Neurology Specific Literature Search   
 
[home][thesaurus]
    

Differential
(Click to cross reference)
abdominal protrusion
abortion, spontaneous
acanthocytosis
agenesis of aqueduct of Sylvius
alpha-fetoprotein
aneurysm
aneurysm, asymptomatic
aneurysm, intracranial
angiography, cerebral
aniridia
anterior tibial muscle weakness
antibodies to voltage-gated calcium channels
apraxia of eye movements
aqueduct of Sylvius, stenosis
aqueductal stenosis
areflexia
arenavirus
ataxia
ataxia telangiectasia
ataxia, cerebellar
ataxia, congenital
ataxia, paroxysmal
ataxia, sensory
ataxia, truncal
ataxic gait
bacterial endocarditis, neurologic manifestations of
Balint's syndrome
Bassen-Kornzweig syndrome
blindness
blindness, sudden
blood cultures
blue tongue virus
brain biopsy
brainstem, atrophy
brainstem, lesion of
bulbar palsy
bulbar palsy, progressive
calcification, intracranial
calcification, periventricular
calcium channel dysfunction
carcinoembryonic antigen
carcinoma
CAT scan
CAT scan, abnormal
CAT scan, emission
CAT scan, emission, abnormal
cataracts
cataracts, congenital
central core disease
central nervous system, infection of
cerebellar ataxia, children
cerebellar ataxia, hereditary
cerebellar ataxia, primary
cerebellar atrophy, primary
cerebellar atrophy, secondary
cerebellar degeneration
cerebellar hypoplasia
cerebellar infarction
cerebellar lesion
cerebellar vermis
cerebral cortical atrophy
cerebral embolism
cerebral infarction
cerebral infarction, hemorrhagic
cerebral ischemia
cerebral palsy
cerebrospinal fluid
cerebrospinal fluid, abnormal
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, gammaglobulin of
cerebrospinal fluid, oligoclonal IgG in
cerebrospinal fluid, red cells in
cerebrovascular accident
cerebrovascular accident, bilateral
children
chloride channel dysfunction
chorea
choreoathetosis
chorioretinitis
chromosomal abnormality
chromosome 11
Clinical Pathologic Conference(C.P.C.)
Coats syndrome
Cockayne's syndrome
coma
congenital infection, CNS
congenital infection, viral
congenital malformation
congenital myopathy
congenital paresis
consanguinity
contactin associated protein like 1 antibodies
contactin associated protein like 1 auto antibodies.(CNTN1)
cornea, abnormal
cyst
cyst, parenchymal
cyst, porencephalic
cyst, subcortical
Dandy Walker malformation
Dandy Walker malformation, adult
deafmute
deafness
degenerative diseases of CNS
dementia
dental procedure, neurologic complications with
diabetes mellitus
difficulty climbing stairs
distal muscle weakness
drooling
dwarfism
dysarthria
dysphagia
dyspnea
dystonia
electroencephalogram, abnormalities of
electromyogram
electron microscopy
embolism
embolism, septic
embolism, systemic
embryogenesis
encephalitis
encephalitis, viral
encephalopathy
endocarditis
endocarditis, neurologic manifestations with
endocarditis, subacute bacterial
endovascular therapy
eye movement, disorders of
facial weakness
facial weakness, bilateral
facioscapulohumeral syndrome
familial
familial hemiplegic migraine
fever
fibrillations
foot deformity
foot drop
Friedreich's ataxia
gait disorder
gait, spastic
gammaglobulin therapy, intravenous, refractory
gargoylism
gene
gene mutation
genetic linkage
genetic neurologic disorders
Gillespie syndrome
glaucoma
growth retardation
Hallgren's syndrome
hand flapping
head circumference
headache
hearing loss
heart block
hematoma, intracerebral
hepatosplenomegaly
herpes simplex virus
histochemistry of muscle
Hurler's syndrome
hydranencephally
hydrocephalus
hydrocephalus, congenital
hydrocephalus, non-communicating(obstructive)
hydrocephalus, treatment of
hypokalemic periodic paralysis
hypotonia
immunodeficiency
immunohistochemistry
immunosuppression
incoordination
influenza A virus
intellectual deterioration
intracerebral hemorrhage
intrauterine
intrauterine infection
intrauterine infection, viral
intrauterine infection, viral of CNS
iris, abnormal
jittery baby
juvenile paresis
Kearns-Sayre syndrome
keratoconus
Laurence-Moon-Bardet-Biedl syndrome
leukemia
lid closure, weakness of
lymphocytic choriomeningitis
lymphoma
maculopathy
malformation, CNS, congenital
malignant hyperpyrexia
Marinesco-Sjogren syndrome
mental retardation
microcephaly
migraine
migraine, hemiplegic
mimics
misdiagnosis
mitral valve lesion
mitral valve prolapse
mitral valve regurgitation
monoclonal gammopathy
mortality
movement disorder
movement disorder, extrapyramidal
MRI
MRI, abnormal
mucopolysaccharidoses
multiple system atrophy
mumps virus
muscle biopsy
muscle weakness
muscle weakness, proximal
muscular dystrophy
muscular dystrophy, differential diagnosis of
muscular dystrophy, facioscapulohumeral
myasthenic syndrome
mycotic aneurysm
myelomalacia
myeloschisis
myoclonic jerks
myoclonus, epilepsy
myopathy
myopia
myotonia congenita
nausea and vomiting
neck pain
nemaline rod myopathy
nemaline rod myopathy, adult onset
neonatal infection, viral
neuritis
neurocutaneous disease
neuroendocrinology
neurologic disease
neurologic disease, diagnoses of
neurologic signs
neuropathology
neuropathology, brain
neuropathy
neuropathy, autoimmune
nodopathy, autoimmune
nystagmus
obesity
occipital lobe, infarction
occipital lobe, infarction, bilateral
ocular motility, disorders of
ocular myopathy
old age, neurology of
optic ataxia
pachygyria
pain, neuropathic
papilledema
paramyotonia congenita
paraspinal muscle
paraspinal muscle weakness
parietal lobe, infarction
paroxysmal neurologic deficits
parvovirus
pathology
periodic paralysis
personality change
pleocytosis of cerebrospinal fluid
polydactyly
Poretti-Boltshauser syndrome
posterior cerebral artery occlusion
posterior fossa, lesion of
potassium channel antibodies
potassium channel dysfunction
progeria
prognosis
progressive neurologic disorder
pseudoaneurysm
pseudoretinitis pigmentosa
psychiatric disorder
psychomotor retardation
radiation hypersensitivity
rapidly progressing neurologic illness
respiratory failure
retinal degeneration
retinitis pigmentosa
retinopathy
review article
rituximab
rubella encephalitis
rubella encephalitis, progressive
rubella syndrome
rubella virus
rubeola virus
schizophrenia
seizure
serologic testing
serologic testing of cerebrospinal fluid
shunt procedure, ventricular
shunt procedure, ventriculo-peritoneal
simultanagnosia
skin, lesions in neurologic disorders
sloped shoulders
slow virus infection of CNS
sodium channel dysfunction
spasticity
Spielmeyer Vogt syndrome
spinal muscular atrophy
spinocerebellar ataxia
spinocerebellar ataxia type 6
standing difficulty
stem cell transplantation
stooped posture
subacute sclerosing panencephalitis(S.S.P.E.)Dawson's disease
subarachnoid hemorrhage
superior cerebellar artery infarction
sweating
telangiectases
teratogenesis
teratogenesis, viral
thrombectomy
thyroiditis
titubation
transplacental virus infections
transverse smile
treatment of neurologic disorder
unconsciousness
urinary incontinence
Usher's syndrome
vasculitides
vertigo
viral infection
viral infection, CNS
viral isolation
virus, slow
visual field defect
visual fields, constricted
visual loss
walking, difficulty with
weakness
weakness, progressive
weakness, proximal
weight loss
wheelchair
white matter disease
wide based gait
winging of scapula
Showing articles 150 to 200 of 2289 << Previous Next >>

