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Differential
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abdominal distention
abducens nerve paralysis
adverse drug reaction
alopecia
amenorrhea
anasarca
anemia
anorexia
arteriopathy
arteritides
arteritis, temporal
arthralgia
arthritis
ascites
aspirin
ataxia
ataxia telangiectasia
ataxic gait
autonomic dysfunction
B 12 deficiency
bacterial infection
basal ganglia, lesion of
Beau's lines
biologic markers
biotin deficiency
biotinidase deficiency
brain atrophy
brain scan, abnormal
brainstem, lesion of
breast feeding
cafe au lait spots
carcinoma
cardiomyopathy
Castleman's disease
CAT scan, emission, abnormal
cataracts
cerebral arteries
cerebral atherosclerosis
cerebral autosomal recessive arteriopathy with subcortical infarction and leukoencephalopathy
cerebral cortical atrophy
cerebral infarction
cerebral infarction, subcortical
cerebral ischemia
cerebral peduncle
cerebral vasculature
cerebral venous infarction
cerebral venous thrombosis
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, gammaglobulin of
cerebrospinal fluid, pressure increased
cerebrovascular accident
cerebrovascular accident, familial occurrence
cerebrovascular accident, young adult
children
chorea
chromosome 8
Clinical Pathologic Conference(C.P.C.)
clubbing of fingers
coma
comorbidities
confusion
confusional state, acute
congestive heart failure
conjunctival injection
conjunctivitis
Coombs test, positive
cortical vein thrombosis
corticotropin level
corticotropin-releasing factor
cortisol, elevated
cranial nerve palsies
cranial neuropathy, multiple
Cushing's syndrome
cytoid bodies
degenerative diseases of CNS
delirium
developmental milestones, loss of
developmental retardation
diabetes insipidus
diabetes mellitus
diet
diplopia
dural sinus thrombosis
dyspnea
echocardiogram
echocardiogram, LVH
edema, pedal
ejection fraction
ejection fraction, abnormal
electrocardiogram, abnormal
electroencephalogram
electroencephalogram, abnormalities of
electromyogram
emergencies, neurologic
encephalopathy
enzyme, defect
erythema nodosum
evoked potentials
eye movement, disorders of
facial hair, excessive
facial pain
facial weakness
failure to thrive
false positive VDRL
familial
fatigue
fever
fingernails, abnormal
fingernails, white
foot drop
fornix, lesion of
gait disorder
gammaglobulin therapy, intravenous
gene
gene mutation
genetic linkage
genetic neurologic disorders
genetic testing
glaucoma
glycosuria
gray hair
Griscelli syndrome
growth retardation
gynecomastia
hair analysis
hair, loss
hallucination
hand pain
headache
hearing loss
hemifacial atrophy
hepatomegaly
hepatosplenomegaly
herniated disc, thoracic
hirsutism
Horner's syndrome
HTRA1 gene
hypercoagulable state
hyperhidrosis
hyperhomocysteinemia
hyperpigmentation of skin
hypertension
hypertrichosis
hypocomplementemia
hypogonadism
hypokalemia
hyponatremia
hypothermia
hypotonia
immunodeficiency
immunoelectrophoresis, serum
immunosuppression
impotence
infant, evaluation of
infantile tremor syndrome
infection
internal capsule
intracranial pressure, increased
jaw pain
Kawasaki disease
leg swelling
leukemia
leuko-araiosis
leukocytosis
leukoencephalopathy
leukopenia
life expectancy
liver disease
liver function enzymes
low back pain
lymphadenopathy
lymphadenopathy, hilar
lymphohistiocytosis
lymphoma involving CNS
lymphopenia
meningitis
meningitis, aseptic
meningoencephalitis
mental status, abnormal
mesial temporal lobe
metabolic acidosis
metabolic alkalosis
microhemorrhage, intracerebral
midbrain, lesion of
middle cerebellar peduncle
middle cerebellar peduncle, lesion
middle cerebellar peduncle, lesion, bilateral
mimics
misdiagnosis
mitoxantrone
monoclonal gammopathy
mononeuritis multiplex
mononeuropathy
mortality
MRI
MRI, abnormal
MRI, diffusion weighted
multiple myeloma
multiple sclerosis
multiple sclerosis, treatment of
muscle pain
muscle weakness, proximal
myelination of nervous system
myelitis
myeloma, osteosclerotic
myelopathy
myocardial injury
myocarditis
myoclonus
myocytolysis
myositis
nausea and vomiting
neck trauma
neonatal screening, genetic neurologic disorders
neoplasm, hormone producing, ectopic
nephritis
nerve biopsy
neuroendocrinology
neurologic complications of, systemic disease
neurologic disease, diagnoses of
neuropathy
neuropathy, motor, multifocal
neuropathy, peripheral
neutropenia
night sweats
nystagmus
nystagmus, rotary
nystagmus, spontaneous
oculocutaneous albinism
ophthalmoplegia
optic atrophy
optic neuritis
P300
pain, back
palpitations
papilledema
paranoia
pericarditis
photophobia
pink eye
plasmacytoma
pleocytosis of cerebrospinal fluid
pleural effusion
pleurisy
POEMS syndrome
poliosis
polymyalgia rheumatica
polyneuropathy
pons, lesion of
postpartum
pregnancy, neurologic complications in
progeria
prognosis
progressive neurologic disorder
psychiatric problems in neurologic disorders
psychosis
ptosis
pulmonary embolism
purpura
quadriparesis
radiation therapy, CNS treatment and complications with
rash
Raynaud's phenomenon
retinal detachment
reversible neurologic disorder
review article
risk factors
scalp necrosis
schizophrenia
scleroderma
scleroderma, neurologic involvement with
scotoma
screening
sedimentation rate, elevated
seizure
seizure, children
seizure, drug resistance
seizure, neonatal
short stature
skin cancer
skin, lesions in neurologic disorders
skin, pale
skin, thickened
slurred speech
small vessel disease
somatosensory evoked potentials
spinal cord, lesion of
splenomegaly
spondylolysis
spondylosis
steroid psychosis
steroid therapy, CNS treatment and complications with
subcortical U fibers
subcutaneous nodules
substantia nigra
symmetric brain lesions
systemic illness
systemic lupus erythematosus
systemic lupus erythematosus, neurologic complications with
systemic lupus erythematosus, skin changes in
temporal lobe, lesion
term infant
thirst
thrombocytopenia
thrombocytosis
thrombotic thrombocytopenia purpura
tinnitus
treatment of neurologic disorder
tremor
tremor, intention
trichopoliodystrophy
tuberculosis
tuberculosis, miliary
urinary frequency
urinary tract infection
urticaria
uveitis
vasculitides
vegetarianism
Venereal Disease Research Laboratory test
vertigo
vision, blurred
visual acuity, decreased
visual loss
vitamin deficiency
vitiligo
Vogt-Koyanagi-Harada syndrome
weakness, generalized
weight loss
Werner's syndrome
white hair
white matter disease
whites
Showing articles 100 to 150 of 1370 << Previous Next >>

