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acute disseminated encephalomyelitis
acute necrotizing encephalitis
advances in neurology
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altered states of consciousness
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anemia
anorexia
anti GQ1b IgG antibody
anti Hu antibody
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anti Mi2 antibody
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anti signal recognition particle antibody
antibodies to voltage-gated calcium channels
anticonvulsants, untoward effects of
antiendomysial antibodies
antiviral agents
aphasia
arbovirus
area postrema
area postrema syndrome
areflexia
arteritides
ascending paralysis
ataxia
ataxia, cerebellar
ataxia, sensory
autoantibodies
autoimmune basal ganglia encephalitis
autoimmune disease
autoimmune GFAP astrocytopathy
autonomic dysfunction
B 12 deficiency
Babinski sign
Barkhof MR criteria for MS
basal ganglia
basal ganglia, lesion of
basal ganglia, lesion, bilateral
behavioral disorder
behavioral disorder, acute
Bickerstaff's brainstem encephalitis
biologic markers
brain biopsy
brain scan
brainstem
brainstem, infarction of
brainstem, lesion of
bulbar palsy
calcification, intracranial
campylobacter infection
CAR syndrome
carcinoma
carcinoma of breast
carcinoma of lung
carcinoma of pancreas
carpal tunnel syndrome
CAT scan, abnormal
CAT scan, chest
cataracts, congenital
catatonia
cauda equina, enhancement
celiac disease, adult
central nervous system, infection of
cerebellar degeneration
cerebellar lesion
cerebral cortex
cerebral cortical encephaliis
cerebral edema
cerebrospinal fluid, abnormal
cerebrospinal fluid, cytology
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, gammaglobulin of
cerebrospinal fluid, oligoclonal bands, absent
cerebrospinal fluid, oligoclonal IgG in
cerebrospinal fluid, protein of
cerebrospinal fluid, proteincytologic dissociation
cerebrospinal fluid, xanthochromia of
cerebrovascular accident
cerebrovascular accident, mimics
cerebrovascular accident, young adult
cerebrovascular disease
children
chorea
choreoathetosis
chorioretinitis
chronic lymphocytic inflammation with pontine perivascular enhancement responsive to steroids
chrysotherapy, neurologic complications of
Clinical Pathologic Conference(C.P.C.)
collagen vascular disease
collapsin response mediator protein 5 IgG
coma
comorbidities
complications
confusion
conus medullaris, lesion of
corneal reflex, abnormal
corpus callosum
corpus callosum, lesion of
cranial nerve palsies
cranial neuropathy
cranial neuropathy, multiple
creatine phosphokinase(CPK)elevated
cyclophosphamide
cyst, porencephalic
cytomegalic inclusion disease
cytosine arabinoside
deep gray nuclei
dementia
demyelinating disease
depression
depression, psychotic
dermatomyositis
diagnostic criteria
diarrhea
diencephalon
differential diagnosis
diplopia
disability, neurological
disorientation
DPPX, antibodies, encephalitis
drowsiness
dysarthria
dyskinesia
dyskinesia, facial
dysphagia
dyspnea
electroencephalogram
electroencephalogram, abnormalities of
electromyogram
electromyogram, incremental response
electron microscopy
ELISA
encephalitis
encephalitis, autoimmune
encephalitis, brainstem
encephalitis, etiology
encephalitis, paraneoplastic
encephalitis, recurrent
encephalitis, viral
encephalomyelitis
encephalomyelitis, paraneoplastic
encephalopathy
enteritis
eosinophilia
epidemiology of neurology
exercise-related muscle strength increase
eye movement, painful
eye, pain in
facial nerve palsy
facial weakness, bilateral
faciobrachial dystonic seizure
false negative
false positive
familial
fatigue
fever
fibrillations
Fisher's syndrome
flaccid paralysis
fluorescent treponema antibody absorption/false positive
fourth ventricle, floor
gadolinium
gait disorder
gamma amino butyric acid receptor antibody
gammaglobulin therapy, intravenous
ganglionitis
gastrointestinal disease, neurologic complications
gender
GFAP-IgG
gliadin antibodies
glioblastoma multiforme(astrocytoma Gr.III)
