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acrocyanosis
advances in neurology
aggression
agitation
Aicardi-Goutieres syndrome
alcohol
algorithm
alternative medicine
alveolar hypoventilation
aminoacidurias
amnesia
Angelman syndrome
angiitis
angiitis, granulomatous of CNS
angiitis, isolated of CNS
angiography, cerebral
angiography, cerebral, negative
ankle edema
ankle, swelling of
anomic aphasia
aphasia
aphasia, children
aphasia, progressive, primary
apraxia
apraxia, speech
artificial intelligence
ascites
Asperger's syndrome
ataxia
ataxia, cerebellar
ataxic gait
attention deficit disorder with hyperactivity
attention span
atypical
auditory processing, impaired
autism
autism, screening for
autoantibodies
autoimmune disease
autonomic dysfunction
Babinski sign
basal ganglia
basal ganglia, calcification of
basal ganglia, degeneration
basal ganglia, lesion of
basal ganglia, lesion, bilateral
behavior
behavior, combative
behavioral disorder
behavioral disorder, acute
Benedict's solution test
bias
bifid uvula
biologic markers
brachycephaly
bradykinesia
brain atrophy
brain biopsy
cafe au lait spots
calcification, intracranial
calf hypertrophy
callosal angle
carbon monoxide poisoning
carcinoma
CAT scan, abnormal
CAT scan, angiography
CAT scan, chest
CAT scan, emission, abnormal
catatonia
cerebellar atrophy, primary
cerebellar disease, eye movement disorder in
cerebellar hypoplasia
cerebral cortical atrophy
cerebral palsy
cerebral palsy, associated problems with
cerebral palsy, pure ataxic
cerebrospinal fluid, abnormal
cerebrovascular accident
cerebrovascular accident, mimics
chest x-ray
chest x-ray, abnormal
chilbran skin lesions
children
chorea
choreoathetosis
chromosomal abnormality
chromosome 15
cleft palate
Clinical Pathologic Conference(C.P.C.)
cognition
comorbidities
complications
compulsivity
computers, neurologic diagnosis and
confabulation
confusion
confusional state, acute
congenital bilateral perisylvian syndrome
consanguinity
constipation
contractures, joint
controversies in neurology
conversion reaction
copper metabolism, abnormal
cornea, abnormal
corpus callosum, hypoplastic
cortical-basal ganglionic degeneration
C-reactive protein, elevated
creatine phosphokinase(CPK)elevated
crying, pathologic
cyclophosphamide
deep learning
degenerative diseases of CNS
delay in diagnosis
dementia
dementia, frontotemporal
dementia, presenile
dentate nuclei, lesion of
depression
developmental disability
developmental evaluation
developmental milestones
developmental milestones, loss of
developmental retardation
diagnostic criteria
dichotic hearing
differential diagnosis
difficulty climbing stairs
dinitrophenylhydrazine(D.N.P.H.)reaction
diplegia, atonic
diplegia, spastic cerebral
disability, neurological
dopa responsive dystonia
drooling
dysarthria
dyskinesia
dyskinesia, buccal lingual facial
dysmorphic
dysphagia
dysphonia
dysplasia of C.N.S.
dyspraxia
dystonia
dystonia, children
dystrophin
efficacy
electroencephalogram
electroencephalogram, abnormalities of
electromyogram
ELISA
emergencies, neurologic
emotional lability
encephalitis
encephalitis, autoimmune
encephalitis, etiology
encephalitis, viral
encephalopathy
encephalopathy, delayed
encephalopathy, post anoxic
encephalopathy, progressive
enuresis
enzyme, defect
epidemiology of neurology
episodic disorders
episodic neurologic deficits
executive dysfunction
exome sequencing
eye movement, disorders of
face, inexpressive
facial appearance, abnormal
facial expression abnormality
facial weakness
facial weakness, bilateral
falling
familial
fatigue
feeding disorder
ferric chloride test
fetal alcohol syndrome
fetus
fever
fine motor function, impaired
fish
fluorescene in situ hybridization
folic acid
fundus, abnormality of
funduscopic exam
gait disorder
galactorrhea
gaze palsy, vertical
gene
gene mutation
Generative Pretrained Transformer 4
genetic counselling
genetic diagnosis, prenatal
genetic neurologic disorders
genetic testing
glabellar sign
globus pallidus
globus pallidus, lesion of
Gowers maneuver
growth retardation
Hallervorden Spatz disease
handwriting
head circumference
head lag
headache
headache, severe
hearing loss
hearing problems in children
hepatolenticular degeneration(Wilson's disease)
hippocampus
hydrocephalus
hydrocephalus, normal pressure
hyperactivity
hyperpyrexia, CNS disorder causing
hyperreflexia
hypertension
hypertonia
hypoglycemia
hypopigmentation of skin
hyporeflexia
hypotonia
hypotonia, infants
imbalance
immunosuppression
immunosuppressive agents
inattention
information technology
insomnia
insular cortex
insulinoma
intellectual deficit
intellectual deficit, treatable causes of
intellectual deterioration
intelligence quotient
interferon alpha
intracerebral hemorrhage
intrauterine
iris, abnormal
iron, brain
irritability
jaundice
karyotyping
