmune disease
bacterial infection
biologic markers
blindness, transient
calcification, gyral
calcification, intracranial
calf hypertrophy
carcinoembryonic antigen
carcinoma
cardiopulmonary bypass
carpal tunnel syndrome
CAT scan, abnormal
CAT scan, venography
central nervous system, infection of
cerebellar ataxia, children
cerebellar ataxia, hereditary
cerebellar degeneration
cerebral edema
cerebral embolism
cerebral infarction
cerebral venous infarction
cerebral venous thrombosis
cerebral venous thrombosis, deep
cerebral venous thrombosis, etiology
cerebral venous thrombosis, recurrent
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, gammaglobulin of
cerebrospinal fluid, gold sol.curve of
cerebrovascular accident
cerebrovascular accident, acute management of
cerebrovascular accident, atrial myxoma
cerebrovascular accident, non atherosclerotic cause of
cerebrovascular accident, prevention of
cerebrovascular accident, thrombolytic agents in treatment
cerebrovascular accident, young adult
cerebrovascular disease
children
chorea
chorea, causes of
choreoathetosis
chromosomal abnormality
chromosome 11
Clinical Pathologic Conference(C.P.C.)
collagen vascular disease
complications
confusion
conversion reaction
coronary artery disease
coronavirus
cortical blindness
coumarin
COVID-19
cranial nerve palsies
cranial neuropathy
cranial neuropathy, multiple
craniectomy, decompressive
crawl regression
C-reactive protein, elevated
creatine phosphokinase(CPK)elevated
D-dimer
decision analysis
delay in diagnosis
dementia
dementia, frontotemporal
developmental milestones, loss of
developmental retardation
diabetes mellitus
diagnostic criteria
difficulty climbing stairs
drooling
dural sinus thrombosis
dysarthria
dyskinesia
dyskinesia, drug induced
dyspnea
dystonia
dystonia, drug induced
dystrophin
echoencephalogram
embolism
encephalitis
encephalitis, focal
encephalopathy
encephalopathy, metabolic
endocarditis, marantic
endovascular therapy
epidemiology of neurology
erythema migrans
evidence-based research
eye movement, disorders of
Factor V Leiden
falling
false positive
false positive VDRL
familial
fever
fibrinolytic agents
fibrinolytic agents, intra-venous local infusion
fine motor function, impaired
fungal infection, CNS
gadolinium
gait disorder
gammaglobulin therapy, intravenous
gender
gene
gene mutation
genetic linkage
genetic neurologic disorders
genetic testing
glaucoma
Gowers maneuver
growth retardation
Guillain Barre syndrome
headache
heart murmur
heparin
heparin, low-molecular-weight
hepatomegaly
heralding manifestation
Horner's syndrome
Horner's syndrome, childhood
Huntington's chorea
hydrocephalus
hypergammaglobulinemia
hypotonia
hypoxia
immunodeficiency
immunosuppression
incidence
inclusion body myositis
infection
intellectual deficit
intracranial pressure, increased
iritis
Jakob-Creutzfeldt disease
juvenile idiopathic inflammatory myopathy
learning disability
learning disability, in children
leukemia
leukocytosis
level of consciousness, decreased
Lewy body disease, diffuse
livedo reticularis
liver disease
liver function enzymes
lupus anticoagulant
Lyme disease
lymphadenopathy
lymphadenopathy, axillary
lymphadenopathy, paraaortic
lymphoma
malformation, vascular
meningeal enhancement
meningitis
meningitis, aseptic
mental retardation
microangiopathy, brain
misdiagnosis
mitral valve lesion
mortality
movement disorder
movement disorder, drug induced
movement disorder, extrapyramidal
MRI
MRI, abnormal
MRI, CAT scan compared to
MRI, contrast enhanced
MRI, functional
MRI, venography
multiple organ failure
multiple system atrophy
multisystem inflammatory syndrome in children
muscle pain
muscle weakness
muscular dystrophy
muscular dystrophy, central nervous system abnormality
muscular dystrophy, Duchenne
myelopathy
myocardial infarction
myocardial injury
myoglobinuria
myopathy
myopathy inflammatory, classification
myopathy, inflammatory
myopathy, inflammatory, classification
myositis
myositis specific autoantibody
myositis, juvenile
neurocutaneous disease
neuroendocrinology
neurologic complications
neurologic complications of, systemic disease
neurologic disease
neurologic disease, diagnoses of
neurologic examination, focal
neurologic signs
neurologic symptoms
neuroophthalmology
neuropathology
neuropathy
neuropathy, vasculitic, systemic
neurotoxin
obstetric complications
ocular motility, disorders of
ophthalmoplegia
ophthalmoplegia, painful
optic atrophy
optic neuropathy
oral contraceptives
pain
pandemic
papilledema
Parkinson disease
pars planitis
partial thromboplastin time, prolonged
pathology
peripheral blood smear
petechiae
photosensitivity, skin
pitfalls
plasmapheresis
platelet inhibiting drugs
polycythemia, primary
polymerase chain reaction
port wine nevus
postinfectious
postpartum
practice guidelines
pregnancy, neurologic complications in
prethrombotic state
prevention of neurologic disorders
progeria
prognosis
progressive neurologic disorder
protein C deficiency
protein S deficiency
pulmonary embolism
pupil
pupil, abnormality in neurologic disorders
quadriparesis
radiation hypersensitivity
rash
Raynaud's phenomenon
Red flags
renal failure
renal infarct
renal vein thrombosis
review article
risk factors
schistocytes
scleroderma
scleroderma, neurologic involvement with
screening
sedimentation rate, elevated
seizure
seizure, children
serologic testing
seronegative
serositis
severe acute respiratory syndrome
skin, lesions in neurologic disorders
speech disorder, childhood
speech, delayed development of
spinal cord, lesion of
spinal muscular atrophy
spirochete infection
splenomegaly
spontaneous remission
steroid therapy, CNS treatment and complications with
stiff joints
strokelike episodes
Sturge-Weber syndrome
syncope
systemic illness
systemic juvenile idiopathic arthritis
systemic lupus erythematosus
telangiectases
third nerve palsy
thrombocytopenia
thrombocytosis
thrombophlebitis
thrombotic microangiopathy
tissue plasminogen activator, intravenous
Tolosa Hunt syndrome
toxins, nervous system
transient ischemic attack
transient neurologic deficit
treatment of neurologic disorder
trigeminal neuropathy
tripping
trochlear nerve palsy
uveitis
valvulopathy
vasculopathy
venous thrombosis, non-cerebral
viral infection
viral infection, CNS
visual field defect
walking, difficulty with
weakness
weakness, progressive
weight loss
wheelchair
white matter disease
workup
Showing articles 300 to 350 of 5387 << Previous Next >>

