Neurology Specific Literature Search   
 
[home][thesaurus]
    

Differential
(Click to cross reference)
abdominal x-ray
abducens nerve paralysis
abducens nerve paralysis, bilateral
acquired immunodeficiency syndrome
acquired immunodeficiency syndrome dementia complex
acquired immunodeficiency syndrome, infants and children
Addison's disease
adducted thumb
adrenoleukodystrophy
adrenoleukodystrophy, adult onset
adrenoleukodystrophy, carrier
adrenomyeloneuropathy
adverse drug reaction
affect, flat
affect, inappropriate
aggression
akinetic mute
algorithm
aminoacidurias
amniocentesis
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, diagnosis of
amyotrophic lateral sclerosis, differential diagnosis
amyotrophic lateral sclerosis, misdiagnosis
anemia
anti Hu antibody
antibiotics
antithyroid antibodies
areflexia
arthralgia
arthritis
astrocytoma
asymptomatic
ataxia
ataxia, cerebellar
ataxic gait
attention deficit disorder with hyperactivity
autism
autoantibodies
autonomic dysfunction
Babinski sign
bacterial infection
Balint's syndrome
basal ganglia, calcification of
basilar impression
Bassen-Kornzweig syndrome
behavioral disorder
bilateral periventricular nodular heterotopia
bismuth
blindness
blood transfusion
bone biopsy
bone density
bone density, increased
bone marrow transplantation
bone pain
brain atrophy
brain biopsy
brain scan, abnormal
buphthalmos
cachexia
CAG repeats
calcification, intracranial
carcinoma
carcinoma of breast
carcinoma of lung
carcinoma of pancreas
carcinoma of stomach
cardiomyopathy
CAT scan
CAT scan, abnormal
CAT scan, brain scan compared to
CAT scan, chest
CAT scan, contrast enhanced
CAT scan, false negative
CAT scan, hare's ears sign on
cataracts
central nervous system, infection of
cerebellar atrophy, primary
cerebellar degeneration
cerebellar hypoplasia
cerebellar lesion
cerebral cortical atrophy
cerebro hepato renal syndrome
cerebrospinal fluid
cerebrospinal fluid, abnormal
cerebrospinal fluid, cytology
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, enzymes in
cerebrospinal fluid, oligoclonal IgG in
cerebrospinal fluid, pressure increased
cerebrovascular accident
Chamberlane's line
chemotherapy, CNS treatment and complications with
chest x-ray, abnormal
children
chromosomal abnormality
chromosome 28
Clinical Pathologic Conference(C.P.C.)
clinodactyly
Cockayne's syndrome
cognition
color vision
color vision, impaired
comorbidities
confusion
congenital malformation
controversies in neurology
cornea, abnormal
cornea, opacity of
corpus callosum, hypoplastic
corpus callosum, lesion of
cortical blindness
cost effectiveness
counselling
cranial nerve palsies
cranial neuropathy, multiple
creatine phosphokinase(CPK)elevated
crying, pathologic
cultured skin fibroblasts
cyst, arachnoid, infant
cyst, benign intracranial
cyst, porencephalic
Danon disease
deafness
decerebrate posture
degenerative diseases of CNS
dementia
dementia, childhood
dementia, presenile
dementia, rapidly progressive
demyelinating disease
depression
developmental evaluation
developmental milestones, loss of
developmental retardation
diabetes insipidus
diarrhea
differential diagnosis
digits, abnormal
diplopia
disability, neurological
disorientation
dizziness
DNA probes
drug induced neurologic disorders
dwarfism
dysarthria
dysmorphic
dysphagia
dystonia
ear, abnormal
electroencephalogram
electroencephalogram, abnormalities of
electron microscopy
electronystagmography
electroretinograph
encephalitis
encephalitis, autoimmune
encephalomyelitis
encephalopathy
evoked potentials
exome sequencing
eye movement, disorders of
face, elongated
facial appearance, abnormal
facial nerve palsy
facial nerve palsy, bilateral
