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Differential
(Click to cross reference)
abscess, intracerebral
abscess, intracranial
abscess, sphenoid sinus
anemia
angiography, cerebral
angiography, posterior fossa
anhidrosis
anti MAG antibodies
aqueduct of Sylvius, stenosis
aqueductal stenosis
area postrema
area postrema syndrome
areflexia
arteriopathy
arthrogryposis multiplex
arylsulfatase B
atlanto-axial subluxation
autoantibodies
autoimmune disease
band keratopathy
basal ganglia
basal ganglia, calcification of
birth injury
blindness
bone marrow transplantation
brainstem, lesion of
calcification, intracranial
carcinoma
carotid artery occlusion, neck
CAT scan
CAT scan pattern
CAT scan, abnormal
CAT scan, cloud-like pattern
cataracts
cataracts, congenital
cavernous sinus, syndrome
central nervous system, infection of
cerebellar hypoplasia
cerebellar peduncle
cerebral ischemia
cerebral palsy
cerebral venous infarction
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
corpus callosum, lesion of
cultured skin fibroblasts
cytomegalovirus infection
cytomegalovirus infection, congenital
deafness
deep gray nuclei
demyelinating disease
developmental retardation
diagnostic criteria
diarrhea
differential diagnosis
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
epidemiology of neurology
epidermal nevus syndrome
Fabry's disease
facial appearance, abnormal
false negative
false positive
fatty acid, elevated plasma content
fever
fungal infection, CNS
gammaglobulin therapy, intravenous
gangliosidosis GM1
gangliosidosis GM2
genetic diagnosis
genetic diagnosis, prenatal
genetic neurologic disorders
genu valgum
glaucoma
hearing loss
hemiparesis
hemorrhoids
hepatomegaly
hepatosplenomegaly
hiccoughs
Hurler's syndrome
hydrocephalus
hydrocephalus, congenital
hydronephrosis
hypertension
hypopyon
hypothalamus, lesion of
hypotonia
hypotonia, infants
immunosuppressive agents
immunotherapy
inappropriate antidiuretic(A.D.H.)hormone
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
medulla oblongata
medulla oblongata, lesion of
memory, impairment of
meningitis
mental retardation
metabolic disorder, primary
metachromatic leukodystrophy
microcephaly
micropolygyria
micropthalmia
middle cerebellar peduncle
middle cerebellar peduncle, lesion
middle cerebellar peduncle, lesion, bilateral
mineralization
monoclonal antibodies
Morquio syndrome
mortality
MRI
MRI, abnormal
MRI, contrast enhanced
MRI, contrast enhanced, cloud-like
MRI, paramagnetic effect
MRI, spinal cord
MRI, susceptibility weighted
mucopolysaccharidoses
myelitis
myelitis, longitudinal
myelitis, transverse
myelopathy
nasal stuffiness
nausea and vomiting
neck pain
neoplasm, metastatic to eye
nerve conduction studies
neurocutaneous disease
neurofibromatosis 2
neurolipidosis IV
neurologic disease, diagnoses of
neuromyelitis optica (Devic's disease)
neuromyelitis optica spectrum disorder
neuropathology
neuropathology, brain
neuropathy
neuropathy, hereditary peripheral
neuropathy, peripheral
nevus
Niemann-Pick disease
ophthalmoplegia
optic atrophy
optic chiasm
optic chiasm, lesion of
optic nerve
optic nerve, hypoplasia of
optic nerve, lesion 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
prevention of neurologic disorders
prognosis
proteinuria
pseudohypopyon
psychological testing
psychological testing, children
psychomotor retardation
pupil, abnormality in neurologic disorders
quadriparesis
rash
recurrent
red eye
remote effect of cancer on the nervous system
respiratory failure
retinal degeneration
retinal detachment
retinal dysplasia
retinitis pigmentosa
retinopathy
review article
rituximab
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
spinal cord, lesion of
splenomegaly
stem cell transplantation
steroid therapy, CNS treatment and complications with
stillbirth
sweating, abnormality of
symmetric brain lesions
Tangier's disease
thalamus, lesion of
third nerve palsy
tongue, enlarged
torticollis
treatment of neurologic disorder
uremia
uveitis
varicose veins
vasculopathy
venous ischemia
vertebral-basilar insufficiency
viral infection, CNS
vision, failure of in childhood
visual acuity
visual acuity, decreased
visual impairment
visual loss
vomiting, intractable
Walker-Warburg syndrome
water channel antibodies
white matter disease
Showing articles 0 to 27 of 27

Neuromyelitis Optica Spectrum Disorder
NEJM 387:631-639, Wingerchuk, D.M. & Lucchinetti, C.F., 2022

Pathogeneses and Imaging Features of Cerebral White Matter Lesions of Vascular Origins
Aging Dis 12:2031-2051, Wu,X.,et al, 2021

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

Treatment Approaches for MOG-Ab-Associated Demyelination in Children
Curr Treat Options Neurol 21:2, Hacohen, Y. & Banweil, B., 2019

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

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

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



Showing articles 0 to 27 of 27