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Differential
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abducens nerve paralysis
acrocyanosis
acute disseminated encephalomyelitis
acute disseminated encephalomyelitis, multiphasic
Addison's disease
adrenoleukodystrophy
adrenoleukodystrophy, adult onset
adrenoleukodystrophy, carrier
adrenomyeloneuropathy
adult polyglucosan body disease
adult-onset leukodystrophy, with neuroaxonal spheroids
advances in neurology
aggression
Aicardi-Goutieres syndrome
albendazole
Alexanders disease
Alexanders disease, adult onset
ANA
anatomy of
angiitis
angiitis, granulomatous of CNS
angiitis, isolated of CNS
animal exposure
anterior tibial muscle weakness
antibiotics
antiviral agents
aphasia
apraxia
areflexia
arthritis
aspartate aminotransferase
ataxia
ataxia, cerebellar
ataxia, sensory
atherosclerosis, generalized
attention deficit disorder with hyperactivity
atypical
auditory evoked brainstem potentials
autonomic dysfunction
axonal degeneration
axonal spheroid
Babinski sign
bacterial infection
bacterial infection, CNS
Bannayan-Riley-Ruvalcaba syndrome
basal ganglia, calcification of
basal ganglia, lesion of
basal ganglia, lesion, bilateral
baylisascariasis
bedridden
behavioral disorder
Bickerstaff's brainstem encephalitis
bladder dysfunction
bone marrow transplantation
brain atrophy
brain biopsy
brainstem, atrophy
brainstem, ischemia
brainstem, lesion of
Brown Sequard syndrome
brucellosis
brucellosis, nervous system involvement with
bulbar palsy
calcification, intracranial
calcifications, intracranial, punctate
carphology
CAT scan
CAT scan, abnormal
CAT scan, myelogram with
CAT scan, serial
CAT scan, spinal cord
CAT scan, spine
central nervous system, infection of
cerebellar lesion
cerebral cortex
cerebral cortical atrophy
cerebrospinal fluid
cerebrospinal fluid, abnormal
cerebrospinal fluid, cell count, normal
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, pressure increased
cerebrospinal fluid, proteincytologic dissociation
cerebrovascular accident
Charcot-Marie-Tooth
chest x-ray, abnormal
chilbran skin lesions
children
Clinical Pathologic Conference(C.P.C.)
cognition
coma
confusion
congenital malformation
consanguinity
coronavirus
corpus callosum
corpus callosum, lesion of
corpus callosum, thinning
cough
COVID-19
cry, abnormal
cultured skin fibroblasts
cyst
cyst, parenchymal
DARS
deafness
deep gray nuclei
degenerative diseases of CNS
dementia
dementia, childhood
dementia, subcortical
demyelinating disease
dentate nuclei
dentate nuclei, lesion of
developmental disability
developmental milestones, loss of
developmental retardation
diagnostic criteria
diet
differential diagnosis
difficulty going down stairs
diplopia
distal muscle atrophy
distal muscle weakness
drooling
dropped head syndrome
dysarthria
dysphagia
dyspraxia
dystonia
dystonia, children
ecchymoses
electroencephalogram, abnormalities of
electromyogram
ELISA
encephalitis
encephalitis, bornavirus
encephalitis, brainstem
encephalitis, viral
encephalopathy
encephalopathy, progressive
endemic area
enzyme, defect
enzyme, muscle disease
eosinophilia
epicanthal folds
epidemiology of neurology
episodic neurologic deficits
evoked potentials
exome sequencing
face, numbness of
facial appearance, abnormal
falling
false negative
familial
fatty acid, elevated plasma content
feeding disorder
fever
flu-like illness
fundus, abnormality of
gait disorder
gait, spastic
galactocerebrosidase
gangliosidosis GM2
gastroenteritis
gene
gene mutation
gene therapy
genetic counselling
genetic diagnosis, prenatal
genetic neurologic disorders
genetic testing
glioma
gliomatosis cerebri
globoid cells
glycogen storage disease
gram negative rod
Guillain Barre syndrome
hallucination
hammertoes
hands, fisted
head lag
headache
headache, recurrent
hearing loss
hearing problems in children
helminthic infection of CNS
hemangioma
hemiparesis
hemiplegia
hemiplegia, progressive
hepatic failure
hepatic failure, acute
hepatitis
hepatolenticular degeneration(Wilson's disease)
hexosaminidase-A
high arched feet
homocystinuria
hot, red, angry babies
human immunodeficiency virus type 1
human parechovirus
human T-lymphotropic virus type I(HTLV-I)
hyperhomocysteinemia
hyperpyrexia, CNS disorder causing
hyperreflexia
hypertension
hypertonia
hypogonadism
hypomyelination
hyporeflexia
hypotension, systemic
hypotonia
hypoxia
hypoxic encephalopathy
hypoxic-ischemic leukoencephalopathy
imbalance
immunosuppression
immunosuppressive agents
impulsivity
in situ hybridization
inclusion bodies
infection
inferior occipitofrontal fasciculus
intellectual deficit
intellectual deterioration
interferon alpha
internal capsule
intrauterine
intrinsic hand muscles, wasting of
irritability
Jakob-Creutzfeldt disease
Jewish
Krabbe's disease
lactate
lactic dehydrogenase(LDH)
laughing
laughing, pathologic
leg weakness, bilateral
lethargy
leuko-araiosis
leukocyte enzyme abnormality
