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Differential
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acalculia
agenesis of corpus callosum
akinesia of eyelid function
alien hand syndrome
alpha-fetoprotein
aphasia
aphasia, progressive, primary
applause sign
apraxia
apraxia of eye movements
apraxia of eyelid opening
apraxia, constructional
areflexia
arm swing, reduced
ataxia
ataxia telangiectasia
ataxia, cerebellar
ataxia, truncal
ataxic gait
automobile accidents
Balint's syndrome
basilar artery
basilar artery occlusion
behavioral disorder
biologic markers
blepharospasm
border zone infarct
bradykinesia
bradyphrenia
brainstem, infarction of
carcinoembryonic antigen
carcinoma
CAT scan, abnormal
CAT scan, emission, abnormal
cerebellar ataxia, children
cerebellar ataxia, hereditary
cerebellar ataxia, primary
cerebellar degeneration
cerebellar hypoplasia
cerebellar lesion
cerebral cortex
cerebral cortical atrophy
cerebral embolism
cerebrovascular accident
cerebrovascular accident, agitated delirium following
Charcot's sign
children
chorea
choreoathetosis
chromosomal abnormality
chromosome 11
cirrhosis
Clinical Pathologic Conference(C.P.C.)
cogwheel rigidty
Collier's sign
confusion
congenital ocular motor apraxia
convergence, impaired
cortical blindness
cortical-basal ganglionic degeneration
crying
cyst
cyst, parenchymal
cyst, subcortical
degenerative diseases of CNS
delay in diagnosis
dementia
dementia, age at onset
developmental milestones, loss of
developmental retardation
diabetes mellitus
diagnostic criteria
diplopia
disconnection syndrome
downward gaze
drooling
dysarthria
dyskinesia, buccal lingual facial
dysphagia
dyspraxia
dystonia
electroencephalogram, abnormalities of
electron microscopy
embolism
embolism, vertebral-basilar artery
enzyme, defect
extrapyramidal movement disorder, progressive
eye movement, disorders of
falling
familial
fine motor function, impaired
finger nose finger test
fourth ventricle, enlargement of
frontal behavioral spatial syndrome
gait disorder
gait, apraxic
Gaucher's disease
gaze palsy
gaze palsy, horizontal
gaze palsy, supranuclear
gaze palsy, vertical
gene
gene mutation
genetic linkage
genetic neurologic disorders
glabellar sign
glucocerebrosidase
growth retardation
hallucination
hallucination, visual
hand flapping
head jerks
headache
hepatic encephalopathy
heralding manifestation
hyperreflexia
hyponatremia
hypophonia
hypotonia
ideomotor apraxia
imbalance
imbalance, postural
immunodeficiency
immunosuppression
inattention
inclusion bodies
inclusion bodies, intracytopasmic
incoordination
irritability
jaw jerk, abnormal
Joubert syndrome
L-dopa
leukemia
levitation
Lewy body
Lewy body disease, diffuse
lymphoma
masked facies
meningitis
mental retardation
mesencephalic artery syndrome
metamorphopsia
midbrain
midbrain, atrophy
midbrain, infarction of
mild cognitive impairment
misdiagnosis
molar tooth sign
mortality
movement disorder
movement disorder, extrapyramidal
MRI
MRI, abnormal
MRI, abnormal, seizure causing
MRI, diffusion weighted
multiple system atrophy
myoclonic jerks
myopia
neurocutaneous disease
neuroendocrinology
neurologic disease, diagnoses of
neurologic disease, tempo
neurologic signs
neuroophthalmology
neuropathology
neuropathology, brain
neuropathy
nystagmus
occipital lobe, infarction
occipital lobe, infarction, bilateral
occipital lobe, lesion of
ocular motility, disorders of
ocular myopathy
ocular myopathy, differential diagnosis
ophthalmoplegia
optokinetic nystagmus, abnormal
Parkinson disease
Parkinson disease, atypical
Parkinson disease, axial symptoms
Parkinson disease, dementia with
Parkinson disease, L-dopa nonresponsive
Parkinson disease, tremor, absence of
Parkinsonism syndrome
pathology
peduncular hallucinosis
penguin silhouette sign
personality change
Poretti-Boltshauser syndrome
posterior cortical atrophy
preclinical
pretectal area
pretectal syndrome
progeria
prognosis
progressive neurologic disorder
progressive supranuclear palsy
pseudoabducens palsy
pseudobulbar palsy
psychomotor retardation
ptosis
pupil, ectopic-acquired
radiation hypersensitivity
reading disorder, acquired
reading problem, causes of
REM sleep
retinal degeneration
retrocollis
retropulsion
review article
rigidity
rigidity, axial
saccadic eye movements
saccadic eye movements, abnormal
salivation, excessive
seizure, nonconvulsive
seizure, occipital lobe
sensory loss
sensory loss, cortical
sequencing difficulty
simultanagnosia
sinemet
single photon emission computed tomography
skew deviation
skin, lesions in neurologic disorders
spinal muscular atrophy
status epilepticus, nonconvulsive
strabismus
suck, poor
superior cerebellar peduncle
symmetric brain lesions
tau protein
tauopathy
telangiectases
thalamoperforating arteries
titubation
top of the basilar syndrome
treatment of neurologic disorder
tremor
upgaze, paralysis of
vision, blurred
visual impairment
visual symptoms
visuospatial disturbance
walking, difficulty with
wheelchair
wide based gait
WORLD spelling test
Showing articles 400 to 450 of 2319 << Previous Next >>

