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Differential
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abortion, spontaneous
acquired immunodeficiency syndrome
acquired immunodeficiency syndrome, infants and children
acute ataxia of childhood
acute disseminated encephalomyelitis
acute disseminated encephalomyelitis, relapsing
adolescent medicine
advances in neurology
adverse drug reaction
albendazole
algorithm
alternating hemiplegia
alternating hemiplegia of childhood
AMPA receptor antibodies
anemia
angiitis, isolated of CNS
angiitis, isolated of CNS, tumefactive
angiography, cerebral, beaded vessels
angiography, cerebral
angiotensin-converting enzyme
animal exposure
anti GQ1b IgG antibody
antibiotics
antibodies to measles
anticardiolipin antibodies
anticoagulant, treatment
antiphospholipid antibodies
antiphospholipid antibody syndrome
antitoxin
antiviral agents
aphasia
areflexia
arteritides
arthritis
arylsulfatase A
aspartate aminotransferase
aspirin
ataxia
ataxia, acute onset
ataxia, cerebellar
ataxic gait
ATP1A3 gene
attention deficit disorder with hyperactivity
atypical lymphocytes
auditory evoked brainstem potentials
autism
autoantibodies
autoimmune basal ganglia encephalitis
autoimmune disease
autonomic dysfunction
bacterial infection
basal ganglia, calcification of
basal ganglia, lesion of
basal ganglia, lesion, bilateral
baylisascariasis
behavioral disorder
behavioral disorder, acute
botulinum toxin
botulism
botulism antitoxin
botulism immune globulin
botulism, infant
brain atrophy
brain biopsy
brainstem, lesion of
bulbar palsy
burning feet
burning hands
burning paresthesia
calcification, gyral
calcification, intracranial
calf hypertrophy
carcinoma
cardiomyopathy
cardiopulmonary bypass
carpal tunnel syndrome
CAT scan
CAT scan, abnormal
CAT scan, emission, abnormal
CAT scan, venography
catalepsy
cataplexy
cataracts
catatonia
cauda equina, enhancement
caudate nucleus, atrophy
celiac disease, adult
celiac disease, childhood
central nervous system, infection of
cerebellar degeneration
cerebellitis
cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy
cerebral cortex
cerebral cortical atrophy
cerebral infarction, hemorrhagic
cerebral infarction, subcortical
cerebral venous infarction
cerebral venous thrombosis
cerebral venous thrombosis, deep
cerebral venous thrombosis, etiology
cerebral venous thrombosis, recurrent
cerebrospinal fluid
cerebrospinal fluid, abnormal
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, lactic acid concentration
cerebrospinal fluid, oligoclonal IgG in
cerebrovascular accident
cerebrovascular accident, acute management of
cerebrovascular accident, bilateral
cerebrovascular accident, multiple
cerebrovascular accident, nonvascular territory
cerebrovascular accident, prevention of
cerebrovascular accident, three territory involvement
cerebrovascular accident, thrombolytic agents in treatment
cerebrovascular accident, topographic pattern
cerebrovascular accident, young adult
cerebrovascular disease
chest x-ray, abnormal
children
cholestasis
chorea
chorea, causes of
choreoathetosis
chorioretinitis
chromosomal abnormality
chronic progressive external ophthalmoplegia
Clinical Pathologic Conference(C.P.C.)
cognition
collagen vascular disease
collapsin response mediator protein 5 IgG
coma
complications
confusion
congenital birth defects
congenital infection, CNS
congenital infection, viral
controversies in neurology
conversion reaction
conversion reaction, children
cortical blindness
cortical infarction
cortical infarction, small
cortical ribbon sign
coryza
cough
coumarin
cranial nerve palsies
cranial neuropathy
cranial neuropathy, multiple
craniectomy, decompressive
crawl regression
creatine phosphokinase(CPK)elevated
cry, abnormal
cry, weak
crying
cytomegalic inclusion disease
cytomegalovirus infection
cytomegalovirus infection, congenital
D-dimer
deafness
decision aids
decision analysis
deep gray nuclei
degenerative diseases of CNS
delay in diagnosis
dementia
dementia, childhood
dementia, presenile
dementia, rapidly progressive
dermatitis herpetiformis
dermatographism
developmental disability
developmental milestones, loss of
developmental retardation
diabetes mellitus
diagnostic criteria
diarrhea
differential diagnosis
difficulty climbing stairs
disability rating scale, neurological
disability, neurological
disease modifying agents
disorientation
DPPX, antibodies, encephalitis
dural sinus thrombosis
dysarthria
dyskinesia
dyskinesia, drug induced
dyskinesia, facial
dysphagia
dystonia
dystonia, drug induced
dystrophin
electroencephalogram, abnormalities of
electroencephalogram, periodic complexes
electromyogram
electron microscopy
emotional lability
encephalitis
encephalitis, autoimmune
encephalitis, brainstem
encephalitis, etiology
encephalitis, human immunodeficiency virus type 1
encephalitis, paraneoplastic