facial nevus
facial weakness
familial
fetus
fever
fontanel, bulging
Fragile-X associated tremor/ataxia-syndrome
fragile-X syndrome
fragile-X syndrome, carrier
frontal lobe, pathologic signs of
fundus, abnormality of
gait disorder
gamma amino butyric acid receptor antibody
gaze palsy
gaze palsy, supranuclear
gender
gene
gene mutation
genetic counselling
genetic diagnosis, prenatal
genetic linkage
genetic neurologic disorders
genetic screening
genetic testing
genital ulcerations
gingival hyperplasia
gingivitis
glaucoma
granulomatous disease
grasp reflex
growth retardation
Guillain Barre syndrome
gum disease
Hallervorden Spatz disease
Hand-Schuller-Christian disease
head circumference
head injury
head injury, prognosis in
headache
hearing loss
hearing problems in children
hemiatrophy
hemiparesis
hemoglobin abnormality, neurologic complications of
hepatomegaly
hepatosplenomegaly
heralding manifestation
heterotopia
hippocampus, hyperintense
hirsutism
hoarseness
Hodgkin's disease, neurologic involvement with
hydrocephalus
hydrocephalus, congenital
hydrocephalus, fetal
hydrocephalus, intrauterine
hydrocephalus, normal pressure
hyperactivity
hyperostosis
hyperostosis corticalis generalisata familiaris
hyperpigmentation of skin
hypocalcemia
hypoglycorrhachia
hypoparathyroidism, idiopathic
hypotonia
imbalance
immunohistochemistry
immunosuppressive agents
inattention
inborn errors of metabolism
inclusion bodies
inclusion bodies, intranuclear
infantile spasm
infertility
intellectual deficit
intellectual deterioration
intelligence quotient
intestinal biopsy
intracranial hemorrhage
intracranial pressure, increased
intrathecal chemotherapy
irritability
joint hypermobility
karyotyping
Kearns-Sayre syndrome
Laurence-Moon-Bardet-Biedl syndrome
learning disability
learning disability, in children
leukodystrophy
leukoencephalopathy
leukoencephalopathy, differential diagnosis
life expectancy
limbic encephalitis
limbic system
lissencephaly
Lowe's syndrome
lung biopsy
lymphadenopathy
lymphadenopathy, hilar
lymphocyte fingerprint profiles
lymphoma
lymphoma involving CNS
macrocephaly
macular degeneration
malformation, CNS, congenital
melanoma, malignant
memory, defect of recent
memory, impairment of
meningeal enhancement
meningismus
meningitis
meningitis, aseptic
meningitis, carcinomatous
meningitis, chronic
meningitis, granulomatous
meningitis, lymphomatous
meningitis, rheumatoid
meningoencephalitis
mental retardation
mental retardation, etiology of
mental retardation, familial
mental status, abnormal
metabolic acidosis
metabolic disorder, primary
metabolic disorder, primary-screening tests
microcephaly
middle cerebellar peduncle
middle cerebellar peduncle, lesion
middle cerebellar peduncle, lesion, bilateral
Mini Mental Status Examination
misdiagnosis
molecular genetics
mortality
motor neuron disease
movement disorder
movement disorder, extrapyramidal
MRI
MRI, abnormal
MRI, contrast enhanced
MRI, diffusion weighted
MRI, spinal cord
mucopolysaccharidoses
multinucleated giant cell
multiple system atrophy
muscle biopsy
muscle pain
muscle weakness, proximal
muscular dystrophy
muscular dystrophy, Becker
myelogram
myelomalacia
myelopathy
myoclonic jerks
myoclonus
myopathy
myopathy, mitochondrial
myopia
nausea and vomiting
neck pain
necrotizing granuloma
neonatal screening, genetic neurologic disorders
neoplasm, primary of CNS
nerve biopsy
nerve conduction studies
neuroendocrinology
neurofibromatosis 1
neurologic complications of, systemic cancer
neurologic complications of, systemic disease
neurologic disease
neurologic disease, diagnoses of
neurologic evaluation
neurologic examination
neurologic testing
