Neurology Specific Literature Search   
 
[home][thesaurus]
    

Differential
(Click to cross reference)
abscess, intracerebral
abscess, intracranial
abscess, sphenoid sinus
anemia
angiography, cerebral
angiography, posterior fossa
anhidrosis
aqueduct of Sylvius, stenosis
aqueductal stenosis
areflexia
arteriopathy
arthrogryposis multiplex
arylsulfatase B
atlanto-axial subluxation
band keratopathy
basal ganglia
basal ganglia, calcification of
birth injury
blindness
bone marrow transplantation
calcification, intracranial
carcinoma
carotid artery occlusion, neck
CAT scan
CAT scan, abnormal
cataracts
cataracts, congenital
cavernous sinus, syndrome
central nervous system, infection of
cerebellar hypoplasia
cerebral ischemia
cerebral palsy
cerebral venous thrombosis
cerebro hepato renal syndrome
cerebrovascular accident
cerebrovascular accident, infancy and childhood
cerebrovascular accident, non atherosclerotic cause of
cerebrovascular accident, recurrent
cerebrovascular accident, young adult
cerebrovascular disease
cervical spine
children
chorioretinitis
chromosomal abnormality
chronic graft versus host disease
Clinical Pathologic Conference(C.P.C.)
Cockayne's syndrome
congenital heart disease
congenital infection, CNS
conjunctival injection
contractures, joint
cornea
cornea, abnormal
cornea, opacification in infancy-causes of
cornea, opacity of
corneal dystrophy
corneal edema
corpus callosum
corpus callosum, hypoplastic
cultured skin fibroblasts
cytomegalovirus infection
cytomegalovirus infection, congenital
deafness
deep gray nuclei
developmental retardation
diarrhea
dissociated sensory loss
donut sign
dural sinus thrombosis
dwarfism
dysmorphic
dysostosis multiplex
dyspraxia
ear, abnormal
ectatic basilar artery
edema, pedal
empyema, epidural
empyema, subdural
encephalocele
enzyme treatment
enzyme, defect
epidermal nevus syndrome
Fabry's disease
facial appearance, abnormal
fatty acid, elevated plasma content
fever
fungal infection, CNS
gangliosidosis GM1
gangliosidosis GM2
genetic diagnosis
genetic diagnosis, prenatal
genetic neurologic disorders
genu valgum
glaucoma
hearing loss
hemiparesis
hemorrhoids
hepatomegaly
hepatosplenomegaly
Hurler's syndrome
hydrocephalus
hydrocephalus, congenital
hydronephrosis
hypertension
hypopyon
hypotonia
hypotonia, infants
inclusion bodies
inclusion bodies, intracytopasmic
intelligence quotient
intracerebral hemorrhage
intraocular pressure, increase
intrauterine
intrauterine infection
intrauterine infection, viral
intrauterine infection, viral of CNS
iritis
jugular foramen syndrome
Krabbe's disease
kyphoscoliosis, neurologic causes of
life expectancy
lipid storage disorder of CNS
lissencephaly
lymphadenopathy
lymphoma
lymphoma, ocular
lymphoma, systemic
lysosomal storage disease
lysosomes, abnoral
macrocephaly
magnetic susceptibility
malformation, CNS, congenital
malformation, vascular
malformation, vascular, cerebral
mastoiditis
memory, impairment of
meningitis
mental retardation
metabolic disorder, primary
metachromatic leukodystrophy
microcephaly
micropolygyria
micropthalmia
mineralization
Morquio syndrome
mortality
MRI
MRI, abnormal
MRI, paramagnetic effect
MRI, susceptibility weighted
mucopolysaccharidoses
myelopathy
nasal stuffiness
neck pain
neoplasm, metastatic to eye
nerve conduction studies
neurocutaneous disease
neurofibromatosis 2
neurolipidosis IV
neurologic disease, diagnoses of
neuropathology
neuropathology, brain
neuropathy
neuropathy, hereditary peripheral
neuropathy, peripheral
nevus
Niemann-Pick disease
ophthalmoplegia
optic atrophy
optic nerve
optic nerve, hypoplasia of
optic nerve, neoplasm of
optic neuritis
orbit, lesions of
osteomyelitis
osteomyelitis, skull
osteoporosis
otitis, neurologic complications with
pachygyria
pain
pain, head
papilledema
paraparesis, spastic
patent ductus arteriosus
pectus carinatum
periventricular leukomalacia
photosensitivity, skin
polycystic kidneys
pregnancy, neurologic complications in
premature infant
prenatal diagnosis by amniocentesis
prognosis
proteinuria
pseudohypopyon
psychological testing
psychological testing, children
psychomotor retardation
pupil, abnormality in neurologic disorders
quadriparesis
rash
red eye
respiratory failure
retinal degeneration
retinal detachment
retinal dysplasia
retinitis pigmentosa
retinopathy
review article
rubella syndrome
sarcoidosis
seizure
seizure, neonatal
sensorineural hearing loss
short neck
short stature
sinusitis
skin, biopsy
skin, lesions in neurologic disorders
skull x-ray, bony defect on
spinal cord, compression of
splenomegaly
stem cell transplantation
stillbirth
sweating, abnormality of
Tangier's disease
third nerve palsy
tongue, enlarged
torticollis
treatment of neurologic disorder
uremia
uveitis
varicose veins
vasculopathy
vertebral-basilar insufficiency
viral infection, CNS
vision, failure of in childhood
visual acuity
visual acuity, decreased
visual impairment
visual loss
Walker-Warburg syndrome
white matter disease
Showing articles 300 to 350 of 974 << Previous Next >>

