4.7 Article

GPR56-related bilateral frontoparietal polymicrogyria: further evidence for an overlap with the cobblestone complex

Related references

Note: Only part of the references are listed.
Article Pediatrics

LISSENCEPHALY(AGYRIA-PACHYGYRIA): CLINICAL FINDINGS AND SERIAL EEG STUDIES

H. Gastaut et al.

DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY (2010)

Review Biochemistry & Molecular Biology

Abnormal glycosylation of dystroglycan in human genetic disease

Jane E. Hewitt

BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE (2009)

Article Neurosciences

GPR56-Regulated Granule Cell Adhesion Is Essential for Rostral Cerebellar Development

Samir Koirala et al.

JOURNAL OF NEUROSCIENCE (2009)

Editorial Material Genetics & Heredity

Diversifying microtubules in brain development

Andrew P. Jackson

NATURE GENETICS (2009)

Article Clinical Neurology

Midbrain-hindbrain involvement in lissencephalies

Patrice Jissendi-Tchofo et al.

NEUROLOGY (2009)

Review Genetics & Heredity

Tubulin-related cortical dysgeneses: microtubule dysfunction underlying neuronal migration defects

Xavier H. Jaglin et al.

TRENDS IN GENETICS (2009)

Article Neurosciences

GPR56 regulates pial basement membrane integrity and cortical lamination

Shihong Li et al.

JOURNAL OF NEUROSCIENCE (2008)

Article Biochemistry & Molecular Biology

Disease-associated mutations affect GPR56 protein trafficking and cell surface expression

Zhaohui Jin et al.

HUMAN MOLECULAR GENETICS (2007)

Article Genetics & Heredity

POMT2 mutations cause α-dystroglycan hypoglycosylation and Walker-Warburg syndrome

J van Reeuwijk et al.

JOURNAL OF MEDICAL GENETICS (2005)

Article Clinical Neurology

Genotype-phenotype analysis of human frontoparietal polymicrogyria syndromes

XH Piao et al.

ANNALS OF NEUROLOGY (2005)

Review Genetics & Heredity

Genetics of the polymicrogyria syndromes

A Jansen et al.

JOURNAL OF MEDICAL GENETICS (2005)

Article Biochemistry & Molecular Biology

Localization and functional analysis of the LARGE family of glycosyltransferases: significance for muscular dystrophy

M Brockington et al.

HUMAN MOLECULAR GENETICS (2005)

Article Multidisciplinary Sciences

G protein-coupled receptor-dependent development of human frontal cortex

XH Piao et al.

SCIENCE (2004)

Review Neurosciences

Targeting dystroglycan in the brain

F Montanaro et al.

NEURON (2003)

Article Genetics & Heredity

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)

Article Genetics & Heredity

An autosomal recessive form of bilateral frontoparietal polymicrogyria maps to chromosome 16q12.2-21

XH Piao et al.

AMERICAN JOURNAL OF HUMAN GENETICS (2002)

Review Neurosciences

Neuronal migration disorders: from genetic diseases to developmental mechanisms

JG Gleeson et al.

TRENDS IN NEUROSCIENCES (2000)