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Differential
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abdominal cramps
acral sensory symptoms
activated protein C resistance
alopecia
alpha galactosidase A deficiency
amyloid angiopathy, cerebral
amyloid angiopathy, hereditary cystatin C
amyloidosis
aneurysm
aneurysm, intracranial
aneurysm, intracranial, familial
angina pectoris
angiography, cerebral
anhidrosis
antiphospholipid antibodies
aphasia
arrhythmia, cardiac
arterial dissection
arterial dissection, carotid
arterial dissection, ruptured
arterial dissection, vertebral
arteriopathy
arteriovenous malformation
arteriovenous malformation, cerebral
asymptomatic
atrial fibrillation
atrial myxoma
autonomic dysfunction
basal ganglia, calcification of
basal ganglia, infarction
basal ganglia, lesion of
Binswanger disease
brain biopsy
brainstem, infarction of
brainstem, lesion of
burning paresthesia
calcification, intracranial
cardiomyopathy
carotid angiogram
carotid artery disease
CAT scan
CAT scan, abnormal
cavernous hemangioma
cerebral atherosclerosis
cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy
cerebral autosomal recessive arteriopathy with subcortical infarction and leukoencephalopathy
cerebral embolism
cerebral embolism, cardiac origin
cerebral infarction
cerebral infarction, hemorrhagic
cerebral infarction, small, deep
cerebral infarction, subcortical
cerebral ischemia
cerebral vasculature, calcification
cerebral venous thrombosis
cerebral venous thrombosis, etiology
cerebrospinal fluid, gammaglobulin of
cerebrovascular accident
cerebrovascular accident, cardiac disease causing
cerebrovascular accident, familial occurrence
cerebrovascular accident, genetic
cerebrovascular accident, infancy and childhood
cerebrovascular accident, location of
cerebrovascular accident, multiple
cerebrovascular accident, non atherosclerotic cause of
cerebrovascular accident, prevention of
cerebrovascular accident, recurrent
cerebrovascular accident, women
cerebrovascular accident, work up for
cerebrovascular accident, young adult
cerebrovascular disease
cerebrovascular disease, cardiovascular disease with
cerebrovascular disease, risk factors in
children
chromosomal abnormality
chromosome 12
chromosome 19
chromosome 5
Clinical Pathologic Conference(C.P.C.)
coagulopathy
cognition
collagen vascular disease
congestive heart failure
corpus callosum
corpus callosum, infarction of
corpus callosum, lesion of
cortical blindness
cystic infarction
deep gray nuclei
dementia
dementia, cerebrovascular disease causing
dementia, subcortical
depression
diarrhea
differential diagnosis
diplopia
DNA probes
dural sinus thrombosis
dysarthria
echocardiogram
Ehlers-Danlos syndrome
electroencephalogram, pediatric patients
encephalopathy
enzyme, defect
epidemiology of neurology
Fabry's disease
Factor V Leiden
factor V, deficiency
familial
familial hemiplegic migraine
fever
fibrinogen
fibromuscular dysplasia
fistula, arterio-venous
fistula, arterio-venous, carotid-cavernous
fistula, arterio-venous, pulmonary
gene
gene mutation
genetic linkage
genetic neurologic disorders
genetic screening
genetic testing
glioblastoma multiforme(astrocytoma Gr.III)
glioma
granular osmiphilic material
headache
headache, thunderclap
hearing loss
hemianopia, homonymous
hemiparesis
hemoglobin abnormality, neurologic complications of
hereditary hemorrhagic telangiectasia(HHT)
herpes simplex encephalitis
herpes simplex encephalitis, differential diagnosis of
homocystinuria
HTRA1 gene
human genome
hypercoagulable state
hyperlipidemia
hypertension
hypertension, cerebrovascular disease with
hypertrophic cardiomyopathy
ileus, paralytic
infantile hemiplegia
intellectual deficit
intellectual deterioration
intracerebral hemorrhage
intracerebral hemorrhage, familial
intracerebral hemorrhage, young adult
intracranial hemorrhage
lactic acidemia
lacunar infarction
leukoencephalopathy
lipid storage disorder of CNS
livedo reticularis
lupus anticoagulant
malformation, vascular
malformation, vascular, cerebral
malformation, vascular, familial
malformation, vascular, screening for
mania
manic-depressive
Marfan syndrome
marihuana
MELAS syndrome
microangiopathy, brain
middle cerebral artery territory infarction
middle cerebral artery, occlusion of
migraine
migraine with aura
migraine, hemiplegic
misdiagnosis
mitochondrial disease
mitochondrial encephalomyopathy
mitral valve lesion
mitral valve prolapse
molecular genetics
mortality
moyamoya
MRI
MRI, abnormal
MRI, black holes on
MRI, diffusion weighted
MRI, serial
multiple sclerosis
multiple sclerosis, differential diagnosis of
multiple sclerosis, familial
multiple sclerosis, misdiagnosis
myocardial infarction
myopathy
myopathy, mitochondrial
neoplasm, primary intracerebral
neoplasm, primary of CNS
neoplasm, primary of CNS-familial occurrence
neurocutaneous disease
neurofibromatosis 1
neurologic complications of, systemic disease
neurologic disease, diagnoses of
neurons
neuropathology
Notch3 gene
obesity
occipital lobe
osteogenesis imperfecta
PAS positive
PAS positive material in the brain
patent foramen ovale
polycythemia, primary
polymerase chain reaction
prethrombotic state
prognosis
protein C deficiency
protein S deficiency
pseudobulbar palsy
pseudoxanthoma elasticum
psychosis
psychosis, acute
pulmonary embolism
quadriparesis
ragged-red fibers
Red flags
renal failure
review article
risk factors
screening
seizure
sensorineural hearing loss
short stature
sibling
sick sinus syndrome
sickle cell disease
skin, biopsy
skin, lesions in neurologic disorders
small vessel disease
Sneddon's syndrome
spinal cord, infarction of
spondylosis
straight sinus
subarachnoid hemorrhage
sudden death
superior sagittal sinus thrombosis
syncope
systemic illness
telangiectases
telangiectases, retinal
temporal lobe, lesion
temporal lobe, lesion, bilateral
thrombocytopenia
thrombophlebitis
transient ischemic attack
treatment of neurologic disorder
tuberous sclerosis
twins
vasculopathy
visual loss
visual loss, transient
Von Hippel Lindau
white matter disease
white matter disease, location
workup
Showing articles 100 to 150 of 12504 << Previous Next >>