A Woman with Progressive Painless Sequential Monocular Vision Loss
Neurol 101:e2197-e2201, Ditrapani,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

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

A Teenager With Right-Sides Headache and Periorbital Changes
Neurol 100:144-150, Lax,D.M.,et al, 2023

Extrapulmonary Manifestations of Sarcoidosis
Rheum Dis Clin North Am 39:277-297, Rao,D.A. & Dellaripa,P.F., 2023

Cavernous Sinus Thrombosis
StatPearls PMID:28846357, Plewa,M.C.,et al, 2023

Progressive Camptocormia with Head Drop and Dysphagia
JAMA Neurol 80:209-210, El-Wahsh,S., et al, 2023

Clinicopathologic Conference, Functional Seiaures
NEJM 388:1210-1218, Case 10-2023, 2023

Myelin Oligodendrocyte Glycoprotein Antibody-Associated Disease (MOGAD): Clinical Features and Diagnosis
UptoDate.com, March, Flanagan,E.P. & Tillema,J-M, 2023

A Teenager with Chronic Meningitis-Does Occams Razor Apply?
Neurol 100:828-835, Havuluri,H.,et al, 2023

Clinicopathologic Conference, Factitious Disorder
NEJM 388:1609-1615, Case 13-2023, 2023

Clinicopathologic Conference, Facioscapulohumeral Muscular Dystrophy
NEJM 388:2379-2387, Case 19-2023, 2023

Paroxysmal Exercise-Induced Dyskinesias Due to Pyruvate Dehydrogenase Deficiency
Neurol 101:46-49, deGusmao,C.M.,et al, 2023

Clinicopathologic Conference, Systemic Immunoglobulin Light-Chain (AL) Amyloidosis
NEJM 389:166-175, Case 21-2023, 2023

An 82-Year-Old Woman with Subacute Ophthalmoparesis and Ataxia
Neurol 101:e570-e575, Rodrigo-Gisbert,M.,et al, 2023

Idiopathic Orbital Inflammation and Tolosa-Hunt Syndrome with Intracranial Extension
Neurol 101:371-374, Yu,S. & Chen,T., 2023

Magnetic Resonance Imaging of the Cranial Nerves in Infectious, Neoplastic, and Demyelinating Diseases, as Well as Other Inflammatory Diseases:A Pictorial Essay
Radiol Bras 55:38-46, Dalaqua,M.,et al, 2022

