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abducens nerve paralysis
acoustic nerve
acquired immunodeficiency syndrome
acquired immunodeficiency syndrome, medical precautions with
acute ataxia of childhood
acute cerebellar ataxia
adolescent medicine
advances in neurology
akinetic mute
alcohol intolerance
algorithm
alkylating agents
alpha-fetoprotein
alpha-synuclein
altered states of consciousness
alternating hemiplegia
alternating hemiplegia of childhood
alternating rapid movement, impaired
AMPA receptor antibodies
amphiphysin antibodies
anemia
angiotensin-converting enzyme
ankle edema
anti GQ1b IgG antibody
anti Hu antibody
anti Ri antibody
anti Yo antibody
antiamphiphysin
antibiotics
antimetabolite
aphasia
apraxia of eye movements
areflexia
arthralgia
arthritis
ascites
asparginase
ataxia
ataxia telangiectasia
ataxia, acute onset
ataxia, cerebellar
ataxia, hereditary
ataxia, progressive
ataxia, sensory
ataxia, truncal
ataxic gait
atonic bladder
ATP1A3 gene
atypical
autoantibodies
autoimmune basal ganglia encephalitis
autoimmune cerebellar ataxia
autoimmune disease
autonomic dysfunction
autonomic neuropathy
Babinski sign
bacterial infection
behavioral disorder
blindness
blood dyscrasias, neurologic findings with
Borrelia burgdorferi infection
brachial plexus neuropathy
bradykinesia
callosal angle
cane
carcinoembryonic antigen
carcinoma
carcinoma of breast
carcinoma of cervix
carcinoma of lung
carcinoma of ovary
carcinoma of uterus
cardiomyopathy
CAT scan
CAT scan, abnormal
cataracts
cauda equina, enhancement
celiac disease, adult
central nervous system, infection of
cerebellar ataxia, children
cerebellar ataxia, hereditary
cerebellar atrophy, primary
cerebellar atrophy, secondary
cerebellar degeneration
cerebellar lesion
cerebellar vermis
cerebral cortex
cerebral venous thrombosis
cerebrospinal fluid
cerebrospinal fluid, abnormal
cerebrospinal fluid, drainage of
cerebrospinal fluid, gammaglobulin of
cerebrospinal fluid, oligoclonal IgG in
cerebrospinal fluid, pressure low
cerebrovascular accident
cerebrovascular accident, recurrent
cerebrovascular disease
ceruloplasmin, serum
chairbound
Charcot-Marie-Tooth
chemotherapy, CNS treatment and complications with
chest pain
chest x-ray, abnormal
children
chorea
choreoathetosis
chromosomal abnormality
chromosome 11
chromosome 9
cisternogram, radionuclide
Clinical Pathologic Conference(C.P.C.)
clubfoot as related to neurologic disease
cognition
cognition, slowed
coinfection
collapsin response mediator protein 5 IgG
coma
complications
consanguinity
contactin associated protein like 2 antibodies
cough
cranial nerve palsies
cranial neuropathy
cranial neuropathy, multiple
Creutzfeldt-Jakob disease, genetic
deep gray nuclei
deep tendon reflexes
degenerative diseases of CNS
dementia
dementia, childhood
dementia, familial
dementia, rapidly progressive
dementia, reversible
depression
dermatitis
dermatomyositis
developmental retardation
dexterity, impaired
diabetes mellitus
diagnostic criteria
diarrhea
diarrhea, bloody
diet
differential diagnosis
difficulty climbing stairs
diplopia
dizziness
dopa responsive dystonia
drooling
dysarthria
dysdiadochokinesia
dyskinesia
dysmetria
dysmorphic
dysphagia
dystonia
edema, pedal
efficacy
electroencephalogram, abnormalities of
electromyogram
emotional lability
encephalitis
encephalitis, autoimmune
encephalitis, brainstem
encephalitis, paraneoplastic
encephalitis, viral
encephalomyelitis
encephalomyelitis, postinfectious
encephalopathy
encephalopathy, parainfectious
Epstein-Barr virus
erythema migrans
esophageal varices
evoked potentials
executive dysfunction
external lumbar drainage
eye movement, disorders of
facial expression abnormality
facial nerve palsy
facial nerve palsy, bilateral
facial nerve palsy, recurrent
facial pain
falling
familial
fever
finger nose finger test
Fisher's syndrome
fluorouracil
flush syndrome
foot drop
frataxin
Friedreich's ataxia
frontal lobe, pathologic signs of
