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Differential
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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 0 to 50 of 968 Next >>

Bilateral Pseudohypopyon Causing White Eyes in a Patient with Lymphoma
Lancet 395:e74, Radhakrishnan Iyer, S.S.,et al, 2020

Mineralization of the Deep Gray Matter with Age: A Retrospective Review with Susceptibility-Weighted MR Imaging
AJNR 29:176-183, Harder,S.L.,et al, 2008

Insights Into the Diagnosis and Treatment of Lysosomal Storage Diseases
Arch Neurol 60:322-328, Wegner,D.A.,et al, 2003

Follow-up of Nine Patients with Hurler Syndrome After Bone Marrow Transplantation
J Pediatr 133:119-125, 71998., Guffon,N.,et al, 1998

Mucolipidosis Type IV; Characteristic MRI Findings
Neurol 51:565-569, Frei,K.P.,et al, 1998

Cerebrovascular Complications of Fabry's Disease
Ann Neurol 40:8-17, Mitsias,P.&Levine,S.R., 1996

Visual Impairment in Patients with Neurofibromatosis 2
Neurol 43:622-623, Bouzas,E.A.,et al, 1993

Lethal Cytomegalovirus Infection in Preterm Infants:Clinical, Radiological, and Neuropathological Findings
Ann Neurol 31:64-68, Perlman,J.M.&Argyle,C., 1992

Ocular Complications of Tangier Disease
Am J Med 83:991-994, Pressley,T.A.,et al, 1987

Tangier Disease (Hypo-a-Lipoproteinemia)
Textbook of Child Neurology, 3rd Ed. , Phila, Lea & Febiger, Ch 1, p 86, Menkes,J.H., 1985

The Cerebrohepatorenal (Zellweger) Syndrome
NEJM 310:1141-1146, Moser,A.E.,et al, 1984

Congenital Hydrocephalus & Eye Abnormalities with Severe Developmental Brain Defects:Warburg's Syndrome
Ann Neurol 16:60-65, Bordarier,C.,et al, 1984

Cerebro-ocular Dysgenesis (Walker-Warberg Syndrome) :Neuropathologic & Etiologic Analysis
Neurol 34:1531-1541, Williams,R.S.,et al, 1984

Clinicopathological Conference
Maroteaux-Lamy Syndrome, Case 44-1983, NEJM 309:1109-1117983., , 1983

Mucopolysaccaridosis IV (Morquio Syndrome) , in The Metabolic Basis of Inherited Disease
(Ed) 5th Ed. , McGraw-Hill, New York, p. 766, Stanbury,J.B., 1983

Cockayne Syndrome:Unusual Neuropathological Findings & Review of the Literature
Ann Neurol 6:340-348, 1979, Soffer,D.,et al, 1979

Neurological Involvement in the Epidermal Naevus Syndrome
JNNP 41:466, McAuley,D.L.,et al, 1978

Sarcoidosis & Its Ophthalmic Manifestations
Am J Ophthmol 86:648-655, Obenauf,C.D.,et al, 1978

Globoid cells, Glial nodules, & Peculiar Fibrillary Changes in the cerebro-hepato-renal Syndrome of Zellweger
Ann Neurol 2:473, deLeon,G.A.,et al, 1977

Neurological Complications of Infections of the Head & Neck
Otolaryng Clin North Am 9:729, Kaplan,R.J., 1976

Corneal Opacification in Infancy
MCV Quart 8:230, Ching,F., 1972

Mucopolysaccaridosis IV (Morquio Syndrome) , in Heritable Disorders of Connective Tissue
(Ed) 4th Ed, The C. V. Mosby Co, St. Louis, p. 583, McKusick,V.A., 1972

Rubella, Clinical Manifestations & Management
Am J Dis Child 118:18-29, Cooper,L.Z.,et al, 1969

Angiokeratoma Corporis Diffusum
Quart J Med 31:177, 1962 April., Wise,D.,et al, 1962

Changing Trends in Demographics, Risk Factors, and Clinical Features of Patients with Infective Endocarditis-Related Stroke, 2005-2015
Neurol 100:e1555-e1564, Ridha,M.,et al, 2023

