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Differential
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agraphia
akinesia
akinesia of eyelid function
alexia
alpha-fetoprotein
Alzheimer's disease, visual variant
aminoacidurias
ANA
anomic aphasia
anterior cerebral artery
anterior cerebral artery territory infarction
anterior cerebral artery, occlusion, language disorder with
aphasia
aphasia, children
aphasia, progressive, primary
aphasia, transcortical
aphasia, transcortical-sensory
apraxia
apraxia of eye movements
apraxia of eyelid closure
apraxia of eyelid opening
apraxia, constructional
apraxia, speech
arthritis
ataxia
ataxia telangiectasia
ataxia, cerebellar
ataxia, truncal
attention deficit disorder with hyperactivity
autism
automobile accidents
Benedict's solution test
bifid uvula
blepharospasm
brain biopsy
bruxism
calcification, intracranial
carcinoembryonic antigen
carcinoma
carotid artery disease
carotid artery occlusion, bilateral
carotid artery occlusion, neck
carphology
CAT scan
CAT scan, abnormal
CAT scan, emission, abnormal
cerebellar ataxia, children
cerebellar ataxia, hereditary
cerebellar degeneration
cerebral arteries, territory of
cerebral cortical atrophy
cerebral infarction
cerebral palsy
cerebral palsy, associated problems with
cerebral palsy, pure ataxic
cerebrovascular accident
cerebrovascular accident, bilateral
Charcot's sign
children
chorea
choreoathetosis
chromosomal abnormality
chromosome 11
cleft palate
Clinical Pathologic Conference(C.P.C.)
cogwheel rigidty
confusion
cortical-basal ganglionic degeneration
degenerative diseases of CNS
dementia
dementia, childhood
dementia, frontotemporal
dementia, presenile
diabetes mellitus
dinitrophenylhydrazine(D.N.P.H.)reaction
diplegia, atonic
diplegia, spastic cerebral
drooling
dysarthria
dysphagia
dysplasia of C.N.S.
dystonia
ecchymoses
electroencephalogram
encephalitis
encephalitis, viral
executive dysfunction
extrapyramidal movement disorder, progressive
eye closure
eye movement, disorders of
familial
ferric chloride test
fever
frontal lobe, pathologic signs of
gag reflex, depressed
gait disorder
gait, apraxic
gaze palsy
gaze palsy, vertical
gene
gene mutation
genetic linkage
genetic neurologic disorders
genetic testing
glabellar sign
growth retardation
handwriting
hearing problems in children
hemianopia, homonymous
hemiparesis
hypertension
hypotonia
immunodeficiency
immunosuppression
immunosuppressive agents
in situ hybridization
insular cortex
intellectual deficit
intellectual deficit, treatable causes of
intelligence quotient
jaw jerk, abnormal
karyotyping
klippel feil syndrome
language disorder in adults
language disorders in children
L-dopa
leukemia
lid
lid abnormalities
lobar atrophy
lymphoma
maple syrup urine disease
masked facies
memory, impairment of
mental retardation
microaneurysm, retinal
micrographia
midline defect in children
misdiagnosis
mortality
movement disorder
movement disorder, extrapyramidal
MRI
MRI, abnormal
MRI, serial
multiple system atrophy
mutism
myelodysplasia
myoclonus
myoclonus, stimulus sensitive
nasal speech
neglect
neurocutaneous disease
neuroendocrinology
neurologic disease, diagnoses of
neurologic examination, focal
neuropathology
neuropathology, brain
neuropathy
ocular motility, disorders of
ocular myopathy
ocular myopathy, differential diagnosis
operculum syndrome
operculum syndrome, bilateral
ophthalmoplegia
palatopharyngeal incompetence
Parkinson disease
Parkinsonism syndrome
pathology
personality change
phenylketonuria
Pick bodies
Pick's disease
pneumonia
polymerase chain reaction
posterior cortical atrophy
progeria
prognosis
progressive multifocal leucoencephalopathy
progressive neurologic disorder
progressive supranuclear palsy
pseudobulbar palsy
psychological testing, neurologic problems
psychomotor retardation
psychosis
psychosis, childhood
psychosocial aspects
ptosis
pure akinesia
radiation hypersensitivity
release phenomena
respirations in CNS disease
retropulsion
Rett's syndrome
review article
rigidity
rocking
scoliosis
seizure
seizure, advice to parents and teachers regarding
seizure, psychosocial aspects of
seizure, treatment of
semantic dementia
simultanagnosia
single photon emission computed tomography
skin, lesions in neurologic disorders
somnolence
speech disorder
speech disorder, childhood
speech, loss of
spina bifida
spinal muscular atrophy
steroid therapy, CNS treatment and complications with
stuttering
systemic lupus erythematosus
tachycardia
tauopathy
telangiectases
temporal lobe, atrophy
thrombocytopenia
urinary incontinence
urine test for metabolic disorders
visual field defect
visuospatial disturbance
walking, difficulty with
wheelchair
white matter disease
word-finding difficulty
Showing articles 0 to 50 of 599 Next >>

