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Differential
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acetazolamide
Addison's disease
adrenoleukodystrophy
adrenoleukodystrophy, adult onset
adrenoleukodystrophy, carrier
akinetic mute
alternating rapid movement
alternating rapid movement, impaired
amyotrophic lateral sclerosis
anorexia
areflexia
arm swing, reduced
arrhythmia, cardiac
aspiration
astrocytoma
asymptomatic
ataxia
ataxia telangiectasia
ataxia, cerebellar
ataxia, hereditary
ataxia, paroxysmal
ataxia, progressive
ataxia, sensory
ataxia, truncal
ataxic gait
ataxic hemiparesis
atrial fibrillation
attention deficit disorder with hyperactivity
attention span
Babinski sign
basal ganglia, degeneration
basal ganglia, lesion of
basal ganglia, lesion, bilateral
biologic markers
bone marrow transplantation
bradykinesia
brain atrophy
brainstem, infarction of
brainstem, lesion of
brainstem, neoplasms of
brainstem, syndrome
cardiomyopathy
CAT scan
CAT scan, abnormal
cataplexy
cerebellar ataxia, autosomal recessive
cerebellar ataxia, hereditary
cerebellar ataxia, neuropathy and vestibular areflexia syndrome
cerebellar atrophy, primary
cerebellar atrophy, secondary
cerebellar degeneration
cerebellar hemorrhage
cerebellar infarction
cerebellum, disease of
cerebral cortex
cerebral cortical atrophy
cerebral embolism
cerebral embolism, cardiac origin
cerebral palsy
cerebral palsy, associated problems with
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, gammaglobulin of
cerebrovascular accident
Charcot-Marie-Tooth
children
chorea
chromosomal abnormality
Clinical Pathologic Conference(C.P.C.)
cognition
congestive heart failure
consanguinity
corona radiata
cortical-basal ganglionic degeneration
cough
cranial neuropathy
cultured skin fibroblasts
deep gray nuclei
degenerative diseases of CNS
delay in diagnosis
dementia
dementia, rapidly progressive
depression
developmental milestones, loss of
dexterity, impaired
diabetes mellitus
diarrhea
diplopia
dizziness
down-beat nystagmus
down-beat nystagmus, primary position of gaze
drooling
dying
dysarthria
dysarthria-clumsy hand syndrome
dysdiadochokinesia
dysmetria
dysphagia
dyspraxia
dystonia
dystonia musculorum deformens
dystonia, cervical
electroencephalogram, abnormalities of
electromyogram
electrophoretic pattern, CSF
embolism
encephalitis
encephalopathy
epileptic encephalopathy
exome sequencing
eye movement, disorders of
failure to thrive
falling
familial
familial periodic ataxia
FARS2 deficiency
fatigue
fine motor function, impaired
finger nose finger test
finger numbness
foam cells
foot drop
Friedreich's ataxia
Friedreich's ataxia, late onset
gait disorder
gaze palsy
gaze palsy, supranuclear
gaze palsy, vertical
gene
gene mutation
genetic counselling
genetic diagnosis, prenatal
genetic neurologic disorders
genetic screening
genetic testing
Gerstmann-Straussler-Scheinker disease
glabellar sign
granular osmiphilic material
hammertoes
handwriting
head nodding
headache
hearing loss
heel-knee-shin test
hepatic failure
hepatolenticular degeneration(Wilson's disease)
hepatosplenomegaly
heralding manifestation
hormone replacement
hydrocephalus
hyperreflexia
hypersomnia
hypertension
hypertonia
hypogonadism
hypogonadism, hypogonadotropic
hypometric saccades
hypotonia
iatrogenic neurologic disorders
imbalance
immunohistochemistry
inattention
incoordination
inferior olivary nucleus
insomnia
intellectual deficit
intellectual deterioration
intelligence quotient
internal capsule
introverted
Jakob-Creutzfeldt disease
Jakob-Creutzfeldt disease, cerebellar variant
Jakob-Creutzfeldt disease, variant
jaundice
Kayser-Fleischer ring
lacunar infarction
lacunar infarction, differential diagnosis of
lateropulsion
leg weakness, bilateral
leukodystrophy
leukoencephalopathy
lipid storage disorder of CNS
liver disease
Lorenzo's oil
lymphoma
lymphoma involving CNS
lymphoma, primary of CNS
medulla oblongata, neoplasm of
memory, defect of recent
memory, impairment of
meningitis, CSF cell count-normal
microcephaly
midbrain, atrophy
misdiagnosis
mitochondrial disease
molecular genetics
motor neuron disease
movement disorder
movement disorder, extrapyramidal
MRI
MRI, abnormal
MRI, contrast enhanced
MRI, diffusion weighted
MRI, false negative
MRI, negative
MRI, spinal cord
MRI, spine
multiple sclerosis, differential diagnosis of
multiple sclerosis, misdiagnosis
myelomalacia
myelopathy
myelopathy, chronic progressive
myoclonic jerks
myoclonus
nausea and vomiting
neoplasm, primary of CNS
neoplasm, primary of CNS-children
nerve conduction studies
neurofibrillary degeneration
neurofibromatosis 1
neurologic disease, diagnoses of
neurologic signs
neurologic symptoms
neuronal ceroid-lipofuscinosis
neuropathology
neuropathy
neuropathy, demyelinating
neuropathy, hereditary peripheral
neuropathy, sensory
next-generation sequencing
Niemann-Pick disease
numb clumsy hands syndrome
nystagmus
ocular motility, disorders of
olivary degeneration, hypertrophic
optic atrophy
ovarian dysgenesis
palatal myoclonus
paraparesis
paraparesis, familial spastic
paraparesis, spastic
Parkinson disease
Parkinsonism syndrome
Perrault syndrome
personality change
pes cavus
pons, infarction of
pontine hemorrhage
positional head-hanging test
prevention of neurologic disorders
prion disease
prion protein gene
prognosis
progressive ataxia and palatal tremor
progressive myoclonic epilepsy
progressive neurologic disorder
proprioception, abnormal
protein 14-3-3, cerebrospinal fluid
psychiatric disorder
psychiatric problems in neurologic disorders
psychological testing
psychological testing, neurologic problems
psychosis
pure dysarthria
pure motor hemiplegia
pursuit eye movements, abnormal
pyramidal tract dysfunction
rapidly progressing neurologic illness
reading disorder, acquired
real-time quaking-induced conversion
release phenomena
retropulsion
review article
rigidity
risk factors
Romberg's sign
rubella encephalitis
rubella encephalitis, progressive
rubella virus
saccadic eye movements, abnormal
scoliosis
seizure
seizure, children
sensorimotor stroke
sensorineural hearing loss
sensory loss
serologic testing
serologic testing of cerebrospinal fluid
slit lamp examination
slurred speech
spastic ataxia
spastic diplegia
spasticity
speech disorder
speech disorder, non aphasic
spinal cord
spinal cord, lesion of
spinocerebellar ataxia
splenomegaly
spontaneous remission
square wave jerks
staggering
strokelike episodes
suck reflex
superior cerebellar artery infarction
superior cerebellar artery syndrome
symmetric brain lesions
tandem gait, ataxic
tau protein
tauopathy
thalamus, lesion of-bilateral
titubation
toe walking
transient neurologic deficit
treatment of neurologic disorder
tremor
tremor, cerebellar
tremor, intention
trinucleotide repeats
upgaze, paralysis of
vertigo
vertigo, episodic
very long chain fatty acids
vestibulopathy
vibratory sensation, abnormal
viral infection, CNS
vision, blurred
vitamin E deficiency
voice, abnormality of
walking frame
walking, difficulty with
weakness
weakness, progressive
weight loss
white matter disease
wide based gait
workup
Showing articles 200 to 250 of 1070 << Previous Next >>