A Randomized Trial of Focused Ultrasound Thalamotomy for Essential Tremor
NEJM 375:730-739,792, Elias, W.J.,et al, 2016

Clinicopathologic Conference, Homocystinuria caused by Cystathionine B-Synthase Deficiency
NEJM 375:1879-1890, Case 34-2016, 2016

A Young Man with Progressive Vision and Hearing Loss
JAMA Neurol 73:880-883, Kung, N.H.,et al, 2016

Neuromyelitis Optica Spectrum Disorders
UpToDate, May, Glisson,C.C., 2016

A 44-Year-Old Man with Eye, Kidney, and Brain Dysfunction
Ann Neurol 79:507-519, Vodopivec, I.,et al, 2016

Non-Alzheimers Dementia 1 Frontotemporal Dementia
Lancet 386:1672-1682, Bang, Jee.,et al, 2015

Characyeristic features and progression of abnormalities on MRI for CARASIL
Neurol 85:459-463, Sekine, Y., etal, 2015

Percutaneous Left Atrial Appendage Closure:Technical Aspects and Prevention of Periprocedural Complications with the Watchman Device
Workd J Cardiol 26:65-75, Mobius-Winkler,S.,et al, 2015

Disturbances of Cerebrospinal Fluid, Including Hydrocephalus, Pseudotumor Cerebri, and Low-Pressure Syndromes, Pseudotumor Cerebri
Adams & Victors Principles of Neurology, Chp 30, pg 628, Ropper, A.H.,et al, 2014

Degenerative Diseases of the Nervous System, Parkinson Disease
Adams & Victors Principles of Neurology, Chp 39, pg 1082, Ropper, A.H.,et al, 2014

Degenerative Diseases of the Nervous System, Friedreich Ataxia
Adams & Victors Principles of Neurology, Chp 39, pg 1102, Ropper, A.H.,et al, 2014

