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acquired immunodeficiency syndrome
acquired immunodeficiency syndrome, heralded by neurologic invol
acute intermittant porphyria
advances in neurology
algorithm
allodynia
amyloid
amyloidosis
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, atypical
amyotrophic lateral sclerosis, diagnosis of
amyotrophic lateral sclerosis, differential diagnosis
amyotrophic lateral sclerosis, epidemiology of
amyotrophic lateral sclerosis, etiology of
amyotrophic lateral sclerosis, familial
amyotrophic lateral sclerosis, misdiagnosis
amyotrophic lateral sclerosis, prognosis
amyotrophic lateral sclerosis, treatment of
amyotrophic lateral sclerosis, work up
amyotrophic lateral sclerosis-like syndrome
anemia
angiostrongylus cantonensis
anterior horn cell disease
anti citrullinated antibody
anti IgLON5
antiviral agents
aphasia
aphasia, progressive, primary
aphonia
apnea
areflexia
arm atrophy
arm weakness
ascending paralysis
ataxia
ataxia, progressive
ataxic gait
autoantibodies
autonomic dysfunction
Babinski sign
basophilic stippling of red blood cells
behavioral disorder
BiPAP
bone marrow biopsy
botulism
brachial amyotrophic diplegia
bulbar palsy
bulbar palsy, acute
bulbar palsy, progressive
burning feet
burning paresthesia
cachexia
CAG repeats
cane
carcinoma
CAT scan, emission, abnormal
CD4 counts
central nervous system, infection of
cerebellar atrophy, primary
cerebrospinal fluid
cerebrospinal fluid, abnormal
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, eosinophilia of
cerebrospinal fluid, proteincytologic dissociation
cervical osteophyte
cervical spine
cervical spondylosis
cervical spondylosis, differential diagnosis of
cervical spondylosis, misdiagnosis
Chinese paralytic syndrome
chondroitin sulfate C
ciguatera poisoning
Clinical Pathologic Conference(C.P.C.)
cognition
coma, episodic
conduction block
confusion
constipation
conversion reaction
cranial neuropathy
creatine phosphokinase(CPK)elevated
crying, pathologic
cyclophosphamide
degenerative diseases of CNS
delay in diagnosis
delusion
dementia
dementia, age at onset
dementia, frontotemporal
dementia, presenile
denervation of muscle
denervation potentials
depression
dexterity, impaired
diabetes mellitus
diagnostic criteria
differential diagnosis
diphtheria
diplegia, atonic
diplegia, brachial
disorientation
distal muscle atrophy
distal muscle weakness
drooling
dying
dysarthria
dysphagia
dysphonia
dyspnea
electromyogram
electrophoretic pattern, serum
emotional lability
encephalitis
encephalitis, autoimmune
encephalopathy
endemic area
eosinophilia
epidemiology of neurology
episodic disorders
episodic neurologic deficits
episodic unconsciousness
evoked potentials
exercise
facial weakness
facial weakness, bilateral
falling
familial
fasciculation
fatigue
fever
fibrillations
fine motor function, impaired
finger weakness
fish poisoning
flaccid paralysis
fluency
foot drop
frontotemporal dementia, behavioral variant
F-wave response
gag reflex, depressed
gait disorder
gait, waddling
gammaglobulin therapy, intravenous
gene
gene mutation
genetic counselling
genetic neurologic disorders
genetic screening
genetic testing
GM1 ganglioside antibodies
Guillain Barre syndrome
Guillain Barre syndrome, differential diagnosis of
Guillain Barre syndrome, variant forms of
gynecomastia
hallucination
hand weakness
headache
headache, progressive
heavy metal intoxication
helminthic infection of CNS
heralding manifestation
highly active antiretroviral therapy
hoarseness
hospice
human immunodeficiency virus type 1
human T-lymphotropic virus type I(HTLV-I)
hypercalcemia
hyperparathyroidism
hyperreflexia
hypersomnia
hyperthyroidism
hypoglycorrhachia
hypophonia
hyporeflexia
imbalance
immunohistochemistry
immunosuppressive agents
immunotherapy
inclusion bodies
inclusion bodies, eosinophilic intranuclear
inclusion body myositis
inflexibility, mental
intellectual deficit
internuclear ophthalmoplegia
intrinsic hand muscles, wasting of
laminectomy, cervical
laughing, pathologic
lead and the nervous system
lead poisoning
leg atrophy
leg weakness, bilateral
leg weakness, unilateral
lid closure, weakness of
life expectancy
lobar atrophy
locked-in syndrome
Lyme disease
lymphoma