Clinicopathologic Conference, Posterior Cortical Atrophy with Frontotemporal Lobe Dementia with Gene Mutation
JAMA Neurol 74:114-118, , 2017

A Young Man with Progressive Language Difficulty and Early-Onset Dementia
JAMA Neurol 73:595-599, Botha, H.,et al, 2016

Infarction in the Territory of the Anterior Cerebral Artery
Neurol 51:620-622, Klatka,L.A.,et al, 1998

Identification of Brain Region for Coordianting Speech Articulation
Lancet 394:221-222, Donnan,G.A.,et al, 1997

Unusual Clinical Presentations of Cortical-Basal Ganglionic Degeneration
Ann Neurol 40:893-900, Bergeron,C.,et al, 1996

Clinicopath Conf
Progressive Multifocal Leukoencephalopathy & Systemic Lupus Erythematosus, Case 20-1995, NEJM 332:17, 3-17995., 1995

The Syndrome of'Pure Akinesia'and Its Relationship to Progressive Supranuclear Palsy
Neurol 44:1025-1029, Riley,D.E.,et al, 1994

Ataxia-Telangiectasia:An Interdisciplinary Approach to Pathogenesis
Medicine 70:99-117, Gatti,R.A.,et al, 1991

Anterior Operculum Syndrome
Neurol 39:1169-1172, Mao,C.C.,et al, 1989

Diagnostic Criteria for Rett Syndrome
The Rett Syndrome Diagnostic Criteria Work Group, Ann Neurol 23:425-4281988., , 1988

Progressive Supranuclear Palsy-Case Study
NEJM 293:346, Richardson,E.P., 1975

Pediatric Neurology
Psych Annals 2:1, , 1972

A Young Woman With Hypertonia, Severe Scoliosis, and Encephalopathy
JAMA Neurol 81:83-84, Hua,L.,et al, 2024

Multidisciplinary End-of-Life Care for a Patient with Amyotrophic Lateral Sclerosis Requesting Euthanasia
Lancet 402:484, Kruithof,W.J.,et al, 2023

Progressive Cranial Neuropathy
JAMA Neurol 80:1375-1376, Buchberger,D.S.,et al, 2023

Clinicopathologic Conference, Antiphospholipid Syndrome due to SLE with Hypocomplimentemia
NEJM 389: 2277-2285, Case 38-2023, 2023

A 47-Year-Old Man With an Upper Respiratory Infection, Acute Confusion, Dysarthria, and Ataxia
Neurol 100:978-983, Kubicki,K.,et al, 2023

Current and Emerging Issues in Wilsons Disease
NEJM 389:922-938, Roberts,E.A. & Schilsky, M.L., 2023

Clinicopathologic Conference, Noncirrhotic hyperammonemia after Roux-en-Y Gastric Bypass
NEJM 389:1221-1230, Case 30-2023, 2023

Manganese Accumulation in the Brain
NEJM 389:1320, Sherman,S.V., 2023

A 48-Year-Old Man With Spasticity and Progressive Ataxia
Neurol 101:e1747-e1752, Vizcarra,J.A.,et al, 2023

