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Differential
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acquired immunodeficiency syndrome
acquired immunodeficiency syndrome-related complex
acrocyanosis
Aicardi-Goutieres syndrome
akathisia
alcohol
alcohol, neurologic complications with
alien hand syndrome
altered states of consciousness
anemia
anorexia
anti basal ganglia antibodies
anti IgLON5
anticholinergic drugs
anxiety
apraxia
apraxia of eye movements
apraxia, constructional
astrocytoma
asymptomatic
ataxia
athetosis
atypical
autoantibodies
B 12 deficiency
ballismus, bilateral
basal ganglia
basal ganglia, calcification of
basal ganglia, infarction
basal ganglia, lesion of
basal ganglia, lesion, bilateral
benign essential tremor
beta adrenergic blocker
blepharospasm
blinking, reduced
bradykinesia
brain atrophy
brain biopsy
bruxism
calcification, intracranial
carbon monoxide poisoning
cardiomyopathy
CAT scan
CAT scan, abnormal
CAT scan, chest
CAT scan, emission, abnormal
cataracts
central nervous system, infection of
cerebral cortical atrophy
cerebrospinal fluid, abnormal
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, gold sol.curve of
cerebrospinal fluid, xanthochromia of
cerebrovascular accident
cerebrovascular accident, complications with
cerebrovascular accident, young adult
ceruloplasmin, serum
chilbran skin lesions
children
chorea
chorea, treatment of
choreoathetosis
choreoathetosis, paroxysmal
chromosomal abnormality
chromosome 7
chronic progressive external ophthalmoplegia
cisternogram, radionuclide
Clinical Pathologic Conference(C.P.C.)
clonazepam
coccidioidomycosis
cold intolerance
conjugate gaze, forced
consanguinity
conversion reaction
copper metabolism, abnormal
cortical-basal ganglionic degeneration
crying
delay in diagnosis
dementia
dentate nuclei, lesion of
depression
developmental retardation
dexterity, impaired
diabetes mellitus
diagnostic criteria
differential diagnosis
disability, neurological
drooling
dysarthria
dyskinesia
dyskinesia, buccal lingual facial
dyskinesia, drug induced
dysphagia
dyspraxia
dystonia
dystonia, children
dystonia, delayed onset
dystonia, face
dystonia, focal
dystonia, psychogenic
dystonia, treatment of
dystonic reaction, acute
electroencephalogram
electromyogram
emergencies, neurologic
encephalitis
encephalitis lethargica
encephalitis, paraneoplastic
encephalitis, viral
encephalopathy
encephalopathy, post anoxic
epileptic encephalopathy
epsilon sarcoglycan gene
extralimbic encephalitis
face, contractions
faciobrachial dystonic seizure
familial
feeding disorder
fever
frontal lobe, pathologic signs of
gait disorder
gamma amino butyric acid receptor antibody
gaze palsy
gaze palsy, supranuclear
gene
gene mutation
genetic diagnosis, prenatal
genetic neurologic disorders
granuloma, pulmonary
grasp reflex
handedness
head injury
head lag
head nodding
headache
hearing loss
heart block
hemiballismus
hemichorea
hemiparesis
hepatic failure
hepatolenticular degeneration(Wilson's disease)
heralding manifestation
human immunodeficiency virus type 1
hydrocephalus
hydrocephalus, normal pressure
hyperekplexia
hyperpyrexia, CNS disorder causing
hyperreflexia
hypoglycorrhachia
hypotonia
hypotonia, infants
hypoxia, newborn
hypoxic encephalopathy
imbalance
immunotherapy
intellectual deficit
interferon alpha
intestinal pseudoobstruction
intracerebral hemorrhage
intrauterine
irritability
Kayser-Fleischer ring
Kearns-Sayre syndrome
L-dopa
Leber's hereditary optic neuropathy
left handedness
Leigh's disease
leucine rich glioma inactivated 1 antibodies
leukodystrophy
leukoencephalopathy
levitation
Lewy body disease, diffuse
liver disease
lobar atrophy
masked facies
mediastinum, mass of
medical-legal aspects of neurology
MELAS syndrome
memory, defect of recent
memory, impairment of
meningismus
meningitis
meningitis, fungal
meningitis, syphilitic
meningitis, TB
MERRF syndrome
microcephaly
misdiagnosis
mitochondrial disease
mitochondrial encephalomyopathy
molecular genetics
mortality
movement disorder
movement disorder, delayed onset
movement disorder, drug induced
movement disorder, extrapyramidal
movement disorder, paroxysmal
movement disorder, psychogenic
movement disorder, treatment of
MRI
MRI, abnormal
myelopathy
myoclonic dystonia
myoclonic jerks
myoclonus
myoclonus, action
myoclonus, cortical
myoclonus, segmental
myopathy
myopathy, mitochondrial
myorhythmia
mysoline
neoplasm, intracranial
neoplasm, primary intracerebral
neoplasm, primary of CNS
neurologic complications of, systemic cancer
neurologic disease, diagnoses of
neurologic disease, diagnoses of, clinical bedside
neurologic disease, multifocal
neurologic signs
neurologic symptoms
neuropathology
neuropathy
oculogyric crisis
ophthalmoplegia
optic neuropathy
pancytopenia
Parkinson disease
Parkinson disease, differential diagnosis of
Parkinson disease, drug induced
Parkinson disease, L-dopa nonresponsive
Parkinson disease, postencephalitic
Parkinson disease, psychogenic
Parkinson disease, tremor, absence of
Parkinsonism syndrome
paroxysmal dystonic choreoathetosis
paroxysmal kinesigenic dyskinesia
paroxysmal neurologic deficits
paroxysmal nonkinesigenic dyskinesia
pathognomonic
penicillamine
pigmentary retinopathy
pleocytosis of cerebrospinal fluid
pneumoencephalogram(PEG)
prenatal
prognosis
progressive neurologic disorder
propranolol
psychiatric problems in neurologic disorders
psychomotor retardation
ptosis
pyramidal tract dysfunction
ragged-red fibers
remote effect of cancer on the nervous system
retinopathy
Rett's syndrome
review article
rigidity
salivation, excessive
seizure
seizure, dystonic
seizure, stimulus sensitive
sensorineural hearing loss
sensory loss
sensory loss, cortical
short stature
skin, lesions in neurologic disorders
sleep apnea, obstructive
sleep pathology and physiology
somnolence
spastic dysphonia
speech disorder
speech disorder, childhood
spinocerebellar ataxia type 16
spongy degeneration of brain
startle reaction
status dystonicus
status epilepticus, intractable
stereotypy
steroid therapy, CNS treatment and complications with
subarachnoid hemorrhage
suck, poor
tardive dyskinesia
tardive dystonia
tauopathy
term infant
thalamic tumors
thalamus, lesion of
thymoma
tic
tonic spasms
torticollis
toxoplasmosis, CNS
treatment of neurologic disorder
tremor
tremor, jaw
tremor, leg
tremor, psychogenic
tremor, treatment of
tremor, writing
viral infection
viral infection, CNS
visuospatial disturbance
weight loss
Whipple's disease
white matter disease
wrist drop
writers cramp
writing
Showing articles 0 to 50 of 847 Next >>

