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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
cardiomyopathy
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
cerebrospinal fluid, lactic acid concentration
cerebrovascular accident
cerebrovascular accident, acute management of
cerebrovascular accident, atrial myxoma
cerebrovascular accident, non atherosclerotic cause of
cerebrovascular accident, nonvascular territory
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
deafness
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 screening
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
lactic acidemia
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
MELAS syndrome
meningeal enhancement
meningitis
meningitis, aseptic
mental retardation
microangiopathy, brain
misdiagnosis
mitochondrial disease
mitochondrial encephalomyopathy
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, diffusion weighted
MRI, functional
MRI, venography
multiple organ failure
multiple system atrophy
multisystem inflammatory syndrome in children
muscle biopsy
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
next-generation sequencing
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
ragged-red fibers
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
sensorineural hearing loss
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
temporal lobe, lesion
temporal lobe, lesion, bilateral
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
whole genome sequencing
workup
Showing articles 150 to 200 of 5474 << Previous Next >>

Brain Arteriovenous Malformation Multiplicity Predicts the Diagnosis of Hereditary Hemorrhagic Telangiectasia Quantitive Assessment
Stroke 43:72-78, Bharatha, A.,et al, 2012

Brain Abnormalities in Neuromyelitis Optica Spectrum Disorder
Multiple Sclerosis International ID 735486, Kim, W.,et al, 2012

Neuro-Sweets Disease
Pract Neurol 12:126-130, Maxwel,G.,et al, 2012

Intraventricular Hemorrhage
UpToDate, Sept, Cucchiara B.L. and Pacelli, J.P., 2011

PANDAS
www.medlink.com,Feb, Erfe,M.C.B., 2011

Encephalitis and antibodies to synaptic and neuronal cell surface proteins
Neurol 77:179-189, Lancaster, E.,et al, 2011

Hereditary Hemorrhagic Telangiectasia (Osler-Weber-Rendu Syndrome)
UpToDate, Feb, Shovlin, C., 2011

MR Imaging of Vogt-Koyanagi-Harada Syndrome with Leptomeningeal Enhancement
AJNR 32:E169-E171, Lohman, B.D.,et al, 2011

Clinical Characteristics of Pediatric-onset Neuro-Behcet Disease
Neurol 77:1900-1905, Uludiz, D.,et al, 2011

Late onset autism and anti-NMDA-receptor encephalitis
Lancet 378:98;378, Creten, C.,et al, 2011

Presentation, Diagnosis, Pathophysiology, and Treatment of the Neurological Features of Sturge-Weber Syndrome
The Neurologist 17:179-184, Comi, A.M., 2011

Redefining the Guillain-Barre Spectrum in Children: Neuroimaging Findings of Cranial Nerve Involvement
AJNR 32:639-42, Zuccoli, G.,et al, 2011

Recognizing Guillain-Barr� Syndrome in Preschool Children
Neurol 76:807-810, Roodbol,J.,et al, 2011

Clinical and Genetic Spectrum of Mitochondrial Neurogastrointestinal Encephalomyopathy
Brain 134:3326-3332, Garone, C.,et al, 2011

Brain Biopsy in Children With Primary Small-Vessel Central Nervous System Vasculitis
Ann Neurol 68:602-610, 573, Elbers,J.,et al, 2010

Glucose Transporter-1 Deficiency Syndrome: The Expanding Clinical and Genetic Spectrum of a Treatable Disorder
Brain 133:655-670, Leen,W.G., et al, 2010

Tourettes Syndrome
NEJM 363:2332-2338, Kurlan,R., 2010

Clinical Presentation, Pathologic Features, and Diagnosis of Primary Central Nervous System Lymphoma
Up to Date Sept 2010, Hochberg,F.H.,et al, 2010

Cogan Syndrome
www.medlink.com, Feb, Ramachandran, T.S., 2010

Periarteritis Nodosa
www.MedLink.com, June, Ramachandran, T. & Roos, R., 2010

Clinicopath Conf, Infantile Krabbe Disease
NEJM 362:346-356, Case 3-2010, 2010

A Comparison of MRI Criteria for Diagnosing Pediatric ADEM and MS
Neurol 74:1412-1415, 1404, Ketelslegers,I.A., et al, 2010