Degenerative Diseases of the Nervous System, Amyotrophic Lateral Sclerosis
Adams & Victors Principles of Neurology, Chp 39, pg 1109, Ropper, A.H.,et al, 2014

Clinical Manifestations and Diagnosis of Bicuspid Aortic Valve in Adults
UpToDate Nov, Braverman, D.C., 2014

Sturge-Weber Syndrome
UptoDate , Nov, Bodensteiner, J.B., 2014

Cerebral Abnormalities in Adults with Ataxia-Telangiectasia
AJNR 35:119-123, Lin, D.D.M.,et al, 2014

Neuronal Intranuclear Inclusion Disease Cases with Leukoencephalopathy Diagnosed via Skin Biopsy
JNNP 85:354-356, Sone, J.,et al, 2014

Autism
Lancet 383:896-910, Lai, M.C.,et al, 2014

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

Parkinson Disease Subtypes
JAMA 71:499-504, Thenganatt, M. & Jankovic, J., 2014

Imaging Findings in MR Imaging-Guided Focused Ultrasound Treatment for Patients with Essential Tremor
AJNR 35:891-896, Wintermark, M.,et al, 2014

Familial Risk of Cerebral Palsy: Population Based Cohort Study
BMJ 349:g4294, g4514, Tollanes, M.C.,et al, 2014

Red Papules on the Tongue of a Patient with Hemiparesis
JAMA 312:741-742, Chiu, H.Y. & Lin, S.J., 2014

A 52-year-old Woman with Progressive Proximal Weakness
Neurol 83:e106-e109, Enduri, S.,et al, 2014

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

Vertebral Artery Dissection in Patients with Autosomal Dominant Polycystic Kidney Disease
J Stroke Cerebrovasc Dis 23:441-443, Kuroki, T.,et al, 2014

A Pilot Study of Focused Ultrasound Thalamotomy for Essential Tremor
NEJM 369:640-648, Elias, W.J.,et al, 2013

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

Sturge-Weber Syndrome
MedLink Neurology, July, Comi, A.M., 2013

Intracranial Lesions with High Signal Intensity on T1-weighted MR images - Review of Pathologies
Pol J Radiol 78:36-46, Zimmy, Anna.,et al, 2013

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

Cerebral Amyloid Angiopathy
eMedicine, Jan, Menon, R.S., 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

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

Screening Patients with a Family History of Subarachnoid Haemorrhage for Intracranial Aneurysms: Screening Uptake, Patient Characteristics and Outcome
JNNP 83:86-88, Miller, T.D.,et al, 2012

LMNA Cardiomyopathy:Cell Biology and Genetics Meet Clinical Medicine
Disease Models & Mechanisms 4:562-568, Lu,J.T., et al, 2011

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

Differential Diagnosis of Bilateral Abnormalities of the Basal Ganglia and Thalamus
RadioGraphics 31:5-30, Hegde,A.N.,et al, 2011

An unusual cause of stroke and hypoxia
BMJ 342:c7200, Bell, S.L. & Eveson, D.J., 2011

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

Association Between Familial Atrial Fibrillation and Risk of New-Onset Atrial Fibrillation
JAMA 304:2263-2269, Lubitz,S.A.,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

Whole-Genome Sequencing in a Patient with Charcot-Marie-Tooth Neuropathy
NEJM 362:1181-1191, Lupski,J.R., et al, 2010

Optimal Screening Strategy for Familial Intracranial Aneurysms: A Cost-Effectiveness Analysis
Neurol 74:1671-1679, Bor,A.S.E., et al, 2010

Familial Mediterranean Fever and Central Nervous System Involvement: A Case Series
Medicine 89:75-84, Kalyoncu,U.,et al, 2010

Pediatric Moyamoya Disease: An Analysis of 410 Consecutive Cases
Ann Neurol 68:92-101, Kim,S.-K., et al, 2010

A Hereditary Moyamoya Syndrome With Multisystemic Manifestations
Neurol 75:259-264, Herv�,D., et al, 2010

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

Aicardi-Gouti�res Syndrome: Neuroradiologic Findings and Follow-up
AJNR 30:1971-1976, Uggetti,C.,et al, 2009



Showing articles 100 to 150 of 12504 << Previous Next >>