lymphoma involving CNS
Man-In-The-Barrel syndrome
masseter muscle wasting
meningismus
meningitis, eosinophilic
mimics
misdiagnosis
monoclonal gammopathy
monomelic amyotrophy
mortality
motor neuron disease
motor neuron disease, misdiagnosis
motor neuron disease, spontaneous recovery
MRI
MRI, abnormal
MRI, spinal cord
MRI, spinal cord, increased intramedullary cord signal
multiple sclerosis
multiple sclerosis, differential diagnosis of
multiple sclerosis, misdiagnosis
muscle atrophy, progressive
muscle biopsy
muscle cramp
muscle stiffness
muscle wasting, diffuse
muscle weakness
muscle weakness, insidious onset of
muscle weakness, proximal
myasthenia gravis
myasthenia gravis, diagnosis
myasthenia gravis, differential diagnosis
myasthenia gravis, misdiagnosis of
myelogram
myelomalacia
myelopathy
myelopathy, ischemic
myelopathy, chronic progressive
myeloradiculopathy
myoclonus
myopathy
myopathy, autoimmune
myopathy, quadriceps
myopathy, steroid responsive
myositis
nasal speech
nausea and vomiting
neck weakness
nerve biopsy
nerve conduction studies
nerve conduction studies, motor
neuroendocrinology
neurologic complications of, surgery
neurologic disease, diagnoses of
neurologic symptoms
neuromuscular disease, electrodiagnosis of
neuromuscular junction, abnormality of
neuronopathy
neuropathology
neuropathology, peripheral nerves
neuropathy
neuropathy, acute
neuropathy, amyloid
neuropathy, diphtheritic
neuropathy, motor
neuropathy, motor, multifocal
neuropathy, multifocal
neuropathy, painful
neuropathy, peripheral, treatment
neuropathy, toxic
neuroprotective agents
neurotoxin
next-generation sequencing
osteomalacia
pain
pain, abdominal
pain, increased response
palliative care
paralysis, acute
paralysis, acute areflexic
paralysis, asymmetric
paranoia
paraparesis, familial spastic
paraparesis, familial spastic, classification
paraparesis, spastic
paraproteinemia
parasitic infection
parasitic infection, CNS
paraspinal muscle
parathormone
parathyroid adenoma
paresthesias
Parkinsonism syndrome
pathology
patient information and support
personality change
Pick's disease
pleocytosis of cerebrospinal fluid
poison, mercury
poliomyelitis
poliomyelitis-like illness
polyglucosan body disease
polymerase chain reaction
polymyositis
polyneuropathy
polyneuropathy, chronic inflammatory demyelinating
polyradiculoneuropathy
porphyria
positive sharp waves
primary lateral sclerosis
prognosis
progressive neurologic disorder
progressive spinal muscular atrophy
proximal muscle atrophy
pseudobulbar palsy
psychiatric problems in neurologic disorders
psychomotor retardation
pyramidal tract dysfunction
quadriceps atrophy
quadriceps weakness
quadriparesis
quadriplegia
radial nerve, palsy of
raw fish ingestion
release phenomena
REM sleep behavior disorder
remote effect of cancer on the nervous system
renal cell carcinoma
renal stones
respirator
respiratory failure
respiratory tract infection
retrovirus
review article
rheumatoid arthritis
rheumatoid arthritis, neurologic complications of
riluzole
risk factors
screening
seizure
sensory symptoms
shell fish poisoning
single photon emission computed tomography
sleep
sleep pathology and physiology
snail
somatosensory evoked potentials
somatosensory evoked potentials, dermatomal
spastic ataxia
spasticity
speech disorder
speech, loss of
spinal cord, cervical
spinal cord, compression of
spinal cord, lesion of
spinal muscular atrophy
spondylosis
stereotyped behavior
sternocleidomastoid muscle
steroid
steroid therapy, CNS treatment and complications with
sushi
syringomyelia
tandem gait, ataxic
tick paralysis
tongue, atrophy
tongue, fasciculations of
tongue, impaired movements of
toxins, nervous system
trauma
travel history
travel, foreign
treatment of neurologic disorder
tremor
tremor, postural
trinucleotide repeats
tripping
unconsciousness
unconsciousness, episodic
unconsciousness, transient
urinary incontinence
viral infection
viral infection, CNS
viral isolation
vocalizations
Waldenstrom's macroglobulinemia
walking, difficulty with
weakness
weakness, generalized
weakness, progressive
weight loss
wheelchair
word-finding difficulty
wrist drop
X-linked bulbospinal neuronopathy
Showing articles 1400 to 1450 of 4087 << Previous Next >>

