Home
About
Overview
Sharing Data
ORCID
Help
History (65)
Autosomal recessive mutations in nuclear transport factor KPNA7 are associated with infantile spasms and cerebellar malformation.
Association of Vitamin D Deficiency and Treatment with COVID-19 Incidence.
High survival and organ function rates after primary chemoradiotherapy for intermediate-stage squamous cell carcinoma of the head and neck treated in a multicenter phase II trial.
Phenotypic heterogeneity between different mutations of MODY subtypes and within MODY pedigrees.
Clinical and imaging heterogeneity of polymicrogyria: a study of 328 patients.
See All 65 Pages
Find People
Find Everything
Login
to edit your profile (add a photo, awards, links to other websites, etc.)
Edit My Profile
My Person List (
0
)
Return to Top
Clinical and imaging heterogeneity of polymicrogyria: a study of 328 patients.
Clinical and imaging heterogeneity of polymicrogyria: a study of 328 patients. Brain. 2010 May; 133(Pt 5):1415-27.
View in:
PubMed
subject areas
Age of Onset
Child, Preschool
Cohort Studies
Developmental Disabilities
Epilepsy
Female
Humans
Infant
Infant, Newborn
Magnetic Resonance Imaging
Male
Malformations of Cortical Development
Microcephaly
Muscle Spasticity
Prevalence
Sex Distribution
authors with profiles
William B. Dobyns