Clinicopathologic Conference, Borrelia Miyamotoi Infection
NEJM 383:1578-1586, Case 32-2020, 2020

Bornavirus Encephalitis Shows a Characteristic Magnetic Resonance Phenotype in Humans
Ann Neurol 88:723-735, Finck, T.,et al, 2020

Central Nervous System Involvement in Erdheim-Chester Disease
Neurol 95:e2746-e2754, Aubart,F.C.,et al, 2020

An 11-year-old girl with focal seizures, fevers, and unilateral, enhancing cortical lesions
Neurol 95:e3153-e3159, Russ, J.B.,et al, 2020

Clinical and Radiologic Findings of Acute Necrotizing Encephalopathy in Young Adults
AJNR 41:2250-2254, Vanjare, H.A.,et al, 2020

A 22-Year-Old Man with Progressive Bilateral Visual Loss
Neurol 94:625-630, Yang, S.L.,et al, 2020

Infection Risks Among Patients with Multiple Sclerosis Treated with Fingolimod, Natalizumab, Rituximab, and Injectable Therapies
JAMA Neurol 77:184-191, Luna, G.,et al, 2020

Delayed Leukoencephalopathy: A Rare Complication after Coiling of Cerebral Aneurysms
AJNR 41:286-292, Ikemura, A.,et al, 2020

Progressive Multifocal Leukoencephalopathy in a Patient with Primary Amyloid Light-Chain Amyloidosis
Clin Neurol Neurosurg 192:doi105709, Katsuse, K.,et al, 2020

"CHOICES": An Acronym to Aid in Delineating Potential Causes of Non-Metabolic, Non-Infectious Acute Toxic Leukoencephalopathy
EJR OPEN 6:243-257, Koksel, Y.,et al, 2019

A Case of Acute Encephalopathy and Rigidity in a 30-Year-Old Man
Neurol 93:759-763, Hurtubise, B. & MacLellan, A., 2019

Treatment Approaches for MOG-Ab-Associated Demyelination in Children
Curr Treat Options Neurol 21:2, Hacohen, Y. & Banweil, B., 2019

Human Parechovirus Meningoencephalitis: Neuroimaging in the Era of Polymerase Chain Reaction-Based Testing
AJNR 40:1418-1421, Sarma, A.,et al, 2019

Basa Ganglia Calcifications (Fahrs Syndrome): Related Conditions and Clinical Features
Neurol Sci 40:2251-2263, Donzuso,G.,et al, 2019

Acute Toxic Leukoencephalopathy: Etiologies, Imaging Findings, and Outcomes in 101 Patients
AJNR 40:267-275, Ozutemiz, C.,et al, 2019

Pembrolizumab Treatment for Progressive Multifocal Leukoencephalopathy
NEJM 380:1597-1605, Cortese, I.,et al, 2019