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

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

Recurrent Involuntary Contractions of the Face, Arm, and Leg in an Elderly Man
JAMA Neurol 76:728-729, Kim, D.D.,et al, 2019

A Middle-Aged Man with New Onset Seizures and Myoclonic Jerks
Neurol 92:e274-e281, Chen, Z. & Neo, S., 2019

IgLON5-mediated neurodegeneration is a differential diagnosis of CNS Whipple disease
Neurol 90:1113-1115, Morales-Briceno, H.,et al, 2018

Choreoathetosis, Dystonia, and Myoclonus in 3 Siblings with Autosomal Recessive Spinocerebellar Ataxia Type 16
JAMA Neurol 73:888-890, Kawarai, T.,et al, 2016

A 56-year-old Man with Cognitive Impairment and Difficulty Tying his Necktie
Neurol 85:e116-e122, Baker, J.M.,et al, 2015

Viral Infections of the Nervous System, Chronic Meningitis, and Prior Diseases, Encephalitis Lethargica (non Economo Disease, sleeping sickness)
Adams & Victors Principles of Neurology, Chp 33, pg 768, Ropper, A.H.,et al, 2014

Inherited Metabolic Diseases of the Nervous System, Subacute Necrotizing Encephalopathy (Leigh Disease)
Adams & Victors Principles of Neurology, Chp 37, pg 996, Ropper, A.H.,et al, 2014

