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Differential
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aqueduct of Sylvius, stenosis
aqueductal stenosis
arbovirus
areflexia
arthralgia
bilateral periventricular nodular heterotopia
brain biopsy
Brazil
calcification, intracranial
caribbean
CAT scan, abnormal
cataracts
Central America
cerebellar hypoplasia
cerebro hepato renal syndrome
chromosomal abnormality
colpocephaly
congenital malformation
cornea, opacity of
corpus callosum
developmental abnormality of brain
developmental retardation
dysmorphic
dystonia
electroencephalogram
electroencephalogram, abnormalities of
electron microscopy
encephalocele
epidemic
epidemiology of neurology
familial
feeding disorder
fever
flavivirus
gene
genetic counselling
genetic neurologic disorders
Guillain Barre syndrome
headache
hydrocephalus
hydrocephalus, congenital
hypotonia
hypotonia, infants
in situ hybridization
inclusion bodies
inclusion bodies, intracytopasmic
infantile spasm
infection
intrauterine infection
intrauterine infection, viral
karyotyping
lissencephaly
malformation, CNS, congenital
mental retardation
mental retardation, etiology of
mental retardation, familial
microcephaly
micrognathia
micropolygyria
Miller-Dieker syndrome
molecular genetics
mortality
mosquito
MRI
MRI, abnormal
muscle pain
nasal bridge, wide
neuronal migration disorder
neuropathology
omphalocele
optic nerve
optic nerve, hypoplasia of
pachygyria
polycystic kidneys
polymerase chain reaction
prenatal diagnosis by amniocentesis
psychomotor retardation
rash
retinal detachment
retinal dysplasia
seizure
seizure, familial
South America
ultrasonography, head
ultrasonography, head, fetus-neonate
viral infection
Walker-Warburg syndrome
X-linked lissencephaly
x-linked mental retardation
Zika virus infection
Showing articles 0 to 10 of 10

Zika Virus Associated with Microcephaly
NEJM 374: DOI:10.1056/NEJMoa1600651, Mlakar, J.,et al, 2016

Mental Retardation
Neurol 61:156-157, Patterson,M.C. &Zoghbi,H.Y., 2003

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

Lissencephaly:A Human Brain Malformation Associated with Deletion of the LIS1 Gene Located at Chromosome 17p13
JAMA 270:2838-2842, Dobyns,W.B.,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

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

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

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

The Lissencephaly, (Agyria) Syndrome in Siblings
Arch Neurol 35:608-611, Garcia,C.A.,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



Showing articles 0 to 10 of 10