Rapid Diagnosis of Bacterial Meningitis with Reagent Strips
Lancet 345:1290-1291, Moosa,A.A.,et al, 1995

Cytokine Elevations in Infants with Bacterial and Aseptic Meningitis
J Pediatr 126:872-876, Dulkerian,S.J.,et al, 1995

Takayasu's Arteritis
Stroke Syndromes, Eds Bogousslavsky & Caplan, Cambridge Univ Press, Chp 48, p 439-442, Naritomi,H., 1995

Mutation Analysis in Patients with Possible but Apparently Sporadic Huntington's Disease
Lancet 344:714-717, Davis,M.B.,et al, 1994

Visual Morbidity in Giant Cell Arteritis:Clinical Characteristics and Prognosis for Vision
Ophthalmology 101:1779-1785, Liu,G.T.,et al, 1994

Trinucleotide Repeat Expansion in Neurological Disease
Ann Neurol 36:814-822, LaSpada,A.R.,et al, 1994

Advances in Molecular Analysis of Fragile X Syndrome
552, Warren,W.T.&Nelson,D.L.JAMA 271:536-553, 1994

Evaluation of Recurrent Pediatric Syncope:Role of Tilt Table Testing
Pediatrics 93:660-662, Strieper,M.J.,et al, 1994

Clinical Usefulness of CSF Bacterial Antigen Studies
J Pediatr 125:235-238, Maxson,S.,et al, 1994

A Worldwide Study of the Huntington's Disease Mutation, The Sensitivity & Specificity of Measuring CAG Repeats
NEJM 330:1401-1406, 14501994., Kremer,B.,et al, 1994

Medical Aspects of the Persistent Vegetative State
NEJM 330:1499-1508, 1572-15791994., Annas,G.J.,et al, 1994

The Effect of a Recent Previous Visit to a Physician on Outcome after Childhood Bacterial Meningitis
JAMA 272:787-791, Kallio,M.J.T.,et al, 1994

Enteroviral Meningitis in Infancy:Potential Role for Polymerase Chain Reaction in Patient Management
Pediatr 94:157-162, Schlesinger,Y.,et al, 1994

Stroke and Cerebral Infarcts in Children Infected with Human Immunodeficiency Virus
Arch Pediatr Adolesc Med 148:965-970, Philippet,P.,et al, 1994

Magnetic Resonance Imaging of the Cauda Equina in Guillain-Barre Syndrome
Neurol 44:1334-1336, Crino,P.B.,et al, 1994

Takayasu Arteritis
Ann Int Med 120:919-929, Kerr,G.S.,et al, 1994

Takayasu Arteritis
Ann Intern Med 120:919-929, Kerr, G.S.,et al, 1994

Shaken Baby Syndrome:Inflicted Cerebral Trauma
Pediatrics 92:872-875, Krugman,R.D.,et al, 1993

