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Differential
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adverse drug reaction
aggression
agitation
akathisia
alcohol
alpha agonists
alternating hemiplegia
alternating hemiplegia of childhood
amnesia
amphetamines
Angelman syndrome
anti IgLON5
apraxia of eye movements
areflexia
ataxia
ataxia, cerebellar
ataxia, progressive
ataxic gait
ATP1A3 gene
attention deficit disorder with hyperactivity
attention span
atypical
autoantibodies
autonomic dysfunction
Balint's syndrome
basal ganglia, lesion of
behavior
behavior, combative
behavioral disorder
behavioral disorder, acute
botulinum toxin
brachycephaly
catecholamine
cerebellar atrophy, primary
cerebral cortex
cerebral cortical atrophy
cerebral ischemia
cerebrospinal fluid
cerebrospinal fluid, abnormal
cerebrovascular accident
chewing movements
children
chorea
chorea, Sydenham's
chorea, Sydenham's, recurrent
chromosomal abnormality
chromosome 15
cirrhosis
Clinical Pathologic Conference(C.P.C.)
clonidine
cognition
coma
concerta
confabulation
confusion
confusional state, acute
controversies in neurology
conversion reaction
coprolalia
C-reactive protein, elevated
delay in diagnosis
dementia
dementia, rapidly progressive
developmental retardation
diagnostic criteria
differential diagnosis
dopamine
dopamine antagonist
drooling
drug induced neurologic disorders
drug interactions
drug overdose
dysarthria
dysmetria
dysmorphic
dysphagia
dystonia
dystonia musculorum deformens
echolalia
electroencephalogram, abnormalities of
emotional lability
encephalitis, autoimmune
encephalopathy
encephalopathy, anoxic
encephalopathy, delayed
encephalopathy, post anoxic
epidemiology of neurology
episodic disorders
episodic neurologic deficits
eye movement, disorders of
facial appearance, abnormal
facial expression abnormality
falling
fatal familial insomnia
feeding disorder
fish
fluorescene in situ hybridization
gait disorder
gamma amino butyric acid
gene mutation
genetic neurologic disorders
genetic testing
Gilles de la Tourette syndrome
guanfacine
hallucination
haloperidol
headache
hearing loss
hepatic encephalopathy
hepatic encephalopathy, treatment of
homovanillic acid
hyperactivity
hyperreflexia
hypersomnia
hypoglycemia
hyponatremia
hypopigmentation of skin
hypotonia
hypoxia
hypoxic encephalopathy
imbalance
imbalance, postural
impulsivity
inattention
incontinence, fecal
insight, loss
insomnia
insulinoma
intellectual deficit
intellectual deterioration
laughing, pathologic
L-dopa
learning disability, in children
macrognathia
memory, defect of recent
memory, impairment of
meningitis, carcinomatous
mental retardation
mental status, abnormal
microcephaly
misdiagnosis
monoamines
movement disorder
movement disorder, hyperkinetic
movement disorder, psychogenic
MRI, abnormal
MRI, abnormal, seizure causing
MRI, diffusion weighted
MRI, disappearing lesion on
MRI, negative
multiple sclerosis
myoclonic jerks
myoclonus
myoclonus, action
myoclonus, post anoxic
neurochemistry
neuroendocrinology
neuroglycopenia
neuroleptic
neuroleptic, atypical
neurologic disease, diagnoses of
neurologic examination
neurologic history
neurotransmitter
next-generation sequencing
norepinephrine
nystagmus
nystagmus, monocular
nystagmus, vertical
obsessive-compulsive disorder
occipital lobe, lesion of
optic atrophy
orthostatic hypotension
palilalia
parasomnia
Parkinson disease
Parkinson disease, dystonia with
Parkinsonism syndrome
paroxysmal hemiplegia
paroxysmal neurologic deficits
patient information and support
pediatric autoimmune neuropsychiatric disorders associated with streptococcal infection
personality change
phenylketonuria
pimozide
postural abnormality
practice guidelines
precipitating factors
prion disease
prognathism
prognosis
progressive neurologic disorder
psychiatric problems in neurologic disorders
psychological testing
psychological testing, children
psychosis
rapid onset dystonia parkinsonism
rapidly progressing neurologic illness
recurrent
respiratory failure
review article
rigidity
Riley-Day syndrome
risk factors
ritalin
Romberg's sign
sedimentation rate, elevated
seizure
seizure, differential diagnosis of
seizure, nonconvulsive
seizure, occipital lobe
selective serotonin reuptake inhibitors
sensorineural hearing loss
serotonin
serotonin syndrome
shivering
simultanagnosia
sleep
sleep pathology and physiology
smiling
speech disorder
speech disorder, childhood
speech, delayed development of
status epilepticus
status epilepticus, nonconvulsive
stereotyped behavior, drug induced
stimulant drugs
stimulation, deep brain
sweating
symmetric brain lesions
tandem gait, ataxic
tardive dyskinesia
teeth, wide-spaced
tic
tic, chronic multiple
tic, classification of
tic, motor
tic, recurrent
tic, sensory
tic, vocal
tongue, protrusion of
torticollis
transient neurologic deficit
trauma
trazodone
treatment of neurologic disorder
undiagnosed
urinary incontinence
vasospasm, cerebral
visual impairment
walking, difficulty with
weight loss
Showing articles 0 to 50 of 17348 Next >>