glutamic acid decarboxylase, antibody
gluten sensitivity
gluten-free diet
Guillain Barre syndrome
Guillain Barre syndrome, axonal form
Guillain Barre syndrome, differential diagnosis of
Guillain Barre syndrome, variant forms of
gynecomastia
headache
hearing loss
heavy metal intoxication
hemiparesis
hemiplegia
hemophagocytic lymphohistiocytosis, cerebromeningeal
hemophagocytosis
hepatomegaly
hepatosplenomegaly
heralding manifestation
herpes labialis
herpes simplex encephalitis
herpes simplex encephalitis, differential diagnosis of
herpes simplex encephalitis, recurrent
herpes simplex encephalitis, treatment of
herpes simplex myelitis
herpes simplex virus
herpes simplex virus infection, immunosuppressed patient
herpes simplex virus, human nervous system and
herpes simplex virus, localization of
herpes simplex virus, malignancy with
herpes simplex virus, pathogenesis of
herpes simplex virus, pathology of
herpes simplex, neurocutaneous lesions in
herpes virus
herpes zoster
herpes, genital
hiccoughs
hippocampal atrophy
HLA
Horner's syndrome
H-reflex testing
H-sign, spinal cord
human T-lymphotropic virus type I(HTLV-I)
hydrocephalus
hyperekplexia
hyperreflexia
hypersomnia
hyperthyroidism
hypertriglyceridemia
hypofibrinogenemia
hypoglycorrhachia
hypokalemia
hypokalemic periodic paralysis
hyponatremia
hypothalamus
hypothalamus, damage to
hypothalamus, lesion of
idiopathic
immunofluorescent exam of CSF cells
immunologic disease
immunology and the nervous system
immunosuppression
immunosuppressive agents
immunotherapy
impotence
inappropriate antidiuretic(A.D.H.)hormone
inclusion bodies, intranuclear
inclusion body myositis
infection
infectious mononucleosis
insomnia
intellectual deficit
interferon
interferon inducer
internal capsule
intestinal biopsy
intracranial hypertension, benign
intracranial pressure, increased
intrauterine infection, viral
intrauterine infection, viral of CNS
iododeoxyuridine
irritability
leg numbness
leg weakness, bilateral
leucine rich glioma inactivated 1 antibodies
level of consciousness, decreased
limbic encephalitis
limbic system
linear lesion
lymphadenopathy
lymphoma
malabsorption
malformation, CNS, congenital
malignancy screen
medulla oblongata
medulla oblongata, lesion of
memory, defect of recent
memory, impairment of
meningeal enhancement
meningismus
meningitis
meningitis, aseptic
meningitis, neutrophilic
meningoencephalitis
meningoencephalomyelitis
mental status, abnormal
mesial temporal lobe
microcephaly
micropthalmia
middle cerebellar peduncle, lesion
middle cerebellar peduncle, lesion, bilateral
mimics
misdiagnosis
monoamines
monoamines, brain
monoclonal antibodies
mononeuritis multiplex
mononeuropathy
mortality
mosquito
motor neuron disease
movement disorder
MRI
MRI pattern
MRI, abnormal
MRI, contrast enhanced
MRI, contrast enhanced, cloud-like
MRI, diffusion weighted
MRI, false negative
MRI, FLAIR
MRI, linear enhancement
MRI, muscle
MRI, negative
MRI, optic nerve
MRI, spinal cord
MRI, spinal cord, increased intramedullary cord signal
MRI, sulcal hyperintensity
MRS
multiple sclerosis
multiple sclerosis, differential diagnosis of
multiple sclerosis, misdiagnosis
muscle cramp
muscle pain
muscle stiffness
muscle strength, testing
muscle weakness
muscle weakness, proximal
muscle weakness, sudden onset of
myasthenia gravis
myasthenic syndrome
myelitis
myelitis, autoimmune
myelitis, longitudinal
myelitis, transverse
myelitis, transverse, idiopathic
myelitis, transverse, recurrent
myeloneuropathy
myelopathy
myelopathy, ischemic
myelopathy, chronic progressive
myelopathy, necrotizing
myelopathy, paraneoplastic
myoclonus
myopathy
myositis
nausea and vomiting
neck weakness
neoplasm, primary intracerebral
nerve conduction studies
nerve conduction studies, motor
nerve root enhancement
neurexin-3 alpha antibodies
neuroinfectious diseases
neurologic complications of, systemic cancer
neurologic complications of, systemic disease
neurologic disease, diagnoses of
neurologic signs
neurologic symptoms
neuromuscular disease, electrodiagnosis of
