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alpha-fetoprotein
alternating hemiplegia
alternating hemiplegia of childhood
alternating rapid movement
aminoacidurias
anti MAG antibodies
anti Yo antibody
aphasia
aphasia, children
apraxia, speech
aspiration
ataxia
ataxia telangiectasia
ataxia, cerebellar
ataxia, progressive
ataxia, truncal
ataxic gait
ataxic hemiparesis
attention deficit disorder with hyperactivity
attention span
autism
autoantibodies
Babinski sign
basal ganglia, degeneration
basilar artery stenosis
behavioral disorder
Benedict's solution test
bifid uvula
bradykinesia
brainstem, atrophy
brainstem, lesion of
calcification, intracranial
carcinoma
carcinoma of breast
carcinoma of ovary
CAT scan, emission, abnormal
catalepsy
cataplexy
cerebellar ataxia, children
cerebellar atrophy, secondary
cerebellar degeneration
cerebellar lesion
cerebral cortex
cerebral cortical atrophy
cerebral palsy
cerebral palsy, associated problems with
cerebral palsy, pure ataxic
cerebrospinal fluid, abnormal
cerebrospinal fluid, oligoclonal IgG in
cerebrovascular accident
chairbound
chemotherapy, CNS treatment and complications with
children
chorea
choreoathetosis
cleft palate
Clinical Pathologic Conference(C.P.C.)
cognition
complications
confusion
consanguinity
cortical-basal ganglionic degeneration
cranial nerve palsies
cranial nerve palsies, bilateral
cranial neuropathy, multiple
crying, pathologic
cryptococcal antigen
cryptococcal meningitis
cultured skin fibroblasts
deep gray nuclei
degenerative diseases of CNS
dementia
dementia, presenile
demyelinating disease
developmental milestones, loss of
diagnostic criteria
dinitrophenylhydrazine(D.N.P.H.)reaction
diplegia, atonic
diplegia, spastic cerebral
diplopia
disability, neurological
disease modifying agents
dizziness
drooling
drowsiness
dysarthria
dysdiadochokinesia
dysmetria
dysphagia
dysphonia
dysplasia of C.N.S.
dyspraxia
dystonia
electroencephalogram
electromyogram
emotional lability
encephalitis
encephalitis, autoimmune
encephalopathy
encephalopathy, acute
epileptic encephalopathy
exome sequencing
eye movement, disorders of
facial nerve palsy
failure to thrive
falling
familial
FARS2 deficiency
ferric chloride test
fine motor function, impaired
foam cells
fungal infection
fungal infection, CNS
gait disorder
gaze palsy
gaze palsy, supranuclear
gaze palsy, vertical
gene
gene mutation
genetic counselling
genetic neurologic disorders
genetic testing
glabellar sign
grasp reflex
head nodding
headache
headache, intractable
hearing loss
hearing problems in children
heel-knee-shin test
hemiplegia
hepatic failure
hepatolenticular degeneration(Wilson's disease)
hepatosplenomegaly
hyperreflexia
hypoglycorrhachia
hypotonia
iatrogenic neurologic disorders
imbalance
immunocompetent
immunodeficiency
immunomodulation
immunotherapy
inattention
incontinence, fecal
incoordination
infection
intellectual deficit
intellectual deficit, treatable causes of
intellectual deterioration
intelligence quotient
jaundice
karyotyping
Kayser-Fleischer ring
klippel feil syndrome
language disorders in children
laughing, pathologic
lethargy
leukemia
lipid storage disorder of CNS
liver disease
locked-in syndrome
lysosomal storage disease
maple syrup urine disease
masked facies
memory, impairment of
meningeal enhancement
meningeal enhancement, nodular
meningitis
meningitis, CSF cell count-normal
meningitis, fungal
meningitis, neutrophilic
meningitis, neutrophilic, persistent
mental retardation
mental status, abnormal
methotrexate
microcephaly
midbrain
midbrain, infarction of
midline defect in children
mimics
misdiagnosis
mitochondrial disease
monoclonal antibodies
monoparesis
motor neuron disease
movement disorder
movement disorder, extrapyramidal
MRI
MRI, abnormal
MRI, angiography
MRI, contrast enhanced
MRI, disappearing lesion on
MRI, negative
MRI, nodular enhancement
multiple system atrophy
mutism
myelodysplasia
nasal speech
nausea and vomiting
negative
neurofibrillary degeneration
neurologic disease, diagnoses of
neurologic examination, focal
neurologic signs
neurologic symptoms
neuropathology
neuropathy
neurotoxic
neurotoxicity, acute
Niemann-Pick disease
ocular motility, disorders of
palatopharyngeal incompetence
paraneoplastic cerebellar degeneration
paraparesis, familial spastic
paraparesis, spastic
Parkinson disease
Parkinsonism syndrome
personality change
phenylketonuria
pleocytosis of cerebrospinal fluid
pleocytosis of cerebrospinal fluid, neutrophilic
pneumonia
primary lateral sclerosis
prognosis
progressive neurologic disorder
progressive supranuclear palsy
pseudobulbar palsy
psychiatric disorder
psychiatric problems in neurologic disorders
psychological testing
psychological testing, neurologic problems
psychosis
psychosis, childhood
psychosocial aspects
ptosis
ptosis, unilateral
pulmonary infection
pure motor hemiplegia
pursuit eye movements, abnormal
pyramidal tract
pyramidal tract dysfunction
quadriparesis
quadriplegia
recurrent
release phenomena
remote effect of cancer on the nervous system
review article
rigidity
saccadic eye movements, abnormal
salivation, excessive
seizure
seizure, advice to parents and teachers regarding
seizure, children
seizure, psychosocial aspects of
seizure, treatment of
single photon emission computed tomography
skin, lesions in neurologic disorders
slit lamp examination
spastic diplegia
spasticity
speech disorder
speech disorder, childhood
speech, loss of
spina bifida
splenomegaly
stare
stuttering
suck reflex
telangiectases
third nerve palsy
third nerve palsy, bilateral
third nerve palsy, partial
toe walking
tongue, impaired movements of
transient neurologic deficit
treatment of neurologic disorder
tremor
upgaze
upgaze, paralysis of
urinary incontinence
urine test for metabolic disorders
vertigo
walking, difficulty with
weight loss
wheelchair
wide based gait
Showing articles 250 to 300 of 15263 << Previous Next >>

