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Differential
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advances in neurology
adverse drug reaction
alpha-synuclein
alternating rapid movement
alternating rapid movement, impaired
amyotrophic lateral sclerosis, differential diagnosis
amyotrophic lateral sclerosis, misdiagnosis
amyotrophic lateral sclerosis-like syndrome
ANA
anemia
anterior horn cell disease
anti citrullinated antibody
anti IgLON5
anti Tr antibodies
anticonvulsants
anticonvulsants, untoward effects of
apnea
applause sign
areflexia
arm swing, reduced
arm weakness
astereognosis
ataxia
ataxia, cerebellar
ataxia, progressive
ataxia, sensory
ataxic gait
athetosis
autoantibodies
autoimmune cerebellar ataxia
axonal degeneration
B 12 deficiency
Babinski sign
behavioral disorder
benign essential tremor
benign essential tremor, refractory
blepharospasm
blindness
brachial neuritis
brachial plexus neuropathy, familial
brachial plexus neuropathy, recurrent
bradykinesia
brain atrophy
breast feeding
bulbar palsy
calf hypertrophy
cerebellar atrophy, secondary
cerebellar degeneration
cerebellum, disease of
cerebral palsy
cerebral palsy, associated problems with
Charcot-Marie-Tooth
children
chromosomal abnormality
chromosome 17
Clinical Pathologic Conference(C.P.C.)
clubfoot as related to neurologic disease
cognition
coin rotation test
cold intolerance
coma, episodic
complications
conduction block
consanguinity
creatine phosphokinase(CPK)elevated
cyclophosphamide
degenerative diseases of CNS
delay in diagnosis
delayed muscle relaxation
dementia
developmental disability
developmental evaluation
developmental milestones
developmental milestones, loss of
developmental retardation
dexterity, impaired
diagnostic criteria
differential diagnosis
difficulty climbing stairs
diplegia, brachial
diplopia
disability, neurological
distal muscle atrophy
distal muscle weakness
dopamine agonist
downward gaze
dysarthria
dysarthria-clumsy hand syndrome
dysdiadochokinesia
dysmetria
dysphagia
dyspraxia
dystonia
dystonia musculorum deformens
dystonia, cervical
dystrophin
electroencephalogram, abnormalities of
electromyogram
encephalitis
encephalitis, autoimmune
encephalopathy
epileptic encephalopathy
episodic disorders
episodic neurologic deficits
episodic unconsciousness
eye movement, disorders of
failed medical management
failure to thrive
falling
familial
FARS2 deficiency
fasciculation
fatigue
fetal tissue
fibrillations
fine motor function, impaired
finger numbness
foot deformity
foot drop
gait disorder
gait, apraxic
gammaglobulin therapy, intravenous
ganglionitis
gaze palsy
gaze palsy, supranuclear
gaze palsy, vertical
gene
gene mutation
genetic counselling
genetic neurologic disorders
genetic testing
Gowers maneuver
granular osmiphilic material
hammertoes
hand deformity
hand numbness
hand weakness
handwriting
hearing loss
high arched feet
hoarseness
homocysteine, serum
hydrocephalus
hyperreflexia
hypersomnia
hypometric saccades
hypophonia
hyporeflexia
hypotonia
ideomotor apraxia
imbalance
imbalance, postural
immunologic disease
immunosuppressive agents
immunotherapy
incoordination
infant, evaluation of
inferior olivary nucleus
intellectual deficit
intellectual deterioration
intelligence quotient
intrauterine
intrinsic hand muscles, wasting of
introverted
lateropulsion
L-dopa
learning disability
learning disability, in children
leg numbness
leg weakness, bilateral
Lewy body
Lhermitte's sign
liver disease
liver function enzymes
low birth weight
lymphoma
lymphoma involving CNS
lymphoma, primary of CNS
masked facies
memory, impairment of
meningitis
meningitis, bacterial
meningitis, children
meningitis, CSF cell count-normal
meningitis, factors influencing mortality in
meningitis, late neurologic sequelae in
meningitis, neurologic aspects and complications of
methylmalonic acid, serum
microcephaly
midbrain
midbrain, atrophy
misdiagnosis
mitochondrial disease
molecular genetics
motor development
motor dysfunction
motor neuron disease
motor neuron disease, misdiagnosis
motor symptoms
motor system
movement disorder
MRI
MRI, abnormal
MRI, brachial plexus
MRI, contrast enhanced
MRI, disappearing lesion on
MRI, spinal cord
MRI, spine
multiple sclerosis
muscle cramp
muscle stiffness
muscle twitching
muscular dystrophy
muscular dystrophy, central nervous system abnormality
muscular dystrophy, Duchenne
musicians
myelopathy
myelopathy, chronic progressive
myoclonus
myoglobinuria
mysoline
nerve conduction studies
nerve conduction studies, motor
nerve conduction studies, sensory
nerve hypertrophy
neurologic complications of, systemic disease
neurologic disease, diagnoses of
neurologic examination
neurologic testing
neuromuscular disease, electrodiagnosis of
neuromyotonia
neuromyotonia and axonal neuropathy
neuronal ceroid-lipofuscinosis
neuronopathy
neuronopathy, sensory
neuroophthalmology
neuropathology
neuropathy
neuropathy, hereditary peripheral
neuropathy, hypertrophic
neuropathy, motor
neuropathy, motor, multifocal
next-generation sequencing
numb clumsy hands syndrome
numbness, extremity
nystagmus
occupational neurologic disorders
olivary degeneration, hypertrophic
overuse syndrome
pain
pain, arm
pain, severe
palatal myoclonus
paraparesis
paraparesis, familial spastic
paraparesis, spastic
paraplegia
paresthesias
Parkinson disease
Parkinson disease, axial symptoms
Parkinson disease, diagnosis
Parkinson disease, nonmotor problems of
Parkinson disease, pathogenesis of
Parkinson disease, treatment of
Parkinson disease, tremor, absence of
Parkinsonism syndrome
penguin silhouette sign
pes cavus
pianist
placebo effect
position sensation
positive sharp waves
posterior column disease
pregnancy, anticonvulsants during
pregnancy, neurologic complications in
premature infant
prenatal
prognosis
progressive ataxia and palatal tremor
progressive myoclonic epilepsy
progressive neurologic disorder
progressive supranuclear palsy
propranolol
proprioception
pseudoathetosis
pseudobulbar palsy
psychological testing
psychological testing, children
psychomotor retardation
pyramidal tract dysfunction
rapidly progressing neurologic illness
recruitment
recruitment, reduced
recurrent
REM sleep behavior disorder
remote effect of cancer on the nervous system
respiratory tract infection
retrocollis
retropulsion
review article
rheumatoid arthritis
rheumatoid arthritis factor(R.A.factor)
rheumatoid arthritis, neurologic complications of
rigidity
rigidity, axial
risk factors
Romberg's sign
saccadic eye movements, abnormal
sedimentation rate, elevated
seizure
seizure, children
seizure, treatment of, polytherapy
sensorineural hearing loss
sensory loss
sensory loss, asymmetric
sequencing difficulty
shooting pain
sinemet
Sjogren's syndrome
sleep pathology and physiology
slurred speech
spastic diplegia
spasticity
speech disorder, childhood
speech, delayed development of
spinal cord
spinal cord, lesion of
spontaneous remission
stem cell transplantation
steppage gait
stimulation, deep brain
systemic illness
tandem gait, ataxic
tau protein
thalamotomy
thalamus, focused ultrasound ablation
toe walking
tone, muscle, increased
treatment of neurologic disorder
tremor
tremor, intention
tremor, postural
tremor, surgical treatment of
tremor, treatment of
tripping
unconsciousness
unconsciousness, episodic
unconsciousness, transient
useless hand
vibratory sensation
vibratory sensation, abnormal
violinist
vision, blurred
visual loss
visual symptoms
vitiligo
vocalizations
walking, difficulty with
weakness
weakness, progressive
weight loss
wheelchair
wide based gait
winging of scapula
writing
Showing articles 50 to 100 of 8886 << Previous 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

