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Differential
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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 200 to 250 of 2289 << Previous Next >>

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

Leg Weakness and Stiffness at the Emergency Room
Neurol 92:e622-e625, af Edholm, K.,et al, 2019

Fibromuscular Dysplasia and Its Neurologic Manifestations
JAMA Neurol 76:217-226, Touze, E.,et al, 2019

A 54-year-old man with Dyspnea and Muscle Weakness
Neurol 92:e1136-e1140, Chertcoff, A.,et al, 2019

Management of Stroke in Neonates and Children
Stroke 50:e51-e96, Ferriero, D.M.,et al, 2019

Toxic Diffuse Isolated Cerebellar Edema from Over-the-Counter Health Supplements
Neurol 92:965-966, Kim, D.D.,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

Antiepileptic Drug Treatment Patterns in Women of Childbearing Age with Epilepsy
JAMA Neurol 76:783-790, Kim, H.,et al, 2019

Risk of 23 Specific Malformations Associated with Prenatal Exposure to 10 Antiepileptic Drugs
Neurol 93:e167-e180, Blotiere, P.O.,et al, 2019

Kelch-Like Protein 11 Antibodies in Seminoma-Associated Paraneoplastic Encephalitis
NEJM 381:47-54, Mandel-Brehm, C.,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

Declining Malformation Rates with Changed Antiepileptic Drug Prescribing, An Observational Study
Neurol 93:e831-e840, Tomson,T.,et al, 2019

Characteristic Head Jerks in Congenital Oculomotor Apraxia due to Joubert Syndrome
Neurol 93:e1125-e1126, Borngraber, F.,et al, 2019

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

Stridor in Multiple System Atrophy
Neurol 93:630-639, Cortelli, P.,et al, 2019

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

A 55-Year-Old Woman Presenting with Ataxia and Numbness 1 Year After Ileum Resection
Neurol 93:675-679, Cassano, V.,et al, 2019

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

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

Clinicopathologic Conference, Creutzfeldt-Jakob Disease
NEJM 381:1569-1578, Case 32-2019, 2019

Progressive Neurological Impairment and an Enhancing Brainstem Lesion in a Middle-Aged Man
JAMA Neurol 76:1397-1398, Gupta, S.,et al, 2019

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

Muscular Dystrophies
Lancet 394:2025-2038, Mercuri, E.,et al, 2019

Orofacial Dyskinesia in a Young Man
JAMA Neurol 76:1517-1518, Tian, X.,et al, 2019

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

Pediatric HIV Infection: Classification, Clinical Manifestations, and Outcome
www.UptoDate.com, June, Gillespie, S.L., 2018

Bilateral Cavernous Carotid Aneurysms: Atypical Presentation of a Rare Cause of Mass Effect
Front Neurol doi:10.3389/fneur.2018.0069, Gagliardi, D.,et al, 2018

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

Heart Transplantation in a Patient with Myotonic Dystrophy Type 1 and End-Stage Dilated Cardiomyopathy: A Short Term Follow-up
Acta Myologica 37:267-271, Papa, A.A.,et al, 2018

Congenital Asymmetric Crying Facies Syndrome, A Case Report
Medicine 97:31(e11403), Liang,X. & He,B., 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

The Laser Shoes
Neurol 90:e164-e171, Barthel, C.,et al, 2018

Recurrent Dysarthria and Ataxia in a Young Girl
JAMA Neurol 75:125-126, Romba, M.,et al, 2018

Clinical Reasoning: Siblings with Progressive Weakness, Hypotonia, Nystagmus, and Hearing Loss
Neurol 90:e625-e631, Set, K.K.,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

Subacute Paresis in a 28-year-old man with HIV
Neurol 90:432-435, Harada, Y.,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

Long-Term Risk of Hemorrhagic Stroke In Young Patients with Congenital Heart Disease
Stroke 49:1155-1162, Giang, K.W.,et al, 2018

A 60-year-old woman with ataxia
Neurol 90:e1627-e1630, Dandapat, S.,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

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

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

Dyke-Davidoff-Masson syndrome
Neurol 90:e2097-e2098, Durcan, R.,et al, 2018

IgLON5-mediated neurodegeneration is a differential diagnosis of CNS Whipple disease
Neurol 90:1113-1115, Morales-Briceno, H.,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

Progressive Weakness and Memory Impairment in a Middle-aged Man
JAMA 320:197-198, DeFilippis, E.M.,et al, 2018



Showing articles 200 to 250 of 2289 << Previous Next >>