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Differential
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abdominal protrusion
abducens nerve paralysis
abscess, intracerebral
acquired immunodeficiency syndrome
acquired immunodeficiency syndrome dementia complex
acquired immunodeficiency syndrome, infants and children
acquired immunodeficiency syndrome-related complex
acute necrotizing encephalitis
adolescent medicine
agenesis of corpus callosum
Aicardi's syndrome
airway obstruction
algorithm
alien hand syndrome
altered states of consciousness
alveolar hypoventilation
amaurosis fugax
amniotic fluid, infection
aneurysm
aneurysm, berry
aneurysm, cavernous sinus
aneurysm, infraclinoid
aneurysm, internal carotid artery
aneurysm, intracranial
aneurysm, posterior communicating artery
aneurysm, supraclinoid
aneurysm, vertebral basilar system
angiography, cerebral
angiography, posterior fossa
ankle clonous
anterior horn cell disease
anterior spinal artery infarction
anterior tibial muscle weakness
antiviral agents
Apgar score
aphasia
apraxia
apraxia of eye movements
areflexia
arm weakness
arrhythmia, cardiac
arteritides
artery of Adamkiewicz
arthritis
arthrogryposis multiplex
asymmetric crying facies
ataxia
atrial fibrillation
autoimmune disease
bacterial infection
baldness
basilar artery occlusion
behavioral disorder
birth injury
blood transfusion
botulism
bradykinesia
brain atrophy
brain biopsy
brain scan
brainstem
brainstem, hypoplasia
brainstem, infarction of
brainstem, lesion of
brainstem, malformation
breech delivery
bruit
bruit, asymptomatic
bulbar palsy
bulbar palsy, progressive
burst suppression pattern, electroencephalogram
calcification, intracranial
camptocormia
carcinoma of lung
cardiomyopathy
carotid artery
carotid artery disease
carotid artery occlusion, intracranial
carotid artery occlusion, neck
carotid artery stenosis
CAT scan
CAT scan, abnormal
cataracts
cataracts, congenital
cavernous sinus, syndrome
central cord syndrome
central core disease
central hypoventilation, congenital
central nervous system, infection of
cerebellar peduncle
cerebral cortical atrophy
cerebral palsy
cerebral palsy, risk factors
cerebrospinal fluid
cerebrospinal fluid, cytology
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, gammaglobulin of
cerebrospinal fluid, xanthochromia of
cerebrovascular accident
cerebrovascular accident, clinical diagnosis
cerebrovascular accident, infancy and childhood
cerebrovascular accident, mimics
cerebrovascular accident, young adult
cerebrovascular disease
cerebrovascular disease, cardiovascular disease with
cervical spine injury
children
chiropractic manipulation
chiropractic manipulation, neurologic complications with
chorea
chorioamnionitis
chorioretinitis
chromosomal abnormality
chromosome 11
chromosome 5
chronic progressive external ophthalmoplegia
cleft palate
clubfoot as related to neurologic disease
Coats syndrome
cognition
coloboma
congenital bilateral perisylvian syndrome
congenital birth defects
congenital heart disease
congenital heart disease, CNS complications with
congenital infection, CNS
congenital infection, viral
congenital malformation
congenital malformation, non CNS
congenital myasthenic syndromes
congenital myopathy
congenital myopathy, inflammatory
congenital ocular motor apraxia
congenital paresis
conjunctivitis
consanguinity
contractures, joint
conus medullaris, lesion of
conversion reaction
corneal reflex, abnormal
corpus callosum
corpus callosum, thinning
cortical-basal ganglionic degeneration
cost effectiveness
cranial nerve palsies
creatine phosphokinase(CPK)elevated
cyst, porencephalic
cytomegalic inclusion disease
cytomegalovirus infection
cytomegalovirus infection, congenital
cytosine arabinoside
deafness
deafness, unilateral
delay in diagnosis
delirium
delivery, complicated
dementia
dementia, childhood
depression
depression, psychotic
developmental abnormality of brain
developmental disability
developmental milestones, loss of
developmental retardation
differential diagnosis
difficulty climbing stairs
diplegia, brachial
diplopia
disability, neurological
disconnection syndrome
dislocated hip, congenital
doppler
drooling
dropped head syndrome
Duane syndrome
dysarthria
dyskinesia, buccal lingual facial
dysphagia
dyspnea
dyspraxia
dystonia
dystrophin
echocardiogram
Ehlers-Danlos syndrome
electrocardiogram, abnormal
electroencephalogram
electroencephalogram, abnormalities of
electromyogram
electron microscopy
ELISA
embolism
emergency room
encephalitis