Can We Prevent Cerebral Palsy?
NEJM 349:1765-1769, Nelson,K.B., 2003

Seizure Exacerbation Associated with Oxcarbazepine in Idiopathic Focal Epilepsy of Childhood
Neurol 61:1012-1013, Chapman,K.,et al, 2003

"Economy Class" Stroke Syndrome?
Neurol 58:960-961, Isayev,Y.,et al, 2002

Death in Children with Epilepsy: A Population-based Study
Lancet 359:1891-1985, Camfield,C.S.,et al, 2002

Hemodynamic Studies in Early Ischemic Stroke
Stroke 33:1274-1279, Akopov,S. &Whitman,G.T., 2002

Neonatal Cerebral Infarction Diagnosed by Diffusion-Weighted MRI
Stroke 33:1142-1145, Mader,I.,et al, 2002

A Practical Approach to the Diagnosis and Management of MELAS: Case Report and Review
The Neurologist 8:302-312, Thambisetty,M.,et al, 2002

Cardiac Papillary Fibroelastoma as a Cause of Recurrent Ischemic Strokes: The Diagnostic Value of Serial Transesophageal Echocardiography
Cerebrovasc Dis 14:256-259, Baba, Y.,et al, 2002

Hyperhomocysteinemia and Other Inherited Prothrombotic Conditions in Young Adults With a History of Ischemic Stroke
Stroke 33:51-56, Madonna,P.,et al, 2002

Spontaneous Intracranial Internal Carotid Artery Dissection
Arch Neurol 59:977-981, Chaves,C.,et al, 2002

Sudden Death in Epilepsy: A Wake-up Call for Management
Lancet 359:1790-1791, Pedley, T.A. &Hauser,W.A., 2002

Deaths from Stroke in US Children, 1979-1998
Neurol 59:34-39,6, Fullerton,H.J.,et al, 2002

Clinical Outcome in 287 Consecutive Young Adults (15-45 Years) With Ischemic Stroke
Neurol 59:26-33,6, Leys,D.,et al, 2002

Minor Head Injury as Cause and Co-Factor in the Aetiology of Stroke in Childhood: A Report of Eight Cases
JNNP 73:13-16, Kieslich,M.,et al, 2002

Clinicopath Conf, Neuronal Ceroid Lipofuscinosis, Late-Onset Infantile Subtype
NEJM 347:672-680, Case 27-2002, 2002

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

Progressive Stroke Following Soccer Playing
Arch Neurol 59:1484-1485, Haussermann,P.,et al, 2002

Antiphospholipid Antibodies and Stroke in Young Women
Stroke 33:2396-2401, Brey,R.L.,et al, 2002

Prospective Assessment of Risk Factors for Recurrent Stroke During Childhood--A 5-year Follow-up Study
Lancet 360:1540-1545,1526, Strater,R.,et al, 2002

Posterior Circulation Stroke in Childhood
Neurol 59:1552-1556, Ganesan,V.,et al, 2002

