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acetazolamide
advances in neurology
agitation
amnesia
AMPA receptor antibodies
amphiphysin antibodies
anti GQ1b IgG antibody
anti IgLON5
antibodies to voltage-gated calcium channels
arrhythmia, cardiac
ataxia
ataxia, cerebellar
ataxia, paroxysmal
atypical
autoantibodies
autoimmune basal ganglia encephalitis
autoimmune disease
autoimmune encephalopathy
autoimmune epilepsy
autonomic dysfunction
autonomic neuropathy
basal ganglia
basal ganglia, lesion of
basal ganglia, lesion, bilateral
behavioral disorder
behavioral disorder, acute
bradykinesia
brain atrophy
brain biopsy
burning feet
calcium channel dysfunction
carcinoma
carcinoma of lung
CAT scan, emission, abnormal
catatonia
caudate nucleus, lesion of
caudate nucleus, lesion of, bilateral
central core disease
cerebellar degeneration
cerebral cortex
cerebral cortical atrophy
cerebrospinal fluid, abnormal
cerebrospinal fluid, childhood
cerebrospinal fluid, oligoclonal IgG in
children
chloride channel dysfunction
chorea
chorea, senile
choreoathetosis
ciguatera poisoning
Clinical Pathologic Conference(C.P.C.)
cognition
cogwheel rigidty
cold hands sign
collapsin response mediator protein 5 IgG
coma
complications
confabulation
confusion
constipation
contactin associated protein like 2 antibodies
controversies in neurology
cytochrome c oxidase
deep gray nuclei
dementia
dementia, rapidly progressive
dementia, reversible
dementia, treatment of
depression
dermatomyositis
diagnostic criteria
diarrhea
dichlorphenamide
differential diagnosis
disability, neurological
DPPX
DPPX, antibodies
DPPX, antibodies, encephalitis
dyskinesia
dyskinesia, facial
dystonia
efficacy
electroencephalogram, abnormalities of
electromyogram
encephalitis
encephalitis, autoimmune
encephalitis, brainstem
encephalitis, clinical picture and treatment of
encephalitis, etiology
encephalitis, paraneoplastic
encephalitis, viral
encephalomyelitis
encephalopathy
episodic neurologic deficits
faciobrachial dystonic seizure
false negative
familial hemiplegic migraine
fasciculation
fever
flu-like illness
gait disorder
gamma amino butyric acid receptor antibody
gammaglobulin therapy, intravenous
gastrointestinal disease, neurologic complications
gender
gene
gene mutation
genetic neurologic disorders
glutamic acid decarboxylase, antibody
glycine receptor antibodies
hallucination
hallucination, olfactory
headache
hemimyoclonic jerks
heralding manifestation
herpes simplex encephalitis
hippocampus
Hodgkin's disease
hyperekplexia
hyperhidrosis
hyperkalemic periodic paralysis
hypersomnia
hypertension
hypokalemic periodic paralysis
hyponatremia
hyponatremia with cerebral disorders
immunologic disease
immunology and the nervous system
immunomodulation
immunosuppressive agents
immunotherapy
inappropriate antidiuretic(A.D.H.)hormone
inappropriate antidiuretic(A.D.H.)hormone, CNS involvement with
insomnia
intellectual deficit
intellectual deterioration
Jakob-Creutzfeldt disease
lateropulsion
leucine rich glioma inactivated 1 antibodies
leukemia, neurologic findings assoc.with
level of consciousness, decreased
limbic encephalitis
limbic system
malignancy screen
malignancy, occult
malignant hyperpyrexia
masked facies
memory
memory, defect of recent
memory, impairment of
meningeal enhancement
mental status, abnormal
mesial temporal lobe
mesial temporal sclerosis
mexiletine
migraine
mild cognitive impairment
mimics
misdiagnosis
molecular genetics
monoclonal antibodies
mood change
mortality
Morvan's fibrillary chorea
movement disorder
movement disorder, extrapyramidal
MRI
MRI pattern
MRI, abnormal
MRI, diffusion weighted
MRI, disappearing lesion on
MRI, false negative
MRI, FLAIR
MRI, negative
muscle diseases, characteristics of
muscle spasm
muscle stiffness
muscle twitching
myasthenia gravis, paraneoplastic
myasthenic syndrome
myelitis, transverse, recurrent
myoclonic jerks
myoclonus
myokymia
myotonia
myotonia congenita
near syncope
negative
neurexin-3 alpha antibodies
neurologic disease, diagnoses of
neurologic disease, multifocal
neuromuscular junction
neuromyotonia
neuronal cell surface antigen
neuronopathy, sensory
neuropathy, paraneoplastic
night sweats
NMDA antagonists
old age, neurology of
onconeural antibodies
ophelia syndrome
opsoclonus-myoclonus syndrome
pain
paralysis
paramyotonia congenita
paraneoplastic cerebellar degeneration
paresthesias
Parkinsonism syndrome
paroxysmal neurologic deficits
pediatric autoimmune neuropsychiatric disorders associated with streptococcal infection
periodic paralysis
peripheral nerve, lesion of
personality change
plasmapheresis
pleocytosis of cerebrospinal fluid
potassium channel antibodies
potassium channel dysfunction
practice guidelines
precipitating factors
prognosis
progressive neurologic disorder
pruritus
psychiatric problems in neurologic disorders
psychological testing
psychosis
psychosis, acute
recurrent
Red flags
remote effect of cancer on the nervous system
retinopathy
reversible neurologic disorder
review article
rippling muscle disease
rituximab
safety
screening
seizure
seizure, adult onset
seizure, drug resistance
seizure, focal
seizure, intractable
seizure, intractable, treatment of
seizure, psychomotor-temporal lobe
seizure, treatment of
seizure, unknown origin
serologic testing
serologic testing, false negative
seronegative
Sjogren's syndrome
Sjogren's syndrome, neurologic manifestations of
sleep pathology and physiology
sodium channel dysfunction
spinocerebellar ataxia
spinocerebellar ataxia type 6
status epilepticus
steroid
steroid therapy, CNS treatment and complications with
striatal encephalitis
striatum, lesion of
striatum, lesion of, bilateral
symmetric brain lesions
tangential
temporal lobe
temporal lobe, lesion
temporal lobe, lesion, bilateral
teratoma
teratoma, ovarian
thiazide diuretic
thymoma
transient neurologic deficit
treatment of neurologic disorder
tremor
unconsciousness
undiagnosed
visual loss
weight loss
wheelchair
white matter disease
white matter disease, subcortical
wide based gait
workup
Showing articles 400 to 450 of 4347 << Previous Next >>