encephalitis, brainstem
encephalitis, viral
encephalopathy
encephalopathy, neonatal
endocarditis, neurologic manifestations with
endocarditis, subacute bacterial
episodic disorders
episodic neurologic deficits
erythema migrans
exome sequencing
eye closure
eye movement, disorders of
eye, pain in
face, inexpressive
face, numbness of
facial appearance, abnormal
facial asymmetry
facial expression abnormality
facial nerve palsy
facial nerve palsy, bilateral
facial nerve palsy, causes of
facial nerve palsy, congenital
facial nerve palsy, prognosis of
facial nerve, lesion of
facial pain
facial weakness
facial weakness, bilateral
facioscapulohumeral syndrome
false negative
familial
fasciculation
fatigue
fever
fibrillations
fibromuscular dysplasia
floppy infant
fluorescent treponema antibody absorption(FTA-ABS)
fluorescent treponema antibody absorption/false positive
foot drop
forceps delivery
fourth ventricle, enlargement of
fourth ventricle, floor
frontal balding
gag reflex, depressed
gait disorder
gait, waddling
ganglioneuroma
gaze palsy
gaze palsy, congenital horizontal
gaze palsy, horizontal
gaze palsy, horizontal-bilateral
gaze palsy, supranuclear
gene
gene mutation
genetic counselling
genetic neurologic disorders
genetic screening
genetic testing
glioblastoma multiforme(astrocytoma Gr.III)
Gowers maneuver
Guillain Barre syndrome
hair, straight-unilateral
hallucination
headache
hearing loss
heart murmur
hemianopia
hemiparesis
hemiplegia
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 infection, newborn
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
heterochromia iridis
heterotopia
HGPPS
high arched feet
high arched palate
highly active antiretroviral therapy
Hirschprung's disease
histochemistry
histochemistry of muscle
hoarseness
Holt-Oram syndrome
Horner's syndrome
Horner's syndrome, bilateral
Horner's syndrome, congenital
Horner's syndrome, painful
human immunodeficiency virus type 1
hydrocephalus
hyperreflexia
hypertension
hypoglycorrhachia
hyporeflexia
hypotonia
hypotonia, infants
hypoxia
hypoxia, newborn
hypoxic encephalopathy
iatrogenic neurologic disorders
IFA
imbalance
immunofluorescent exam of CSF cells
immunohistochemistry
immunosuppression
inclusion bodies, intranuclear
infantile spasm
infectious mononucleosis
insular cortex
intellectual deficit
intellectual deterioration
interferon
interferon inducer
internal carotid artery
internuclear ophthalmoplegia
intracerebral hemorrhage
intracranial pressure, increased
intrauterine
intrauterine infection
intrauterine infection, viral
intrauterine infection, viral of CNS
iododeoxyuridine
ipsilateral hemiplegia
jaw pain
joint hypermobility
juvenile paresis
Kearns-Sayre syndrome
klippel feil syndrome
kyphoscoliosis, neurologic causes of
language disorders in children
leg weakness, bilateral
leg weakness, unilateral
level of consciousness, decreased
levitation
lid closure, weakness of
limbic encephalitis
limbic system
Lyme disease
lymphadenopathy
macrocephaly
malformation, CNS, congenital
malignant hyperpyrexia
Man-In-The-Barrel syndrome
meconium staining
median neuropathy
medulla oblongata
medulla oblongata, lesion of
medulla oblongata, malformation
Melkersson's syndrome
memory, impairment of
meningitis
meningitis, aseptic
mental retardation
mental status, abnormal
merosin
mestinon
microcephaly
micrognathia
micropthalmia
migraine
mimics
misdiagnosis
mitral valve prolapse
Moebius syndrome
molecular genetics
monoamines
monoamines, brain
monoclonal gammopathy
mononeuropathy
motor neuron disease
MRI
MRI, abnormal
MRI, contraindications
MRI, diffusion tensor
MRI, diffusion weighted
MRI, spinal cord
MRI, spine
multiple sclerosis
multiple sclerosis, differential diagnosis of
muscle atrophy, progressive
muscle atrophy, static
muscle biopsy
muscle weakness
muscle weakness, proximal
muscular dystrophy
muscular dystrophy, central nervous system abnormality
muscular dystrophy, classification
muscular dystrophy, congenital
muscular dystrophy, congenital, Fukuyama type
muscular dystrophy, differential diagnosis of
muscular dystrophy, facioscapulohumeral
muscular dystrophy, LAMA2
muscular dystrophy, neurogenic hypothesis of
myasthenia gravis
myasthenia gravis, congenital
myasthenia gravis, etiology of
myasthenia gravis, familial incidence of
myasthenia gravis, neuromuscular junction in
myasthenia gravis, treatment of
myasthenic syndrome
myelitis
myelomalacia
myelopathy
myoclonic jerks
myopathy
myopathy, centronuclear
myositis
myotonia
myotonia congenita
myotonia dystrophica