Hippocampal Sclerosis in Children with Intractable Temporal Lobe Epilepsy:Detection with MR Imaging
AJR 161:1045-1048, Grattan-Smith,J.D.,et al, 1993

Molecular Genetics in Neurology
Ann Neurol 34:757-773, Martin,J.B., 1993

The Polymerase Chain Reaction:Application to Nervous System Disease
Ann Neurol 34:513-523, Darnell,R.B., 1993

Clinical Consequences of Isolating the Gene for Huntington's Disease
BMJ 307:397-398, Harper,P.S., 1993

The Spectrum of Neurologic Involvement in Wegener's Granulomatosis
Neurol 43:1334-1337, Nishino,H.,et al, 1993

Atypical Leber's Hereditary Optic Neuropathy with Molecular Confiramtion
Arch Neurol 50:470-473, Weiner,N.C.,et al, 1993

Head-Upright Tilt Table Testing in Children with Unexplained Syncope
Pediatr 92:426-430, Samoil,D.,et al, 1993

Serial Changes of Cerebral Glucose Metab & Caudate Size in Persons at Risk for Huntington's Dis
Arch Neurol 49:1161-1167, Grafton,S.T.,et al, 1992

The Psychological Consequences of Predictive Testing for Huntington's Disease
NEJM 327:1401-1405, 14491992., Wiggins,S.,et al, 1992

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

The Persistent Vegetative State in Children:Report of the Child Neurology Society Ethics Committee
Ann Neurol 32:570-576, Ashwal,S.,et al, 1992

Antiphospholipid Antibody Syndrome
JAMA 268:1451-1453, Lockshin,M.D., 1992

Clinicopath Conf
Cat-Scratch Disease, with Encephalopathy, Case 22-1992, NEJM 326:1480-148992., , 1992

Cerebral Cysticercosis and Stroke. Alarcon
F. , et al, Stroke 23:224-22892., , 1992

A Follow-Up Study of Isolated Cases of Suspected Huntington's Disease
Ann Neurol 31:293-298, Bateman,D.,et al, 1992

Headaches in Children Younger than 7 Years of Age
Arch Neurol 49:79-82, Chu,M.L.&Chinnar,S., 1992

A Clinical Study of Noonan Syndrome
Arch Dis Child 67:178-183, Sharland, M.,et al, 1992

Plasmapheresis in Children with Guillain-Barre Syndrome
Neurol 41:1928-1931, Lamont,P.J.,et al, 1991

Clinical Analysis of Isolated Angiitis of the Central Nervous System, A Report of 11 Cases
Arch Int Med 151:2290-2294, Crane,R.,et al, 1991

Sarcoidosis of the Nervous System, A Clinical Approach
Arch Int Med 151:1317-1321, Sharma,Om.P.&Sharma,A.D., 1991

CIDP of Childhood:Treatment with High-Dose Intravenous Immunoglobulin
Neurol 41:828-830, Vedanarayanan,V.V.,et al, 1991

Clinical and Electrophysiological Aspects of Acute Paralytic Disease of Children and Young Adults in Northern China
Lancet 338:593-597, McKhann,G.M.,et al, 1991

Head-up Tilt for the Evaluation of Syncope of Unknown Origin in Children
J Pediatr 118:676-679, Lerman-Sagie,T.,et al, 1991

Guillain-Barre Syndrome and Plasmapheresis in Childhood
(Letters) , Ann Neurol 29:688-68991., , 1991

Mitochondril Encephalopathies:Molecular Genetic Diagnosis from Blood Samples
Lancet 337:1311-1313, Hammans,S.R.,et al, 1991

Relevance of Common Tests of Cerebrospinal Fluid in Screening for Bacterial Meningitis
J Pediatr 119:363-369, Bodewald,L.E.,et al, 1991

Tourette Syndrome and Other Tic Disorders, Diagnosis, Pathophysiology, and Treatment
Medicine 70:15-32, Singer,H.S.&Walkup,J.T., 1991

Inflammatory Demyelinating Polyneuropathy in a Child with Symptomatic Human Immunodeficiency Virus Infection
J Pediatr 118:242-245, Raphael,S.A.,et al, 1991

Cat Scratch Disease, Acute Encephalopathy & Other Neurologic Manifestations
Am J Dis Child 145:98-101, Carithers,H.A.&Margileth,A.M., 1991

Genetic Testing for Huntington's Disease
BMJ 300:1089-1090, Harper,P.,et al, 1990

Crohn Disease in an Infant with Central Nervous System Thrombosis and Protein-Losing Enteropathy
J Pediatr 117:436-439, Mezoff,A.G.,et al, 1990

Clinical Uses of Intravenous Immunoglobulins
Ann Int Med 112:278-292, Berkman,S.A.,et al, 1990



Showing articles 300 to 350 of 5387 << Previous Next >>