Brain and Skin Involvement in Erdheim-Chester Disease
Neurol 96:e1590-e1592, Budhram, A.,et al, 2021

Cervical Spondylotic Myelopathy Secondary to Ochronotic Vertebral Arthropathy
Neurol 96:627-628, Pinto, W.,et al, 2021

A Triad of Tremor, Ataxia, and Cognitive Impairment
Neurol 96:e1802-e1803, Au, L.W.C.,et al, 2021

Clinicopathologic Conference, Normal Pressure Hydrocephalus
NEJM 384:1350-1358, Case 10-2021, 2021

A 7-Year-Old Boy with Acute-Onset Altered Mental Status
Neurol 96:e2774-e2778, Wong, G.J.,et al, 2021

A 71-Year-Old Man with Horizontal Gaze Palsy, Anarthria, and Quadriparesis
Neurol 96:1146-1150, Cheema, I.,et al, 2021

A 29-Year-Old Man with Fevers and Rapidly Progressive Cranial Neuropathies
Neurol 97:95-98, Dessy, A.,et al, 2021

A 13-Year-Old Boy with Subacute-Onset Spastic Gait
JAMA Neurol 78:e1-e2, Xie, N.,et al, 2021

Clinicopathologic Conference, Cerebellar Ataxia, Neuropathy and Vestibular Areflexia Syndrome
NEJM 385:165-175, Case 20-2021, 2021

Progressive Ataxia and Doenbeat Nystagmus in an Adult
JAMA Neurol 78:1018-10019, Fernandez, A.C.,et al, 2021

Immunocompetent Patient with Multiple Cranial Nerve Palsies, Ataxia, and Cognitive Decline
Neurol 94:e225-e229, Nigam, M.,et al, 2020

Acute Ischemic Stroke in Adolescents
Neurol 94:e158-e169, Rambaud, R.,et al, 2020

Feasibility, Safety, and Outcome of Endovascular Recanalization in Childhood Stroke
JAMA Neurol 77:25-34, Sporns, P.B.,et al, 2020

Rapidly Progressive Gait Disorder and Cranial Nerves Involvement in a 9-year-old boy
Neurol 94:e330-e334, Lipp, A.,et al, 2020