myotonia dystrophica, classification
nasal speech
nausea and vomiting
neck weakness
nemaline rod myopathy
nemaline rod myopathy, adult onset
neoplasm, intracranial
neoplasm, metastatic to CNS
neoplasm, primary intracerebral
neoplasm, primary of CNS
neoplasm, primary of CNS-infants
nerve conduction studies
nerve injury
neurologic disease, diagnoses of
neurologic disease, diagnoses of, clinical bedside
neurologic examination, focal
neuromuscular junction
neuroophthalmology
neuropathology
neurosyphilis
nonverbal
nusinersen
nystagmus
nystagmus, vertical
obstetric neurologic injuries
ocular motility, disorders of
ocular myopathy
Ondine's curse
opened mouth
operculum syndrome
operculum syndrome, bilateral
ophthalmoplegia
opportunistic infection
opportunistic infection, CNS
optic atrophy
optic nerve
optic nerve, lesion of
optic neuritis
optokinetic nystagmus, abnormal
orbicularis oculi muscle
pacemaker, cardiac-transvenous
pain, back
palpitations
papilledema
paralysis
paranoia
paraplegia
paraplegia, acute
parasitic infection, CNS
paraspinal muscle
paraspinal muscle weakness
paratrigeminal syndrome
peroneal nerve palsy
peroneal nerve, lesion of
personality change
photophobia
phrenic nerve
phrenic nerve pacemaker
phrenic nerve, injury of
pitfalls
placenta
placenta, infection of
pleocytosis of cerebrospinal fluid
polyinosinic cytidic acid(poly IC)
polymicrogyria
polymyositis
polymyositis, infantile
pons, hypoplasia
positive sharp waves
posterior spinal artery infarction
pregnancy, neurologic complications in
prognosis
progressive neurologic disorder
pseudobulbar palsy
psychiatric problems in neurologic disorders
psychological testing
psychomotor retardation
psychosis
ptosis
ptosis, bilateral
ptosis, unilateral
pulmonary infiltrates
pulse oximeter
pupil, abnormality in neurologic disorders
pyramidal tract dysfunction
pyramidal tract, uncrossed
quadriparesis
quadriplegia
quality of life
rash
remote effect of cancer on the nervous system
renal artery stenosis
respiratory failure
retinopathy
review article
rheumatic heart disease
rigidity
risk factors
rubella encephalitis
rubella encephalitis, progressive
rubella syndrome
rubella virus
rubeola virus
sciatic neuropathy
scoliosis
scoliosis, neurologic association with
scotoma
screening
sedimentation rate, elevated
seizure
seizure, children
seizure, neonatal
seizure, psychomotor-temporal lobe
seizure, recurrent
sensory ganglia
sensory loss
sensory loss, cortical
septicemia
serologic testing
skin, lesions in neurologic disorders
sloped shoulders
SMN1 gene
speech disorder
spina bifida
spinal cord
spinal cord vasculature
spinal cord, enlargement
spinal cord, infarction of
spinal cord, injury of
spinal cord, injury, New Born
spinal cord, intramedullary cyst of
spinal cord, ischemic lesion of
spinal cord, neoplasm
spinal cord, neoplasm, infants and children
spinal cord, transection
spinal cord, vascular disorders Affecting
spinal muscular atrophy
spinal muscular atrophy, classification
spirochete infection
standing difficulty
stem cell transplantation
stent, carotid artery
steroid therapy, CNS treatment and complications with
stooped posture
strokelike episodes
subacute myelo-opticoneuropathy(S.M.O.N.)complex
subacute sclerosing panencephalitis(S.S.P.E.)Dawson's disease
subarachnoid hemorrhage
subtemporal decompression
symmetric brain lesions
syncope
syphilis, congenital
syphilis, diagnosis and treatment
syphilis, neurologic complications with
syringomyelia
talk
temporal lobe, lesion
temporal lobe, lesion, bilateral
temporalis muscle wasting
term infant
third nerve palsy
tinnitus
tongue, fasciculations of
tongue, impaired movements of
TORCH infections
torticollis
torticollis, infants and children
toxic encephalopathy
toxoplasmosis, CNS
toxoplasmosis, congenital
transient ischemic attack
transient neurologic deficit
transluminal angioplasty, carotid artery
transplacental virus infections
transposition of the great vessels
transverse smile
trauma
treatment of neurologic disorder
tremor
trigeminal neuralgia
trinucleotide repeats
ulnar nerve
ulnar neuropathy
ultrasonography
ultrasonography, carotid artery
vasculopathy
vertebral artery
vertigo
viral infection
viral infection, CNS
viral isolation
viral myopathy
weakness
weakness, congenital
weakness, fatiguable
weakness, focal
weakness, generalized
weakness, progressive
weakness, proximal
weight loss
wheelchair
white matter disease
wide based gait
Wildervanck's syndrome
winging of scapula
workup
xerostomia
Showing articles 0 to 50 of 2137 Next >>

