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Differential
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abortion, spontaneous
advances in neurology
agenesis of corpus callosum
Aicardi's syndrome
anatomy of
anosmia
atomic bomb
autism
basal ganglia, lesion of
behavioral disorder
bilateral periventricular nodular heterotopia
brain biopsy
burst suppression pattern, electroencephalogram
carphology
CAT scan
CAT scan, abnormal
CAT scan, emission
CAT scan, emission, abnormal
CAT scan, false negative
cataracts
cerebellar hypoplasia
cerebral dominance
cerebral hemisphere left-right asymmetry
cerebral palsy
cerebrovascular accident
cerebrovascular accident, bilateral
cerebrovascular accident, intrauterine
chewing movements
children
chorioretinitis
chromosomal abnormality
chromosome 28
cleft lip
cleft palate
Clinical Pathologic Conference(C.P.C.)
clinodactyly
cocaine
coloboma
colpocephaly
congenital malformation
congenital malformation, non CNS
corpus callosum
corpus callosum, hypoplastic
cortical dysplasia, focal
cyst, porencephalic
cytoarchitectonics, cerebral cortex
degenerative diseases of CNS
developmental abnormality of brain
developmental retardation
digits, abnormal
double-cortex syndrome
drug abuse
dyslexia
dysmorphic
dysplasia of C.N.S.
ear, abnormal
electroencephalogram
electroencephalogram, abnormalities of
encephalitis, focal
encephalitis, Rasmussen's
epidemiology of neurology
epilepsia partialis continua
exome sequencing
facial anomalies
facial asymmetry
familial
feeding disorder
fetal alcohol syndrome
fragile-X syndrome
gadolinium
gene
gene mutation
genetic counselling
genetic linkage
genetic neurologic disorders
genetic screening
genetic testing
globus pallidus, lesion of
globus pallidus, lesion of, bilateral
gonadotropin-releasing hormone
hamartoma
handedness
head circumference
heavy metal intoxication
hemihypertrophy, congenital
hemiparesis
hemispherectomy
heterotopia
hippocampus
histopathology
human genome
Huntington's chorea
hypertelorism
hypogonadism
hypomelanosis of Ito
hypopigmentation of skin
hypotonia
hypotonia, infants
immunologic disease
infantile spasm
intellectual deficit
intellectual deterioration
intelligence quotient
intrauterine
intrauterine growth retardation
intrauterine infection
Kallmann's syndrome
karyotyping
lissencephaly
macrocephaly
malabsorption
malformation, CNS, congenital
malformation, vascular
megalencephaly
mental retardation
mental retardation, familial
mesial temporal lobe
mesial temporal sclerosis
microcephaly
micrognathia
micropthalmia
molecular genetics
mortality
MRI
MRI, abnormal
MRI, CAT scan compared to
MRI, contrast enhanced
MRS
muscular dystrophy
myopathy
myotonia dystrophica
nasal bridge, wide
neoplasm, primary intracranial
neoplasm, primary of CNS
neoplasm, primary of CNS-children
neural tube defect
neurocutaneous disease
neurofibromatosis 1
neurologic disease
neurologic disease, diagnoses of
neuronal migration disorder
neuroophthalmology
neuropathology
neuropathology, brain
neuropathy
non-dominant hemisphere
olfactory bulb
operculum syndrome
operculum syndrome, bilateral
optic nerve
optic nerve, lesion of
pachygyria
paroxysmal nonkinesigenic dyskinesia
pneumoencephalogram(PEG)
poison, mercury
poison, neurologic problems with
polymerase chain reaction
polymicrogyria
Potter syndrome
pregnancy, neurologic complications in
premature infant
prognosis
pseudobulbar palsy
psychological testing
psychological testing, children
psychomotor retardation
pyramidal tract dysfunction
radiation therapy, CNS treatment and complications with
radiation, ionizing
radiation, ionizing, intrauterine
review article
schizencephaly
scoliosis
screening
seizure
seizure, adult onset
seizure, children
seizure, diagnosis of
seizure, equivalents
seizure, etiology of
seizure, familial
seizure, focal
seizure, intractable
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seizure, neonatal
seizure, prognosis in childhood
seizure, psychomotor-temporal lobe
seizure, surgical treatment of
seizure, treatment of
seizure, workup of
skin, biopsy
skin, lesions in neurologic disorders
spinocerebellar degeneration
status epilepticus
stillbirth
Sturge-Weber syndrome
sudden infant death syndrome
syndactyly
synkinesis
temporal lobe, lesion
temporal lobe, status
temporal lobectomy
teratogenesis
teratogenic drugs
treatment of neurologic disorder
trinucleotide repeats
tuberous sclerosis
ultrasonography
ultrasonography, head, fetus-neonate
vertebral anomalies
whistling
Wood's light
X-linked bulbospinal neuronopathy
X-linked lissencephaly
x-linked mental retardation
Showing articles 0 to 50 of 12880 Next >>

