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Differential
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acoustic neurinoma
acoustic neurinoma, bilateral
acquired immunodeficiency syndrome
adrenoleukodystrophy
adrenomyeloneuropathy
advances in neurology
adverse drug reaction
Alexanders disease
algorithm
alopecia
alpha-fetoprotein
Alzheimer's disease
Alzheimer's disease, diagnosis of
Alzheimer's disease, early onset
Alzheimer's disease, familial
amniocentesis
amyloid angiopathy, cerebral
amyloid angiopathy, hereditary cystatin C
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, familial
anemia
anemia, hemolytic
anesthesia, general
anosmia
apolipoprotein E
APP gene
apraxia of eye movements
arteriopathy
ataxia
ataxia telangiectasia
ataxia, cerebellar
ataxia, hereditary
ataxia, truncal
attention deficit disorder with hyperactivity
autonomic dysfunction
basal ganglia, degeneration
basal ganglia, lesion of
Bassen-Kornzweig syndrome
benign familial neonatal convulsions
brachial neuritis
brachial plexus neuropathy
brachial plexus neuropathy, familial
brain biopsy
brainstem, lesion of
brainstem, neoplasms of
bulbar palsy, progressive
cafe au lait spots
carcinoembryonic antigen
carcinoma
carcinoma of pancreas
CAT scan
CAT scan, abnormal
cataracts
cavernous hemangioma
cerebellar ataxia, children
cerebellar ataxia, hereditary
cerebellar degeneration
cerebellar lesion
cerebellum, neoplasms of
cerebral atherosclerosis
cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy
cerebral autosomal recessive arteriopathy with subcortical infarction and leukoencephalopathy
cerebral infarction
cerebral infarction, subcortical
cerebral ischemia
cerebro hepato renal syndrome
cerebrovascular accident
cerebrovascular accident, familial occurrence
cerebrovascular accident, young adult
Charcot-Marie-Tooth
chorea
choreoathetosis
choreoathetosis, paroxysmal
chromosomal abnormality
chromosome 11
chromosome 14
chromosome 17
chromosome 2
chromosome 22
chromosome 3
chromosome 7
chromosome 9
clindamycin
clonazepam
clubfoot as related to neurologic disease
Cockayne's syndrome
coma
compression neuropathy
compression neuropathy, recurrent
cost effectiveness
creatine phosphokinase(CPK)elevated
Creutzfeldt-Jakob disease, genetic
cryptococcal meningitis
cyst, neoplastic cerebellum
cytomegalovirus infection
degenerative diseases of CNS
dementia
dementia, familial
dementia, presenile
dementia, rapidly progressive
dementia, transmissible
dentate nuclei
dentate nuclei, lesion of
developmental retardation
diabetes mellitus
DNA probes
drooling
drug induced neurologic disorders
dysarthria
dysmorphic
dystonia
dystonia musculorum deformens
dystonia, paroxysmal
dystrophin
ear, abnormal
electroencephalogram
electronystagmography
electroretinograph
encephalitis
encephalitis, focal
encephalitis, Rasmussen's
encephalitis, viral
enzyme, muscle disease
epidemiology of neurology
ethics in neurology
eye movement, disorders of
face, elongated
facial appearance, abnormal
familial
fasciculation
fatal familial insomnia
fragile-X syndrome
Friedreich's ataxia
fundus, abnormality of
gadolinium
gait disorder
gaze palsy
gaze palsy, supranuclear
gene
gene mutation
genetic counselling
genetic diagnosis
genetic diagnosis, prenatal
genetic linkage
genetic neurologic disorders
genetic screening
genetic testing
Gerstmann-Straussler-Scheinker disease
GFAP gene
gonadotropin-releasing hormone
growth retardation
gynecomastia
Hallervorden Spatz disease
hallucination
hamartoma
headache
headache, positional
hearing loss
hemangioblastoma
hemiparesis
hepatic failure
hepatolenticular degeneration(Wilson's disease)
hepatolenticular degeneration(Wilson's disease), presymptomatic
hepatosplenomegaly
Hispanics
HTRA1 gene
Hunter's syndrome
huntingtin
Huntington's chorea
Huntington's chorea, genetic counselling
Huntington's chorea, presymptomatic detection of
hyperactivity
hyperekplexia
hyperhidrosis
hyperkalemic periodic paralysis
hyperreflexia
hyperthermia
hypogonadism
hypotelorism
hypotonia
hypotonia, infants
imbalance
immunodeficiency
immunohistochemistry
immunoperoxidase staining
immunosuppression
in situ hybridization
inclusion bodies, intracytopasmic
insomnia
intracerebral hemorrhage
intracerebral hemorrhage, familial
intracerebral hemorrhage, young adult
Jakob-Creutzfeldt disease