Clinicopathologic Conference, Borrelia Miyamotoi Infection
NEJM 383:1578-1586, Case 32-2020, 2020

Burning Pain in the Legs
NEJM 383:e18, Sacks, C.A., 2020

Clinicopathologic Conference, AA Amyloidosis, Complicated by Cerebral Mucormycosis
NEJM 382:1457-1466, Case 11-2020, 2020

A 42-year-old Woman with Progressive Cognitive Difficulties and Gait Imbalance
Neurol 94:e1219-e1226, Slama, M.C.C.,et al, 2020

An 81-year-old Woman with Decreased Consciousness and Fluctuating Right Facial Droop
Neurol 94:843-848, Van Ommeren, R.,et al, 2020

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

Involuntary Hand-Shaking: Transient Ischemic Attack, Seizure, or Psychogenic?
Ann Neurol 88:12-13, Sharma, V.K. & Sinha, A.K., 2020

Palatal Myoclonus, Abnormal Eye Movements, and Olivary Hypertrophy in GAD65-Related Disorder
Neurol 94:273-275, Macaron, G.,et al, 2020

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

A 65-year-old man with Asymmetric Weakness and Parethesias
Neurol 93:856-861, Harada, Y.,et al, 2019

Hand Posture as Localizing Sign in Adult Focal Epileptic Seizures
Ann Neurol 86:793-800, Ferando, I.,et al, 2019

Orofacial Dyskinesia in a Young Man
JAMA Neurol 76:1517-1518, Tian, X.,et al, 2019

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

Clinicopathologic Conference, Ingestion of Isopropyl Alcohol
NEJM 380:1657-1665, Case 13-2019, 2019

Toxic Diffuse Isolated Cerebellar Edema from Over-the-Counter Health Supplements
Neurol 92:965-966, Kim, D.D.,et al, 2019

Subacute Progressive Sensorimotor Symptoms
BMJ 365:doi:10.1136/bmj.l1923, Francis, A.,et al, 2019

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

A 26-Year Old Man with Right Hand and Arm Weakness
Neurol 93:e927-e933, Elliott,E.J.&Smith,J.D., 2019