encephalitis, viral
encephalomyelitis, postinfectious
encephalopathy
encephalopathy, metabolic
encephalopathy, progressive
endocarditis, marantic
endovascular therapy
enterovirus
eosinophilia
epidemiology of neurology
Epstein-Barr virus
evidence-based research
evoked potentials
exercise intolerance
exome sequencing
eye movement, disorders of
facial nerve palsy
faciobrachial dystonic seizure
Factor V Leiden
falling
false negative
false positive
false positive VDRL
familial
fatal familial insomnia
fatigue
feeding disorder
fever
fibrinolytic agents
fibrinolytic agents, intra-venous local infusion
fine motor function, impaired
Fisher's syndrome
flaccid paralysis
food poisoning
food-borne infection
frontal lobe, pathologic signs of
fundus, abnormality of
fungal infection, CNS
gadolinium
gait disorder
gamma amino butyric acid receptor antibody
gammaglobulin therapy, intravenous
gastrointestinal disease, neurologic complications
gaze palsy
gaze palsy, supranuclear
gaze palsy, vertical
gender
gene mutation
genetic neurologic disorders
genetic screening
genetic testing
geographic location
Gilles de la Tourette syndrome
glaucoma
glutamic acid decarboxylase, antibody
gluten ataxia
gluten sensitivity
gluten-free diet
Gowers maneuver
granulomatous disease
gray matter
growth retardation
Guillain Barre syndrome
Guillain Barre syndrome, variant forms of
H1N1 influenza
hallucination
head bobbing
headache
hearing loss
heart block
helminthic infection of CNS
heparin
heparin, low-molecular-weight
hepatic failure
hepatitis
hepatomegaly
hepatosplenomegaly
heralding manifestation
herpes simplex encephalitis
herpes virus
HLA
hoarseness
Hodgkin's disease
honey
human immunodeficiency virus type 1
human immunodeficiency virus type 1, acute infection
Huntington's chorea
Huntington's disease, children
hydrocephalus
hyperactivity
hyperbilirubinemia
hyperekplexia
hyperreflexia
hypertension
hypertension, children and adolescents
hypertonia
hypogonadism
hyponatremia
hyporeflexia
hypothalamus
hypothalamus, disturbance of
hypotonia
hypotonia, infants
hypoxia
immunization, neurologic complications with
immunotherapy
impaired vigilance
incidence
inclusion bodies
inclusion bodies, eosinophilic cytoplasmic
inclusion bodies, eosinophilic intranuclear
inclusion body myositis
incoordination
infant, evaluation of
infection
infectious mononucleosis
infectious mononucleosis, neurologic findings with
influenza
influenza A virus
influenza immunization
insomnia
intellectual deficit
intellectual deterioration
intestinal pseudoobstruction
intracerebral hemorrhage
intracranial pressure, increased
intrauterine infection
intrauterine infection, viral
irritability
irritable baby
jaundice
Kearns-Sayre syndrome
lactic acidemia
learning disability
learning disability, in children
Leber's hereditary optic neuropathy
Leigh's disease
lethargy
leucine rich glioma inactivated 1 antibodies
leukocytosis
leukoencephalopathy
level of consciousness, decreased
limbic encephalitis
lipid storage disorder of CNS
livedo reticularis
liver disease
liver function enzymes
lupus anticoagulant
lymphadenopathy
lymphadenopathy, axillary
lymphadenopathy, paraaortic
lymphoma
lymphomatoid granulomatosis
lysosomal storage disease
malabsorption
malaise
malformation, vascular
MELAS syndrome
memory, defect of recent
memory, impairment of
meningeal enhancement
meningismus
meningitis
meningitis, aseptic
meningitis, carcinomatous
meningitis, eosinophilic
meningoencephalitis
mental status, abnormal
MERRF syndrome
mesial temporal lobe
metachromatic leukodystrophy
metachromatic leukodystrophy, juvenile
microangiopathy, brain
microcephaly
migraine
migraine, seizures in
misdiagnosis
mitochondrial disease
mitochondrial disease, pathogenesis
mitochondrial encephalomyopathy
mitral valve lesion
molecular genetics
monoclonal antibodies
mortality
movement disorder
movement disorder, drug induced
movement disorder, hyperkinetic
MRI
MRI, abnormal
MRI, angiography
MRI, CAT scan compared to
MRI, contrast enhanced
MRI, diffusion weighted
MRI, disappearing lesion on
MRI, FLAIR
MRI, negative
MRI, punctate pattern
MRI, ring sign, open
MRI, spinal cord
MRI, venography
MRI, volumetry
multiple organ failure
multiple sclerosis
multiple sclerosis, differential diagnosis of
multiple sclerosis, misdiagnosis
muscle biopsy
muscle wasting, diffuse
muscle weakness
muscular dystrophy
muscular dystrophy, central nervous system abnormality
muscular dystrophy, Duchenne
mutism
mycoplasma
mycoplasma pneumoniae
myelitis
myelitis, transverse
myelitis, transverse, recurrent
myelopathy
myocardial infarction
myoclonus
myoglobinuria
myopathy
myopathy, critically ill
myopathy, mitochondrial
myositis
myotonia dystrophica
neonatal infection, viral
neoplasm, primary of CNS
nerve biopsy
nerve conduction studies
neurexin-3 alpha antibodies
neurocutaneous disease
neurologic complications of, systemic cancer