Iatrogenic Cerebral Amyloid Angiopaty Post Neurosurgery:Frequency, Clinical Profile, Radiological Features, and Outcome
Stroke 54:1214-1223, 1224, Kaushik,K.,et al, 2023

Neonatal Seizures
NEJM 388:1692-1700, Ropper.A.H., 2023

Early Detection of Underlying Cavernomas in Patients with Spontaneous Acute Intracerebral Hematomas
AJNR 44:807-813, Bani-Sadr,A.,et al, 2023

Unpacking the CNS Manifestations of Epstein-Barr Virus:An Imaging Perspective
AJNR 44:1002-1008, Soni,N.,et al, 2023

Brain Calcification in a Young Woman With Seizures, Explore the Rare Differentials
Neurol 100:397-398, Menon,B.,et al, 2023

Updates on Sturge-Weber Syndrome
Stroke 53:3769-3779, Yeom,S.E.&Comi,A.M., 2022

Clinicopathologic Conference, Neurosyphilis
NEJM 386:583-590, Case 4-2022, 2022

Contemporary Trends in the Nationwide Incidence of Primary Intracerebral Hemorrhage
Stroke 53:e70-e74, Bako, A.T.,et al, 2022

Cerebrovascular Ischemic Events in Patients with Takayasu Arteritis
Stroke 53:1550-1557, Mirouse, A.,et al, 2022

Cerebrovascular Ischemic Events in Patients with Takayasu Arteritis
Stroke 53:1550-1557, Mirouse, A.,et al, 2022

Case Report of Lambl Excrescences in a Pediatric Patient with Multifocal Strokes
Neurol 99:73-76, Robertson, D.M.,et al, 2022

Neuroimaging Findings in Parechovirus Encephalitis: A Case Series of Pediatric Patients
Pediatr Neurol 130:41-45, Tierradentro-Garcia, L.O.,et al, 2022

Clinical Manifestations and Diagnosis of Listeria Monocytogenes Infection
UptoDate Aug, Gelfand, M.S.,et al, 2022

Atypical Presentation of Primary Angiitis of Central Nervous System Responsive to Rituximab
Stroke 53:e490-e494, Kesav, P.,et al, 2022

Congenital Cytomegalovirus Infection
BMJ 373:m1212, Pesch, M.H.,et al, 2021

A Rare Treatable and Under Recognized Cause of Recurrent Convexity Subarachnoid Hemorrhage:Lupus anticoagulant Hypoprothombinemia Syndrome
Ann Indian Acad Neurol 24:986-989, Jain, S.,et al, 2021

Body Mass Index in 1.9 Million Adolescents and Stroke in Young Adulthood
Stroke 52:2043-2052, Bardugo, A.,et al, 2021

A 7-Year-Old Boy with Acute-Onset Altered Mental Status
Neurol 96:e2774-e2778, Wong, G.J.,et al, 2021

Vagus Nerve Stimulation and Seizure Outcomes in Pediatric Refractory Epilepsy
Neurol 96:1041-1051, Jain, P. & Arya, R., 2021

When Should a Brain MRI Be Performed in Children with New-Onset Seizures? Results of a Large Prospectice Trial
AJNR 42:1645-1701, Hourani, R.,et al, 2021

Clinicopathologic Conference, Vascular Ehlers-Danlos Syndrome
NEJM 385:1317-1325, Case 30-2021, 2021

Efficacy and Safety of Adjunctive Lacosamide in the Treatment of Primary Generalised Tonic-Clonic Seizures: A Double-Blind, Randomised, Placebo-Controlled Trial
JNNP 91:1067-1075, Vossler, D.G.,et al, 2020

Large-Vessel Stroke as a Presenting Feature of Covid-19 in the Young
NEJM 382:e61-e63, Oxley, T.J., et al, 2020

FDA Approves Fenfluramine for Treatment of Seizures Associated with Dravet Syndrome
FDA June2020, , 2020



Showing articles 0 to 50 of 968 Next >>