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A 17-Year-Old Girl with Progressive Cognitive Impairment
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Progressive Camptocormia with Head Drop and Dysphagia
JAMA Neurol 80:209-210, El-Wahsh,S., et al, 2023

Spinal Muscular Atrophy
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Myotonic Dystrophy: Etiology, Clinical Features, and Diagnosis
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Subacute Paresis in a 28-year-old man with HIV
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A Child with Arthrogryposis
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Congenital Asymmetric Crying Facies Syndrome, A Case Report
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A Child with Delayed Motor Milestones and Ptosis
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A 64-year-old Man with Progressive Paraspinal Muscle Weakness
Neurol 86:e4-e9, Schneider, R.,et al, 2016

An 11-year-old Boy with Language Disorder and Epilepsy
Neurol 86:e48-e53, Dong, L. & Zhou, X., 2016

A Neonate with Micrognathia and Hypotonia
Neurol 86:e80-e84, Vawter-Lee, M.M.,et al, 2016

Performance of Bedside Stroke Recognition Tools in Discrimination Childhood Stroke from Mimics
Neurol 86:2154-2161, Mackay, M.T.,et al, 2016

A 51-year-old Woman with Weakness and Stiff Neck
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Spinal Cord Ischemia: Practical Imaging Tips, Pearls, and Pitfalls
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Stroke and NonStroke Brain Attacks in Children
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Ipsilateral Stroke in a Patient with Horizontal Gaze Palsy with Progressive Scoliosis and a Subcortical Infarct
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Diagnosis and Etiology of Congenital Muscular Dystrophy
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Segmental Zoster Paresis of Limbs: Report of Three Cases and Review of Literature
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Neurologic Features of Horizontal Gaze Palsy and Progressive Scoliosis with Mutations in ROBO3
Neurol 64:1196-1203, Bosley, T.M.,et al, 2005