neuromuscular junction, abnormality of
neuromyelitis optica (Devic's disease)
neuromyelitis optica (Devic's disease), screening
neuromyelitis optica spectrum disorder
neuromyelitis optica, IgG
neuronal cell surface antigen
neuronopathy, sensory
neuropathology
neuropathy
neuropathy, peripheral
neuropathy, sensory
neuropathy, vasculitic, systemic
neutropenia
NMDA antagonists
NMDA receptors
nystagmus
ophthalmoplegia
ophthalmoplegia, total
opisthotonus
opsoclonus-myoclonus syndrome
optic atrophy
optic chiasm
optic chiasm, lesion of
optic disc edema
optic nerve sheath enhancement
optic nerve, enlarged
optic nerve, lesion of
optic neuritis
optic neuritis, bilateral
optic neuritis, recurrent
optic neuropathy
optical coherence tomography
owl's eye sign of spinal cord
pain
pain, abdominal
pain, back
pain, leg
pain, neuropathic
pancytopenia
papilledema
papillitis
paralysis, acute
paralysis, acute areflexic
paraneoplastic cerebellar degeneration
paraparesis
paraparesis, flaccid
paraparesis, spastic, tropical
paresthesias
periaqueductal lesion
pericarditis
perineuritis
perineuritis, optic
periodic paralysis
periodic paralysis, thyrotoxic
perioral numbness
perivascular enhancement
personality change
pitfalls
pleocytosis of cerebrospinal fluid
polyinosinic cytidic acid(poly IC)
polymerase chain reaction, false negative
polymyositis
pons, lesion of
positive sharp waves
posterior inferior cerebellar artery syndrome
posterior leukoencephalopathy syndrome
potassium
precipitating factors
prevention of neurologic disorders
prognosis
progressive multifocal leucoencephalopathy
psychiatric problems in neurologic disorders
psychomotor retardation
psychosis
ptosis
ptosis, bilateral
ptosis, unilateral
pupil, abnormality in neurologic disorders
pupil, light reflex, abnormal
pyramidal tract
quadriparesis
quadriplegia
quadriplegia, transient
rapidly progressing neurologic illness
recurrent
Red flags
remote effect of cancer on the nervous system
repetitive nerve stimulation
respirator
respiratory failure
respiratory tract infection
review article
rheumatoid arthritis
rheumatoid arthritis, neurologic complications of
rituximab
rubella virus
sarcoidosis
sarcoidosis, CNS
scleroderma
scleroderma, neurologic involvement with
screening
seizure
seizure, psychomotor-temporal lobe
sensory level
serologic testing
serologic testing, false negative
seronegative
seropositive
Sjogren's syndrome
Sjogren's syndrome, neurologic manifestations of
skin, lesions in neurologic disorders
slurred speech
spinal cord, biopsy
spinal cord, compression of
spinal cord, lesion of
spinal cord, neoplasm
splenium of corpus callosum
splenomegaly
steroid responsive encephalopathy
steroid therapy, CNS treatment and complications with
stool culture
striatal encephalitis
striatum, lesion of
striatum, lesion of, bilateral
strokelike episodes
subacute myelo-opticoneuropathy(S.M.O.N.)complex
subarachnoid hematoma, spinal
subarachnoid hemorrhage
subtemporal decompression
systemic lupus erythematosus
systemic lupus erythematosus, neurologic complications with
talk
temporal lobe, lesion
temporal lobe, lesion, bilateral
teratoma
teratoma, ovarian
thalamus, infarction, bilateral
thalamus, lesion of
thalamus, lesion of-bilateral
third ventricle, wall
thrombocytopenia
thymoma
thyrotoxicosis
tongue, impaired movements of
transplacental virus infections
treatment of neurologic disorder
tremor
tremor, postural
trigeminal neuralgia
trigeminal neuropathy
tumefactive lesion
urinary retention
viral infection
viral infection, CNS
vision loss, sequential
vision, blurred
visual acuity
visual loss
visual loss, progressive
visual loss, sudden
vomiting, intractable
walking, difficulty with
water channel antibodies
weakness
weakness, acute
weakness, episodic
weakness, generalized
weakness, progressive
weakness, proximal
weight loss
West Nile fever
wheelchair
white matter disease
white matter disease, periventricular
white matter disease, subcortical
workup
xerophthalmia
xerostomia
Showing articles 0 to 50 of 1617 Next >>