Ictal Whistling Associated with Dominant Parahippocampal Gyrus Cortical Dysplasia
Neurol 103:e209489, Hartnett,P.,et al, 2024

Histopathological Findings in Brain Tissue Obtained during Epilepsy Surgery
NEJM 377:1648-1656, Blumcke, I.,et al, 2017

Somatic Mutations in Cerebral Cortical Malformations
NEJM 371:733-743, Jamuar, S.S.,et al, 2014

Gray Matter Heterotopia
Neurol 55:1603-1608, Barkovich,A.J. & Kuzniecky,R.I., 2000

Focal Cortical Dysplasia:Appearance on MR Images
Radiology 203:553-559, Yagishita,A.,et al, 1997

Why Would You Remove Half a Brain? Outcome of 58 Children after Hemispherectomy-Johns Hopkins 1968-96
Pediatrics 100:163-171, Vining,E.P.G.,et al, 1997

Bilat Periventricular Nodular Heterotopia with Mental Retard & Syndactyly in Boys:New X-Linked MR Synd
Neurol 49:1042-1047, Dobyns,W.B.,et al, 1997

Proton Magnetic Resonance Spectroscopy of a Gray Matter Heterotopia
Neurol 47:1571-1574, Marsh,L.,et al, 1996

Clinicopath Conf
Focal Cortical Dysplasia, Case 7-1996, NEJM 334:586-592996., , 1996

Subcortical Heterotopia:A Distinct Clinicoradiologic Entity
AJNR 17:1315-1322, Barkovich,A.J., 1996

X-Linked Malformation of Neuronal Migration
Neurol 47:331-339, Dobyns,W.B.,et al, 1996

Periventricular Heterotopia and Epilepsy
Neurol 44:51-55, Huttenlocher,P.R.,et al, 1994

Neuronal Migration Disorders:Positron Emission Tomography Correlations
Ann Neurol 35:290-297, Lee,N.,et al, 1994

Subependymal Heterotopia:A Distinct Neuronal Migration Disorder Associated with Epilepsy
JNNP 57:1195-1202, Raymond,A.A.,et al, 1994

Life Threatening Focal Status Epilepticus Due to occult Cortical Dysplasia
Arch Neurol 50:695-700, Desbiens,R.,et al, 1993

Magnetic Resonance Imaging in Childhood Intractable Partial Epilepsies:Pathologic Correlations
Neurol 43:681-687, Kuzniecky,R.,et al, 1993

Molecular Genetics in Neurology
Ann Neurol 34:757-773, Martin,J.B., 1993

Hypomelanosis of Ito
Editorial, Lancet 339:651-6521992., , 1992

Gray Matter Heterotopias:MR Characteristics & Correlation with Develop & Neurologic Manifest
Radiology 182:493-499, Barkovich,A.J.&Kjos,B.O., 1992

Effect of Cocaine Use On the Fetus
NEJM 327:399-407, Volpe,J.J., 1992

MR Imaging of Tuberous Sclerosis:Pathogenesis of This Phakomatosis, Use of Gadopenetate, & Literature Review
Radiology 183:227-238, Braffman,B.H.,et al, 1992

Brief Report:Intragenic Deletion of the Kalig-1 Gene in Kallmann's Syndrome
NEJM 326:1752-1755, 17751992., Bick,D.,et al, 1992