Duchenne Muscular Dystrophy
BMJ 368:L7012, Fox, H.,et al, 2020

Palatal Myoclonus, Abnormal Eye Movements, and Olivary Hypertrophy in GAD65-Related Disorder
Neurol 94:273-275, Macaron, G.,et al, 2020

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

A 59-year-old Woman with Multiple Myeloma and Lower Extremity Weakness and Numbness
Neurol 94:794-800, Gadot, R.,et al, 2020

Balance, Falls, and Hearing Loss: Is It Time for a Paradigm Shift?
JAMA Otolaryngol Head Neck Surg doi:10.1001/JAMAoto.2020.0415, Lubetzky, A.V., 2020

Homonymous Hemianopia with Normal Magnetic Resonance Imaging
JAMA Ophthalmol doi:10.1001/JAMAOphthalmol.2020.0447, Cai, S.,et al, 2020

A 47-year-old Man with Rapidly Progressive Ataxia and Vitiligo
Neurol 94:e1664-e1669, Han, F.,et al, 2020

Rapid Progression of Prion Disease Associated with Transverse Myelitis
Neurol 94:e1670-e1672, Hussein, O.,et al, 2020

Clinicopathologic Conference, AA Amyloidosis, Complicated by Cerebral Mucormycosis
NEJM 382:1457-1466, Case 11-2020, 2020

Ondine Curse Syndrome Cause by Dorsolateral Medullary Stroke
Neurol 94:e1557-e1558, Fiedler, E. & Gill, R., 2020

Progressive Ataxia and Palatal Tremor
Neurol 94:e1445-e1447, Pradeep, S.,et al, 2020

A 45-Year-Old Man with Progressive Insomia and Psychiatric and Motor Symptoms
Neurol 94:e1213-e1218, Lima, J.E.E.,et al, 2020

A 42-year-old Woman with Progressive Cognitive Difficulties and Gait Imbalance
Neurol 94:e1219-e1226, Slama, M.C.C.,et al, 2020

A 16-year-old Girl with Ataxia, Oscillopsia, and Behavioral Changes
Neurol 94:713-717, Silverman, A.,et al, 2020

Wall-Eyed Bilateral Internuclear Ophthalmoplegia by Ischemic Stroke
Neurologist 25:82-84, Uzawa, A.,et al, 2020

Pernicious Anaemia
BMJ 369:m1319, Mohamed, M.,et al, 2020

Functional Gait Disorders
Neurol 94:1093-1099, Nonnekes, J.,et al, 2020

Complex Ataxia
Neurol 95:136-141, Abkur, T.,et al, 2020

Burning Pain in the Legs
NEJM 383:e18, Sacks, C.A., 2020

Clinicopathologic Conference, HIV Type 2 Infection & Cerebral Toxoplasmosis
NEJM 383:859-866, Case 27-2020, 2020

An Adolescent Girl Presenting with Worsening Vertigo, Headache, and Ataxia
Neurol 95:e1760-e1763, Brigham, E.,et al, 2020

Opsoclonus in Anti-Ma2 Brain-Stem Encephalitis
NEJM 383:e84, Sacks, C.A.,et al, 2020

A 57-Year-Old Woman with Progressive Ataxia and Falls
Neurol 95:650-656, Badahdah, A., 2020

Sensory Ganglionopathy
NEJM 383:1657-1662, Amato, A.A. & Ropper, A.H., 2020

Hypointensity of the Basal Ganglia in Adults with Glucose Transporter Protein Type 1 Deficiency Syndrome: A Novel Magnetic Resonance Imaging Finding
Ann Neurol 87:10-11, Van Samkar, A.,et al, 2020

A 72-year-old Man with a Progressive Cognitive and Cerebellar Syndrome
Neurol 95:e2707-e2710, Lad, M. & Griffiths, T.D., 2020

Bithalamic Lesions
Stroke 51:e355-e358, Chen, P.M.,et al, 2020

Clinical features, prognostic factors, and antibody effects in anti-mGluR1 encephalitis
Neurol 95:e3012-e3025, Spatola, M.,et al, 2020

Clinicopathologic conference, Vitamin D deficiency
NEJM 383:2462-2470, Case 39-2020, 2020

Cyclic Vomiting Syndrome in Children
AJGH 2:doi:10.33552/AJGH.2020, Al-Ansari, N., 2020

Progressive Proximal Weakness in a 61-Year-Old Man
Neurol 98:122-127, Yu, M.,et al, 2020

Vessel Wall MR Imaging for the Detection of Intracranial Inflammatory Vasculopathies
Cardiovasc Diagn Ther 10:1108-1119, Edjlali,M.,et al, 2020

Paraoxysmal Tonic Upgaze in Children, Three Case Reports and a Review of the Literature
Pediatr Emer Care 35:e67-e69, Kartal,A., 2019

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

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

Challenging Diagnosis of Gerstmann-Straussler-Scheinker Disease
Neurol 92:101-103, Kang, M.J.,et al, 2019



Showing articles 150 to 200 of 2289 << Previous Next >>