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Differential
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abortion, spontaneous
abstinence syndrome
aciduria
acquired immunodeficiency syndrome
acquired immunodeficiency syndrome dementia complex
acquired immunodeficiency syndrome, congenital
acquired immunodeficiency syndrome, infants and children
acquired immunodeficiency syndrome-related complex
acrocyanosis
acromicria
acute necrotizing encephalitis
addiction, heroin
advances in neurology
adverse drug reaction
agenesis of aqueduct of Sylvius
agenesis of corpus callosum
aggression
Aicardi-Goutieres syndrome
Aicardi's syndrome
alcohol
alcohol, neurologic complications with
Alexanders disease
Alexanders disease, adult onset
algorithm
altered states of consciousness
anemia
Angelman syndrome
angiotensin-converting enzyme, inhibitors
anticoagulant, complications of
anticoagulant, treatment
antiviral agents
aphasia, conduction
apnea
aqueduct of Sylvius, stenosis
aqueductal stenosis
areflexia
arenavirus
aspartocyclase
astrogliopathy
ataxia
ataxia, cerebellar
ataxic gait
atomic bomb
attention deficit disorder with hyperactivity
attention span
atypical
autism
autoimmune epilepsy
autonomic dysfunction
Bannayan-Riley-Ruvalcaba syndrome
basal ganglia, calcification of
basal ganglia, lesion of
basal ganglia, lesion, bilateral
behavior, combative
behavioral disorder
blindness
blue tongue virus
bone marrow transplantation
brachycephaly
bradycardia
brain atrophy
brain biopsy
brain scan
brain weight
brainstem, atrophy
bruising
bulbar palsy
burst suppression pattern, electroencephalogram
cachexia
cafe au lait spots
calcification, intracranial
calcification, periventricular
Canavan's disease
carcinoma
carcinoma of lung
CAT scan
CAT scan, abnormal
cataracts
cataracts, congenital
cavum Vergae
central nervous system, infection of
cerebellar atrophy, primary
cerebellar atrophy, secondary
cerebellar degeneration
cerebellar hypoplasia
cerebellar lesion
cerebellar vermis
cerebral cortical atrophy
cerebral palsy
cerebral venous thrombosis
cerebrospinal fluid
cerebrospinal fluid, abnormal
cerebrospinal fluid, cytology
cerebrospinal fluid, gammaglobulin of
cerebrospinal fluid, xanthochromia of
cerebrovascular accident
cerebrovascular accident, intrauterine
cerebrovascular accident, neonatal
chilbran skin lesions
children
chorea
choreoathetosis
chorioretinitis
chromosomal abnormality
chromosome 15
cisterna magna, enlarged
cleft lip
cleft palate
Clinical Pathologic Conference(C.P.C.)
cocaine
cocaine, intrauterine exposure
Cockayne's syndrome
cognition
cognitive delay
cold hands sign
coloboma
complications
congenital birth defects
congenital heart disease
congenital infection, CNS
congenital infection, viral
congenital malformation
congenital malformation, non CNS
consanguinity
constipation
contractures, joint
cornea, opacification in infancy-causes of
cornea, opacity of
corpus callosum
corpus callosum, atrophy of
corpus callosum, thinning
cortical blindness
coumarin
cranial neuropathy, multiple
cry, abnormal
cry, high-pitched
cultured skin fibroblasts
cyanosis
cyst
cyst, parenchymal
cyst, porencephalic
cytomegalic inclusion disease
cytomegalovirus infection
cytomegalovirus infection, congenital
cytosine arabinoside
Dandy Walker malformation
deafness
deafness, congenital
deep gray nuclei
degenerative diseases of CNS
dementia
dementia, childhood
dentate nuclei
dentate nuclei, lesion of
depression
depression, psychotic
dermatitis
dermatoglyphics
developmental abnormality of brain
developmental disability
developmental evaluation
developmental milestones
developmental milestones, loss of
developmental retardation
diabetes mellitus
diagnostic criteria
diarrhea
differential diagnosis