leukocytosis
leukodystrophy
leukoencephalitis, acute necrotizing hemorrhagic
leukoencephalopathy
leukoencephalopathy, adult onset, sporadic
leukoencephalopathy, differential diagnosis
lipid storage disorder of CNS
lipomatosis
liver function enzymes
Lorenzo's oil
lysosomal storage disease
macrocephaly
magnetic transfer imaging
meconium staining
memory, defect of recent
memory, impairment of
meningeal enhancement
meningismus
meningitis, aseptic
meningitis, brucellosis
meningitis, eosinophilic
meningitis, noninfectious
meningoencephalitis
mental status, abnormal
metachromatic leukodystrophy
metachromatic leukodystrophy, late-infantile
Meyer's loop
microaneurysm, retinal
microcephaly
microdontia
midbrain, lesion of
middle cerebellar peduncle
middle cerebellar peduncle, lesion
middle cerebellar peduncle, lesion, bilateral
mimics
misdiagnosis
mortality
motor neuron disease
movement disorder
MRI
MRI, abnormal
MRI, contrast enhanced
MRI, demyelinating disease
MRI, diffusion tensor
MRI, diffusion weighted
MRI, disappearing lesion on
MRI, false negative
MRI, FLAIR
MRI, high signal foci on
MRI, high signal intensity of basal ganglia
MRI, hypointense signal foci on
MRI, lesion burden
MRI, negative
MRI, perfusion
MRI, serial
MRI, spinal cord
MRI, spinal cord, increased intramedullary cord signal
MRI, spine
MRI, T1 weighted high signal foci
MRI, volumetry
MRS
multiple sclerosis
multiple sclerosis, differential diagnosis of
multiple sclerosis, misdiagnosis
muscle spasm
mutism
mycoplasma
mycoplasma pneumoniae
myelitis
myelitis, longitudinal
myelomalacia
myeloneuropathy
myelopathy
myelopathy, ascending
myelopathy, chronic progressive
neoplasm, primary of CNS
nerve biopsy
nerve conduction studies
nerve root enhancement
neuroaxonal leukodystrophy
neurogenic bladder
neurologic disease, diagnoses of
neurologic examination
neurologic signs
neurological intensive care
neuropathology
neuropathology, brain
neuropathy
neuropathy, demyelinating
neuropathy, sensory
night blindness
numbness, ascending
nystagmus
oculodentodigital dysplasia
opisthotonus
optic ataxia
optic chiasm, enlarged
optic nerve, enlarged
optic radiation
pain
pain, foot
palatal myoclonus
paralysis
paraparesis
paraparesis, familial spastic
paraparesis, spastic
paraparesis, spastic, tropical
parechovirus encephalitis
Parkinson disease
Parkinson disease, arteriosclerotic
PAS positive material in the brain
pediatric neurology
Pelizaeus Merzbacher
penis, pigmented macules
peroxisomal disease
personality change
pes cavus
phenylketonuria
pigmented macules
pleocytosis of cerebrospinal fluid
pneumonia
polyglucosan body
polyglucosan body disease
polymerase chain reaction
polyps, gastrointestinal tract
pons, lesion of
posterior column disease
prenatal
prenatal diagnosis by amniocentesis
prognosis
progressive multifocal leucoencephalopathy
progressive neurologic disorder
pseudobulbar palsy
psychiatric problems in neurologic disorders
psychological testing
psychological testing, neurologic problems
psychomotor retardation
pulmonary infiltrates
pyramidal
pyramidal tract
pyramidal tract dysfunction
raccoon
radiculopathy
rapidly fatal neurologic illness
rapidly progressing neurologic illness
rash
rash, hand
recurrent
release phenomena
respiratory failure
respiratory tract infection
retrovirus
reversible neurologic disorder
review article
rigidity
Romberg's sign
Rosenthal fibers
roundworm
Saudi Arabia
Schilder's disease
scissors gait
screening
season
sedimentation rate, elevated
seizure
seizure, neonatal
sensory loss
septicemia
serologic testing
severe acute respiratory syndrome
skin, darkening of
skin, lesions in neurologic disorders
somatosensory evoked potentials
somnolence
spasticity
speech disorder, childhood
speech, loss of
spinal cord, herniation
spinal cord, lesion of
spinal cord, pathologic exam of
spontaneous remission
startle reaction
steroid therapy, CNS treatment and complications with
subcortical U fibers
suck, poor
symmetric brain lesions
syndactyly
systemic lupus erythematosus
tachycardia
tandem gait, ataxic
Tay-Sachs disease
teeth, abnormal
temporal lobe, lesion
temporal lobe, lesion, bilateral
term infant
testicular atrophy
thalamus, lesion of
thalamus, lesion of-bilateral
thrombocytopenia
toe walking
tone, muscle, increased
tractography
transient neurologic deficit
trauma
treatment of neurologic disorder
tremor
tremor, intention
tremulousness
tripping
uncal herniation
uncinate fasciculus
urinary incontinence
vaccination, neurologic complications with
vasculitides
vasogenic edema
vibratory sensation, abnormal
viral infection
viral infection, CNS
Virchow-Robin spaces, dilated
visual loss
walking, delayed
walking, difficulty with
Wallerian degeneration
weakness
weakness, generalized
weakness, progressive
wheelchair
white matter disease
white matter disease, periventricular
white matter tracts
wide based gait
Showing articles 250 to 300 of 2347 << Previous Next >>