Strokelike Episodes in a Patient with Chronic Gait Abnormalities
JAMA Neurol 76:621-622, Santoro, J.D. & Chitnis, T., 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 47-year-old Man with Diffuse White Matter Disease and Rapidly Progressive Dementia
Neurol 92:e2832-e2837, Di Luca, D.G.,et al, 2019

A 65-year-old Woman with Subacute Hemiballism
Neurol 92:345-349, Cacic, K.,et al, 2019

Acute Convexity Subarachnoid Hemorrhage
Neurol 93:e524-e525, Theodorou, A.,et al, 2019

Cytotoxic Lesions of the Corpus Callosum Caused by Thermogenic Dietary Supplements
AJNR 40:1304-1308, Galnares-Olalde, J.A.,et al, 2019

Pes Cavus and Neuropathy
Neurol 93:e823-e826, Alderson,J.,& Ghosh,P.S., 2019

Bilateral Alopecia as Clue to Diagnosis of Gomez-Lopez-Hernandez Syndrome in a 38-Year-Old Man
Neurol 93:408-410, Kronlage,C.&Healy,D.G., 2019

Predicting Developmental Outcomes in Preterm Infants
Neurol 93:e1231-e1240, Cayam-Rand, D.,et al, 2019

Clinicopathologic Conference, Adenovirus Meningoencephalitis
NEJM 381:1459-1470, Case 31-2019, 2019

A Rare Case of Metachromatic Leukodystrophy with Multiple Bilateral Cranial Nerve Enhancement
Neurol 93:e1742-e1743, Sonowal, P.,et al, 2019

When MRI is a Clue in Episodic Ataxia
Neurol 93:e2074-e2075, Dhawan, S.R.,et al, 2019

GGC Repeat Expansion of NOTCH2NLC in Adult Patients with Leukoencephalopathy
Ann Neurol 86:962-968,809, Okubo, M.,et al, 2019

Lyme Disease: What the Neuroradiologist Needs to Know
AJNR 40:1998-2000, Valand, H.A.,et al, 2019

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

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

Misdiagnosis of Multiple Sclerosis
Neurol 92:15-16, Brownlee, W.J., 2018

Adult-Onset Leukoencephalopathy with Axonal Spheroids and Pigmented Glia: An MRI Study of 16 French Cases
AJNR 39:1657-1661, Codjia, P.,et al, 2018

Distinctive Imaging in a Paucisymptomatic Child with Leukodystrophy
Neruol 91:e1368-e1369, Sharawat, I.K.,et al, 2018

Selenium Toxicity Associated with Reversible Leukoencephalopathy and Cortical Blindness
JAMA Neurol 75:1282-1283, Rae, W.,et al, 2018

Clinicopathologic Conference, Pulmonary Adenocarcinoma, Complicated by a Hypercoagulable State with a Nonbacterial Thrombotic Endocarditis
NEJM, Case 33-2018, 2018

White Matter Lesion Related to Decompression Sickness Following Extreme Breath-Hold Diving
Neurol 91:847-848, Guerreiro, C.,et al, 2018

Neuronal Intranuclear Inclusion Disease Showing Intranuclear Inclusions in Renal Biopsy 12 Years Earlier
Neurol 91:884-886, Motoki, M.,et al, 2018

Neuro-Sweet Disease Presenting as Ischemic Stroke and Aseptic Meningitis
Neurol 91:e2197-e2199, Das, A.S.,et al, 2018

Cerebral Atrophy and Leukoencephalopathy in a Young Man Presenting with Encephalitic Episodes
JAMA Neurol 75:1563-1564, Xiao, F.,et al, 2018

Rapid Progression of Reversible Cognitive Impairment in an 80-year-old Man
Neurol 91:1109-1113, Bouthour, W.,et al, 2018

Clinicopathologic Conference, Vitamin C Deficiency (Scurvey), Vitamin B6 & Folate Deficiencies
NEJM 379:282-289, Case 22-2018, 2018

Alexander Disease with Features of Both Frontal and Bulbospinal Involvement
Neurol 91:e396-e397, Nam,T-S.,et al, 2018

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

Teaching NeuroImages: Acute Necrotizing Encephalopathy of Childhood
Neurol 90:e177-e178, Biswas, A.,et al, 2018

Seizures and Encephalitis in Myelin Oligodendrocyte Glycoprotein IgG Disease vs Aquaporin 4 IgG Disease
JAMA Neurol 75:65-71, Hamid, S.H.M.,et al, 2018

Multiple Sclerosis
NEJM 378:169-180, Reich, D.S.,et al, 2018

Mystery Case: A 48-year-old Woman with Bizarre Behavior, Neurologic Symptoms, and Progressive Decline
Neurol 90:242-247, Kesari, N.K.,et al, 2018

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



Showing articles 100 to 150 of 1370 << Previous Next >>