Kayser-Fleischer ring
klippel feil syndrome
language
language delay
language development, neurologic basis of
language disorder in adults
language disorders in children
laughing, pathologic
L-dopa
learning disability
learning disability, in children
lenticular nucleus, lesion of, bilateral
leukodystrophy
leukoencephalopathy
lid
lid abnormalities
Lisch nodules
liver biopsy
liver disease
liver function enzymes
lobar atrophy
locked-in syndrome
long bone lesion
lymphoma
machine learning
macrocephaly
macrognathia
magnetoencephalography
maple syrup urine disease
medical errors
medical-legal aspects of neurology
megalencephaly
megalencephaly, idiopathic
memory, impairment of
meningeal enhancement
mental retardation
mental status, abnormal
microcephaly
midline defect in children
misdiagnosis
monoclonal antibodies
mood change
mortality
motor neuron disease
movement disorder
movement disorder, extrapyramidal
movement disorder, psychogenic
MRI
MRI, abdomen
MRI, abnormal
MRI, angiography
MRI, automated reading
MRI, diffusion tensor
MRI, disappearing lesion on
MRI, functional
MRI, negative
MRI, paramagnetic effect
MRI, pelvis
MRI, serial
MRI, vessel wall enhancement
multiple sclerosis, differential diagnosis of
muscle stiffness
muscular dystrophy
muscular dystrophy, central nervous system abnormality
muscular dystrophy, Duchenne
mutism
myelodysplasia
myoclonus
myoclonus, stimulus sensitive
myoglobinuria
nasal speech
neoplasm, metastatic
neoplasm, primary of CNS
neuroendocrinology
neurofibroma
neurofibromatosis 1
neuroglycopenia
neurologic disease, diagnoses of
neurologic evaluation
neurologic examination
neurologic examination, focal
neurologic signs
neurologic symptoms
neuroophthalmology
neuropathology
neuropathology, brain
NMDA antagonists
nonverbal
nystagmus
nystagmus, vertical
ocular fundus photography
ocular motility, disorders of
opened mouth
operculum syndrome
operculum syndrome, bilateral
opisthotonus
optic atrophy
palatopharyngeal incompetence
PANK2 mutation
papilledema
paraparesis, spastic
Parkinson disease
Parkinsonism syndrome
patient information and support
personality change
phenylketonuria
pheochromocytoma
philtrum, tented
Pick bodies
Pick's disease
pleocytosis of cerebrospinal fluid
pneumoencephalogram(PEG)
postural abnormality
precipitating factors
pregnancy, neurologic complications in
prenatal
prevention of neurologic disorders
primary lateral sclerosis
prognathism
prognosis
progressive neurologic disorder
prolactin, elevated
pruritus
pseudobulbar palsy
psychiatric disorder
psychiatric problems in neurologic disorders
psychological testing
psychological testing, children
psychological testing, neurologic problems
psychomotor retardation
psychosis
psychosis, childhood
psychosocial aspects
pyramidal tract
pyramidal tract dysfunction
quadriparesis
quadriplegia
rapidly progressing neurologic illness
recurrent
release phenomena
remote effect of cancer on the nervous system
ReNU syndrome
respirator
retinitis pigmentosa
review article
rhabdomyolysis
rigidity
risk factors
risk-benefit assessment
rituximab
saccadic eye movements, abnormal
safety
scoliosis
screening
sea-blue histiocytes
sedimentation rate, elevated
seizure
seizure, advice to parents and teachers regarding
seizure, differential diagnosis of
seizure, hysterical
seizure, psychosocial aspects of
seizure, recurrent
seizure, treatment of
semantic dementia
sensory loss
sexual behavior, disorder of
short stature
sign language
skin, lesions in neurologic disorders
sleep pathology and physiology
slit lamp examination
smiling
socialisation
spasticity
speech disorder
speech disorder, childhood
speech disorder, non aphasic
speech lateralization
speech therapy
speech, absence of
speech, delayed development of
speech, loss of
speech, slowed
spina bifida
spinal cord, lesion of
stammering
startle reaction
stereotyped behavior, drug induced
steroid therapy, CNS treatment and complications with
stuttering
substantia nigra
suck reflex
sweating
symmetric brain lesions
systemic illness
tauopathy
teeth, wide-spaced
temporal lobe, atrophy
temporal lobe, lesion
temporal lobe, lesion, bilateral
teratoma
teratoma, ovarian
thrombocytopenia
titubation
tongue, impaired movements of
tongue, protrusion of
transient neurologic deficit
treatment of neurologic disorder
tremor
tremor, intention
tripping
tumefactive lesion
tyrosine hydroxylase deficiency
upgaze, paralysis of
urinary incontinence
urine test for metabolic disorders
urine, dark
validation
vasculitides
virtual assistant
visual evoked response
visual field defect
visual impairment
vitamin supplementation
walking, difficulty with
weakness, functional
weakness, progressive
weight loss
wheelchair
white matter disease
whole genome sequencing
word-finding difficulty
workup
Showing articles 350 to 400 of 2349 << Previous Next >>

