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Differential
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abdominal x-ray
adverse drug reaction
affect, flat
agitation
akathisia
alcohol intolerance
alternating rapid movement
aluminum
anorexia
anti IgLON5
anticonvulsants
anticonvulsants, selection of
antithyroid antibodies
apnea
apraxia
arm swing, reduced
arm weakness
asterixis
ataxia
ataxia, cerebellar
ataxia, progressive
ataxia, truncal
ataxic gait
autoantibodies
autonomic dysfunction
axonal spheroid
Babinski sign
basal ganglia, calcification of
basal ganglia, degeneration
basal ganglia, lesion of
basal ganglia, lesion, bilateral
behavioral disorder
bismuth
bradykinesia
brain atrophy
brain biopsy
brainstem, atrophy
brainstem, lesion of
bulbar palsy
CAG repeats
carbon monoxide poisoning
cardiomyopathy
CAT scan
CAT scan, abnormal
CAT scan, emission
CAT scan, emission, abnormal
cataracts
celiac disease, adult
central nervous system, infection of
cerebellar atrophy, primary
cerebellar atrophy, secondary
cerebellar degeneration
cerebral cortex
cerebral glucose metabolism
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, gammaglobulin of
cerebrospinal fluid, lactic acid concentration
cerebrospinal fluid, oligoclonal IgG in
cerebrovascular accident
cerebrovascular accident, young adult
cherry red spot-myoclonus syndrome
chewing movements
children
choking
chorea
chorea, familial
choreoathetosis
chronic progressive external ophthalmoplegia
Clinical Pathologic Conference(C.P.C.)
clonus
coenzyme Q10 deficiency
cognition
color vision, impaired
coma
coma, episodic
confabulation
confusion
congenital infection, CNS
congenital paresis
cranial nerve palsies
Creutzfeldt-Jakob disease, genetic
deep gray nuclei
degenerative diseases of CNS
delay in diagnosis
dementia
dementia, differential diagnosis of
dementia, rapidly progressive
dementia, transmissible
dementia, treatment of
dentate nuclei, lesion of
dentatorubral-pallidoluysian atrophy
depression
developmental milestones, loss of
diabetes mellitus
dialysis
dialysis dementia
diet
differential diagnosis
diplopia
doll's head maneuver
Dravet syndrome
dysarthria
dysdiadochokinesia
dysmetria
dysphagia
dysphasia
dyssynergia cerebellaris myoclonica
dystonia
electroencephalogram, abnormalities of
electroencephalogram, triphasic delta waves
electromyogram
encephalitis
encephalitis, autoimmune
encephalitis, brainstem
encephalitis, paraneoplastic
encephalitis, viral
encephalomyelitis
encephalopathy
encephalopathy, delayed
encephalopathy, Hashimoto's
enterovirus
enterovirus infection of CNS
epidemic
episodic disorders
episodic neurologic deficits
episodic unconsciousness
eye movement, disorders of
faciobrachial dystonic seizure
falling
familial
fasciculation
fatal familial insomnia
fatigue
fever
fine motor function, impaired
finger nose finger test
flaccid paralysis
gait disorder
gait, apraxic
gaze palsy, vertical
gene mutation
gene therapy
genetic counselling
genetic neurologic disorders
genetic testing
globus pallidus, lesion of
glutamic acid decarboxylase, antibody
gluten ataxia
gluten sensitivity
gluten-free diet
granular osmiphilic material
grasp reflex
gray matter
gyrus, abnormal
hallucination
hand-foot-mouth disease
handwriting
headache
hearing loss
heart block
heel-knee-shin test
hemimyoclonic jerks
hepatosplenomegaly
heralding manifestation
hoarseness
hyperreflexia
hypersomnia
hyperthyroidism
hypometric saccades
hyponatremia
hypophonia
hypothyroidism
hypotonia
imbalance
imbalance, postural
immunohistochemistry
immunotherapy
inattention
incontinence, fecal
incoordination
insight, loss
insomnia
intellectual deficit
intellectual deterioration
intestinal pseudoobstruction
intrauterine infection
intrauterine infection, viral of CNS
introverted
Jakob-Creutzfeldt disease
Jakob-Creutzfeldt disease, cerebellar variant
Jakob-Creutzfeldt disease, variant
juvenile paresis
Kearns-Sayre syndrome
Lafora's disease
lateropulsion
Leber's hereditary optic neuropathy
Leigh's disease
Leigh's disease, adult variety
leucine rich glioma inactivated 1 antibodies
leukocyte enzyme abnormality