joint hypermobility
Kallmann's syndrome
Kearns-Sayre syndrome
KRIT1 gene
Kugelberg-Welander syndrome
Laurence-Moon-Bardet-Biedl syndrome
leukemia
leukodystrophy
leukoencephalopathy
lymphoma
macrocephaly
macular degeneration
malformation, vascular
malformation, vascular, cerebral
malformation, vascular, familial
malignant hyperpyrexia
manic-depressive
medulla oblongata
medulla oblongata, atrophy
medulla oblongata, lesion of
meningitis
meningitis, recurrent
meningitis, relapse
mental retardation
mental retardation, familial
Mexican
Mexico
misdiagnosis
molecular genetics
mongolism
mononeuropathy
mononeuropathy, recurrent
mortality
motor neuron disease
movement disorder
movement disorder, extrapyramidal
MRI
MRI, abnormal
MRI, contrast enhanced
MRI, spinal cord
MRI, spinal cord, increased intramedullary cord signal
mucopolysaccharidoses
mucopolysacchariduria
multiple sclerosis
multiple sclerosis, differential diagnosis of
multiple sclerosis, familial
multiple sclerosis, misdiagnosis
multiple system atrophy
muscle biopsy
muscle spasm
muscle stiffness
muscular dystrophy
muscular dystrophy, Becker
muscular dystrophy, differential diagnosis of
muscular dystrophy, Duchenne
muscular dystrophy, Duchenne, carrier
muscular dystrophy, Duchenne, neonatal screening
muscular dystrophy, Duchenne, presymptomatic detection
muscular dystrophy, female occurrence of
muscular dystrophy, limb-girdle
myelin basic protein gene
myoclonus
myopathy
myopathy, mitochondrial
myopathy, proximal
myopia
myotonia
myotonia dystrophica
neonatal screening, genetic neurologic disorders
neoplasm, metastatic to CNS
neoplasm, posterior fossa
neoplasm, primary intracranial
neoplasm, primary of CNS
neurocutaneous disease
neuroendocrinology
neurofibroma
neurofibromatosis 1
neurofibromatosis 2
neurofibromatosis 2, presymptomatic
neurologic disease
neurologic disease, diagnoses of
neuronal ceroid-lipofuscinosis
neuronal migration disorder
neuropathology
neuropathology, brain
neuropathy
neuropathy, amyloid
neuropathy, hereditary peripheral
neuropathy, peripheral
night blindness
Notch3 gene
ocular motility, disorders of
oculopharyngeal muscular dystrophy
olfactory bulb
optic atrophy
optic glioma
optic nerve
optic neuropathy
pain
pain, flank
paraparesis
paraparesis, familial spastic
paraparesis, spastic
paroxysmal dystonic choreoathetosis
paroxysmal neurologic deficits
pathology
patient information and support
periodic paralysis
peroxisomal disease
pheochromocytoma
pigmentary retinopathy
polycystic kidneys
polymerase chain reaction
polyneuropathy, familial
posterior fossa, lesion of
practice guidelines
prenatal diagnosis by amniocentesis
prion disease
progeria
prognosis
progressive multifocal leucoencephalopathy
progressive spinal muscular atrophy
proximal myotonic myopathy
radiation hypersensitivity
recombinant DNA
recurrent
refractive errors
Refsum's disease
renal cell carcinoma
renal cyst
retinal degeneration
retinal hemangioma
retinal lesion
retinal tumor
retinitis pigmentosa
retinopathy
review article
RFLPs
rigidity
risk factors
Rosenthal fibers
seizure
seizure, familial
seizure, focal
seizure, intractable, treatment of
seizure, neonatal
sensorineural hearing loss
simian crease
skin, lesions in neurologic disorders
skull x-ray, abnormal
sleep pathology and physiology
small vessel disease
Southern immunoblot test
spasticity
spinal cord
spinal cord, lesion of
spinal cord, neoplasm
spinal muscular atrophy
spine, metastasis to
spinocerebellar ataxia
spinocerebellar ataxia type 3/Machado Joseph disease
spinocerebellar degeneration
spondylosis
spongy degeneration of brain
startle reaction
stuporous
subarachnoid hemorrhage
synkinesis
tapetoretinal degeneration
telangiectases
testicular enlargement
thalamus, lesion of
tinnitus
tomaculous neuropathy
trauma
treatment of neurologic disorder
trinucleotide repeats
Usher's syndrome
ventricular garlands
vibratory sensation, abnormal
viral infection
viral infection, CNS
visual field defect
visual loss
Von Hippel Lindau
Von Hippel Lindau, carrier
Von Hippel Lindau, screening protocol for
walking, difficulty with
Werdnig-Hoffman disease
Western immunoblot test
wheelchair
white matter disease
X-linked bulbospinal neuronopathy
x-linked mental retardation
X-linked neuropathy
Showing articles 150 to 200 of 349 << Previous Next >>