PML Diagnostic Criteria
Neurol 80:1430-1438, Berger, J.,et al, 2013

Clinical Reasoning: A Woman with Rapidly Progressive Apraxia
Neurol 80:e162-e165, Pressman, P.,et al, 2013

Longitudinally Extensive Transverse Myelitis in Neuro-Beh�et Disease
Neurol 80:e189-e190, Graham, D.,et al, 2013

CNS-Immune Reconstitution Inflammatory Syndrome in the Setting of HIV Infection, Part 1: Overview and Discussion of Progressive Multifocal Leukoencephalopathy-Immune Reconstitution Inflammatory Syndrome and Cryptococcal-Immune Reconstitution Inflammatory Syndrome
AJNR 34:1297-1307, Post, M.J.D.,et al, 2013

Combined Retinal and Cerebral Hyperperfusion Syndrome after Carotid Thromboendarterectomy
Neurol 81:e166-e167, Ketteler, S.,et al, 2013

Bilateral Cerebellar Peduncle Lesions in JC Virus Encephalitis
IJID 17:e1086-e1087, , 2013

Spectrum of Neurologic Complications in Chronic Lymphocytic Leukemia
Clin Lymphoma Myeloma Leuk 12:164-179, Lopes da Silva, R., 2012

Early Diffusion MR Imaging Findings and Short-Term Outcome in Comatose Patients with Hypoglycemia
AJNR 33:904-909, Johkura, K.,et al, 2012

The Many Faces of Posterior Reversible Encephalopathy Syndrome
Br J Radiol 85:1566-1575, Stevens, C.J. & Heran, M.K.S., 2012

Cerebral Fat Embolism Syndrome in Sickle Cell Anaemia/�-Thalassemia: Importance of Susceptibility-weighted MRI
Clin Radiol 67:1023-1026, Mossa-Basha, M.,et al, 2012

Persistent Diffusion-Restricted Lesions in Bevacizumab-Treated Malignant Gliomas are Associated with Improved Survival Compared with Matched Controls
AJNR 33:1763-1770, Mong, S.,et al, 2012

PML-IRIS in a patient treated with Brentuximab
Neurol 79:2075-2077, Geldern, G.,et al, 2012

Gradient Echo T2*-weighted Magnetic Resonance Imaging Revealing Cerebral Microbleeds in a Patient with Microscopic Polyangiitis Complicated by Cerebrovascular Disease
J Stroke Cerebrovas Dis 21:904.e7-904.e9, Yamashiro, K.,et al, 2012

A Young Man with Progressive Subcortical Lesions and Optic Nerve Atrophy
Neurol 79:e63, Komatsuzaki, S.,et al, 2012

Clinical Reasoning: A Young Man with Reversible Paralysis, Cerebral White Matter Lesions, and Peripheral Neuropathy
Neurol 79: e70-e72, Zhong, L.,et al, 2012

Neurologic Manifestations of E Coli infection - induced Hemolytic-Uremic Syndrome in Adults
Neurol 79:1466-1473, Weissenborn, K.,et al, 2012

The Cerebral Autosomal-Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL) Scale
Stroke 43:2871-2876, Pescini, F.,et al, 2012

Clinical Reasoning: A 33-year-old Woman with Severe Postpartum Occipital Headaches
Neurol 78:366-369, Maalouf,N. and Harik,S.I., 2012

Characteristics of Intravascular Large B-Cell Lymphoma on Cerebral MR Imaging
AJNR 33:292-296, Yamamoto,A.,et al, 2012