A Clinical Prediction Rule for Ambulation Outcomes After Traumatic Spinal Cord Injury: A Longitudinal Cohort Study
Lancet 377:1004-1010, 972, van Middendorp,J.J,et al, 2011

Brainstem Lesion in Clinically Isolated Syndromes
Neurol 75:1933-1938, Tintore,M.,et al, 2010

Pregnancy and Fetal Outcomes After Interferon-b Exposure in Multiple Sclerosis
Neurol 75:1794-1802, Amato,M.P.,et al, 2010

Retrospective Analysis of NMDA Receptor Antibodies in Encephalitis of Unknown Origin
Neurol 75:1735-1739, Pr�ss,H.,et al, 2010

Successful Management of Natalizumab-Associated Progressive Multifocal Leukoencephalopathy and Immune Reconstitution Syndrome in a Patient With Multiple Sclerosis
Arch Neurol 67:1391-1394, Schr�der,A.,et al, 2010

Evidence for Acute Neurotoxicity After Chemotherapy
Ann Neurol 68:806-815, Petzold,A.,et al, 2010

Dysexecutive Syndrome: Diagnostic Criteria and Validation Study
Ann Neurol 68:855-864, Godefroy,O.,et al, 2010

Safety and Efficacy of Natalizumab in Children With Multiple Sclerosis
Neurol 75:912-917, Ghezzi,A.,et al, 2010

Progressive Multifocal Leukoencephalopathy: Can We Reduce Risk in Patients Receiving Biological Immunomodulatory Therapies?
Ann Neurol 68:271-274, Tyler,K., 2010

A Look Beneath the Surface in a "Typical" Thalamic Hemorrhage
Neurol 75:e40, Volbers,B.,et al, 2010

Hemorrhagic Manifestations of Reversible Cerebral Vasoconstriction Syndrome: Frequency, Features, and Risk Factors
Stroke 41:2505-2511, 2455, Ducros,A.,et al, 2010

Diagnostic Role of Target Lesion on Diffusion-WEighted Imaging, A Case of Cerebral Aspergillosis and Review of the Literature
Neurologist 16:364-367, Finelli,P.F.,et al, 2010

Familial Neuromyelitis Optica
Neurol 75:310-315, Matiello,M., et al, 2010

Rapid Disease Course in African Americans With Multiple Sclerosis
Neurol 75:217-223, Kister,I., et al, 2010

Serial MRI and CSF Biomarkers in Normal Aging, MCI, and AD
Neurol 75:143-151, Vemuri,P., et al, 2010

Paramedic Diagnosis of Stroke: Examining Long-Term Use of the Melbourne Ambulance Stroke Screen (MASS) in the Field
Stroke 41:1363-1366, Bray,J.E., et al, 2010

Neonatal Cerebral Sinovenous Thrombosis From Symptom to Outcome
Stroke 41:1382-1388, Berfelo,F.J., et al, 2010

Agreement Regarding Diagnosis of Transient Ischemic Attach Fairly Low Among Stroke-Trained Neurologists
Stroke 41:1367-1370, Castle,J., et al, 2010

Sporadic Creutzfeldt-Jakob Disease Mimicking Nonconvulsive Status Epilepticus
Neurol 74:1995-1999, Lapergue,B., et al, 2010

Critical Vasospasm During Fingolimod (FTY720) Treatment in a Patient With Multiple Sclerosis
Neurol 74:2022-2024, Schwarz,A., et al, 2010

Does This Patient Have a Hemorrhagic Stroke? Clinical Findings Distinguishing Hemorrhagic Stroke From Ischemic Stroke
JAMA 303:2280-2286, Runchey,S. &McGee,S., 2010

Longitudinal Study of Vision and Retinal Nerve Fiber Layer Thickness in Multiple Sclerosis
Ann Neurol 67:749-760, Talman,L.S., et al, 2010

Cardiotoxicity and Other Adverse Events Associated With Mitoxantrone Treatment for MS
Neurol 74:1822-1826, Kingwell,E., et al, 2010