gait disorder
gait, magnetic
gamma amino butyric acid receptor antibody
gammaglobulin therapy, intravenous
gastrointestinal disease, neurologic complications
gaze palsy, horizontal
gene
gene mutation
genetic counselling
genetic linkage
genetic neurologic disorders
genetic screening
genetic testing
Gerstmann-Straussler-Scheinker disease
glutamic acid decarboxylase, antibody
gluten ataxia
gluten sensitivity
gluten-free diet
granulomatous disease
growth retardation
Guillain Barre syndrome
Guillain Barre syndrome, infantile and childhood form
Guillain Barre syndrome, variant forms of
hallucination
handwriting
headache
headache, severe
hearing loss
heel-knee-shin test
hepatic encephalopathy
hepatic failure
hepatolenticular degeneration(Wilson's disease)
hepatolenticular degeneration(Wilson's disease), presymptomatic
heralding manifestation
herpes virus
high altitude sickness
hoarseness
Hodgkin's disease
human immunodeficiency virus type 1
hydrocephalus
hydrocephalus, normal pressure
hydrocephalus, normal pressure, etiology
hydrocephalus, treatment of
hyperreflexia
hypoalbuminemia
hyponatremia
hyporeflexia
hypothalamus
hypothalamus, disturbance of
hypotonia
imbalance
immune reconstitution inflammatory syndrome
immunodeficiency
immunologic disease
immunology and the nervous system
immunosuppression
immunosuppressive agents
immunotherapy
impotence
inappropriate antidiuretic(A.D.H.)hormone, CNS involvement with
inclusion bodies, eosinophilic intranuclear
inclusion bodies, intranuclear
infection
infectious mononucleosis
infectious mononucleosis, neurologic findings with
intellectual deficit
intellectual deterioration
intracranial hypertension, benign
irritability
isoniazid
Jakob-Creutzfeldt disease
Jakob-Creutzfeldt disease, cerebellar variant
jaw pain
Kayser-Fleischer ring
Korsakoff's psychosis
L-dopa
leg weakness, bilateral
lethargy
leucine rich glioma inactivated 1 antibodies
leukemia
leukemia, neurologic findings assoc.with
leukopenia
limbic encephalitis
liver function enzymes
lumbar drain
lumbar puncture, repeated
Lyme disease
lymphocytic meningoradiculitis
lymphoma
malignancy screen
malignancy, occult
masked facies
Melkersson's syndrome
memory, impairment of
meningismus
meningitis
meningitis, aseptic
meningitis, carcinomatous
meningitis, neurologic aspects and complications of
meningitis, recurrent
meningoencephalitis
meningoencephalopathy
mental retardation
mental status, abnormal
methotrexate
methylhydrazine derivatives
microcephaly
mimics
misdiagnosis
molecular genetics
monoamine oxidase inhibitors
monoclonal antibodies
monoclonal gammopathy
mononeuritis multiplex
mood change
mortality
motor neuron disease
mountain climbing
movement disorder
movement disorder, extrapyramidal
movement disorder, hyperkinetic
MRI
MRI, abnormal
MRI, brachial plexus
MRI, diffusion weighted
MRI, flow void, CSF
MRI, high signal foci on
MRI, negative
MRI, periventricular hyperintensity
MRI, punctate pattern
multiple sclerosis
multiple system atrophy
muscle biopsy
muscle pain
muscle weakness
muscle weakness, proximal
myasthenia gravis
myasthenia gravis, paraneoplastic
myasthenic syndrome
mycoplasma
mycoplasma pneumoniae
myelitis
myelopathy
myelopathy, chronic progressive
myopathy
myopathy, vacuolar
myositis
myositis, ocular
nausea and vomiting
nemaline rod myopathy
nerve conduction studies
neuroaxonal dystrophy
neuroaxonal dystrophy, infantile
neurocutaneous disease
neuroendocrinology
neurologic complications of, surgery
neurologic complications of, systemic cancer
neurologic complications of, systemic disease
neurologic disease
neurologic disease, diagnoses of
neurologic disease, multifocal
neurologic disease, tempo
neurologic signs
neurologic symptoms
neuromuscular junction
neuronal cell surface antigen
neuronal intranuclear inclusion disease
neuronopathy
neuronopathy, sensory
neuropathology
neuropathy
neuropathy, acute
neuropathy, ataxic
neuropathy, painful
