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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 100 to 150 of 5387 << Previous Next >>

Identifying and Managing Common Childhood Language and Speech Impairments
BMJ 350:h2318, Reilly, S.,et al, 2015

Clinicopathologic Conference, CAT Scratch Disease (Encephalopathy Associated with Bartonella Henselae)
NEJM 372:2050-2058, Case 16-2015, 2015

International Consensus Diagnostic Criteria for Neuromyelitis Optica Spectrum Disorders
Neurol 85:177-189, Wingerchuk, D.M.,et al, 2015

Dystonia in Children and Adolescents: A Systematic Review and a New Diagnostic Algorithm
JNNP 86:774-781, Van Egmond, M.E.,et al, 2015

Demyelinating Encephalopathy in Adult Onset Stills Disease: Case Report and Review of the Literatures
Clin Neurol Neurosurg 115:2213-2216, Jie, W., et al, 2015

Molybdenum Cofactor Deficiency
Neurol 85:e175-e178, Nagappa, M.,et al, 2015

IgG4-associated Orbital and Ocular Inflammation
J Ophthalmic Inflamm Infect 5:1-8, Lee,C.S.,et al, 2015

Extraintestinal Manifestations of Coeliac Disease
Nat Rev Gastroenterol Hepatol 12:561-571, Leffler, D.A.,et al, 2015

Computed Tomographic Angiography or Magnetic Resonance Angiography for Detection of Intracranial Vascular Malformations in Patients with Intracerebral Hemorrhage
Stroke 46:e2-e3, Josephson, C.B.,et al, 2014

Clinicopathologic Conference, Dermatomyositis. Malignant Atrophic Papulosis (Degoss Disease), Involving the Skin and Gastrointestinal Tract
NEJM 370:2327-2337, Case 18-2014, 2014

Clinical Manifestations, Pathologic Features, and Diagnosis of Langerhans Cell Histiocytosis
UptoDate Oct. 2014, McClain, K.L., 2014

Clinicopathologic Conference, Chronic Meningoencephalitis Consistent with Rasmussens Encephalitis
NEJM 371:1737-1746, Case 34-2014, 2014

Early-Onset Stroke and Vasculopathy Associated with Mutations in ADA2
NEJM 370:911-920, Zhou, Q.,et al, 2014

Diagnostic and Classification Criteria of Takayasu Arteritis
J Autoimmun 48-49:79-83, deSouza, A.W.S. & deCarvalho, J.F., 2014

The Limbic-Girdle Muscular Dystrophies
Neuro Clin 32:729-749, Wicklund, M.P. and Kissel, J.T., 2014

Juvenile Myasthenia Gravis: Recommendations for Diagnostic Approaches and Treatment
Neuropediatrics 45:75-83, Marina, A.D.,et al, 2014

Tourettes Syndrome
BMJ 347:f4964, Cavanna, A.E. & Seri, S., 2013

Revised Diagnostic Criteria for the Pseudotumor Cerebri Syndrome in Adults and Children
Neurol 81:1159-1165, Friendman, D.I.,et al, 2013

Chediak-Higashi Syndrome: Pathognomonic Feature
Lancet 382:1514, Antunes, H.,et al, 2013

Central Nervous System Involvement in Whipple Disease
Medicine 92:324-330, Compain, C.,et al, 2013

Clinical Reasoning: A Woman with Recurrent Aphasia and Visual Field Defects
Neurol 81:e141-e144, Nourbakhsh, B.,et al, 2013

Mycoplasma Pneumoniae Infection: Neurologic Complications
www.MedLink.com, Oct, Greenlee, J.E., 2013

Paediatric Autoimmune Encephalopathies: Clinical Features, Laboratory Investigations and Outcomes in Patients with or without Antibodies to known Central Nervous System Autoantigens
JNNP 84:748-755, Hacohen, Y.,et al, 2013

Clinicopathologic Conferences, Celiac Disease, Addisons Disease, and Major Depression Disorder
NEJM 368:2015-2024, Case 16-2013, 2013

Diagnosis of Lambert-Eaton Myasthenic Syndrome in Children
Neurol 80:e220-e222, Morgan-Followell,B.& de los Reyes,E., 2013

A Systematic Approach to the Diagnosis of Suspected Central Nervous System Lymphoma
JAMA Neurol 70:311-319, Scott, B.J.,et al, 2013

CNS-Immune Reconstitution Inflammatory Syndrome in the Setting of HIV Infection, Part 1: Overview and Discussion of Progressive Multifocal Leukoencephalopathy-Immune Reconstitution Inflammatory Syndrome and Cryptococcal-Immune Reconstitution Inflammatory Syndrome
AJNR 34:1297-1307, Post, M.J.D.,et al, 2013

Dopa-Responsive Dystonia Revisited
Arch Neurol 69:1558-1562, Tadic, V.,et al, 2012

Cogan Syndrome An Analysis of Reported Neurological Manifestations
The Neurologist 18:55-63, Antonios,N. and Silliman,S., 2012

Evidence-based Guideline: Intravenous Immunoglobulin in the Treatment of Neuromascular Disorders
Neurol 78:1009-1015, Patwa,H.S.,et al, 2012

Guidelines for the Determination of Brain Death in Infants and Children: An Update of the 1987 Task Force Recommendations - Executive Summary
Ann Neurol 71:573-585, Nakagawa,T.A.,et al, 2012

Clinicopathologic Conference, Rocky Mountain Spotted Fever
NEJM 366:1434-1443, Case 11-2011, 2012

Development of a Suspicion Index to Aid Diagnosis of Niemann-Pick Disease Type C
Neurol 78:1560-1567,1546, Wijburg, F.A.,et al, 2012

Intracranial Optic Nerve Enlargement in Infantile Krabbe Disease
Neurol 78: e126, Shah, S.,et al, 2012

Primary Sjogren Syndrome
BMJ 344:e3821, Ramos-Casals, M.,et al, 2012

Heterogeneity of Coenzyme Q10 Deficiency
Arch Neurol 69:978-983, Emmanuele, V.,et al, 2012

Multimodal Imaging of Reversible Cerebral Vasoconstriction Syndrome: A Series of 6 Cases
AJNR 33:1403-1410, Marder, C.P.,et al, 2012

Range of Genetic Mutations Associated with Severe Non-Syndromic Sporadic Intellectual Disability: An Exome Sequencing Study
Lancet 380:1674-1682, Rauch, A.,et al, 2012

Diagnostic Exome, Sequencing in Persons with Severe Intellectual Disability
NEJM 367:1921-1929, Ligt, J.,et al, 2012

Neurologic Complications of Influenza A (H1N1)pdm09
Neurol 79:1474-1481, Khandaker,G.,et al, 2012

The Cerebral Autosomal-Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL) Scale
Stroke 43:2871-2876, Pescini, F.,et al, 2012

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



Showing articles 100 to 150 of 5387 << Previous Next >>