JC Virus Infection of the Brain
AJNR 31:1564-1576, Bag,A.K.,et al, 2010

New Aspects on Patients Affected by Dysferlin Deficient Muscular Dystrophy
JNNP 81:946-953, Klinge,L.,et al, 2010

Clinical Reasoning: Seizures in a Child With Sensorineural Deafness and Agitation
Neurol 74:e61-e63, Auvin,S., et al, 2010

Diagnosis and Management of the Antiphospholipid Syndrome
BMJ 340:1125-1132, Cohen,D., et al, 2010

Natalizumab and Progressive Multifocal Leukoencephalopathy: What are the Causal Factors and Can It be Avoided?
Arch Neurol 67:923-930, Warnke,C., et al, 2010

Population-Based Study of Behavior Immediately After Transient Ischemic Attack and Minor Stroke in 1000 Consecutive Patients: Lessons for Public Education
Stroke 41:1108-1114, Chandratheva,A.,et al, 2010

Neuromyelitis Optica Treatment: Analysis of 36 Patients
Arch Neurol 67:1131-1136, Bichuetti,D.B.,et al, 2010

Evidence Report: The Efficacy and Safety of Mitoxantrone (Novantrone) in the Treatment of Multiple Sclerosis: Report of the Therapeutics and Technology Assessment Subcommittee of the American Academy of Neurology
Neurol 74:1463-1470, Marriott,J.J., et al, 2010

Posterior Reversible Encephalopathy Syndrome After Rituximab Infusion in Neuromyelitis Optica
Neurol 74:1471-1473, S�nchez-Carteyron,A., et al, 2010

Safety of tPA in Stroke Mimics and Neuroimaging-Negative Cerebral Ischemia
Neurol 74:1340-1345, 1336, Chernyshev,O.Y., et al, 2010

Can Electronic Clinical Documentation Help Prevent Diagnostic Errors?
NEJM 362:1066-1069, Schiff,G.D. &Bates,D.W., 2010

Robot-Assisted Therapy for Long-Term Upper-Limb Impairment After Stroke
NEJM 362:1772-1783, 1827, Lo,A.C., et al, 2010

Antibodies to Glutamic Acid Decarboxylase Define a Form of Limbic Encephalitis
Ann Neurol 67:470-478, Malter,M.P., et al, 2010

How Neurologists Think A Cognitive Psychology: Perspective on Missed Diagnoses
Ann Neurol 67:425-433, Vickrey,B.G., et al, 2010

Neuropsychological Dysfunction and Neuroimaging Abnormalities in Neurologically Intact Adults With Sickle Cell Anemia
JAMA 303:1823-1831, Vichinsky,E.P., 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

NMDA Receptor Encephalitis Mimicking Seronegative Neuromyelitis Optica
Neurol 74:1473-1475, Kruer,M.C., et al, 2010

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

Resuscitating the Heart but Losing the Brain: Brain Atrophy in the Aftermath of Cardiac Arrest
Neurol 74:306-312, Horstmann,A.,et al, 2010

A Case of Neuro-Behcet Disease Mimicking Gliomatosis Cerebri
AJNR 31:E1, Varoglu,A.O., 2010

Spinal Cord Sarcoidosis: Clinical and Laboratory Profile and Outcome of 31 Patients in a Case-Control Study
Medicine 89:133-140, Cohen-Aubart,F.,et al, 2010

The Expanding Clinical Profile of Anti-AMPA Receptor Encephalitis
Neurol 74:857-859, Graus,F.,et al, 2010

Ring and Nodular Multiple Sclerosis Lesions: A Retrospective Natural History Study
Neurol 74:851-858, Davis,M.,et al, 2010

Neuromyelitis Optica in France: A Multicenter Study of 125 Patients
Neurol 74:736-742, Collongues,N.,et al, 2010

Neurological Outcomes at 18 Months of Age After Moderate Hypothermia for Perinatal Hypoxic Ischaemic Encephalopathy: Synthesis and Meta-Analysis of Trial Data
BMJ 340:c363, Edwards,A.D.,et al, 2010

Willful Modulation of Brain Activity in Disorders of Consciousness
NEJM 362:579-589,648, Monti,M.M.,et al, 2010

Increased Tissue Damage and Lesion Volumes in African Americans with Multiple Sclerosis
Neurol 74:538-544,532, Weinstock-Guttman,B.,et al, 2010



Showing articles 1400 to 1450 of 4087 << Previous Next >>