digits, abnormal
disability, neurological
drooling
drug abuse
drug abuse, toxic screen In
drug withdrawal
dural sinus thrombosis
dwarfism
dysarthria
dysmorphic
dysostosis multiplex
dystonia
dystonia, children
ear, abnormal
electroencephalogram
electroencephalogram, abnormalities of
electron microscopy
embryogenesis
encephalitis, brainstem
encephalocele
encephalopathy
encephalopathy, metabolic
endoscopic surgery
endoscopy
enophthalmous
enzyme, defect
epicanthal folds
epidemiology of neurology
epidermal nevus syndrome
episodic disorders
ethics in neurology
ethylmalonic aciduria
ethylmalonic encephalopathy
evoked potentials
eye movement, disorders of
facial anomalies
facial appearance, abnormal
facial asymmetry
facial expression abnormality
facial nerve palsy
facial nevus
facial weakness
failure to thrive
familial
feeding disorder
fetal alcohol syndrome
fetus
fever
finger tapping
fish
flavivirus
fluorescene in situ hybridization
fontanel, bulging
frontal bossing
fucosidosis
gait disorder
gender
gene
gene mutation
genetic counselling
genetic diagnosis, prenatal
genetic neurologic disorders
genetic testing
GFAP gene
glioblastoma multiforme(astrocytoma Gr.III)
growth retardation
Guillain Barre syndrome
head bobbing
head circumference
head circumference and brain development
head lag
headache
hemangioma
hemiparesis
hemorrhage, intracranial, newborn
heparin
hepatomegaly
hepatosplenomegaly
herpes labialis
herpes simplex encephalitis
herpes simplex encephalitis, differential diagnosis of
herpes simplex encephalitis, infancy and childhood
herpes simplex encephalitis, prognosis 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
heterotopia
holoprosencephaly
human immunodeficiency virus type 1
Hurler's syndrome
hydranencephally
hydrocephalus
hydrocephalus, congenital
hydrocephalus, non-communicating(obstructive)
hydrocephalus, treatment of
hydroxyglutaric aciduria
hyperactivity
hyperhomocysteinemia
hyperpigmentation of skin
hyperpyrexia, CNS disorder causing
hyperreflexia
hypertelorism
hypertension
hypertonia
hypoglycorrhachia
hypomyelination
hypopigmentation of skin
hypoplastic left heart syndrome
hypotelorism
hypotonia
hypotonia, infants
hypsarrhythmia
immunofluorescent exam of CSF cells
immunosuppression
in situ hybridization
inborn errors of metabolism
inclusion bodies, intranuclear
infantile spasm
infection, recurrent
infectious mononucleosis
influenza A virus
insect repellent
intellectual deficit
intellectual deterioration
intelligence quotient
interferon
interferon alpha
interferon inducer
intracranial hemorrhage
intracranial pressure, increased
intrauterine
intrauterine infection
intrauterine infection, viral
intrauterine infection, viral of CNS
iododeoxyuridine
iris, abnormal
irritability
jittery baby
karyotyping
klippel feil syndrome
kyphosis
laughing, pathologic
learning disability, in children
lens, dislocation of
lethargy
leukodystrophy
leukoencephalopathy
leukoencephalopathy, differential diagnosis
level of consciousness, decreased
life expectancy
limbic encephalitis
limbic system
lip, abnormal
lipomatosis
Lisch nodules
lissencephaly
long bone lesion
low birth weight
lymphadenopathy
lymphocytic choriomeningitis
lymphoma
lysosomal storage disease
lysosomes, abnoral
macrocephaly
macrognathia
malformation, CNS, congenital
malnutrition and brain development
meningitis
meningitis, aseptic
meningocele
meningoencephalitis
mental retardation
mental status, abnormal
mestinon
metabolic disorder, primary
methadone
methylene tetrahydrofolate reductase
methylenetetrahydrofolate reductase deficiency
micrencephaly
microcephaly
micrognathia
micropthalmia
midline defect in children
Miller-Dieker syndrome
misdiagnosis
molecular genetics
molybdenum cofactor deficiency
monoamines
monoamines, brain