Autism
Lancet 374:1627-1638, Levy,S.,et al, 2009

Clinical and Mutational Spectrum of Neurofibromatosis Type 1-Like Syndrome
JAMA 302:2111-2118, 2150, 2170, Messian,L.,et al, 2009

Leukodystrophies: Classification, Diagnosis, and Treatment
Neurologist 15:319-328, Costello,D.,et al, 2009

MRI in the Diagnosis of Pediatric Multiple Sclerosis
Neurol 72:961-967, Callen,D.J.A.,et al, 2009

Clinicopath Conf., Atypical Hemolytic-Uremic Syndrome
NEJM 361:389-400, Case 23-2009, 2009

Lyme Neuroborreliosis: Manifestations of a Rapidly Emerging Zoonosis
AJNR 30:1079-1087, Hildenbrand,P.,et al, 2009

Multiple Bilateral Non-Hemorrhagic Cerebral Infarctions Associated with Microscopic Polyangiitis
Clin Neurol Neurosurg 111:904-906, Ku, B. & Shin, H., 2009

Aicardi-Gouti�res Syndrome
Br Med Bull 89:183-201, Orcesi, S.,et al, 2009

Spinal Muscular Atrophy
Lancet 371:2120-2133, Lunn,M.R. &Wang,C.H., 2008

Diagnosis and Etiology of Congenital Muscular Dystrophy
Neurol 71:312-321,308, Peat,R.A.,et al., 2008

Juvenile Dermatomyositis and Other Idiopathic Inflammatory Myopathies of Childhood
Lancet 371:2201-2212, Feldman,B.M.,et al., 2008

Sports-Related Internal Carotid Artery Dissection: Pathogenesis and Therapeutic Point of View
The Neurologist 14:307-311, Dharmasaroja,P. &Dharmasaroja,P., 2008

Tuberous Sclerosis
Lancet 372:657-658, Curatolo,P.,et al., 2008

Second Consensus Statement on the Diagnosis of Multiple System Atrophy
Neurol 71:670-676, Gilman,S.,et al., 2008

Diagnosis and Management of Attention-Deficit/Hyperactivity Disorder in Children, Young People, and Adults: Summary of NICE Guidance
BMJ 337:751-753, Kendall,T.,et al, 2008

Risk Factors of Cerebral Vein and Sinus Thrombosis
Front Neurol Neurosci 23:23-54, de Freitas, G.R. & Bogousslavsky, J., 2008

Optic Pathway Gliomas in Neurofibromatosis-1: Controversies and Recommendations
Ann Neurol 61:189-198, Listernick,R.,et al, 2007

Predictors of Diagnosis in Huntington Disease
Neurol 68:1710-1717, Langbehn,D.R.,et al, 2007

Magnetic Resonance Imaging of Biceps Femoris Muscles in Benign Acute Childhood Myositis
Arch Neurol 64:1200-1201, Kawarai,T.,et al, 2007

Neonatal Seizures
Ann Neurol 62:112-120, Silverstein,F.S. &Jensen,F.E., 2007

Patterns of Guillain-Barre Syndrome in Children: Results From a Mexican Population
Neurol 69:1665-1671,1647, Nachamkin,I.,et al, 2007

10 Questions About the Clinical Determination of Brain Death
Neurologist 13:380-381, Wijdicks,E.F.M., 2007

Pediatric Encephalitis: What Is the Role of Mycoplasma Pneumoniae
Pediatrics 120:305-313, Christie,L.J., et al, 2007

Whipples Disease
NEJM 356:55-66, Fenollar,F.,et al, 2007

Clinical Prediction Rule for Identifying Children With Cerebrospinal Fluid Pleocytosis at Very Low Risk of Bacterial Meningitis
JAMA 297:52-60, Nigrovic,L.E.,et al, 2007

Narrative Review: Reversible Cerebral Vasoconstriction Syndromes
Ann Intern Med 146:34-44, Calabrese,L.H.,et al, 2007

The Tuberous Sclerosis Complex
NEJM 355:1345-1356, Crino,P.B.,et al, 2006

Diagnostic Evaluation of Clinically Normal Subjects with Chronic hyperCKemia
Neurol 66:1585-1587, Fernandez,C.,et al, 2006



Showing articles 150 to 200 of 5474 << Previous Next >>