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

Clinical and Structural Findings in Patients with Lesion-Induced Dystonia
Neurol 99:e1957-e1967, Corp, D.T.,et al, 2022

Major Neurological Deficit Following Neck Hyperextension During Dental Treatment
Neurologist 6:361-363, El-Hajj, V.G.,et al, 2022

Spinal Muscular Atrophy
UpToDate, Oct, Bodamer,O.A., 2022

Inconsistency and Incongruence: The Two Diagnostic Pillars of Functional Movement Disorder
Lancet 400:328, Hess, C.H.,et al, 2022

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

Clinicopathological Conference, Chronic Candida Albicans Meningitis
NEJM 387:641-650, Case 25-2022, 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

A 51-Year-Old Woman with Diplopia and Headache
Neurol 99:524-530, Kathuria, G.,et al, 2022

Torticollis in a Child with Otalgia
BMJ 378:e070608, Sarathi, C.I.P.,et al, 2022

Horizontal Diplopia Due to Extraocular Muscle Metastasis
Neurol 99:669-670, Atik, M.,et al, 2022

Pulsatile Superficial Temporal Artery
JAMA Neurol 79:414-415, Kasischke, K. & Rose, D.Z., 2022

A 56-Year-Old Man with Unusual Presentation of Subacute Encephalopathy and Seizure
Neurol 98:e95-e102, Wang, T.,et al, 2022

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

Reversible Symmetric Basal Ganglia Lesions in a Patient with Diabetes Undergoing Dialysis
Neurol 98:773-774, Quigley, S., 2022

Bilateral Trigeminal Neuralgia - A Condition of the Upper Neck
Head Pain Disorder, Jan, , 2022

Pontine Owl-Eyes Lesions in a Case of Neuroborreliosis
Neurol 98:e443-e444, Borgeaud, S.,et al, 2022

A 64-Year-Old Man with History of Meningitis Presenting with Proximal Weakness of the Arms
Neurol 98:208-213, Karschnia, P.,et al, 2022

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

Clinicopathologic Conference, Neurosyphilis
NEJM 386:583-590, Case 4-2022, 2022

Myotonic Dystrophy: Etiology, Clinical Features, and Diagnosis
UptoDate 2022 Jan, Darras, B.T., 2022

Leber Hereditary Optic Neuropathy with Longitudinal Spinal Cord Lesion Mimicking Spinal Cord Infarction
Neurol 98:468-469, Zhao, B.,et al, 2022

A Young Man with Daily Episodes of Altered Awareness
Neurol 98:e1197-e1203, Villamar, M.F.,et al, 2022

Sturge-Weber Syndrome
www.UptoDate.com,Dec, Patterson,M.C., 2022

Spontaneous Escherichia Coli Meningitis and Brain Abscess in an Immunocompetent Adult
Cureus doi.10.7759/CUREUS.208728, Jeter,K.et al, 2022

An Unexpected Case of Disseminated Amebiasis with Cerebral Involvement and Successful Recovery in a Non-Endemic Context
Am J Case Rep 22:e934188, Zamora,P.S.,et al, 2021

Choreoathetosis and Focal Dystonia in Vitamin B12 Deficiency
Neurol 97:e1545, Ng, C.F.,et al, 2021

A 55-Year-Odd Man with Old Behavior and Abnormal Movements
Neurol 97:1090-1093, McIntosh, P. & Scott, B., 2021

Shoulder-Tap Test for Functional Gait Disorders
Neurol 97:1070-1071, Coebergh, J.,et al, 2021

A Middle-Aged Man with Progressive Gait Abnormalities
Neurol 97:e2423-e2428, Lin, J.,et al, 2021

Vitamin B12 Deficiency in a 29-Year-Old Woman
Neurol 97:e643-e646, Huddar, A.,et al, 2021



Showing articles 400 to 450 of 2319 << Previous Next >>