Clinical Reasoning: A 13-year-old Boy Presenting with Dystonia,Myoclonus,and Anxiety
Neurol 78:e72-e76, Blackburn,J.S. and Cirillo,M.L., 2012

Movement Disorders Emergencies Part 2 Hyperkinetic Disorders
Arch Neurol 68:719-724, Robottom, B.J.,et al, 2011

Aicardi-Gouti�res Syndrome
Br Med Bull 89:183-201, Orcesi, S.,et al, 2009

Wilson Disease: Description of 282 Patients Evaluated Over 3 Decades
Medicine 86:112-121, Taly,A.B., et al, 2007

Post-Stroke Movement Disorders; Report of 56 Patients
JNNP 75:1568-1574, Alarcon,F.,et al, 2004

HIV-Related Movement Disorders, Epidemiology, Pathogenesis and Management
CNS Drugs 16:663-668, Cardoso,F., 2002

Delayed Movement Disorders After Carbon Monoxide Poisoning
Eur Neurol 42:141-144, Choi,I.S. &Cheon,H.Y., 1999

Localization of a Gene for Myoclonus-Dystonia to Chromosome 7q21-q31
Ann Neurol 46:794-798, Nygaard,T.G.,et al, 1999

Clinical Presentation and Pharmacological Therapy in Corticobasal Degeneration
Arch Neurol 55:957-961, Kompoliti,K.,et al, 1998

Comparison of Extrapyramidal Features in 31 Path Cases of Diffuse Lewy Body Disease & 34 Cases of Parkinson's
Neurol 48:376-380, Louis,E.D.,et al, 1997

Accuracy of the Clinical Diagnosis of Corticobasal Degeneration:A clinicopathologic Study
Neurol 48:119-125, Litvan,I.,et al, 1997

Delayed-Onset Progressive Movement Disorders after Static Brain Lesions
Neurol 46:68-74, Scott,B.L.,et al, 1996

Psychogenic Movement Disorders:Frequency, Clinical Profile and Characteristics
JNNP 59:406-412, Factor,S.A.,et al, 1995

Mitochondrial DNA and Disease
NEJM 333:638-644, Johns,D.R., 1995

The Relationship of Essential Tremor to Other Movement Disorders:Report on 678 Patients
Ann Neurol 35, 717-7231994., Koller,W.C.,et al, 1994

Tardive Stereotype and Other Movement Disorders in Tardive Dyskinesias
Neurol 43:937-941, Stacy,M.,et al, 1993

Movement Disorders in Astrocytomas of the Basal Ganglia and the Thalamus
JNNP 55:1162-1167, Krauss,J.K.,et al, 1992

Extrapyramidal Involvement in Rett's Syndrome
Neurol 40:293-295, FitzGerald,P.M.,et al, 1990

Cortical-Basal Ganglionic Degeneration
Neurol 40:1203-1212, Riley,D.E.,et al, 1990

Movement Disorders & AIDS
Neurol 37:37-41, Nath,A.,et al, 1987

Primary Writing Tremor & Myoclonic Writer's Cramp
Neurol 35:1387-1391, Ravits,J.,et al, 1985

Familial Paroxysmal Dystonic Choreoathetosis & its Differentiation From Related Syndromes
Ann Neurol 2:285, Lance,J.W., 1977

Case Records of MGH-NEJM 285:621
1971., , 1971

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

Severe Amyloid-Related Imaging Abnormalities After Anti-B-Amyloid Monoclonal Antibody Treatment
Neurol 101:1079-1080, Bonami,S.,et al, 2023

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

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

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

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

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

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

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

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

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

A 23-Year-Old Woman Presenting with Cognitive Impairment and Gait Disturbance
Neurol 99:997-1003, Chaity,D.K.,et al, 2022

Clinicopathologic Conference, Anti-IgLON5 IgG-Associated Neurologic Disorder
NEJM 386:173-180, Case 1-2022, 2022

A 6-Year-Old Girl with Progressive Toe Walking
Neurol 98:e769-e773, Libdeh, A.A. & Ibrahim, A., 2022

Clinicopathologic Conference, Genetic Creutzfeldt-Jakob Disease
NEJM 386;674-687, Case 5-2022, 2022



Showing articles 0 to 50 of 847 Next >>