Related references
Note: Only part of the references are listed.LISSENCEPHALY(AGYRIA-PACHYGYRIA): CLINICAL FINDINGS AND SERIAL EEG STUDIES
H. Gastaut et al.
DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY (2010)
Abnormal glycosylation of dystroglycan in human genetic disease
Jane E. Hewitt
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE (2009)
Bilateral frontoparietal polymicrogyria, Lennox-Gastaut syndrome, and GPR56 gene mutations
Elena Parrini et al.
EPILEPSIA (2009)
GPR56-Regulated Granule Cell Adhesion Is Essential for Rostral Cerebellar Development
Samir Koirala et al.
JOURNAL OF NEUROSCIENCE (2009)
Diversifying microtubules in brain development
Andrew P. Jackson
NATURE GENETICS (2009)
Midbrain-hindbrain involvement in lissencephalies
Patrice Jissendi-Tchofo et al.
NEUROLOGY (2009)
Congenital muscular dystrophies with defective glycosylation of dystroglycan A population study
E. Mercuri et al.
NEUROLOGY (2009)
Tubulin-related cortical dysgeneses: microtubule dysfunction underlying neuronal migration defects
Xavier H. Jaglin et al.
TRENDS IN GENETICS (2009)
GPR56 regulates pial basement membrane integrity and cortical lamination
Shihong Li et al.
JOURNAL OF NEUROSCIENCE (2008)
Refining genotype - phenotype correlations in muscular dystrophies with defective glycosylation of dystroglycan
Caroline Godfrey et al.
BRAIN (2007)
Disease-associated mutations affect GPR56 protein trafficking and cell surface expression
Zhaohui Jin et al.
HUMAN MOLECULAR GENETICS (2007)
Orphan G protein-coupled receptor GPR56 plays a role in cell transformation and tumorigenesis involving the cell adhesion pathway
Ning Ke et al.
MOLECULAR CANCER THERAPEUTICS (2007)
Spectrum of brain changes in patients with congenital muscular dystrophy and FKRP gene mutations
E Mercuri et al.
ARCHIVES OF NEUROLOGY (2006)
A developmental and genetic classification for malformations of cortical development
AJ Barkovich et al.
NEUROLOGY (2005)
POMT2 mutations cause α-dystroglycan hypoglycosylation and Walker-Warburg syndrome
J van Reeuwijk et al.
JOURNAL OF MEDICAL GENETICS (2005)
Genotype-phenotype analysis of human frontoparietal polymicrogyria syndromes
XH Piao et al.
ANNALS OF NEUROLOGY (2005)
Genetics of the polymicrogyria syndromes
A Jansen et al.
JOURNAL OF MEDICAL GENETICS (2005)
Localization and functional analysis of the LARGE family of glycosyltransferases: significance for muscular dystrophy
M Brockington et al.
HUMAN MOLECULAR GENETICS (2005)
G protein-coupled receptor-dependent development of human frontal cortex
XH Piao et al.
SCIENCE (2004)
Bilateral frontoparietal polymicrogyria: Clinical and radiological features in 10 families with linkage to chromosome 16
BS Chang et al.
ANNALS OF NEUROLOGY (2003)
Mutations in the O-mannosyltransferase gene POMT1 give rise to the severe neuronal migration disorder Walker-Warburg syndrome
D Beltran-Valero de Bernabé et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2002)
Deletion of brain dystroglycan recapitulates aspects of congenital muscular dystrophy
SA Moore et al.
NATURE (2002)
An autosomal recessive form of bilateral frontoparietal polymicrogyria maps to chromosome 16q12.2-21
XH Piao et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2002)
Neuronal migration disorders: from genetic diseases to developmental mechanisms
JG Gleeson et al.
TRENDS IN NEUROSCIENCES (2000)