leukodystrophy
leukoencephalopathy
leukoencephalopathy, hereditary diffuse
limbic encephalitis
linear lesion
maculopathy
masked facies
MELAS syndrome
memory, defect of recent
memory, impairment of
meningitis
meningitis, aseptic
meningoencephalitis
mental retardation
MERRF syndrome
micrographia
mimics
misdiagnosis
mitochondrial disease
mitochondrial encephalomyopathy
MNGIE syndrome
molecular genetics
monoparesis
mortality
motor cortex
motor neuron disease
motor neuron disease, misdiagnosis
movement disorder
MRI
MRI, abnormal
MRI, diffusion weighted
MRI, false negative
MRI, high signal intensity of basal ganglia
MRI, negative
MRI, pelvis
MRI, spinal cord
MRI, susceptibility weighted
mutism
myelitis
myelitis, longitudinal
myelitis, transverse
myelopathy
myoclonic ataxia
myoclonic jerks
myoclonus
myoclonus, cortical
myoclonus, epilepsy
myoclonus, stimulus sensitive
myoclonus, treatment of
myoclonus-ataxia syndrome
myopathy
myopathy, mitochondrial
nausea and vomiting
neuroaxonal leukodystrophy
neurologic complications of, systemic cancer
neurologic disease
neurologic disease, diagnoses of
neuronal ceroid-lipofuscinosis
neuropathology
neuropathology, brain
neuropathy
neuropathy, ataxia, retinitis pigmentosa
neurotoxic
neurotoxin
next-generation sequencing
ocular motility, disorders of
ophthalmoplegia
ophthalmoplegia, progressive external
opsoclonus
opsoclonus-myoclonus syndrome
optic atrophy
optic atrophy, hereditary
optic neuropathy
oral ulcerations
ovarian tumor
palatal myoclonus
pancytopenia
paralysis, acute
paralysis, acute areflexic
paraparesis, spastic
parasomnia
Parkinsonism syndrome
paroxysmal neurologic deficits
pathologic reflex
personality change
pigmentary retinopathy
pleocytosis of cerebrospinal fluid
polyneuropathy
pontocerebellar atrophy
potassium channel antibodies
prion disease
prognosis
progressive infantile poliodystrophy
progressive myoclonic epilepsy
progressive neurologic disorder
progressive pallidum atrophy
protein 14-3-3, cerebrospinal fluid
protein 14-3-3, cerebrospinal fluid, false negative
pseudobulbar palsy
psychiatric problems in neurologic disorders
psychomotor retardation
psychosis
psychosis, acute
ptosis
pursuit eye movements, abnormal
pyruvate metabolism, abnormality of
quadriparesis
ragged-red fibers
Ramsay Hunt syndrome
rapidly progressing neurologic illness
real-time quaking-induced conversion
release phenomena
REM sleep behavior disorder
remote effect of cancer on the nervous system
renal failure
respiratory failure
retinopathy
review article
rigidity
Romberg's sign
rooting reflex
rubella encephalitis
rubella encephalitis, progressive
rubella syndrome
rubella virus
rubeola virus
saccadic eye movements, abnormal
seizure
seizure, children
seizure, paradoxical
seizure, treatment of
sensorineural hearing loss
serologic testing
serologic testing of cerebrospinal fluid
short stature
sleep pathology and physiology
slow virus infection of CNS
slurred speech
snout reflex
sodium valproate
somnolence
spasticity
speech disorder
spinal cord
spinal cord, lesion of
spinocerebellar ataxia
spinocerebellar ataxia type 7
spongy degeneration of brain
square wave jerks
startle myoclonus
startle reaction
steroid
steroid therapy, CNS treatment and complications with
stiff man syndrome
subacute sclerosing panencephalitis(S.S.P.E.)Dawson's disease
suicide
symmetric brain lesions
tandem gait, ataxic
tau protein
temporal lobe, lesion, bilateral
teratoma, ovarian
thalamus, lesion of-bilateral
thyroiditis
toxins, nervous system
transplacental virus infections
treatment of neurologic disorder
tremor
tremor, intention
tremor, postural
trinucleotide repeats
unconsciousness
unconsciousness, episodic
unconsciousness, transient
Unverricht-Lundborg disease
upgaze, paralysis of
urinary incontinence
vertigo
viral infection
viral infection, CNS
viral isolation
virus, slow
vision, blurred
visual acuity, decreased
visual impairment
vocalizations
walking, difficulty with
weakness, acute
weakness, focal
weight loss
wheelchair
white matter disease
wide based gait
writing
Showing articles 600 to 650 of 3352 << Previous Next >>