A 48-year-old woman with confusion, personality change, and multiple enhancing brain lesions
Neurol 90:e1724-e1729, Hills, J.M.,et al, 2018

Essential Tremor
NEJM 378:1802-1810, Haubenberger, D.,et al, 2018

Progressive cognitive decline, cerebellar ataxia, recurrent myoclonus, and epilepsy
Neurol 90:e1827-e1831, Xiao, F.,et al, 2018

Diagnosis and Management of the Antiphospholipid Syndrome
NEJM 378:2010-2021, Garcia, D. & Erkan, D., 2018

A 23-year-old woman with fever and vertical diplopia
Neurol 90:e2006-e2010, Lin, D.J.,et al, 2018

Encephalitis with mGluR5 antibodies
Neurol 90:e1964-e1972, Spatola, M.,et al, 2018

Cognitive Impairment Before Intracerebral Hemorrhage is Associated with Cerebral Amyloid Angiopathy
Stroke 49:40-45, Banerjee, G.,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

Gummatous Neurosyphilis
Neurol 90:e913-e914, Silva, H.S.,et al, 2018

Clinicopathologic Conference, Homocystinuria due to genetic mutations of the gene encoding cystathionine B-synthase (CBS)
NEJM 378:941-948, Case 7-2018, 2018

A 12-year-old girl with headache and change in mental status
Neurol 90:524-529, Patel, P.,et al, 2018

Headache and Altered Mental Status
Neurol 90:e1267-e1270, Spera, K.M.,et al, 2018

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

Seizures and Encephalitis in Myelin Oligodendrocyte Glycoprotein IgG Disease vs Aquaporin 4 IgG Disease
JAMA Neurol 75:65-71, Hamid, S.H.M.,et al, 2018

Gasperini Syndrome
Neurol 90:e261, Lorio, R., 2018

Practice Guide Update Summary: Mild Cognitive Impairment
Neurol 90:126-135, Petersen, R.C.,et al, 2018

Supplementary Motor Area Stroke Mimicking Functional Disorder
Stroke 49:e28-e30, Mathew, P.,et al, 2018

A 60-year-old man with arm weakness and numbness
Neurol 90:190-196, Foster, L.A.,et al, 2018