Neurosyphilis
NEJM 381:1358-1363, Ropper, A.H.,et al, 2019

Relapsing-Remitting Severe Bickerstaffs Brainstem Encephalitis
BMJ 394:684, Tyrakowska, Z.,et al, 2019

Bilateral Claude Syndrome
Neurol 93:599-600, Witsch, J.,et al, 2019

A 14-Year-Old Girl with Headache, Seizures, and Confusion
Neurol 92:e161-e167, Xiao, L.,et al, 2019

Clinicopathologic Conference, Powassan Virus Encephalitis
NEJM 380:380-387, Case 3-2019, 2019

A 61-Year-Old Woman with Acute Onset Dysgraphia
Neurol 92:e386-e391, Smith, L.R.,et al, 2019

Contemporary Reversal of Oral Anticoagulation in Intracerebral Hemorrhage
Stroke 50:529-536, Bower, M.M.,et al, 2019

Oculodentodigital Dysplasia: A Hypomyelinating Leukodystrophy with a Characteristic MRI Pattern of Brain Stem Involvement
AJNR 40:903-907, Hartin, I.,et al, 2019

A 78-year-old Man with a Gait Disorder
Neurol 93:223-227, Saucedo, M.,et al, 2019

Clinicopathologic Conference, Amyotrophic Lateral Sclerosis
NEJM 380:1566-1574, Case 12-2019, 2019

Limbic-Predominant Age-Related TDP-43 Encephalopathy (LATE): Consensus Working Group Report
Brain DOI: 10.1093/brain/awz099, Nelson, P.T.,et al, 2019

Rare Presentation of Spontaneous, Direct, Carotid Cavernous Fistula in Late Pregnancy:A Case Report
Ophthalmol Clin Res 2:73-77, Agrawal,N.,et al, 2019

Hereditary Spastic Paraplegia:From Diagnosis to Emerging Therapeutic Approaches
Lancet Neurol 18:1136-1146, Shribman,S.,et al, 2019

Pyruvate Dehydrogenase Deficiency (PDCD)
eMedicine.medscape,com, Aug, Frye,R.E.,et al, 2018

Behcet Disease
emedicine.medscape.com Dec, Davey-Ranasinghe, N. & Diamond, H.S., 2018

Subacute Progressive Ptosis, Ophthalmoplegia, Gait Instability, and Cognitive Changes
JAMA Neurol 75:1284-1285, Lin, J.,et al, 2018

Proptosis and Double Vision in a Child
JAMA Neurol 75:1142-1143, Lu, A.J.,et al, 2018

Facial Myokymia and Myorhythmia in Anti-IgLON5 Disease
Neurol 91:e1659, Vetter, E.,et al, 2018

Clinical Presentation and Cranial MRI Findings of Listeria Monocytogenes Encephalitis
Neurologist 23:198-203, Arslan, F.,et al, 2018

Progressive Multifocal Leukoencephalopathy: Epidemiology, Clinical Manifestations, and Diagnosis
www.UptoDate.com, May, Koralnik, I.J., 2018

Clinical Reasoning: A 49-year-old man with Progressive Numbness, Weakness, and Evidence of Leptomeningeal Enhancement
Neurol 90:e90-e93, Lovett, A.,et al, 2018