A Case of Monocytic Pleocytosis in West Nile Virus Encephalitis and Review of the Literature
Case Reports 23:687-688, Villafuerte, B.J.,et al, 2020

Diagnostic and Prognostic Value of Conventional Brain MRI in the Clinical Work-Up of Patients with Amyotrophic Lateral Sclerosis
J Clin Med 9:1-12, Rizzo, G.,et al, 2020

Acetylcholine Receptor-Antibody-Positive Myasthenia Gravis Presenting with Early Atrophy and Nonfluctuating Weakness of Proximal Limb Muscles
J Clin Neurol 16:714-716, Pancheri, E.,et al, 2020

Progressive Multifocal Leukoencephalopathy in a Patient with Primary Amyloid Light-Chain Amyloidosis
Clin Neurol Neurosurg 192:doi105709, Katsuse, K.,et al, 2020

Progressive Proximal Weakness in a 61-Year-Old Man
Neurol 98:122-127, Yu, M.,et al, 2020

Generalized Myoclonus in COVID-19
Neurol 95:e767-e772, Rabano-Suarez, P.,et al, 2020

A 73-Year-Old Man with Recurrent Aphasia, Headaches, and Confusion
Neurol 95:e2595-e2599, Bose, G.,et al, 2020

Bornavirus Encephalitis Shows a Characteristic Magnetic Resonance Phenotype in Humans
Ann Neurol 88:723-735, Finck, T.,et al, 2020

Sensory Ganglionopathy
NEJM 383:1657-1662, Amato, A.A. & Ropper, A.H., 2020

Dressing Apraxia as Initial Manifestation of Creutzfeldt-Jakob Disease
Tremor and Other Hyperkinetic Movements 10:1-3, Heckmann, J.G.,et al, 2020

Bilateral Ptosis, Dysphagia, and Progresive Weakness in a Patient of French-Canadian Background
Neurol 95:933-938, Paul,P.,et al, 2020

Migraine, hearing loss, and blurred vision in a young woman
Neurol 95:e2945-e2950, Sasikumar, S.,et al, 2020

Bithalamic Lesions
Stroke 51:e355-e358, Chen, P.M.,et al, 2020

Clinical features, prognostic factors, and antibody effects in anti-mGluR1 encephalitis
Neurol 95:e3012-e3025, Spatola, M.,et al, 2020

Neurological Impairments in a Patient Returning from Cuba
JAMA Neurol 77:1570-1571, Serlin, Y.,et al, 2020