Neurological Manifestations Among US Government Personnel Reporting Directional Audible and Sensory Phenomena in Havana, Cuba
JAMA 319:1125-1133, 1098, 1079, Swanson, R.L.,et al, 2018

Thrombectomy for Stroke at 6 to 16 Hours with Selection by Perfusion Imaging
NEJM 378:708-718, Albers, G.W.,et al, 2018

Degenerative Cervical Myelopathy
BMJ 360:k186, Davies, B.M.,et al, 2018

Late Window Paradox
Stroke 49:768-771, Albers, G.W., 2018

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

Antibody-Mediated Encephalitis
NEJM 378:840-851, Dalmau, J.,et al, 2018

Clinicopathologic Conference, Homocystinuria due to genetic mutations of the gene encoding cystathionine B-synthase (CBS)
NEJM 378:941-948, Case 7-2018, 2018

A 12-year-old girl with headache and change in mental status
Neurol 90:524-529, Patel, P.,et al, 2018

Tinnitus
NEJM 378:1224-1231, Bauer, C.A., 2018

Acute Brain Lesions on Magnetic Resonance Imaging and Delayed Neurological Sequelae in Carbon Monoxide Poisoning
JAMA Neurol 75:436-443, Jeon, S.B.,et al, 2018

Automated DWI analysis can identify patients within the thrombolysis time window of 4.5 hours
Neurol 90:e1570-e1577, Wouters, A.,et al, 2018

Disability in adults with arthrogryposis is severe, partly invisible, and varies by genotype
Neurol 90:e1596-e1604, Dai, S.,et al, 2018

Coma
Neurol 90:e1638-e1645, Schievink, W.I.,et al, 2018

Progressive cognitive decline, cerebellar ataxia, recurrent myoclonus, and epilepsy
Neurol 90:e1827-e1831, Xiao, F.,et al, 2018

Diagnosis and Management of the Antiphospholipid Syndrome
NEJM 378:2010-2021, Garcia, D. & Erkan, D., 2018

Time to Decision and Treatment with tPA (Tissue-Type Plasminogen Activator) Using Telemedicine Versus an Onboard Neurologist on a Mobile Stroke Unit
Stroke 49:1528-1530, Bowry, R.,et al, 2018

Misdiagnosis of Cerebral Vein Thrombosis in the Emergency Department
Stroke 49:1504-1506, Liberman, A.L.,et al, 2018

Encephalitis with mGluR5 antibodies
Neurol 90:e1964-e1972, Spatola, M.,et al, 2018

MRI-Guided Thrombolysis for Stroke with Unknown Time of Onset
NEJM 379:611-622, 682, Thomalla, G.,et al, 2018