Validation of the 2023 International Diagnostic Criteria for MOGAD in a Selected Cohort of Adults and Children
Neurol 103:e209321, Varley,J.A.,et al, 2024

Glial Fibrillary Acidic Protein Astrocytopathy:Review of Pathogenesis, Imaging Features, and Radiographic Mimics
AJNR 45:1394-1402, Shetty,D.,et al, 2024

Diagnosis of Myelin Oligodendrocyte Glycoprotein Antibody-Associated Disease:International MOGAD Panel Proposed Criteria
Lancet Neurol doi.org110.1016/51474-4422(22)00431-8, Banwell,B.,et al, 2023

Myelin Oligodendrocyte Glycoprotein Antibody-Associated Disease (MOGAD):Clinical Features and Diagnosis
www.UptoDate.com, Sept, Flanagan,E.P. & Tillema,J-M, 2023

Myelin Oligodendrocyte Glycoprotein Antibody-Associated Disease (MOGAD): Clinical Features and Diagnosis
UptoDate.com, March, Flanagan,E.P. & Tillema,J-M, 2023

Severe Hippocampal Atrophy in a Patient with Autoimmune Glial Fibrillary Acidic Protein Astrocytopathy
JAMA Neurol 80:642-643, Bartels,F.,et al, 2023

Neuromyelitis Optica Spectrum Disorder
NEJM 387:631-639, Wingerchuk, D.M. & Lucchinetti, C.F., 2022

Clinical and Neuroimaging Findings in MOGAD-MRI and OCT
Clin Exp Immunol 206:266-281, Bartels,F.,et al, 2021

CNS Demyelinating Attacks Requiring Ventilatory Support With Myelin Oligodendrocyte Glycoprotein or Aquaporin-4 Antibodies
Neurol 97:e1351-e1358, Zhao-Fleming,H.H.,et al, 2021

Paraneoplastic Myeloneuropathies
Neurol 96:e632-e639, Shah, S.,et al, 2021

Paraneoplastic Encephalomyelitis with Glutamic Acid Decarboxylase Antibodies Presenting as Longitudinal Pyramidal Tract Hyperintensity
JAMA Neurol 77:899-900, Miralles, C.,et al, 2020

Imaging Review of Paraneoplastic Neurologic Syndromes
AJNR 41:2176-2187, Madhavan, A.A.,et al, 2020

A 23-Year-Old Man with Headaches, Confusion, and Lower Extremity Weakness
Neurol 92:863-867, Patel, N.M.,et al, 2019

Aquaporin-4 and MOG Autoantibody Discovery in Idiopathic Transverse Myelitis Epidemiology
Neurol 93:e414-e420, Sechi, E.,et al, 2019

Evaluation of Idiopathic Transverse Myelitis Revealing Specific Myelopathy Diagnoses
Neurol 90:e96-102, Zalewski, N.L.,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

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

Glial Fibrillary Acidic Protein Immunoglobulin G as Biomarker of Autoimmune Astrocytopathy: Analysis of 102 Patients
Ann Neurol 81:298-309, Flanagan, E.P.,et al, 2017

A Patient with a History of Encephalomyelitis and Recurrent Optic Neuritis
Neurol 89:e231-e234, Gutman, J.M.,et al, 2017

Clinical Pathologic Conference, West Nile Virus Encephalitis
NEJM 377:1878-1886, Case 34-2017, 2017

Clinical Presentation and Prognosis in MOG-antibody Disease: A UK Study
BRAIN 140:3128-3138, Jurynczyk, M.,et al, 2017

A Man with Rapidly Ascending Paralysis
Neurol 89:e25-e31, Rosenberg, J.,et al, 2017

Neuromyelitis Optica Spectrum Disorders
UpToDate, May, Glisson,C.C., 2016

Autoimmune Glial Fibrillary Acidic Protein Astrocytopathy
JAMA Neurol 73:1297-1307, Fang, B.,et al, 2016