Involuntary Groaning Induced by Levodopa Therapy in a Patient With Progressive Supranuclear Palsy
JAMA Neurol 77:1569, Park, J.E., 2020

Clinicopathologic conference, Vitamin D deficiency
NEJM 383:2462-2470, Case 39-2020, 2020

Clinicopathologic conference, Cryptococcal meningoencephalitis and advanced HIV infection
NEJM 383:2572-2580, Case 40-2020, 2020

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

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

Nusinersen in Adult Patients with Spinal Muscular Atrophy
Neurol 95:e413-e416, Moshe-Lilie, O.,et al, 2020

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

Functional Gait Disorders
Neurol 94:1093-1099, Nonnekes, J.,et al, 2020

FDA Approves Fenfluramine for Treatment of Seizures Associated with Dravet Syndrome
FDA June2020, , 2020

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

Degenerative Cervical Spondylosis
NEJM 383:159-168, Theodore, N., 2020

Long Survival Sporadic Creutzfeldt-Jakob Disease
Neurol 95:87-88, Liu, X.Y.,et al, 2020

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

A 14-Year-Old Boy with Acute Weakness, Parethesias, and Headache
Neurol 95:e1285-e1289, Seese, R.R.,et al, 2020

A Young Generalized Dystonia Patient with Globus-Pallidus-Specific Lesion
Ann Neurol 88:637-638, Wu, H.,et al, 2020

Spinal Xanthomatosis
Neurol 95:e1615-e1616, Valencia-Sanchez, C.,et al, 2020

Opsoclonus in Anti-Ma2 Brain-Stem Encephalitis
NEJM 383:e84, Sacks, C.A.,et al, 2020

"Boule Du Biceps" in Dysferlinopathy
Neurol 94:83-84, El Sherif, R.,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

Hypointensity of the Basal Ganglia in Adults with Glucose Transporter Protein Type 1 Deficiency Syndrome: A Novel Magnetic Resonance Imaging Finding
Ann Neurol 87:10-11, Van Samkar, A.,et al, 2020

A 70-year-old Man with Rapid Stepwise Paraparesis and Sensory Loss
Neurol 94:e651-e655, Krause, M.A.,et al, 2020

Infection Risks Among Patients with Multiple Sclerosis Treated with Fingolimod, Natalizumab, Rituximab, and Injectable Therapies
JAMA Neurol 77:184-191, Luna, G.,et al, 2020

A Rare Presentation of Whipple Disease
Neurol 94:e758-e761, Koek, A.T.,et al, 2020

Hopkins Syndrome
Neurol 94:e996-e997, Sgobbi de Souza, P. V.,et al, 2020

Accuracy of a Machine Learning Muscle MRI - Based Tool for the Diagnosis of Muscular Dystrophies
Neurol 94:e1094-e1102, Verdu-Diaz, J.,et al, 2020

A 59-year-old Woman with Multiple Myeloma and Lower Extremity Weakness and Numbness
Neurol 94:794-800, Gadot, R.,et al, 2020

Balance, Falls, and Hearing Loss: Is It Time for a Paradigm Shift?
JAMA Otolaryngol Head Neck Surg doi:10.1001/JAMAoto.2020.0415, Lubetzky, A.V., 2020

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

A 22-Year-Old Man with Progressive Bilateral Visual Loss
Neurol 94:625-630, Yang, S.L.,et al, 2020

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

Wall-Eyed Bilateral Internuclear Ophthalmoplegia by Ischemic Stroke
Neurologist 25:82-84, Uzawa, A.,et al, 2020

Muscular Dystrophies
Lancet 394:2025-2038, Mercuri, E.,et al, 2019

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

Clinicopathologic Conference, Lymphocytic Choriomeningitis Virus Infection
NEJM 381:2553-2560, Case Record 40-2019, 2019



Showing articles 600 to 650 of 3352 << Previous Next >>