A Fatal Case of Undiagnosed Candida Meningitis-Role of Computer-assisted Diagnosis
Neurologist 23:138-140, Finelli, P.F., 2018

Intravenous Thrombolysis in Unwitnessed Stroke Onset: MR WITNESS Trial Results
Ann Neurol 83:980-993, Schwamm, L.H.,et al, 2018

Neurologic Outcomes in Pediatric Cardiac Arrest Survivors Enrolled in the THAPCA trials
Neurol 91:e123-e131, Ichord, R.,et al, 2018

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

Drug Reaction with Eosinophilia and Systemic Symptoms after Daclizamub Therapy
Neurol 91:e359-e363, Rauer,S.,et al, 2018

A Curable Myopathy Manifesting as Exercixe Intolerance and Respirtory Failure
Neurol 91:187-190, Silva,A.M.S.,et al, 2018

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

Surveillance for Matastatic Hemangiopericytoma-Solitary Fibrous Tumors-Systematic Literature Review on Incidence,Predictors and Diagnosis of Extra-Carnial Disease
J Neurooncol 138:447-467, Ratneswaren,T.,et al, 2018

FARS2 dificiency; new cases, review of clinical, biochemical, and molecular spectra, and variants interpretation based on structural, functional, and evolutionary significance
Mol Genet Metab 125:281-291, Almannai, M.,et al, 2018

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

Unique Gadolinium Enhancement Pattern in Spinal Dural Arteriovenous Fistulas
JAMA Neurol 75:1542-1545, Zalewski, N.L.,et al, 2018

Atrial-Esophageal Fistula Post-Maze Radiofrequency Ablation
ACS Case Reviews in Surg 2:1-4, Montminy,E.M.,et al, 2018

Atrioesophageal Fistula -Clinical Presentation, Procedural Characteristics, Diagnostic Investigations, and Treatment Outcomes
Circ Arrhythrm Electrophysiol doi:10.1161/CIRCEP.117.005579, Han,H-C.,et al, 2017

IGG4-Related Hypertrophic Pachymeningitis Coexpressing Antineutrophil Cytoplasmic Antibodies
Neurol 4:e341-e343, Massey, J., 2017

Menkes Disease Mimicking Child Abuse
Pediat Dermatol 34:e132-e134, Droms, R.J.,et al, 2017

Clinical Presentation and Prognosis in MOG-antibody Disease: A UK Study
BRAIN 140:3128-3138, Jurynczyk, M.,et al, 2017

Huntington Disease: Clinical Features and Diagnosis
UptoDate Dec 2017, Oksana Suchowersky, 2017

A Patient with a History of Encephalomyelitis and Recurrent Optic Neuritis
Neurol 89:e231-e234, Gutman, J.M.,et al, 2017

Clinical Imaging Factors Associated with Infarct Progression in Patients with Ischemic Stroke During Transfer for Mechanical Thrombectomy
JAMA Neurol 74:1361-1367,1298, Boulouis, G.,et al, 2017

Clinicopathologic Conference, Copper Deficiency Myelopathy
NEJM 377:1977-1984, Case 35-2017, 2017

Mobile Interventional Stroke Teams Lead to Faster Treatment Times for Thrombectomy in Large Vessel Occlusion
Stroke 48:3295-3300, Wei, D.,et al, 2017

A 61-year-old woman with Lower Extremity Paralysis and Sensory Loss
Neurol 89:e257-e263, Manners, J.,et al, 2017

Population-based Study of Ischemic Stroke Risk after Trauma in Children and Young Adults
Neurol 89:2310-2316, Fox, C.K.,et al, 2017

Paraneoplastic and Autoimmune Encephalitis
UptoDate July, Dalmau, J.,et al, 2017

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

Neuroimaging Changes in Menkes Disease, Part 1
AJNR 38:1850-1857, Manara, R.,et al, 2017

A 55-year-old Man with Rapidly Progressive Dementia and Parkinsonism
Neurol 89:e182-e187, Tabuas-Pereira, M.,et al, 2017

A 46-year-old man with Persistent Hiccups, Cognitive Dysfunction, and Imbalance
Neurol 89:e193-e196, Lamb, C.J.,et al, 2017

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

Clinicopathologic Conference, Eosinophilic Granulomatosis with Polyangiitis
NEJM 377:1569-1578, Case 32-2017, 2017

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



Showing articles 350 to 400 of 2349 << Previous Next >>