neuronal ceroid-lipofuscinosis
neuronal migration disorder
neuropathology
neuropathology, brain
neuropathy
neuropathy, hereditary peripheral
neuropathy, motor, multifocal
neuropathy, peripheral
neurotoxic
neurotoxin
nevus
night blindness
nystagmus
obesity
old age, neurology of
oligophrenin 1
ophthalmoplegia
opportunistic infection
opportunistic infection, CNS
optic atrophy
optic atrophy, infants
optic foramina
optic foramina, abnormal
optic nerve
optic neuropathy
osteolytic lesion, causes of
osteopetrosis
ovarian insufficiency
Paget's disease
pain
pain, back
papilledema
paraparesis
paraparesis, familial spastic
paraparesis, spastic
Parkinsonism syndrome
paroxysmal nonkinesigenic dyskinesia
PAS positive
peroxisomal disease
peroxisomes
perseveration
personality change
phakomatoses
photosensitivity, skin
pigmentary retinopathy
pineal, shifted
pituitary stalk
pituitary stalk, lesion of
pituitary, enlargement
pituitary, lesion of
PLEDs
PLEDs, bilateral independent
PLEDs, etiology of
pleocytosis of cerebrospinal fluid
pleural effusion
pneumoencephalogram(PEG)
pneumothorax
polymerase chain reaction
port wine nevus
posterior fossa, mass of
practice guidelines
precocious puberty
prenatal diagnosis by amniocentesis
prognosis
progressive neurologic disorder
pseudarthrosis
pseudobulbar palsy
psychiatric disorder
psychological testing
psychomotor retardation
pulmonary infiltrates
pulmonary nodules
pupil, abnormality in neurologic disorders
quadriparesis
quadriplegia
rapidly progressing neurologic illness
rash
refractive errors
Refsum's disease
remote effect of cancer on the nervous system
respirations in CNS disease
reticulum cell sarcoma
retinal degeneration
retinal lesion
retinal tumor
retinitis pigmentosa
retinopathy
Rett's syndrome
review article
rheumatoid arthritis
rheumatoid arthritis factor(R.A.factor)
rheumatoid arthritis, neurologic complications of
rickets
rigidity
root lesion, nerve
sarcoidosis
sarcoidosis, CNS
sarcoma
scoliosis
screening
seizure
seizure, children
seizure, familial
seizure, neonatal
sensorineural hearing loss
serologic testing
short stature
shunt procedure, ventricular
shunt procedure, ventriculo-atrial
simian crease
sinuses, diseases of
skin, biopsy
skin, darkening of
skin, lesions in neurologic disorders
skull fracture
skull x-ray
skull x-ray, abnormal
skull x-ray, bony defect on
somatosensory evoked potentials
Southern immunoblot test
speech, delayed development of
spinal cord, lesion of
spinal cord, pathologic exam of
spinocerebellar degeneration
splenium of corpus callosum
splenomegaly
steroid therapy, CNS treatment and complications with
stimulant drugs
Sturge-Weber syndrome
subdural hematoma
subdural hematoma, bilateral
symmetric brain lesions
syndactyly
systemic illness
tandem gait, ataxic
tantrum
tapetoretinal degeneration
temporal lobe
temporal lobe, lesion
temporal lobe, lesion, bilateral
term infant
testicular enlargement
thalassemia
thalassemia/mental retardation syndrome
thrombocytopenia
tinnitus
toxins, nervous system
toxoplasmosis, CNS
transilumination of skull
treatment of neurologic disorder
tremor
tremor, intention
tremor, postural
tremor, writing
trinucleotide repeats
tuberous sclerosis
Turner's syndrome
ultrasonography
urinary incontinence
Usher's syndrome
uveitis
vertigo
very long chain fatty acids
Virchow-Robin spaces, dilated
visual acuity, decreased
visual field defect
visual loss
weight loss
West disease
Whipple's disease
white matter disease
Wood's light
workup
writing
X-linked bulbospinal neuronopathy
x-linked hydrocephalus
x-linked intellectual deficit
X-linked lissencephaly
x-linked mental retardation
Showing articles 250 to 300 of 5980 << Previous Next >>

