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Differential
(Click to cross reference)
adverse drug reaction
alopecia
alternating rapid movement
anti IgLON5
anticholinergic drugs
anticonvulsants
anticonvulsants, blood level determination of
anticonvulsants, mechanism of action of
anticonvulsants, teratogenicity of
anticonvulsants, untoward effects of
anxiety
apnea
apraxia
ataxia
ataxia, truncal
ataxic gait
athetosis
autoantibodies
autoimmune disease
axonal spheroid
Babinski sign
basal ganglia
basal ganglia, lesion of
behavioral disorder
behavioral disorder, acute
belching
bradykinesia
brain biopsy
brain scan
bulbar palsy
carbamazepine
cardiac arrest
cardiac arrest and resuscitation
CAT scan, abnormal
cerebellar atrophy, primary
cerebellum, disease of
cerebral cortex
cerebral cortical atrophy
cerebrospinal fluid
cerebrospinal fluid, hydroxyindoleacetic acid, 5(5-HIAA)
cerebrospinal fluid, lactic acid concentration
children
chorea
chromosomal abnormality
chromosome 7
Clinical Pathologic Conference(C.P.C.)
clonazepam
clonus
cognition
cogwheel rigidty
coma
coma, episodic
confusion
degenerative diseases of CNS
delay in diagnosis
dementia
dementia, reversible
dementia, treatment of
developmental milestones
developmental milestones, loss of
disability, neurological
drug induced neurologic disorders
drug overdose
dysmetria
dysphagia
dyspnea
dystonia
electroencephalogram
electroencephalogram, abnormalities of
electroencephalogram, periodic complexes
electromyogram
emotional lability
encephalitis
encephalitis, autoimmune
encephalopathy
encephalopathy, anoxic
encephalopathy, delayed
encephalopathy, Hashimoto's
encephalopathy, post anoxic
episodic disorders
episodic neurologic deficits
episodic unconsciousness
epsilon sarcoglycan gene
extrapyramidal
falling
familial
fasciculation
fine motor function, impaired
fingerprint bodies
Fisher C.M.
gait disorder
gamma amino butyric acid
gammaglobulin therapy, intravenous
gene
gene mutation
genetic neurologic disorders
glutamic acid decarboxylase, antibody
glycine
granular osmiphilic material
handwriting
hepatitis
hepatolenticular degeneration(Wilson's disease)
hepatomegaly
hiccoughs
hoarseness
Huntington's chorea
hyperreflexia
hypersomnia
hypertonia
hypophonia
hypoxia
hypoxic encephalopathy
iatrogenic neurologic disorders
imbalance
immunotherapy
inattention
inborn errors of metabolism
inclusion bodies
inclusion bodies, eosinophilic cytoplasmic
incontinence, fecal
infantile spasm
intellectual deficit
Jakob-Creutzfeldt disease
Jakob-Creutzfeldt disease, cerebellar variant
kuru plaques
lactic acidemia
leg spasms, painful
Leigh's disease
leukoencephalopathy
leukoencephalopathy, hereditary diffuse
life support, withdrawal of
lithium
memory, impairment of
mental status, abnormal
misdiagnosis
motor neuron disease
motor neuron disease, misdiagnosis
movement disorder
movement disorder, treatment of
MRI
MRI, abnormal
MRI, disappearing lesion on
muscle spasm
muscle twitching
myoclonic dystonia
myoclonic jerks
myoclonus
myoclonus, action
myoclonus, cortical
myoclonus, epilepsy
myoclonus, post anoxic
myoclonus, sleep
myoclonus, stimulus sensitive
myoclonus, treatment of
negative
neuroaxonal leukodystrophy
neuromuscular disease, electrodiagnosis of
neuronal ceroid-lipofuscinosis
neuropathology
neurotoxic
nystagmus
nystagmus, rotary
old age, neurology of
optic atrophy
orthostatic hypotension
Parkinson disease
Parkinsonism syndrome
paroxysmal neurologic disorder
PAS positive
PAS positive material in the brain
personality change
pheneturide
piracetam
prognosis
progressive encephalomyelitis with rigidity syndrome
progressive neurologic disorder
psychiatric problems in neurologic disorders
pyramidal tract dysfunction
pyruvate metabolism, abnormality of
quadriparesis
REM sleep behavior disorder
respiratory failure
respiratory myoclonus
rigidity
Romberg's sign
seizure
seizure, children
seizure, minor motor
seizure, petit mal
seizure, tonic-clonic
seizure, treatment of
sleep pathology and physiology
sodium valproate
sodium valproate, toxicity
spastic dysphonia
spasticity
speech disorder
speech, loss of
startle myoclonus
startle reaction
status epilepticus
status epilepticus, myoclonic
stiripentol
storage disease of CNS
striatonigral degeneration
striatonigral degeneration, infantile
stuttering
tandem gait, ataxic
thalamus
titubation
treatment of neurologic disorder
tremor
tremor, intention
tremor, writing
unconsciousness
unconsciousness, episodic
unconsciousness, transient
urinary incontinence
urinary retention
viral infection, CNS
vocalizations
walking, difficulty with
wheelchair
writers cramp
writing
Showing articles 0 to 50 of 816 Next >>

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

Spasms and Myoclonus in a Young Woman with Hashimoto Thyroiditis
JAMA Neurol 77:650-651, Shen, D.,et al, 2020

MRI-EEG Correlation for Outcome Prediction in Postanoxic Myoclonus
Neurol 95:e335-e341, Beuchat, I.,et al, 2020