A 65-Year-Old Woman with Cancer History and Wrist Drop
Neurol 99:570-576, Merrill, R.,et al, 2022

Neuroimaging Biomarkers in a Patient with Probable Psychiatric-Onset Prodromal Dementia with Lewy Bodies
Neurol 99:654-657, Urso, D.,et al, 2022

Amyotrophic Lateral Sclerosis
Lancet 400:1363-1380, Feldman, E.L.,et al, 2022

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

Association Between Occupational Exposure to Formaldehyde and Cognitive Impairment
Neurol 98:e633-e640, Letellier, N.,et al, 2022

Clinicopathologic Conference, Diffuse Large B-Cell Lymphoma
NEJM 386:977-986, Case 7-2022, 2022

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

Hypotonia and Delayed Teeth Eruption in a 2-Year-Old Girl
Neurol 97:875-878, Dinov, D.,et al, 2021

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

Clinicopathologic Conference, Cerebral Amyloid Angiopatny-Related Inflammation
NEJM 385:358-368, Case 22-2021, 2021

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

When Should a Brain MRI Be Performed in Children with New-Onset Seizures? Results of a Large Prospectice Trial
AJNR 42:1645-1701, Hourani, R.,et al, 2021

Spontaneous Intracranial Hypotension
NEJM 385:2173-2178, Schievink, W.I., 2021

A Middle-aged Woman with Severe Scoliosis and Encephalopathy
JAMA Neurol 78:251-252, Mohan, G.,et al, 2021

Acute Flaccid Myelitis: Cause, Diagnosis, and Management
Lancet 394:334-397, Murphy, O.C.,et al, 2021

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

Molecular Diagnostic Yield of Exome Sequencing in Patients with Cerebral Palsy
JAMA 325:467-475, Moreno-De-Luca, A.,et al, 2021