Precentral Gyrus Infarct Presenting as Isolated Contralateral Peripheral-Type Facial Palsy
Neurol 91:421-422, Hebant, B.,et al, 2018

Atypical Parkinsonian Syndromes: A General Neurologists Perspective
Eur J Neurol 25:41-58, Deutschlander, A.B.,et al, 2018

A Patient With Multiple Cranial Nerve Palsies and Areflexic Paraparesis
Neurol 91:e392-e395, Garg,R.K.,et al, 2018

Risk of Ischemic and Hemorrhagic Strokes in Occult and Manifest Cancers
Stroke 49:1585-1592, Andersen, K.K. & Olsen, T.S., 2018

Clinicopathologic Conference, Poststroke Mania and the Frontal Lobe Syndrome
NEJM 379:182-189, Case 21-2018, 2018

A 56-year-old woman with acute vertigo and diplopia
Neurol 90:748-752, Sharma, R.,et al, 2018

Review of the Neurological Implications of von Hippel-Lindau Disease
JAMA Neurol 75:620-627, Dornbos, D.,et al, 2018

Diagnosing Stroke in Acute Dizziness and Vertigo
Stroke 49:788-795, Saber Tehrani, A.S.,et al, 2018

Five and 10 Minute Apgar Scores and Risks of Cerebral Palsy and Epilepsy: Population Based Cohort Study in Sweden
BMJ 360:k207, Persson, M.,et al, 2018

A 52-year-old woman with a 3 weeks of progressive gait ataxia and dysarthria
Neurol 90:e985-e989, Ly, C.,et al, 2018

Clinicopathologic Conference, Primary Progressive Aphasia, Semantic Variant, due to TAR DNA Binding Protein 43 associated Frontotemporal Lobar Degen
NEJM 376:158-167, Case 1-2017, 2017

Sudden-Onset Pulsatile Headache in a Previously Healthy Young Man
Neurol 88:e26-e29, Qin, C.,et al, 2017

Cranial Nerve Hypertrophy in IgG4 Anti-Neurofascin 155 Antibody-Positive Polyneuropathy
Neurol 88:e52, Franques, J.,et al, 2017

Acute Hydrocephalus Caused by Radiographically Occult Fourth Ventricular Outlet Obstruction
Neurol 88:e36-e37, Duran, D.,et al, 2017

A Woman in Her 60s with Chronic Meningitis from Aspergillus
JAMA Neurol 74:348-352, Pichler, M.R.,et al, 2017

Cerebellar Ataxia and Hearing Impairment
JAMA Neurol 74:243-244, Lin, C.Y. & Kuo, S.H., 2017

Intracranial Dural Arteriovenous Fistulae
Stroke 48:1424-1431, Reynolds, M.R.,et al, 2017

A 13-year-old boy with Chronic Ataxia and Developmental Delay
Neurol 88:e116-e121, Libdeh, A.A.,et al, 2017

Clinicopathologic Conference, MELAS (mitochondrial encephalopathy, lactic acidosis, and stroke like episodes)
NEJM 376:1668-1678, CASE 13-2017, 2017

Glial Fibrillary Acidic Protein Immunoglobulin G as Biomarker of Autoimmune Astrocytopathy: Analysis of 102 Patients
Ann Neurol 81:298-309, Flanagan, E.P.,et al, 2017

Advances in Progressive Supranuclear Palsy: New Diagnostic Criteria, Biomarkers, and Therapeutic Approaches
Lancet Neurol 16:552-563, Boxer, A.L.,et al, 2017

Clinicopathologic Conference, Biotinthiamine-Responsive Basal Ganglia Disease Due to Mutation SLC19A3
NEJM 377:2376-2385, Case 38-2017, 2017

Intrathecal 2-hydroxypropyl-�-cyclodextrin Decreases Neurological Disease Progression in Niemann-Pick disease, type C1: a non-randomised, open-label, phase 1-2 trial
Lancet 390:1758-1768, Ory, D.S.,et al, 2017

My Weeping Patient
Neurol 89:e202, Peters, J.,et al, 2017

A Case of Ataxia, Seizure, and Choreoathetosis in a 34-year-old Woman
Neurol 89:e220-e223, Xiao, F. & Wang, X.F., 2017

A Middle-aged man with Progressive Ophthalmoparesis, Ataxia, and Spastic Paraparesis
JAMA Neurol 74:733-736, Kung, N.H.,et al, 2017

A 27-year-old man with Acute-Onset Ataxia
Neurol 88:e207-e211, Risco, J. & Weiss, M., 2017

Man with Recurrent Paralysis and Cerebral White Matter Lesions
JAMA Neurol 74:599-600, Xiao, F., 2017

Precipitous Deterioration of Motor Function, Cognition, and Behavior
JAMA Neurol 74:591-596, Fernandez-Fournier, M.,et al, 2017



Showing articles 250 to 300 of 15263 << Previous Next >>