Neurology Specific Literature Search   
 
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Differential
(Click to cross reference)
cerebrovascular accident
cerebrovascular accident, bilateral
Clinical Pathologic Conference(C.P.C.)
clubfoot as related to neurologic disease
congenital bilateral perisylvian syndrome
congenital malformation
creatine phosphokinase(CPK)elevated
cry, weak
cytoarchitectonics, cerebral cortex
developmental abnormality of brain
developmental disability
developmental retardation
double-cortex syndrome
drooling
dysarthria
dyskinesia, buccal lingual facial
dyslexia
dysphagia
dysplasia of C.N.S.
electroencephalogram, abnormalities of
electromyogram
exome sequencing
facial weakness, bilateral
familial
feeding disorder
floppy infant
gag reflex, depressed
gene mutation
genetic neurologic disorders
heterotopia
human genome
hypotonia
hypotonia, infants
intellectual deficit
malformation, CNS, congenital
megalencephaly
mental retardation
merosin
MRI
MRI, abnormal
muscle biopsy
muscular dystrophy
muscular dystrophy, congenital
neurologic disease
neuropathology
neuropathology, brain
nonverbal
operculum syndrome
operculum syndrome, bilateral
pachygyria
polymicrogyria
prognosis
pseudobulbar palsy
pyramidal tract dysfunction
screening
seizure
term infant
Showing articles 0 to 5 of 5

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

Case 35-2006: A Newborn Boy with Hypotonia
NEJM 355:2132-2142, Brown,R.H.,et al, 2006

Congenital Bilateral Perisylvian Syndrome:Study of 31 Patients
Lancet 341:608-612, Kuzniecky,R.,et al, 1993

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

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



Showing articles 0 to 5 of 5