mortality
mosquito
movement disorder
MRI
MRI, abnormal
multiple sclerosis
multiple system atrophy
mumps virus
myelitis
myelomeningocele
myeloschisis
nasal bridge, wide
nasal stuffiness
nausea and vomiting
neonatal abstinence syndrome
neonatal infection, viral
neoplasm, primary intracerebral
neoplasm, primary of CNS
neural tube defect
neurocutaneous disease
neurofibroma
neurofibromatosis 1
neurologic disease
neurologic disease, diagnoses of
neurologic disease, tempo
neurologic examination
neurologic signs
neuronal ceroid-lipofuscinosis
neuronal migration disorder
neuropathology
neuropathology, brain
neuropathy
neuropathy, peripheral
neuroradiology
nevus
nose, abnormal
nutritional deficiency
nystagmus
omphalocele
opiate
opportunistic infection
optic atrophy
optic atrophy, infants
optic nerve
optic nerve, hypoplasia of
optic nerve, lesion of
optic neuropathy
organoid nevus syndrome
osteopetrosis
oxycodone
pachygyria
palatal myoclonus
paraparesis
parotitis
paroxysmal neurologic deficits
parvovirus
pediatric neurology
penis, pigmented macules
personality change
petechiae
pheochromocytoma
photosensitivity, skin
pigmentary retinopathy
pigmented macules
pleocytosis of cerebrospinal fluid
pneumoencephalogram(PEG)
polyinosinic cytidic acid(poly IC)
polyps, gastrointestinal tract
pons, atrophy
postural abnormality
practice guidelines
pregnancy, neurologic complications in
prenatal
prenatal diagnosis by amniocentesis
prevention of neurologic disorders
progeria
prognathism
prognosis
pruritus
psychiatric problems in neurologic disorders
psychological testing
psychological testing, children
psychomotor retardation
psychosis
pupil, abnormality in neurologic disorders
pyramidal tract dysfunction
quadriparesis
quadriplegia
radiation therapy, CNS treatment and complications with
radiation, ionizing
radiation, ionizing, intrauterine
rash
remote effect of cancer on the nervous system
respiratory failure
retinal degeneration
Rett's syndrome
review article
Rosenthal fibers
rubella syndrome
rubella virus
rubeola virus
schizencephaly
scoliosis
scoliosis, neurologic association with
screaming
screening
seizure
seizure, children
seizure, intractable
seizure, neonatal
seizure, psychomotor-temporal lobe
seizure, withdrawal
septo-optic dysplasia
sexually transmitted disease
short neck
short stature
shunt procedure, ventricular
simian crease
skin, darkening of
skin, lesions in neurologic disorders
skull x-ray
skull x-ray, abnormal
skull x-ray, bony defect on
smiling
spastic diplegia
spasticity
speech disorder
speech disorder, childhood
speech, delayed development of
spina bifida
splenomegaly
spongy degeneration of brain
startle reaction
stereotyped behavior
steroid therapy, CNS treatment and complications with
stillbirth
strabismus
subacute myelo-opticoneuropathy(S.M.O.N.)complex
subdural hematoma
subdural hematoma, neonates and infants
subtemporal decompression
sulfite oxidase deficiency
superior sagittal sinus thrombosis
symmetric brain lesions
talk
teeth, wide-spaced
teratogenesis
teratogenesis, viral
teratogenic drugs
thrombocytopenia
tongue, protrusion of
toxoplasmosis, CNS
transplacental virus infections
travel, foreign
treatment of neurologic disorder
tremor
trigeminal neuralgia
trisomes
trisomy 9p
ultrasonography
ultrasonography, head, fetus-neonate
uric acid, low
urine test for metabolic disorders
vaccinia
varicella zoster virus
variola
vasculitides
vein of Galen
ventriculostomy
vertebral anomalies
viral infection
viral infection, CNS
Virchow-Robin spaces, dilated
visual evoked response
visual tracking
vomiting, episodic
vomiting, recurrent
wheelchair
white matter disease
workup
xeroderma pigmentosa
yawning movements
Zika virus infection
Showing articles 0 to 50 of 18011 Next >>