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

The Phenotypic Continuum of ATP1A3-Related Disorders
Neurol 99:e1511-e1526, Vezyroglou,A., et al, 2022

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

Clinicopathological Conference, Insulinoma
NEJM 379:376-384, Case 23-2018, 2018

A 54-year-old woman with Confusion and Visual Disturbances
Neurol 91:363-367, Rossi, K.C.,et al, 2018

Clinical Decision-Making in Functional and Hyperkinetic Movement Disorders
Neurol 88:118-123,114, van der Salm, S.M.A.,et al, 2017

A Case of Altered Mental Status, Not Otherwise Specified
Neurol 89:e154-e158, Swor, D.E.,et al, 2017

Tourettes Syndrome
NEJM 363:2332-2338, Kurlan,R., 2010

The Pediatric Autoimmune Neuropsychiatric Disorders Associated with Streptococcal Infection (PANDAS) Etiology for Tics and Obsessive-Compulsive Symptoms: Hypothesis or Entity? Practical Considerations for the Clinician
Pediatrics 113:883-886, Kurlan,R. &Kaplan,E., 2004

Tourette's Syndrome
NEJM 345:1184-1192, Jankovic,J., 2001

Tourette Syndrome:Update and Review of the Literature
The Neurologist 4:188-195, Feigin,A.&Clarke,H., 1998

Serotonin Syndrome
Neurol 45:219-223, Bodner,R.A.,et al, 1995

Sydenham's Chorea:Physical and Psychological Symptoms of St. Vitus Dance
Pediatrics 91:706-713, Swedo,S.E.,et al, 1993

Angelman Syndrome: Clinical Profile
J Child Neurol 7:270-280, Zori,R.T.,et al, 1992

Tourette Syndrome and Other Tic Disorders, Diagnosis, Pathophysiology, and Treatment
Medicine 70:15-32, Singer,H.S.&Walkup,J.T., 1991

Tourette's Syndrome:Current Concepts
Neurol 39:1625-1630, Kurland,R., 1989

Methylphenidate-induced Chorea:Case Report & Pharmacologic Implications
Neurol 28:1041-1044, Weiner,W.J.,et al, 1978

Catecholamines & Neurologic Diseases
NEJM 293:274, Moskowitz,M.A.,et al, 1975

Juvenile-Onset Dopa-Responsive Dystonia-Until It Isnt
Neurol 104:e213436, Paredes,N.C.,et al, 2025