Clinicopath Conf, Chronic Salicylate Toxicity
NEJM 388:264-272, Case Record 2, 2023

Slowly rogressive Cerebellar Ataxia in a 55-Year-Old Female Patient
JAMA Neurol 80:107-108, Bernaola,M.T.,et al, 2023

A 66-Year-Old Woman With Progressive Encephalopathy and Bilateral Hearing Loss
Neurol 100:254-258, Rivers,D.,et al, 2023

A 77-Year-Old Man with Involuntary Movements, Sleep Changes, Falls, Bulbar Symptoms, and Cognitive Complaints
Neurol 99:26-30, Cao, T.Q.,et al, 2022

More Than a Little Unsteady
NEJM 387:e9, Kraft, A.W.,et al, 2022

Functional Neurological Disorders
Neurologist 27:276-289, Mishra, A. & Pandey, S., 2022

Reversible Parkinsonism Caused by Lumboperitoneal Shunt Overdrainage
Neurol 99:486-488, Takeuchi, H.,et al, 2022

An 80-Year-Old Woman with a Homonymous Hemianopsia
Neurol 99:713-717, Tajfirouz, D.,et al, 2022

COVID-19-Booster Vaccine-Induced Encephalitis
Acta Neurol Belg 122:579-581, Sluyts,Y.,et al, 2022

Confused About Confusion
NEJM 386:80-87, Spanjaart, A.M.,et al, 2022

Rare Cause of Hemiparesis and Ataxia in a 36-Year-Old Man
Neurol 98:251-255, Decker, J. & Singh, M., 2022

A Dizzy Architect
Neurol 98:543-549, Scutelnic, A.,et al, 2022

Clinicopathological Conference, Systemic Lupus Erythematosus with Antiphospholipid Syndrome
NEJM 386:1560-1570, Case 12-2022, 2022

A 37-Year-Old Man with Involuntary Movements, Gait Disturbance, and Hyperasthesia
Neurol 98:851-853, Meng, D.,et al, 2022

Sweet Syndrome
Stat Pearls www.ncbi.nlm.gov, Sept, Goyal,V.P. & Holmes,H, 2022

Miller Fisher Syndrome and Acute Motor and Sensory Axonal Neuropathy (AMSAN) Variant Guillain-Barre Overlap Syndrome (MFS/AMSAN-GBS) After Upper Respiratory Tract Infection (URTI)
Acta Sci Clin Case Reports 3:19-24, Chau,T.C. & Muhamad,N.A.N., 2022

Severe Vitamin B12 Deficiency Presenting as Pancytpenia, Hemolytic Anemia, and Parasthesia:Could Your B12 Be Any Lower?
Cureus doi:10.7759/cureus 29225, Pelling,M.M., et al, 2022

Pediatric Parainfectious Encephalitis Associated with COVID-19
Neurol 96:541-544, Gaughan, M.,et al, 2021

A 71-Year-Old Man Presenting with Acute Onset Dysarthria and Dysphagia
Neurol 96:180-184, Spagni, G.,et al, 2021

Rapidly Progressive Thalamic Dementia
Neurol 96:e809-e813, Rizzo, A.C.,et al, 2021

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

Clinicopathologic Conference, Delayed Postthypoxic Leukoencephalopathy
NEJM 384:2438-2445, Case 19-2021, 2021

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

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

A 59-Year-Old Woman Presenting with Diplopia, Dysarthria, Right-sided Weakness, and Encephalopathy
Neurol 97:e859-e864, Manzano, G.S.,et al, 2021

A 40-Year-Old Woman With Scapular Winging and Dysphonia
Neurol 97:503-507, Aladawi, M.,et al, 2021

Facial Numbness, Dysarthria, Muscle Atrophy, and Weakness in a Young Patient
JAMA Neurol 78:1273-1274, Liu, Y.,et al, 2021

A 28-Year-Old Woman with Vision Loss and an Unusual Gait
Neurol 97:e1860-e1865, Dohlman, J.C.,et al, 2021



Showing articles 0 to 50 of 599 Next >>