Myasthenia Gravis
NEJM 375:2570-2581, Gilhus, N.E.,et al, 2016

Neonatal Abstinence Syndrome
NEJM 375:2468-2479, McQueen, K. & Murphy-Oikonen, J., 2016

Computer-Assisted Diagnostic Checklist in Clinical Neurology
Neurologist 21:23-27, Finelli,P.F. and McCabe, A.L., 2016

Safety and Diagnostic Value of Brain Biopsy in HIV Patients: A Case Series and Meta-Analysis of 1209 Patients
JNNP 87:722-733, Lee, A.M.,et al, 2016

The Effectiveness of Electronic Differential Diagnoses (DDX) Generators: A Systematic Review and Meta-Analysis
PLoS ONE 11:e0148991, Riches, N.,et al, 2016

Encephalitis of Unclear Origin Diagnosed by Brain Biopsy
JAMA Neurol 72:66-72, Gelfand, J.M.,et al, 2015

The Tablet Device in Hospital Neurology and in Neurology Graduate Medical Education: A Preliminary Study
Neurohosp 5:15-21, George, P.,et al, 2015

Beyond Myalgic Encephalomyelitis/Chronic Fatigue Syndrome: An IOM Report on Redefining an Illness
JAMA 313:1101-1102, Clayton, E.W., 2015

Spinal Cord Ischemia: Practical Imaging Tips, Pearls, and Pitfalls
AJNR 36:825-830, Vargas, M.I.,et al, 2015

Stroke Prevention in Atrial Fibrillation
JAMA 313:1950-1962, Lip, G.Y.H. & Lane, D.A., 2015

Care and Outcomes of Patients with In-Hospital Stroke
JAMA Neurol 72:749-755,746, Saltman, A.P.,et al, 2015

Screening with MRI for Accurate and Rapid Stroke Treatment
Neurol 84:2438-2444, 2394, Shah, S.,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

Rapid Assessment and Treatment of Transient Ischemic Attacks and Minor Stroke in Canadian Emergency Departments
Stroke 46:2987-2990, Kamal, N.,et al, 2015

Recognizing Autoimmune-Mediated Encephalitis in the Differential Diagnosis of Limbic Disorders
AJNR 36:2196-2205, da Rocha, A.J.,et al, 2015

Treatment of Brain Metastases
J Clin Oncol 33:3475-3484, Lin, X. & DeAngelis, L.M., 2015

Stroke and Cancer - A Complicated Relationship
J Neurol Transl Neurosci 2:1039-1051, Dearborn, J.L.,et al, 2014

Cerebral Venous Thrombosis
Stroke 45:e16-e18, Gulati, D.,et al, 2014

Neuroimaging in Intracerebral Hemorrhage
Stroke 45:903-908, Macellari, F.,et al, 2014