Diet Quality is Associated with Disability and Symptom Severity in Multiple Sclerosis
Neurol 90:e1-e11, Fitzgerald, K.C.,et al, 2018

Practice Guide Update Summary: Mild Cognitive Impairment
Neurol 90:126-135, Petersen, R.C.,et al, 2018

Persistent Postural-Perceptual Dizziness (PPPD): A Common, Characteristic and Treatable Cause of Chronic Dizziness
Pract Neurol 18:5-13, Popkirov, S.,et al, 2018

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

The Parkinson Pandemic - A Call to Action
JAMA Neurol 75:9-10, Dorsey, E.R. & Bloem, B.R., 2018

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

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

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

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

Toxidrome Recognition in Chemical - Weapons Attacks
NEJM 378:1611-1620, Ciottone, G.R., 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

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

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

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

Wilson Disease
NIDDK Oct2018, , 2018

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

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

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

MRI of the Swallow Tail Sign: A Useful Marker in the Diagnosis of Lewy Body Dementia?
AJNR 38:1737-1741, Shams, S.,et al, 2017

Paraneoplastic and Autoimmune Encephalitis
UptoDate July, Dalmau, 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

Diagnosis and Management of Dementia with Lewy Bodies
Neurol 89:88-100, McKeith, I.G.,et al, 2017

Clinicopathologic Conference, Advanced AIDS Complicated by HSV-1 Encephalopathy. Basal-Cell Carcinoma. Kaposis Sarcoma.
NEJM 376:2580-2589, Case 20-2017, 2017

A New Potential Biomarker for Dementia with Lewy Bodies
Neurol 89:318-326, Donadio, V.,et al, 2017

Amyotrophic Lateral Sclerosis
NEJM 377:162-172, Brown, R.H.,et al, 2017

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

Autoimmune Encephalitis: Pathophysiology and Imaging Review of an Overlooked Diagnosis
AJNR 38:1070-1078, Kelley, B.P.,et al, 2017

Intractable Epilepsy and Progressive Cognitive Decline in a Young Man
JAMA Neurol 74:737-740, Cohen, A.L.,et al, 2017

A Child with Delayed Motor Milestones and Ptosis
Neurol 88:e158-e163, Ghosh, P.S., 2017

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

Outcomes after Diagnosis of Mild Cognitive Impairment in a Large Autopsy Series
Ann Neurol 81:549-559, Abner, E.L.,et al, 2017

Clinical Manifestations of the anti-IgLON5 Disease
Neurol 88:1736-1743,1688, Gaig, C.,et al, 2017

Clinical and Neuroimaging Features in Gorlin-Goltz Syndrome
Neurol 88:e52-e54, da paz Oliveira, G.,et al, 2017

Spontaneous Subarachnoid Haemorrhage
Lancet 389:655-666, Macdonald, R.L. & Schweizer, T.A., 2017

Characteristics in Limbic Encephalitis with Anti-Adenylate Kinase 5 Autoantibodies
Neurol 88:514-524,508, Do, L. & Chanson, E., 2017

Professional Football may be Linked to Brain Injuries Usually Seen in Boxing
BMJ 356:j811, Hawkes, N., 2017

Personality Changes, Executive Dysfunction, and Motor and Memory Impairment
JAMA Neurol 74:245-246, Lopez Chiriboga, A.S.,et al, 2017

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

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

Sugar- and Artificially Sweetened Beverages and the Risks of Incident Stroke and Dementia
Stroke 48:1139-1146, Pase, M.P.,et al, 2017

Primary Angiitis of the Central Nervous System
Stroke 48:1248-1255, Boulouis, G.,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

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

A Woman with Intellectual Disability, Amenorrhoea, Seizures, and Balance Problems
JAMA Neurol 73:1494-1495, Hughes, A.J.C.,et al, 2016

Neurologic Signs and Symptoms Frequently Manifest in Acute HIV Infection
Neurol 87:148-154, Hellmuth, J.,et al, 2016



Showing articles 250 to 300 of 5980 << Previous Next >>