Stroke in the Young in the Northern Manhattan Stroke Study
Stroke 33:2789-2793, Jacobs,B.S.,et al, 2002

Stroke in a Healthy 46-Year-Old Man
JAMA 285:2757-2762, Wityk,R.J., 2001

Chickenpox and Stroke in Childhood
Stroke 32:1257-1262, Askalan,R.,et al, 2001

Fits and Strokes
Lancet 358:120, Sharma,P.,et al, 2001

Cerebral Sinovenous Thrombosis in Children
NEJM 345:417-423, DeVeber,G.,et al, 2001

Sudden Unexplained Death in Children With Epilepsy
Neurol 57:430-434, Donner,E.J.,et al, 2001

Arterial Dissection and Stroke in Children
Neurol 57:1155-1160, Fullerton,H.J.,et al, 2001

Mitochondrial Disease and Stroke
Stroke 32:2507-2510, Martinez-Fernandez,E.,et al, 2001

Silent Infarcts in Children With Sickle Cell Anemia and Abnormal Cerebral Artery Velocity
Arch Neurol 58:2017-2021, Pegelow,C.H.,et al, 2001

Ischemic Stroke and Active Migraine
Neurol 57:1805-1811, Milhaud,D.,et al, 2001

Immediate Surgery for Moyomoya Syndrome?
Arch Neurol 58:130-131,132, Roach,E.S., 2001

Surgery for Moyamoya Syndrome?
Arch Neurol 58:128-129,132, Scott,R.M., 2001

Use of Specialized Coagulation Testing in the Evaluation of Patients with Acute Ischemic Stroke
Neurol 56:624-627, Bushnell,C.,et al, 2001

Stroke Prevention and Treatment in Sickle Cell Disease
Arch Neurol 58:565-568, Adams,R.J., 2001

Is Patent Foramen Ovale a Family Trait?
Stroke 32:1563-1566, Arquizan,C.,et al, 2001

MRI Hyperintensities of the Temporal Lobe and External Capsule in Patients with CADASIL
Neurol 56:628-634, O'Sullivan,M.,et al, 2001

Vertebral Artery Dissection Due to Indirect Neck Trauma: An Underrecognised Entity
Neurol India 49:384-390, Prabhakar,S.,et al, 2001

Amusement park stroke
Neurol 55:564, Burneo, J.G.,et al, 2000

Tonic Seizures are a Particular Risk Factor for Drowning in People with Epilepsy
BMJ 321:975-976, Besag,F.M.C., 2000

Cerebral Infarctin in the Term Newborn: Clinical Presentation and Long-Term Outcome
J Pediatr 137:351-355, Sreenan,C. et al, 2000

Practice Parameter: Evaluating a First Nonfebrile Seizure in Children
Neurol 55:616-623, Hirtz,D. et al, 2000

Stiripentol in Severe Myoclinic Epilepsy in Infancy: A Randomised Placebo-Controlled Syndrome-Dedicated Trial
Lancet 356:1638-1642,1623, Chiron,C.,et al, 2000

Discontinuation of Anticonvulsant Therapy in Children with Partial Epilepsy
Neurol 55:1393-1395, Verrotti,A.,et al, 2000

Homocysteine and Neurologic Disease
Arch Neurol 57:1422-1428, Diaz-Arrastia,R., 2000

Interatrial Septal Abnormalities and Stroke
Neurol 55:1172-1179, Overell,J.R.,et al, 2000

Adverse Cardiovascular and Central Nervous System Events Associated with Dietary Supplements Containing Ephedra Alkaloids
NEJM 343:1833-1838,1886, Haller,C.A. & Benowitz,N.L., 2000

Phenylpropanolamine and the Risk of Hemorrhagic Stroke
NEJM 343:1826-1832,1886, Kernan,W.N.,et al, 2000

Protein C Deficiency Related to Valproic Acid Therapy: A Possible Association with Childhood Stroke
J Pediatr 137:714-718, Gruppo,R.,et al, 2000

De Novo Mutation in the Notch3 Gene Causing CADASIL
Ann Neurol 47:388-391, Joutel,A.,et al, 2000

Early Identification of Refracvtory Epilepsy
NEJM 342:314-319, Kwan,P.&Brodie,M.J., 2000



Showing articles 300 to 350 of 974 << Previous Next >>