A 57-Year-Old Man With Chronic Gait Unsteadiness and Diminished Lower Extremity Sensation
Neurol 104:e213713, Rawat,R.,et al, 2025

Rapidly Progressive Frontotemporal Dementia with Amytrophic Lateral Sclerosis in an Elderly Female
Cureus doi:10.7759/CUREUS.32182, Sweedan,Y.G.,et al, 2025

A 59-Year-Old Man with Progressive Dysarthria and Gait Instability
Neurol 104:e213729, Shen,D.,et al, 2025

Addressing Systemic Complications of Acute Stroke: A Scientific Statement From the American Heart Association
Stroke 56:e15-e29, Kumar,S.,et al, 2025

A 50-Year-Old Man with Ataxia, Dystonia, and Abnormal Ocular Movements
Neurol 103:e210046, Panigrahi,B.,et al, 2024

Clinical Neurologic Features and Evaluation of PTEN Hamartoma Tumor Syndrome, A Systematic Review
Neurol 103:e209844, Dhawan,A.,et al, 2024

Roving Eye and Head in a Patient with Genetic Creutzfeldt-Jakob Disease
Neurol 102:e209385, Nishida,K.,, 2024

Clinicopathologic Conference, Thyrotoxic Periodic Paralysis Associated with Graves Disease
NEJM 390:1514-1522, Case 13-2024, 2024

Wall-Eyed Bilateral Internuclear Ophthalmoplegia Variant Syndrome Caused by Isolated Left Thalamic Infarction
Neurol 102:e209475, Wu,B.P.,et al, 2024

Expanding Clinical Spectrum an Anti-GQ1b Antibody Syndrome, A Review
JAMA Neurol 81:762-770, Lee,S-U.,et al, 2024

Paraneoplastic Calmodulin Kinase-Like Vesicle-Associated Protein (CAMKV) Autoimmune Encephalitis
Ann Neurol 96:21-33, Gilligan,M.,et al, 2024

Clinicopathologic Conference, Paraneoplastic Encephalomyelitis Due to Small-Cell Lung Carcinoma and Concurrent Cerebral Amyloid Angiopathy
NEJM< 391357-369, Case 23-2024, 2024

Parkinsons Disease
NEJM 391:442-452, Tanner,C.M. & Ostrem,J.L., 2024

The "Chameleon Eyes Sign" in Myasthenia Gravis
Neurol 103:e209756, Zara,P.,et al, 2024

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

Clinicopatholigical Conference, Plasmodium Falciparum Malaria
NEJM 309:549-556, Case 4-2024, 2024

Clinicopathologic Conference, Myeloperoxidase antineutrophil cytoplasmic antibody-associated vasculitis
NEJM 390:843-851, Case 7-2024, 2024

Eagle Syndrome
Stat Pearls NBK 430789, Bokhari,M.R.,et al, 2024

A 19-Month Old Girl with Infantile-Onset Myopathy and White Matter Changes
Neurol 102:e209258, Lail,G.,et al, 2024

Rabbit Syndrome
Neurol102:e209275, Huynh,T.U., & Beckley, E.H., 2024

Ocular Myasthenia Gravis, Central Ocular Motor Signs and Unilateral Visual Loss Caused by the Great Neuro-Ophthalmologic Impersonator
Neurol 102:e209260, Young,A. & Johnston,J.L., 2024

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

Tuberous Sclerosis Complex:Clinical Features
www.UptoDate.com, Dec, Randle,S., et al, 2023

Movement Disorders in Patients with Genetic Developmental and Epileptic Encephalopathies
Neurol 101:e1884-e1892, van der Veen,S.,et al, 2023

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

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

Clinicopathologic Conference,Limb-Shaking Transient Ischemia Attacks
NEJM 389:1416-1423, Case 31-2023, 2023

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

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

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



Showing articles 0 to 50 of 17348 Next >>