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

Clinical Reasoning: A Woman with Rapidly Progressive Apraxia
Neurol 80:e162-e165, Pressman, P.,et al, 2013

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

Clinicopathologic Conference, Kufs Disease (Autosomal Dominant) Parry Type Neuronal Ceroid Lypofuscinosis
NEJM 364:1062-1074, Case 8-2011, 2011

Orthostatic Myoclonus: A Contributor to Gait Decline in Selected Elderly
Neurol 68:1826-1830, Glass,G.A.,et al, 2007

Stiripentol in Severe Myoclinic Epilepsy in Infancy: A Randomised Placebo-Controlled Syndrome-Dedicated Trial
Lancet 356:1638-1642,1623, Chiron,C.,et al, 2000

Cortical Myoclonus in Huntington's Disease
Movement Disorders 9:633-641, Thompson,P.D.,et al, 1994

Prognostic Value of Myoclonus Status in Comatose Survivors or Cardiac Arrest
Ann Neurol 35:239-243, Wijdicks,E.F.M.,et al, 1994

Clinicopath Conf
Infantile Striatonigral Regeneration, with Cerebellar Degeneration, Familial, Case 30-1992, NEJM 327, 261-1992., 1992

High-Frequency Diaphragmatic Flutter:Symptoms and Treatment by Carbamazepine
Lancet 339:265-267, Vantrappen,G.,et al, 1992

Myoclonus in Adult Huntington's Disease
Ann Neurol 29:213-215, Vogel,C.M.,et al, 1991

A Creutzfeldt-Jakob Like Syndrome Due to Lithium Toxicity
JNNP 51:120-123, Smith,S.J.M.&Kocen,R.S., 1988

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

Valproic Acid in the Treatment of Nonepileptic Myoclonus
Arch Neurol 39:448-449, Sotaniemi,K.,et al, 1982

Valproic Acid
NEJM 302:661-666, Brown,T.R., 1980

Clin. Path. Conference
Creutzfeldt-Jakob Disease, Ataxic Type, with Kuru Plaques, Case Record 45-1980, NEJM 303:1162-11710., , 1980

Postanoxic Action Myoclonus (Lance-Adams Syndrome) Responding to Valproate
Arch Neurol 36:44-45, Rollinson,R.D.,et al, 1979

Treatment of Myoclonus with Pheneturide
JNNP 41:598-602, Ward,C.D., 1978

Post-anoxic Action Myoclonus:Improvement with Valproic Acid
NEJM 299:313, Fah,S., 1978

Syndrome of Intention of Action Myoclonus as a Sequel to Hypoxic Encephalopathy
Brain 86:111, Lance,J.,et al, 1963

Diseases of the Basal Ganglia-Their Relation to Disorders of Movement
Lancet 1099, 1960, Nov., Denny-Brown,D., 1960

Clinical Picture in Creutzfeldt-Jakob Disease
Trans of Amer Neuro Assn 5:l47, Fisher,C.M., 1960

Efficacy and Safety of IV Thrombolysis for Acute Ischemic Stroke Patients with Moyamoya Disease
Neurol 104:e210243, Chen,H.,et al, 2025

Efficacy and Safety of Sodium Oxybate in Isolated Focal Laryngeal Dystonia:A Phase IIb Double-Blind Placebo-Controlled Cross-Over Randomized Clinical Trial
Ann Neurol 97:329-343, Simonyan,K.,et al, 2025

A 19-Year-Old Woman with Progressive Weakness and Numbness in Her Arms and Legs
Neurol 104:e213495, Alsabah,A-A.,et al, 2025

Postprocedural Brachial Neuritis:Clinical, Electrodiagnostic, and Neuroimaging Features
AJNR 46:1050-1055, Ambati,V.S.,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

Posttransplant Anti-GABAA Receptor Antibody-Associated Autoimmune Encephalitis
Neurol 102:e209245, Togni,C.L.,et al, 2024

Clinicopathological Conference, Glutamic Acid Decarborylase 65 Autoantibody-Associated Stiff-Person Syndrome
NEJM 390:1712-1719, Case 14-2024, 2024

Clinicopathologic Conference, Myasthenia Gravis
NEJM 391:1441-1450, Case 32-2024, 2024

Powassan Virus Encephalitis: A Tertiary Center Experience
Clin Inf Dis 78:80-89, Mendoza,M.A.,et al, 2024

Age-Related Changes in Neurologic Examination and Sensory Nerve Amplitude in the General Population, Aging of the Peripheral Nervous System
Neurol 101:e1351-e1358, Taams,N.E.,et al, 2023

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

Severe Amyloid-Related Imaging Abnormalities After Anti-B-Amyloid Monoclonal Antibody Treatment
Neurol 101:1079-1080, Bonami,S.,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 60-Year Old Man with Asymmetric Weakness and Persistent Fever
Neurol 100:530-536, Zheng,Y.,et al, 2023

A 26-Year-Old Woman with Recurrent Pain, Weakness, and Atrophy in Bilateral Upper Limbs During Pregnancy and Puerperium
Neurol 100:631-637, Zeng,T.f.,et al, 2023

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

Adult Patient Presenting with Spine Pain Following a Motor Vehicle Accident
Neurol 100:1025-1031, Sharma,V. & Soto,O, 2023

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

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

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

A 73-Year-Old Woman with Episodic Dysarthria and Horizontal Binocular Diplopia
Neurol 98:767-772, Bower, A.S.,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

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

A 31-year-Old Man with Bilateral Limited Mobility of Joints
JAMA Neurol 79:1083-1084, Wang, Z.,et al, 2022



Showing articles 0 to 50 of 816 Next >>