neurologic complications of, systemic disease
neurologic disease
neurologic disease, diagnoses of
neurologic disease, tempo
neurologic examination, focal
neurologic signs
neurologic symptoms
neurological intensive care
neuromuscular disease, electrodiagnosis of
neuromuscular junction, abnormality of
neuronal cell surface antigen
neuropathy
neuropathy, acute
neuropathy, peripheral
neuropathy, vasculitic, systemic
neurotoxin
next-generation sequencing
Niemann-Pick disease
NMDA antagonists
Notch3 gene
nystagmus
nystagmus, monocular
obsessive-compulsive disorder
obstetric complications
ophelia syndrome
ophthalmoplegia
ophthalmoplegia, progressive external
opisthotonus
opportunistic infection
opportunistic infection, CNS
optic atrophy
optic disc edema
optic nerve
optic neuritis
optic neuropathy
oral contraceptives
oral ulcerations
osteoporosis
pain
pancytopenia
papilledema
paralysis, acute
paralysis, acute areflexic
Parkinson disease, dystonia with
Parkinsonism syndrome
paroxysmal hemiplegia
paroxysmal neurologic deficits
partial thromboplastin time, prolonged
pediatric autoimmune neuropsychiatric disorders associated with streptococcal infection
peripheral blood smear
persistent vegetative state
personality change
petechiae
pigmentary retinopathy
pitfalls
plasmapheresis
platelet inhibiting drugs
pleocytosis of cerebrospinal fluid
pneumonia
POLG1 gene
poliomyelitis-like illness
polycythemia, primary
polymerase chain reaction
polymerase chain reaction, false negative
polymerase chain reaction, false positive
polyneuritis
polyneuropathy
polyneuropathy, critically ill
polyneuropathy, critically ill, children
port wine nevus
postpartum
posttransplant lymphoproliferation disorder
postural abnormality
potassium channel antibodies
practice guidelines
precipitating factors
pregnancy, neurologic complications in
prethrombotic state
prevention of neurologic disorders
prion disease
prognosis
progressive multifocal leucoencephalopathy
progressive neurologic disorder
protein C deficiency
protein S deficiency
psychiatric disorder
psychiatric problems in neurologic disorders
psychomotor retardation
psychosis
psychosis, childhood
ptosis
ptosis, bilateral
puberty
puberty, delayed
pulmonary embolism
pulmonary infiltrates
quadriparesis
raccoon
ragged-red fibers
rapid onset dystonia parkinsonism
rapidly progressing neurologic illness
rash
Raynaud's phenomenon
recurrent
Red flags
renal failure
renal infarct
renal vein thrombosis
respirator
respiratory failure
respiratory tract infection
retinopathy
review article
rigidity
risk factors
rituximab
roundworm
rubeola virus
runny nose
salivation, excessive
sarcoidosis
sarcoidosis, CNS
schistocytes
scleroderma
scleroderma, neurologic involvement with
screening
sedimentation rate, elevated
seizure
seizure, children
seizure, differential diagnosis of
seizure, hysterical
seizure, neonatal
seizure, nonepileptic
sensorineural hearing loss
septicemia
seroconversion
serologic testing
serologic testing, false negative
seronegative
serositis
serum alanine aminotransferase
short stature
skin, lesions in neurologic disorders
sleep pathology and physiology
slow virus infection of CNS
small for dates infant, problems in
sore throat
spasticity
speech disorder
speech disorder, childhood
speech, delayed development of
spinal cord
spinal cord, lesion of
splenomegaly
spontaneous remission
status epilepticus
steroid
steroid therapy, CNS treatment and complications with
stiff joints
streptococcal infection
striatal encephalitis
striatum, lesion of
striatum, lesion of, bilateral
strokelike episodes
Sturge-Weber syndrome
subacute sclerosing panencephalitis(S.S.P.E.)Dawson's disease
subarachnoid hemorrhage
subarachnoid hemorrhage, cerebral convexity
suck, poor
sural nerve
systemic illness
systemic juvenile idiopathic arthritis
systemic lupus erythematosus
tachycardia
temporal lobe, lesion
temporal lobe, lesion, bilateral
teratoma
teratoma, ovarian
term infant
thalamus, lesion of-bilateral
Three territory sign
thrombocytopenia
thrombocytosis
thrombophlebitis
thrombotic microangiopathy
thymoma
tic
tissue plasminogen activator, intravenous
titubation
toxins, nervous system
transient ischemic attack
transient neurologic deficit
treatment of neurologic disorder
tremor
tremulousness
trigeminal nerve
trigeminal neuropathy
trinucleotide repeats
tripping
ultrasonography, head
urinary retention
vaccination, neurologic complications with
vaccine
valvulopathy
vasculopathy
venous thrombosis, non-cerebral
viral infection
viral infection, CNS
virus, slow
visual acuity, decreased
visual field defect
visual impairment
visual loss
weakness
weakness, generalized
weakness, infant
weakness, progressive
web sites
weight loss
white matter disease
white matter disease, subcortical
whole genome sequencing
workup
Showing articles 750 to 800 of 6734 << Previous Next >>