Griscelli Syndrome and CNS Lymphohistiocytosis
Neurol 82:e122-e123, Saini, A.G.,et al, 2014

ICU-Acquired Weakness and Recovery from Critical Illness
NEJM 370:1626-1635, Kress, J.P. & Hall, J.B., 2014

Use of a Novel High-Resolution Magnetic Resonance Neurography Protocol to Detect Abnormal Dorsal Root Ganglia in Sjogren Patients with Neuropathic Pain
Medicine 93:121-134, Birnbaum, J.,et al, 2014

Traumatic Intracranial Hypertension
NEJM 370:2121-2130, Stocchetti, N. & Maas, A.I.R., 2014

The Treatment of Dystonic Tremor: A Systematic Review
JNNP 85:759-769, Fasano, A.,et al, 2014

Diagnosis of Reversible Causes of Coma
Lancet 384:2064-2076, Edlow, J.A.,et al, 2014

NeurologicDx - Internet Based Differential Diagnostic Checklist in Clinical Neurology
Ann Neurol 74:S5, Finelli, P.F. & McCabe, A.L., 2013

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

PML Diagnostic Criteria
Neurol 80:1430-1438, Berger, J.,et al, 2013

Computed Tomography Angiography in Hyperacute Ischemic Stroke
Stroke 44:1480-1488, Mortimer, A.,et al, 2013

Incidence of Atrial Fibrillation Detected by Implantable Loop Recorders in Unexplained Stroke
Neurol 80:1546-1550, Corter, P.,et al, 2013

Patent Foramen Ovale and Cryptogenic Stroke
Stroke 44:2676-2678, Furlan, A.J. and Jauss, M., 2013

Aggressive Medical Therapy Alone is Not Adequate in Certain Patients with Severe Symptomatic Carotid Stenosis
Stroke 44:2955-2956, Brown, M.M., 2013

Aggressive Medical Therapy Alone is Adequate in Certain Patients with Severe Symptomatic Carotid Stenosis
Stroke 44:2957-2958, Chaturvedi, S.,et al, 2013

Sensitivity of MRI of the Spine Compared with CT Myelography in Orthostatic Headache with CSF Leak
Neurol 81:1789-1792, Starling, A.,et al, 2013

Differential Diagnosis of a Low CSF Glucose in Children and Young Adults
Neurol 81:e178-e181, Leen, W.G.,et al, 2013

Central Nervous System Neuronal Surface Antibody Associated Syndromes: Review and Guidelines for Recognition
JNNP 83:638-645, Zuliani,L.,et al, 2012

Acute Stroke Imaging: What is Sufficient for Triage to Endovascular Therapies?
AJNR 33:790-792, Lev, M.H., 2012

Acute Stroke Imaging: CT with CT Angiography and CT Perfusion before Management Decisions
AJNR 33:792-794, Fox, A.J.,et al, 2012

Risk of Natalizumab-Associated Progressive Multifocal Leukoencephalopathy
NEJM 366:1870-1880,1938, Bloomgren, G.,et al, 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

The Management of Suspected Encephalitis
BMJ 344:e3489, Thwaites, G.E., 2012

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

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

Reliability of Real-Time Video Smartphone for Assessing National Institutes of Health Stroke Scale Scores in Acute Stroke Patients
Stroke 43:3271-3277, Demaerschalk, B.,et al, 2012

The Diagnosis and Treatment of Limbic Encephalitis
Acta Neurol Scand 126:365-375, Asztely, F. & Kumliem, E., 2012

Diagnosis and Management of Cerebral Venous Thrombosis: A Statement for Healthcare Professionals From the American Heart Association/American Stroke Association
Stroke 42:1158-1192, Saposnik,G.,et al, 2011

Etiologic investigation of ischemic stroke in young adults
Neurol 76:1983-1988, Larrue, V.,et al, 2011

Intravenous thrombolysis in acute ischaemic stroke: a systematic review and meta-analysis to aid decision making in patients over 80 years of age
JNNP 82:712-717, Bhatnagar, P.,et al, 2011

Mild Cognitive Impairment
NEJM 362:2227-2234, Peterson, R.C., 2011

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



Showing articles 150 to 200 of 349 << Previous Next >>