neuropathy, paraneoplastic
neuropathy, peripheral
neuropathy, recurrent
neuropathy, sensory
neurotoxin
next-generation sequencing
nitrogen mustard
NMDA antagonists
nystagmus
nystagmus, monocular
ocular motility, disorders of
oculomasticatory myorhythmia
onconeural antibodies
ophelia syndrome
ophthalmoplegia
ophthalmoplegia, progressive external
ophthalmoplegia, recurrent
opsoclonus
opsoclonus-myoclonus syndrome
optic atrophy
optic disc edema
optic nerve
optic neuritis
optic neuropathy
orthostatic hypotension
ovarian tumor
pain
pain, abdominal
pain, back
pain, leg
papilledema
paraneoplastic cerebellar degeneration
paraparesis
paraparesis, familial spastic
paraparesis, familial spastic, classification
paraparesis, spastic
paresthesias
Parkinson disease, dystonia with
Parkinson disease, juvenile
Parkinsonism syndrome
paroxysmal hemiplegia
paroxysmal neurologic deficits
pathology
pediatric autoimmune neuropsychiatric disorders associated with streptococcal infection
penicillamine
peripheral nerve, lesion of
personality change
pes cavus
photophobia
picking at skin
pleocytosis of cerebrospinal fluid
pneumonia
POLG1 gene
poliomyelitis-like illness
polyclonal gammopathy
polymerase chain reaction
polymyositis
polyneuropathy
polyneuropathy, chronic idiopathic
polyneuropathy, chronic idiopathic, ataxic
polyneuropathy, chronic inflammatory demyelinating
polyneuropathy, chronic relapsing
postural abnormality
potassium channel antibodies
practice guidelines
precipitating factors
pregnancy, neurologic complications in
prion disease
prion protein gene
PRKN gene
procarbazine
progeria
prognosis
progressive multifocal leucoencephalopathy
progressive neurologic disorder
proprioception, abnormal
protein 14-3-3, cerebrospinal fluid
psychiatric disorder
psychiatric problems in neurologic disorders
psychomotor retardation
psychosis
ptosis
ptosis, bilateral
pulmonary infiltrates
quadriplegia
radiation hypersensitivity
rapid onset dystonia parkinsonism
rapidly progressing neurologic illness
real-time quaking-induced conversion
recurrent
Red flags
regional enteritis
remote effect of cancer on the nervous system
renal stones
respiratory failure
retinopathy
reversible neurologic disorder
review article
rhinorrhea
rigidity
risk factors
rituximab
safety
sarcoidosis
sarcoidosis, CNS
scoliosis
screening
sedimentation rate, elevated
seizure
sensorineural hearing loss
sensory polyneuropathy
serologic testing
serologic testing, false negative
seronegative
short steps
shunt procedure, lumboperitoneal
shunt procedure, ventricular
shunt procedure, ventricular-complications of
sinemet
skin, biopsy
skin, lesions in neurologic disorders
sleep pathology and physiology
slit lamp examination
spastic ataxia
spasticity
spinal cord
spinal cord, lesion of
spinal muscular atrophy
spirochete infection
splenomegaly
startle myoclonus
status epilepticus
steroid
steroid therapy, CNS treatment and complications with
stiff man syndrome
striatal encephalitis
striatum, lesion of
striatum, lesion of, bilateral
subarachnoid hemorrhage
synucleinopathy
systemic illness
tandem gait, ataxic
telangiectases
temporal lobe, lesion
thrombocytopenia
tick bite
tinnitus
tonic foot response
transglutaminase antibodies
transient ischemic attack
treatment of neurologic disorder
tremor
tremor, postural
trientine dihydrochloride
trinucleotide repeats
ulcerative colitis
upgaze, paralysis of
urinary incontinence
urinary retention
vasculitides
ventricular enlargement
ventriculostomy
vinblastine
vincristine neurotoxicity
viral infection
viral infection, CNS
vision, blurred
vision, failure of in childhood
visual acuity, decreased
visual evoked response
visual impairment
visual loss
vocal cord paralysis
walking frame
walking, difficulty with
weakness
weakness, generalized
weakness, progressive
weakness, proximal
weight loss
wheelchair
Whipple's disease
wide based gait
workup
wrist drop
zinc
Showing articles 200 to 250 of 6548 << Previous Next >>