The Natural History of SLE by Prospective Analysis
Medicine 50:85, Estes,D.,et al, 1971

The Neuropathy of Acute Intermittent Porphyria
Quart J Med 38:307, 1969 July., Ridley,A., 1969

Ataxia In Childhood
Dev Med Child Neurol 10:388-389, Wilson,J., 1968

Huntington's Chorea
Bruyn, G. W. In Vinken & Bruyn, Handbk of Clin Neurol, North-Holland Publ Co, Amsterdam, 6:298, , 1968

The Remote Effects of Cancer on the Nervous System
Proc Roy Soc Med 60:683, Wilkinson,M., 1967

Infectious Mononucleosis:Neurologic & EEG Findings
Medicine 45:5l, Schnell,R.,et al, 1966

Cerebellar Disease in Infectious Monoucleosis
Arch Neurol 15:270, Dowling,M.&Slyck,E., 1966

The Uveomeningoencephalitic Syndrome
Neurol 16, 6031966., Riehl,J.L.,et al, 1966

Central Nervous System Manifestations of Periarteritis Nodosa
Neurol 15:114, Ford,R.G.,et al, 1965

Role of Infection in the Guillain-Barre Syndrome
JNNP 27:395, Melnick,S., 1964

Neurological Complications of Wegener's Granulomatosis
Arch Neurol l8:45, 1963, Drachman,D., 1963

Infectious Neuronitis (Guillain-Barre Syndrome) in Children
Neurol 9:533-539, Peterman,A.F.,et al, 1959

Polyneuritis in Children
Pediatrics 22:972-990, Low,N.L.,et al, 1958

Cerebellar Ataxia in Children
Handout & References., Gilbert,J.J., 1850

Neurology & Psychiatry Section-Year book of Pediatrics
Pediatr Abstract p. 406-449., , 1850

Creutzfeldt-Jakob-Like Presentation in Anti-AMPAR Encephalitis
Ann Neurol 99:1466-1467, Durbano,K.et al, 2026

Using Susceptibility-Based Imaging in Highly Active Late-Onset Multiple Sclerosis
Neurol 106:e214794, Sosa,S.M.,et al, 2026

Unilateral Primary Angiitis of the Central Nervous System: A Rare and Under-Recognized Entity
AJNR 47:589-595, Rai,P.,et al, 2026

Zorevunersen in Children and Adolescents with Dravet Syndrome
NEJM 394:969-982, Laux,L.,et al, 2026

Can AI Say "I Dont Know"?
NEJM 394:1873-1875, Sikora,A.,et al, 2026

A 28-Year-Old Man with Seizures and Thalamic Lesions
Neurol 106:e218065, Santos-Rojo,A.B.,et al, 2026

A 35-Year-Old Patient with Rapidly Progressive Ascending Weakness Leading to Loss of Brainstem Reflexes
Neurol 106:e218059, Lyons,H.J.,et al, 2026