Mystery Case: A 48-year-old Woman with Bizarre Behavior, Neurologic Symptoms, and Progressive Decline
Neurol 90:242-247, Kesari, N.K.,et al, 2018

Clinical Reasoning: Siblings with Progressive Weakness, Hypotonia, Nystagmus, and Hearing Loss
Neurol 90:e625-e631, Set, K.K.,et al, 2018

Neurological Manifestations Among US Government Personnel Reporting Directional Audible and Sensory Phenomena in Havana, Cuba
JAMA 319:1125-1133, 1098, 1079, Swanson, R.L.,et al, 2018

Degenerative Cervical Myelopathy
BMJ 360:k186, Davies, B.M.,et al, 2018

Diagnosing Stroke in Acute Dizziness and Vertigo
Stroke 49:788-795, Saber Tehrani, A.S.,et al, 2018

Wilson Disease
NIDDK Oct2018, , 2018

FARS2 dificiency; new cases, review of clinical, biochemical, and molecular spectra, and variants interpretation based on structural, functional, and evolutionary significance
Mol Genet Metab 125:281-291, Almannai, M.,et al, 2018

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

Bilateral Cavernous Carotid Aneurysms: Atypical Presentation of a Rare Cause of Mass Effect
Front Neurol doi:10.3389/fneur.2018.0069, Gagliardi, D.,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

Hashimotos Thyroiditis and Autoimmune Gastritis
Front Endocrinol 8:00092, Cellini,Miriam,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

Huntington Disease: Clinical Features and Diagnosis
UptoDate Dec 2017, Oksana Suchowersky, 2017

The Useless Hand of Oppenheim
Pract Neurol 17:464-468, Wiblin, L. & Guadagno, J., 2017

Retropharyngeal Abscess
Emedicine.medscape.com Jan, Kahn, J.H. & Shlamovitz, G.Z., 2017

Advances in Progressive Supranuclear Palsy: New Diagnostic Criteria, Biomarkers, and Therapeutic Approaches
Lancet Neurol 16:552-563, Boxer, A.L.,et al, 2017

Clinicopathologic Conference, Primary Progressive Aphasia, Semantic Variant, due to TAR DNA Binding Protein 43 associated Frontotemporal Lobar Degen
NEJM 376:158-167, Case 1-2017, 2017

Infratentorial Dural Arteriovenous Fistula Resulting in Brainstem Edema and Enhancement
Neurol 88:503-504, Emmer, B.J.,et al, 2017

Clinical and Neuroimaging Features in Gorlin-Goltz Syndrome
Neurol 88:e52-e54, da paz Oliveira, G.,et al, 2017

Spontaneous Subarachnoid Haemorrhage
Lancet 389:655-666, Macdonald, R.L. & Schweizer, T.A., 2017

Rheumatoid Pannus of the Cervical Spine
Neurol 88:e51, Weerasinghe, D.,et al, 2017

Characteristics in Limbic Encephalitis with Anti-Adenylate Kinase 5 Autoantibodies
Neurol 88:514-524,508, Do, L. & Chanson, E., 2017

Professional Football may be Linked to Brain Injuries Usually Seen in Boxing
BMJ 356:j811, Hawkes, N., 2017

MRI Findings in Collet-Sicard Syndrome
Neurol 88:811, , 2017

Personality Changes, Executive Dysfunction, and Motor and Memory Impairment
JAMA Neurol 74:245-246, Lopez Chiriboga, A.S.,et al, 2017

Cerebellar Ataxia and Hearing Impairment
JAMA Neurol 74:243-244, Lin, C.Y. & Kuo, S.H., 2017

Acute Spinal Cord Compression
NEJM 376:1358-1369, Ropper, A.E. & Ropper, A.H., 2017

Sugar- and Artificially Sweetened Beverages and the Risks of Incident Stroke and Dementia
Stroke 48:1139-1146, Pase, M.P.,et al, 2017

Intracranial Dural Arteriovenous Fistulae
Stroke 48:1424-1431, Reynolds, M.R.,et al, 2017

Primary Angiitis of the Central Nervous System
Stroke 48:1248-1255, Boulouis, G.,et al, 2017

A Child with Delayed Motor Milestones and Ptosis
Neurol 88:e158-e163, Ghosh, P.S., 2017

Clinicopathologic Conference, MELAS (mitochondrial encephalopathy, lactic acidosis, and stroke like episodes)
NEJM 376:1668-1678, CASE 13-2017, 2017



Showing articles 400 to 450 of 4347 << Previous Next >>