A 58-year-old Man with Hand Tremor and Episodes of Neck Pain
Neurol 93:557-561, Urso, D.,et al, 2019

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

A 61-Year-Old Woman with Acute Onset Dysgraphia
Neurol 92:e386-e391, Smith, L.R.,et al, 2019

A 40-Year-Old Woman Presenting with Distal Leg Weakness
Neurol 92:242-247, Fam, D.,et al, 2019

Clinicopathologic Conference, Pernicious Anemia (Vitamin B12 Deficiency)
NEJM 380:665-674, Case 5-2019, 2019

A 54-year-old man with Dyspnea and Muscle Weakness
Neurol 92:e1136-e1140, Chertcoff, A.,et al, 2019

Clinicopathologic Conference, Ocular Syphilis
NEJM 380:1062-1071, Case 8-2019, 2019

Facial Myokymia and Myorhythmia in Anti-IgLON5 Disease
Neurol 91:e1659, Vetter, E.,et al, 2018

Clinicopathologic Conference, Lyme Meningoradiculitis
NEJM 379:1862-1868, Case 34-2018, 2018

Complex Bilateral Corpus Callosum Infarction after Paradoxical Embolism
Neurol 91:e1947-e1948, Calheiros de Oliveira Costa, G.V.,et al, 2018

A 35-year-old Woman with Diplopia, Ataxia, and Altered Mental Status
Neurol 91:e1942-e1946, Bauer, Z.,et al, 2018

Progressive Gait Difficulty and Incontinence in a 40-year-old Man with HIV
Neurol 91:1065-1070, Silverman, A.,et al, 2018

Clinical Reasoning: A 49-year-old man with Progressive Numbness, Weakness, and Evidence of Leptomeningeal Enhancement
Neurol 90:e90-e93, Lovett, A.,et al, 2018

Clinical Reasoning: Cardioembolic Stroke in a 23-year-old Man with Elbow Contracture
Neurol 90:e172-e176, Roy, B. & Raynor, E., 2018

Recurrent Dysarthria and Ataxia in a Young Girl
JAMA Neurol 75:125-126, Romba, M.,et al, 2018

A 41-year-old man with Thunderclap Headache
Neurol 91:e87-e91, Grossman, S.et al, 2018

Progressive Weakness and Memory Impairment in a Middle-aged Man
JAMA 320:197-198, DeFilippis, E.M.,et al, 2018

Precentral Gyrus Infarct Presenting as Isolated Contralateral Peripheral-Type Facial Palsy
Neurol 91:421-422, Hebant, B.,et al, 2018

A 58-year-old Woman with Systemic Scleroderma and Progressive Cervical Cord Compression
Neurol 91:e1262-e1264, Karschnia, P.,et al, 2018

Antibody-Mediated Encephalitis
NEJM 378:840-851, Dalmau, J.,et al, 2018

A 52-year-old woman with a 3 weeks of progressive gait ataxia and dysarthria
Neurol 90:e985-e989, Ly, C.,et al, 2018

A 42-year-old man with unilateral leg weakness
Neurol 90:e1085-e1090, Schneider, R.,et al, 2018

A 60-year-old woman with ataxia
Neurol 90:e1627-e1630, Dandapat, S.,et al, 2018

Disability in adults with arthrogryposis is severe, partly invisible, and varies by genotype
Neurol 90:e1596-e1604, Dai, S.,et al, 2018

Making Sense of the Clinical Spectrum of Limb Girdle Muscular Dystrophies
Pract Neurol 18:201-210, Khadilkar,S.V.,et al, 2018

Wilson Disease
NIDDK Oct2018, , 2018

Human Parechovirus: An Increasingly Recognized Cause of Sepsis-Like Illness in Young Infants
Clin Microbiol Reviews 31:1-17, Olijve, L.,et al, 2018

Spinocerebellar Ataxia Type 2: Clinicogenetic Aspects, Mechanistic Insights, and Management Approaches
Front Neurol doi:10.3389/fneur.2017.00472, Velazquez-Perez, L.C.,et al, 2017

A Rare Case of Bilateral Optic Neuritis and Guillain-Barre Syndrome Post Mycoplasma Pneumoniae Infection
Neuro Opth 41:41-47, Baheerathan, A.,et al, 2017

Wernekink Commissure Syndrome Secondary to Bilateral Caudal Paramedian Midbrain Infarction Presenting with a Unique "Heart or V" Appearance Sign:Case Report and Review of the Literature
Front Neurol soi.10.3389/fneur.2017.00376,Aug, Zhou,C.,et al, 2017

Clinicopathologic Conference, Biotinthiamine-Responsive Basal Ganglia Disease Due to Mutation SLC19A3
NEJM 377:2376-2385, Case 38-2017, 2017

Safety and Efficacy of Focused Ultrasound Thalamotomy for Patients with Medication-Refractory, Tremor-Dominant Parkinson Disease
JAMA Neurol 74:1412-1418, Bond, A.E.,et al, 2017



Showing articles 200 to 250 of 1070 << Previous Next >>