Autoimmune Encephalitis as Treatment-Responsive Cause of Rapidly Progressive Dementia
Neurol 106:e214933, van Steenhoven,R.W.,et al, 2026

Paramagnetic Rim Lesions and Development of Clinical MS in Radiologically Isolated Syndrome
JAMA Neurol 83:250-258, Lim,T.R.et al, 2026

Polymyalgia Rheumatica
NEJM 394:1097-1109, Dejaco,C.,et al, 2026

Clinical Manifestations of Primary CNS T-Cell Lymphoma, Retrospective Study of Histopathologic, Molecular, and Neuroimaging Fetures
Neurol 106:e24744, Muller,K.J.,et al, 2026

Frequency of AQP4 and MOG Antibodies in Patients with Optic Neuritis Fulfilling Minimal New Multiple Sclerosis MRI Criteria
Neurol 106:e214753, Deschamps,R.,et al, 2026

The 2024 McDonld Criteria for Dignosis of Multiple Sclerosis, The Rubber meets the Road
Neurol 106:e214688, Miller, A.E., 2026

A 41-Year-Old Man Presenting with Right Foot Tingling
Neurol 106:214781, Lu,V.,et al, 2026

Comparison of AI, Diagnostic Generator, and Expert Opinion in Difficult Neurologic Diagnosis; Real-World Case Study
Diagnosis doi.org/10.1515/dx-2026-002, Finelli,P.F., 2026

Diagnostic Value of the Kappa Free light Chain Index to Distinguish MOGAD, NMOSD, and MS
Neurol 106:e214946, Tournier,A.,et al, 2026

Using Susceptibility-Based Imaging in highly ctive Late-Onset Multiple Sclerosis
Neurol 106:e214794, Sosa,S.M.,et al, 2026

Large Language Model Performance and Clinical Reasoning Tasks
JAMA Netw Open 9:e264003, Rao,A.S.,et al, 2026

Deep Venous Dural Arteriovenous Fistula Mimicking Progressive Dementia
Stroke 57:e180-181, Langlois-Therien,T.,et al, 2026

Cerebral Amyloid Angiopathy
NEJM 394:1836-1845, Greenberg,S.M., 2026

Increased Prevalence of Nitrous Oxide-Induced Subacute Combined Degeneration of the Spinal Cord: Clinical and Imaging Findings
AJNR 47:513-520, Bruen,R.,et al, 2026

A 69-Year Old Man With Rapid Cognitive Decline and Abnormal Movements
Neurol 106:e214686;2026, Lim,G.Z.,et al, 2026

Turning Slowly Predicts Future Diagnosis of Parkinsons Disease:A Decade-Long Longitudinal Analysis
Ann Neurol 99:114-123, Elshehabi,M.,, 2026

Restless Legs Syndrome, A Review
JAMA 335:703-714, Winkelmen,J.W. & Wipper, B., 2026

Peripheral Neuropathy, A Review
JAMA 335:255-266, Mauermann,M.L. & Staff,N.P., 2026

Congenital Zika Syndrome
NEJM 394:e2, Bacin,F. & Montenegro,M.A., 2026

CT Perfusion Abnormality in Hypoglycemic Focal Neurological Deficits
Stroke 57:e6-e7, Mikito,S.,et al, 2026

Clinicopathologic Conference, Disseminated Infection with Hypervirulent Klebsiella Pneumoniae
NEJM 394:282-294, Case 202026, 2026

Myelin Oligodendrocyte Glycoprotein Antibody - Associated Cerebral Cortical Encephalitis: A Case Report Highlighting Diagnostic Challenges and Therapeutic Implications
Front Immunol 16:1619807, Liu,M. & Li, D., 2025

AI: Need for Comparative Studies in Complex Neurologic Diagnosis
Ann Neurol doi:10.1002/ana.78068, Finelli,P.F., 2025

Idiopathic Normal-Pressure Hydrocephalus
NEJM 393:2243-2253, 2264, Johnson,M.D.,& Williams, M.A., 2025

A 5-Year-Old Boy with Subacute and Refractory Myoclonus
Neurol 106:e214457, Park,P.S.,et al, 2025

Recurrent Ischemic Strokes Due to Os Odontoideum
Ann Neurol 98:1315-1317, Wang,J.,et al, 2025

A 62-Year-Old Man with Progressive Limb Weakness, Involuntary Movements, and HyperCKemia
JAMA Neurol 82L:1286-1287, Liu,Y.,et al, 2025

Complex Regional Pain Syndrome
NEJM 393:2338-2348, Goebel,A., 2025



Showing articles 750 to 800 of 6734 << Previous Next >>