Natalizumab-Associated PML Identified in the Presymptomatic Phase Using MRI Surveillance
Neurol 78:507-508, Blair,N.F.,et al, 2012

Fatal PML Associated with Efalizumab Therapy
Neurol 78:458-467, Schwab,N.,et al, 2012

The Autosomal Recessive Cerebellar Ataxias
NEJM 366:636-646, Anheim,M.,et al, 2012

CNS Involvement at the Onset of Primary Hemophagocytic Lymphohistiocytosis
Neurol 78:1150-1156, Deiva,K.,et al, 2012

A Prematurely Aging Patient Presenting with Severe Leukoaraiosis and Stroke
Neurol 78:e113-e114, Seixas,J.C.,et al, 2012

Early Diffusion MR Imaging Findings and Short-Term Outcome in Comatose Patients wtih Hypoglycemia
AJNR 33:904-909, Johkura, K.,et al, 2012

Risk of Natalizumab-Associated Progressive Multifocal Leukoencephalopathy
NEJM 366:1870-1880,1938, Bloomgren, G.,et al, 2012

Intracranial Optic Nerve Enlargement in Infantile Krabbe Disease
Neurol 78: e126, Shah, S.,et al, 2012

Progressive Multifocal Leukoencephalopathy in Patient with Transitory Lymphopenia
Neurol 78:2000-2002, Chabwine, J.N.,et al, 2012

Restricted Diffusion in Vanishing White Matter
Arch Neurol 69:723-727, Van de Lei, H.D.W.,et al, 2012

Clinical Reasoning: Encephalopathy in a 10-year-old boy
Neurol 79:e12-e18, Rodan, L. & Tein, I., 2012

Primary Sjogren Syndrome
BMJ 344:e3821, Ramos-Casals, M.,et al, 2012

The Ever-Expanding Spectrum of Congenital Muscular Dystrophies
Ann Neurol 72:9-17, Mercuri, E. & Muntoni, F., 2012

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

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

Sporadic Cerebral Amyloid Angiopathy Revisited: Recent Insights Into Pathophysiology and Clinical Spectrum
JNNP 83:124-137, Charidimou,A.,et al, 2012

Cerebral Amyloid Angiopathy in the Elderly
Ann Neurol 70:871-880, Viswanathan, A. and Greenberg, S.M., 2011

Basal Ganglia Involvement in Wernicke Encephalopathy: Report of 2 Cases
AJNR 32:E129-E131, Zuccoli, G.,et al, 2011

Complete Resolution of Advanced Mycoplasma Pneumoniae Encephalitis Mimicking Brain Mass Lesions: Report of Two Pediatric Cases and Review of Literature
Neuro, Simpkins, A.,et al, 2011

Patient with Unilateral White Matter Involvement Does Not Have Krabbe Disease
Arch Neurol 68:1345, Van der Knaap, M.S. and Wenger, D.A., 2011

Management and Outcome of CSF-JC Virus PCR-negative PML in a Natalizumab-treated Patient with MS
Neurol 77:2010-2016, Kuhle, J.,et al, 2011

Rhombencephalitis A Series of 97 Patients
Medicine 90:256-261, Moragas, M.,et al, 2011

Clinicopathologic conference, Neurologic form of immune reconstitution inflammatory syndrome (neuro-IRIS), without evidence of concurrent opportunistic infection
NEJM 362:2343-2352, Case 18-2011, 2011

Progressive Multifocal Leukoencephalopathy in a Patient without Immunodeficiency
Neurol 77:297-299, Tan, I.L.,et al, 2011

Progressive Multifocal Leukoencephalopathy in Transplant Recipients
Ann Neurol 70:305-322, Mateen, F.J.,et al, 2011

Clinicopathologic Conference, Susacs Syndrome (retinocochleocerebral vasculopathy)
NEJM 365:549-559, Case 24-2011, 2011

Progressive Multifocal Leukoencephalopathy: Prognosis and treatment
UpToDate, June, Koralnik, I.J.,et al, 2011

Rituximab-Associated Progressive Multifocal Leukoencephalopathy in Rheumatoid Arthritis
Arch Neurol 68:1156-1164, Clifford, D.B.,et al, 2011

Immune Reconstitution Inflammatory Syndrome in Natalizumab-Associated PML
Neurol 77:1061-1067,1033, Tan, I.L.,et al, 2011

Unilateral White Matter Involvement in Krabbe Disease
Arch Neurol 68:130-131, Lemmens,R.,et al, 2011

Cerebral Amyloid Angiopathy Related Inflammation: Three Case Reports and a Review
JNNP 82:20-26, Chung,K.K.,et al, 2011



Showing articles 250 to 300 of 2347 << Previous Next >>