A Middle-aged Woman with Severe Scoliosis and Encephalopathy
JAMA Neurol 78:251-252, Mohan, G.,et al, 2021

An Infant with Developmental Delay, Epileptic Spasms, and Acrocyanosis
Neurol 94:939-942, Madaan, P.,et al, 2020

The Syndrome of Cutaneous Photosensitivity, Growth Failure, and Basal Ganglia Calcification
Neurol 87:e56-e57, Saini, A.G.,et al, 2016

Zika Virus as an Emerging Global Pathogen
JAMA Neurol 73:875-879, Beckham, J.D.,et al, 2016

Clinicopathologic Conference, Aqueductal Stenosis with Hydrocephalus
NEJM 375:2583-2593, Case 40-2016, 2016

Neonatal Abstinence Syndrome
NEJM 375:2468-2479, McQueen, K. & Murphy-Oikonen, J., 2016

Molybdenum Cofactor Deficiency
Neurol 85:e175-e178, Nagappa, M.,et al, 2015

Bannayan-Riley-Ruvalcaba Syndrome: MRI Neuroimaging Features in a Series of 7 Patients
AJNR 35:402-406, Bhargava, R.,et al, 2014

Clinicopathologic Conference, Severe Methylenetetrahydrofolate Reductase Deficiency
NEJM 371:847-858, Case 27-2014, 2014

Cognitive Delay in a 7-year-old Girl
Neurol 81: e148-e150, Cachia, D. & Stine, C., 2013

GFAP Mutations, Age at Onset, and Clinical Subtypes in Alexander Disease
Neurol 77:1287-1294, Prust, M.,et al, 2011

Practice Parameter: Evaluation of the Child with Microcephaly (An Evidence-Based Review): Report of the Quality Standards Subcommittee of the American Academy of Neurology and the Practice Committee of the Child Neurology Society
Neurol 73:887-897, Ashwal,S.,et al, 2009

Aicardi-Gouti�res Syndrome
Br Med Bull 89:183-201, Orcesi, S.,et al, 2009

Congenital Lymphocytic Choriomeningitis Virus Infection: Spectrum of Disease
Ann Neurol 62:347-355, Bonthius,D.J.,et al, 2007

Major Congential Malformations After First-Trimester Exposure to ACE Inhibitors
NEJM 354:2443-2451,2498, Cooper,W.O.,et al, 2006

MR Brain Imaging of Fucosidosis Type I
AJNR 22:777-780, Galluzzi,P.,et al, 2001

Pyridostigmine-Induced Microcephaly
Neurol 54:1873-1874, Niesen,C.E.&Shah,N.S., 2000

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

The Epilepsy of Trisomy 9p
Neurol 47:821-824, Stern,J.M., 1996

Canavan Disease:From Spongy Degeneration to Molecular Analysis
J Pediatr 127:511-517, Matalon,R.,et al, 1995

The Synd of Autosomal Recessive Pontocerbellar Hypoplasia, Microcephaly, & Extrapyr Dyskinesia (Pontocereb Hypopl Type 2)
Neurol 45:311-317, Barth,P.G.,et al, 1995

Prenatal Alcohol Exposure and Long-Term Developmental Consequences
Lancet 341:907-910, Spohr,H.,et al, 1993

Miller-Dieker Syndrome:Detection of a Cryptic Chromosome Translocation Using in Situ Hybridization in a Family
Am J Dis Child 147:1291-1294, Alvarado,M.,et al, 1993