Anti-Mog Antibodies with Longitudinally Extensive Transverse Myelitis Preceded by Clippers
Neurol 84:1177-1179, Symmonds, M.,et al, 2015

Short Myelitis Lesions in Aquaporin-4-IgG-Positive Neuromyelitis Optica Spectrum Disorders
JAMA Neurol 72:81-87, Flanagan, E.P.,et al, 2015

Brain Abnormalities as an Initial Manifestation of Neuromyelitis Optica Spectrum Disorder
MSJ 17:1107-1112, Kim, W.,et al, 2013

Aquaporin-4 Antibody-Positive Cases Beyond Current Diagnosis Criteria for NMO Spectrum Disorders
Neurol 80:2210-2216, Sato, D.,et al, 2013

Longitudinally Extensive Transverse Myelitis with and Without Aquaporin 4 Antibodies
JAMA Neurol 70:1375-1381, Kitley, J.,et al, 2013

Current Concept of Neuromyelitis Optica (NMO) and NMO Spectrum Disorders
JNNP doi:10.1136/JNNP-2012-302310, Jacob, A.,et al, 2012

Brain Abnormalities in Neuromyelitis Optica Spectrum Disorder
Multiple Sclerosis International ID 735486, Kim, W.,et al, 2012

Clincopathologic Conference,Graves Disease with Thyrotoxic Periodic Paralysis
NEJM 366:553-560, Case 4-2012, 2012

The Differential Diagnosis of Longitudinally Extensive Transverse Myelitis
Mult Scler 18:271-285, Kitley, J.L.,et al, 2012

Paraneoplastic isolated myelopathy Clinical course and neuroimaging clues
Neurol 76:2089-2095, Flanagan, E.P.,et al, 2011

NMDA Receptor Encephalitis Mimicking Seronegative Neuromyelitis Optica
Neurol 74:1473-1475, Kruer,M.C., et al, 2010

Paraneoplastic Syndromes Affecting Brain and Cranial Nerves
UpToDate May 2009, Dalmau,J. &Rosenfeld,M., 2009

Pathologic and Immunologic Profiles of a Limited Form of Neuromyelitis Optica with Myelitis
Neurol 73:1628-1637, Yanagawa,K.,et al, 2009

To Test or Not to Test: NMO-IgG and Optic Neuritis
Neurol 70:2192-2193, Giovannoni,G., 2008

NMO-IgG Predicts the Outcome of Recurrent Optic Neuritis
Neurol 70:2197-2200, Matiello,M.,et al, 2008

Diagnosis and Treatment of Neuromyelitis Optica
The Neurologist 13:2-11, Wingerchuk,D.M., 2007

Paraneoplastic Encephalomyelitis Associated with Pancreatic Tumor and anti-GAD Antibodies
Neurol 66:450-451, Hernandez-Echebarria,L.,et al, 2006

Neuromyelitis Optica IgG Status in Acute Partial Transverse Myelitis
Arch Neurol 63:1398-1400, Scott,T.F.,et al, 2006

Recurrent Transverse Myelitis Associates with Anti-Ro (SSA) Autoantibodies
Neurol 62:147-149, Hummers,L.K.,et al, 2004

Neurologic Manifestations in Primary Sjogren Syndrome: A Study of 82 Patients
Medicine 83:280-291, Delalande,S.,et al, 2004

Bickerstaff's Brainstem Encephalitis: Clinical Features of 62 Cases and a Subgroup Associated with Guillain-Barre Syndrome
Brain 126:2279-2290, Odaka,M.,et al, 2003

Neurological Complications of Coeliac Disease
Postgrad Med J 78:393-398, Tengah, D.S.N.A.,et al, 2002

Clinicopath Conf,Guillain-Barre Syndrome, Campylobacter Jejuni Enteritis,Case 39-1999
NEJM 341:1996-2003, , 1999

Immunologic Analysis of Spinal Cord-Biopsy Specimen from a Pt with HTLV-I-Associated Neurologic Disease
NEJM 336:839-845, Levin,M.C.,et al, 1997

Myositis:Immunologic Contributions to Understanding Cause, Pathogenesis, and Therapy
Ann Int Med 122:715-724, Plotz,P.H.,et al, 1995



Showing articles 0 to 50 of 1617 Next >>