MR Imaging of Brain-Stem Hypoplasia in Horizontal Gaze Palsy with Progressive Scoliosis
AJNR 25:1046-1048, Rossi, A.,et al, 2004

Fibromuscular Dysplasia
NEJM 350:1862-1871, Slovut,D.P. &Olin,J.W., 2004

MRI Findings in Mobius Syndrome: Correlation with Clinical Features
Neurol 55:1058-1060, Pedraza,S.,et al, 2000

Maternal Infection and Cerebral Palsy in Infants of Normal Birth Weight
JAMA 278:207-211, 2471997., Grether,J.K.&Nelson,K.B., 1997

Congenital Muscular Dystrophy Syndromes Distinguished by Alkaline and Acid Phosphatase, Merosin, & Dystrophin Staining
Neurol 46:810-814, Connolly,A.M.,et al, 1996

Congenital Unilateral Facial Paralysis
Pediatrics 97:261-265, Shapiro,N.L.,et al, 1996

Congenital Muscular Dystrophy with Primary Laminin a2 (Merosin) Deficiency Presenting as Inflammatory Myopathy
Ann Neurol 40:782-791, Pegoraro,E.,et al, 1996

TORCH Infections in the Newborn
Semin Neurol 13:106-115, Donley,D.K., 1993

Congenital Bilateral Perisylvian Syndrome:Study of 31 Patients
Lancet 341:608-612, Kuzniecky,R.,et al, 1993

Diaphragm Pacing in Infants and Children
J Pediatr 120:1-8, Weese-Mayer,D.E.,et al, 1992

Quadriplegia after Chiropractic Manip in Infant with Congen Torticollis by a Spinal Cord Astrocy
J Pediatr 120:266-269, Shafrir,Y.&Kaufman,B.A., 1992

Transsection of the Spinal Cord Associated with Breech Delivery
Am J Dis Child 146:351-352, DiMario,F.J.&Wood,B.P., 1992

Cortical-Basal Ganglionic Degeneration
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Congenital Inflammatory Myopathy
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Phrenic Nerve Pacing in Quadriplegia
Editorial, Lancet 336:88-901990., , 1990

Origins of Cerebral Palsy
Am J Dis Child 143:1154-1160, Naeye,R.L.,et al, 1989

Congenital Muscular Dystrophy
J Pediatr 115:214-221, Leyten,Q.H.,et al, 1989

Human Immunodeficiency Virus-Associated Myopathy:Analysis of 11 Pts
Ann Neurol 24:79-84, Simpson,D.M.&Bender,A.N., 1988

Mobius Syndrome and Transposition of the Great Vessels
Neurol 38:1894-1895, Raroque,H.G.,et al, 1988

Lyme Disease, A Neuro-Ophthalmologic View
J Clin Neuro-ophthalmol 7:185-190, MacDonald,A.B., 1987

Central Core Disease, Clinical Features in 13 Patients
Medicine 66:389-396, Shuaid,A.,et al, 1987

Neurological Manifestations in Three German Children with AIDS
Neuropediatrics 18:99-106, Biggemann,B.,et al, 1987

Facioscapulohumeral Dystrophy, in Myology, Basic & Clinical
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Abnormalities of Eyelid Closure
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Myasthenia Gravis & Myasthenic Syndromes
Ann Neurol 16:519-534, Engel,A.G., 1984

Unilateral Straight Hair in Congenital Horner Syndrome Due to Stellate Ganglion Tumor
Ann Neurol 13:345-346, Shewmon,D.A., 1983

Basilar Artery Occlusion in Childhood
Arch Neurol 36:100-102, Mori,K.,et al, 1979

Congenital Ocular Motor Apraxia
Arch Neurol 36:29-31, Orrison,W.W.,et al, 1979

EEG Recognition of Aicardi's Syndrome
Arch Neurol 34:563, Fariello,R.G.,et al, 1977



Showing articles 0 to 50 of 2137 Next >>