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

Magnetic Resonance Imaging in Epilepsy
Lancet 340:343-344, 1992,, , 1992

MRI in the Diagnosis of Heterotopic Gray Matter, Report of Three Cases First Discovered in Adulthood
Neuroradiology 33:527-528, Zisch,R.&Artmann,W., 1991

Focal Neuronal Migration Disorders and Intractable partial Epilepsy:A Study of 30 Patients
Ann Neurol 30:741-749, Palmini,A.,et al, 1991

Focal Neuronal Migration Disorders and Intractable Partial Epilepsy:Results of Surgical Treatment
Ann Neurol 30:750-757, Palmini,A.,et al, 1991

The Spectrum of Lissencephaly:Report of Ten Patients Analyzed by Magnetic Resonance Imaging
Ann Neurol 30:139-146, Barkovich,A.J.,et al, 1991

Epilepsy and Disorders of Neuronal Migration
Editorial, Lancet 336:10351990., , 1990

High-Intensity Basal Ganglia Lesions on T1-Weighted MR Images in Neurofibromatosis
AJR 154:369-373, Mirowitz,S.A.,et al, 1990

Progress in Tuberous Sclerosis
Editorial, Lancet 336:598-5991990., , 1990

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

Magnetic Resonance Imaging and Neurobehavioral Correlates in Schizencephaly
Arch Neurol 47:911-916, Aniskiewicz,A.S.,et al, 1990

Bilateral Central Macrogyria:Epilepsy, Pseudobulbar Palsy, and Mental Retardation-A Migration Disorder
Ann Neurol 25:547-554, Kuzniecky,R.,et al, 1989

Bilateral Opercular Polymicrogyria
Ann Neurol 25:90-92, Becker,P.S.,et al, 1989

MR of Neuronal Migration Anomalies
AJR 150:179-187, Barkovich,A.J.,et al, 1988

MR Imaging of Heterotopic Gray Matter
J Comput Assist Tomogr 11:878-879, Hayden,S.A.,et al, 1987

Hypomelanosis of Ito, Wood's Light & Magnetic Resonance Imaging as Diagnostic Measures
Arch Neurol 43:848-850, Ardinger,H.H.&Bell,W.E., 1986

Developmental Dyslexia:Four Consecutive Patients with Cortical Anomalies
Ann Neurol 18:222-233, Galaburda,A.M.,et al, 1985

Cerebral Lateralization, Biological Mechanisms, Associations, & Pathology:I
Arch Neurol 42:428-459, 4271985., Geschwind,N.&Galaburda,A.M., 1985

Hypomelanosis of Ito (incontinentia pigmenti achromians) :Macrocephaly & Gray Matter Heterotopias
Neurol 32:1013-1016, Ross,D.L.,et al, 1982

Brain Abnormalities in Infants with Fotter Syndrome (oligohydramnios tetrad)
Neurol 31:1571-1574, Grunnet,M.L.,et al, 1981

Fetal Methylmercury Poisoning:Clinical & Toxicological Data on 29 Cases
Ann Neurol 7:348-353, Marsh,D.O.,et al, 1980

Agenesis of the Corpus Callosum:A Study of the Frequency of Associated Malformations
Ann Neurol 6:349-354, Parrish,M.L.,et al, 1979

Cytoarchitectonic Abnormalities in Developmental Dyslexia:A Case Study
Ann Neurol 6:94-100, Galaburda,A.M.,et al, 1979

The Aicardi Syndrome:Report of 4 Cases & Review of the Literature
Ann Neurol 5:475-482, Bertoni,J.M.,et al, 1979

Human Brain, (Cytoarchitectonic Left-Right Asymmetries in the Temporal Speech Region)
Arch Neurol 35:812-817, Galaburda,A.M.,et al, 1978

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

Validation of the 2023 International Diagnostic Criteria for MOGAD in a Selected Cohort of Adults and Children
Neurol 103:e209321, Varley,J.A.,et al, 2024



Showing articles 0 to 50 of 12880 Next >>