Outlook for the Child with a Cephalocele
Pediatrics 90:914-919, Brown,M.S.,et al, 1992

Causal Heterogeneity in Isolated Lissencephaly
Neurol 42:1375-1388, Dobyns,W.B.,et al, 1992

Angelman Syndrome: Clinical Profile
J Child Neurol 7:270-280, Zori,R.T.,et al, 1992

Brain and Ocular Abnormalities in Infants with In Utero Exposure to Cocaine and other Street Drugs
Am J Dis Child 145:688-695, Dominguez,R.,et al, 1991

Effect of Very Low Brith Weight and Subnormal Head Size on Cognitive Abilities at School Age
NEJM 325:231-237, Hack,M.,et al, 1991

Perinatal Loss and Neurological Abnormalities Among Children of the Atomic Bomb
JAMA 264:605-609, 6221990., Yamazaki,J.N.&Schull,W.J., 1990

Congenital Brain Anomalies Associated with the Hypoplastic Left Heart Syndrome
Pediatrics 85:984-990, Glauser,T.A.,et al, 1990

Infantile CNS Spongy Degeneration-14 Cases:Clinical Update
Neurol 40:1876-1882, Gascon,G.G.,et al, 1990

Sulfite Oxidase Deficiency:Clinical, Neuroradiologic, and Biochemical Features in Two New Patients
Neurol 39:252-257, Brown,G.K.,et al, 1989

Congenital AIDS:Review of Neurological Problems
Child's Nerv Syst 5:9-11, Curles,R.G., 1989

Pediatric Acquired Immunodefieiency Syndrome
Am J Dis Child 142:29-35, Belman,A.L.,et al, 1988

Difference Between Herpes Simplex Virus Type I & Type 2 Neonatal Encephalitis in Neurological Outcome
Lancet 1:1-4, Corey,L.,et al, 1988

The Dandy-Walker Syndrome
In Handbk of Clin Neurology, Elsevier Publ, Amsterdam, 50:32387., Epstein,M.H.&Johanson,C.E., 1987

Neurological Manifestations in Xeroderma Pigmentosum
Ann Neurol 20:70-75, Mimaki,T.,et al, 1986

Cavum Vergae, Association with Neurologic Abnormality & Diagnosis by Magnetic Resonance Imaging
Arch Neurol 43:821-823, Miller,M.E.,et al, 1986

Neurologic Manifestations of the Organoid Nevus Syndrome
Arch Neurol 42:236-240, Clancy,R.R.,et al, 1985

Neurological Complications in Infants & Children with Acquired Immune Deficiency Syndrome
Ann Neurol 18:560-566, Belman,A.L.,et al, 1985

Alexander's Disease, A Disease of Astrocytes
Brain 108:367-385, Borrett,D.&Becker,L.E., 1985

Schizencephaly:A Clinical & CT Study
Neurol 34:997-1001, Miller,G.M.,et al, 1984

Human Cytomegalovirus Infection & Disorders of the Nervous System
Jr. , Arch Neurol 41:310-320984., Bale,J.F., 1984

A Progressive Syndrome of Autism, Dementia, Ataxia, & Loss of Purposeful Hand Use in Girls:Rett's Syndrome
Ann Neurol 14:471-491, Hagberg,B., 1983

Familial Porencephaly
Arch Neurol 40:567-569, Berg,R.A.,et al, 1983

Cockayne Syndrome
J Comput Assist Tomogr 6:1172-1174, Levinson,E.D.,et al, 1982

Santavuori Disease:Diagnosis by Leukocyte Ultrastructure
Neurol 32:1277-1281, Baumann,R.J.,et al, 1982

Septo-optic Dysplasia in an Infant of a Diabetic Mother
Arch Neurol 38:590-591, Donat,J.F.G., 1981

Von Recklinghausen Neurofibromatosis
NEJM 305:1617-1627, Riccardi,V.M., 1981



Showing articles 0 to 50 of 18011 Next >>