Clinicopathologic Conference, Normal Pressure Hydrocephalus
NEJM 384:1350-1358, Case 10-2021, 2021

Adults with Cerebral Palsy Require Ongoing Neurologic Care
Ann Neurol 89:860-871, Smith, S.E.,et al, 2021

Natural History of "Pure" Primary Lateral Sclerosis
Neurol 96:e2231-e2238, Hassan, A.,et al, 2021

National Institute of Neurological Disorders and Stroke Consensus Diagnostic Criteria for Traumatic Encephalopathy Syndrome
Neurol 96:848-863, Katz, D.I.,et al, 2021

Cocaine and Levamisole Cerebral Toxicity
Ann Neurol 89:1253-1254, Allard, J.,et al, 2021

Complete Evaluation of Dementia: PET and MRI Correlation and Diagnosis for the Neuroradiologist
AJNR 42:998-1007, Oldan, J.D.,et al, 2021

Congenital Cytomegalovirus Infection
BMJ 373:m1212, Pesch, M.H.,et al, 2021

The Tolosa-Hunt Syndrome
NJJP 71:577-582, Kline,L.B. & Hoyt,W.F., 2021

Clinicopathologic conference, Frontotemporal Lobar Degeneration with tau-positive inclusions consistent with Picks disease
NEJM 383:2666-2675, Case 41-2020, 2020

Guillain-Barre Syndrome Associated with JEV Infection
NEJM 383:1188-1190, Wang, G.,et al, 2020

A 57-Year-Old Woman with Progressive Ataxia and Falls
Neurol 95:650-656, Badahdah, A., 2020

A 72-year-old Man with a Progressive Cognitive and Cerebellar Syndrome
Neurol 95:e2707-e2710, Lad, M. & Griffiths, T.D., 2020

Fat Embolism Syndrome in Sickle Cell Disease
J Clin Med 9:1-12, Tsitsikas, D.A.,et al, 2020

A 16-year-old Girl with Ataxia, Oscillopsia, and Behavioral Changes
Neurol 94:713-717, Silverman, A.,et al, 2020

An Infant with Developmental Delay, Epileptic Spasms, and Acrocyanosis
Neurol 94:939-942, Madaan, P.,et al, 2020

Ears of the Lynx Magnetic Resonance Imaging Sign
Ann Neurol 88:16-17, Baghbanian, S.M.,et al, 2020

Clinical Characteristics, Risk Factors, and Outcomes of POEMS Syndrome
Neurol 95:e268-e279, Keddie, S.,et al, 2020

A 10-Year-Old Girl with Muscle Stiffness
Neurol 95:e773-e778, Prior, D.E. & Ghosh, P.S., 2020

Melbourne Mobile Stroke Unit and Reperfusion Therapy
Stroke 51:922-930, Zhao, H.,et al, 2020

Immunocompetent Patient with Multiple Cranial Nerve Palsies, Ataxia, and Cognitive Decline
Neurol 94:e225-e229, Nigam, M.,et al, 2020

Telemedicine in Neurology
Neurol 94:30-38,16, Hatcher-Martin, J.M.,et al, 2020

Effects of Tranexamic Acid on Death, Disability, Vascular Occlusive Events and Other Morbidities in Patients with Acute Traumatic Brain Injury (CRASH-3): A Randomised, Placebo-Controlled Trial
Lancet 394:1713-1723,1687, The CRASH-3 trial collaborators, 2019

A 17-year-old Baseball Player with Right Hand Weakness
Neurol 92:e76-e80, Vachon, C. & Libdeh, A.A., 2019

Oculodentodigital Dysplasia: A Hypomyelinating Leukodystrophy with a Characteristic MRI Pattern of Brain Stem Involvement
AJNR 40:903-907, Hartin, I.,et al, 2019

A 47-year-old Man with Diffuse White Matter Disease and Rapidly Progressive Dementia
Neurol 92:e2832-e2837, Di Luca, D.G.,et al, 2019

Relapsing-Remitting Severe Bickerstaffs Brainstem Encephalitis
BMJ 394:684, Tyrakowska, Z.,et al, 2019

Pes Cavus and Neuropathy
Neurol 93:e823-e826, Alderson,J.,& Ghosh,P.S., 2019

Clinicopathologic Conference, Creutzfeldt-Jakob Disease
NEJM 381:1569-1578, Case 32-2019, 2019

Long-Term Treatment Effect in Cerebrotendinous Xanthomatosis Depends on Age at Treatment Start
Neurol 92:e83-e95, Stelten, B.M.L.,et al, 2019

Neurodegeneration with Brain Iron Accumulation
AIAN 22:267-276, Batla, A. & Gaddipati, C., 2019

Hereditary Spastic Paraplegia:From Diagnosis to Emerging Therapeutic Approaches
Lancet Neurol 18:1136-1146, Shribman,S.,et al, 2019

Pyruvate Dehydrogenase Deficiency (PDCD)
eMedicine.medscape,com, Aug, Frye,R.E.,et al, 2018



Showing articles 50 to 100 of 8886 << Previous Next >>