HIV Infection Presenting with Motor Axonal Variant of Guillain-Barre Syndrome
J Clin Neuromusc Dis 9:303-305, Wagner, J.C. and Bromberg, M.B., 2007

Detection of CSF 14-3-3 Protein in Guillain-Barr Syndrome
Neurol 67:2211-2216, Bersano,A.,et al, 2006

MR IMaging and Angiography of Primary CNS Vasculitis of Childhood
AJNR 27:192-199, Aviv,R.I.,et al, 2006

Diagnostic Evaluation of Clinically Normal Subjects with Chronic hyperCKemia
Neurol 66:1585-1587, Fernandez,C.,et al, 2006

Early Clinical Signs and Imaging Findings in Gerstmann-Straussler-Scheinker Syndrome (Pro102Leu)
Neurol 66:1672-1678, Arata,H.,et al, 2006

Plasma Exchange in Neuroimmunological Disorders: Part 2. Treatment of Neuromuscular Disorders
Arch Neurol 63:1066-1071, Lehmann,H.C.,et al, 2006

Isolated Abducens Nerve Palsy as a Regional Variant of Guillain-Barre Syndrome
JNS 243:35-38, Tatsumoto, M.,et al, 2006

Spinal dural arteriovenous fistulas: a congestive myelopathy that initially mimics a peripheral nerve disorder
Brain 129:3150-3164, Jellema, K., et al, 2006

Phenotypic Spectrum Associated with Mutations of the Mitochondrial Polymerase y Gene
Brain 129:1674-1684, Horvath, R.,et al, 2006

Mitochondrial DNA Polymerase-y and Human Disease
Hum Mol Genet 15:R244-R252, Hudson, G.,et al, 2006

Primary Angiitis of the Central Nervous System: Emerging Variants
Q J Med 98:643-654, Maclaren,K.,et al, 2005

Idiopathic Acute Transverse Myelitis: Application of the Recent Diagnostic Criteria
Neurol 65:1950-1953,1857, de Seze,J.,et al, 2005

Guillain-Barre Syndrome
Lancet 366:1653-1666, Hughes,R.C. &Comblath,D.R., 2005

Initial Diagnoses Given to Persons with the Fragile X Associated Tremor/Ataxia Syndrome (FXTAS)
Neurol 65:299-301, Hall,D.A.,et al, 2005

Neurological presentation of intravascular lymphoma: report of two cases and discussion of diagnostic challenges
Eur J Neurol 12:710-714, Lozsadi, D.A.,et al, 2005

Primary Angiitis of the Central Nervous System at Conventional Angiography
Radiology 233:878-882, Kadkhodayan,Y.,et al, 2004

Assessment: Transcranial Doppler Ultrasonography
Neurol 62:1468-1481, Sloan,M.A.,et al, 2004

Intravenous Immunoglobulin in Autoimmune Neuromuscular Diseases
JAMA 291:2367-2375, Dalakas,M.C., 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

Clinicopath Conf., Chronic Inflammatory Demyelinating Polyneuropathy
NEJM 348:735-743, Case 6-2003, 2003

Polymyositis Masquerading as Motor Neuron Disease
Arch Neurol 60:1001-1003, Ryan,A.,et al, 2003

Polymyositis
Neurol 61:316-321, van der Meulen,M.F.G.,et al, 2003

Polymyositis and Dermatomyositis
Lancet 362:971-982, Dalakas,M.C.&Hohlfeld,R., 2003

Spinal Dural Arteriovenous Fistulas: Clinical Features in 80 Patients
JNNP 74:1438-1440, Jellema,K.,et al, 2003

Subacute Inflammatory Demyelinating Polyneuropathy
Neurol 61:1507-1512, Oh,S.J.,et al, 2003

Does This Patient Have Parkinson Disease?
JAMA 289:347-353, Rao,G.,et al, 2003

Diagnostic Criteria for Idiopathic Intracranial Hypertension
Neurol 59:1492-1495, Friedman,D.I. &Jacobson,D.M., 2002

Diagnostic Criteria for Dystonia in DYT1 Families
Neurol 59:1780-1782, Bressman,S.B.,et al, 2002

Polymyalgia Rheumatica and Giant-Cell Arteritis
NEJM 347:261-271, Salvarani,C.,et al, 2002

CADASIL Mimicking Primary Angiitis of the Central Nervous System
Arch Neurol 59:1480-1483, Engelter,S.T.,et al, 2002

Chronic Inflammatory Demyelinating Polyneuropathy Presenting with Features of GBS
Neurol 58:979-982, Mori,K.,et al, 2002

Chronic Idiopathic Axonal Polyneuropathy and Successful Aging of the Peripheral Nervous System in Elderly People
Arch Neurol 59:533-540,520, Vrancken,A.F.J.E.,et al, 2002

Temporal Arteritis
JAMA 287:2996-3000,3034, Hellmann,D.B., 2002

Diagnostic Strategies in Vasculitis Affecting the Central Nervous System
Cleve Clin J Med 69:SII 105-108, Calabrese,L.H., 2002

Recessive Ataxia With Ocular Apraxia
Arch Neurol 58:201-205,173, Barbot,C.,et al, 2001

Clinical and Neuroradiologic Features of Acute Disseminated Encephalomyelitis in Children
Neurol 56:1308-1312,1257, Hynson,J.L.,et al, 2001

Early Electrodiagnostic Findings in Guillain-Barre Syndrome
Arch Neurol 58:913-917, Gordon,P.H. & Wilbourn,A.J., 2001

Reliability of Normal Findings on MR Imaging for Excluding the Diagnosis of Vasculitis of the Central Nervous System
AJR 177:455-459, Wasserman, B.A.,et al, 2001

Inclusiong Body Myositis Mimicking Motor Neuron Disease
Arch Neurol 58:1253-1256, Dabby,R.,et al, 2001

Paraneoplastic Cerebellar Ataxia Due to Autoantibodies Against a Glutamate Receptor
NEJM 342:21-27, Smitt,P.S.,et al, 2000

A Six-Year-Old Girl with Tick paralysis
NEJM 342:90-94, Felz,M.W.,et al, 2000

Hereditary Recurrent Focal Neuropathies, Clinical and Molecular Features
Neurol 54:546-551, Stogbauer,F.,et al, 2000

The DYT1 Phenotype and Guidelines for Diagnostic Testing
Neurol 54:1746-1753,1718, Bressman,S.B.,et al, 2000

Inborn Errors of Metabolism as a Cause of Neurological Disease in Adults: An Approach to Investigation
JNNP 69: 5-12, Gray,R.G.F. et al, 2000

Intravenous Immunoglobulin in the Treatment of Autoimmune Neuromuscular Diseases:Present Status and Practical Therapeutic Guidelines
Muscle & Nerve 22:1479-1497, Dalakas,M.C., 1999

Brain Biopsy in Primary Angiitis of the Central Nervous System
Neurol 53:858-860, Alrawi,A.,et al, 1999

Chronic Cryptogenic Sensory Polyneuropathy,Clinical and Laboratory Characteristics
Arch Neurol 56:540-547, 519, Wolfe,G.I.,et al, 1999

Intravenous Immunoglobulin Treatment in Neurologic Disorders
Arch Neurol 56:1025-1027,1032, Sorensen,P.S., 1999

Is the Routine Use of Intravenous Immunoglobulin Treatment in Neurologic Disorders Justified?
Arch Neurol 56:1028-1032, Karussis,D.&Abramsky,O., 1999



Showing articles 200 to 250 of 6548 << Previous Next >>