Published in Handb Clin Neurol on January 01, 2013
Mutations in WDR62, encoding a centrosome-associated protein, cause microcephaly with simplified gyri and abnormal cortical architecture. Nat Genet (2010) 2.44
Alpha-B-crystallin as a tissue marker of epileptic foci in paediatric resections. Can J Neurol Sci (2009) 1.39
Deletion of chromosome 21 disturbs human brain morphogenesis. Genet Med (2006) 1.02
Fetal brain mTOR signaling activation in tuberous sclerosis complex. Cereb Cortex (2012) 0.98
Population meta-analysis of low plasma glucose thresholds in full-term normal newborns. Am J Perinatol (2006) 0.96
Fetal brain lesions in tuberous sclerosis complex: TORC1 activation and inflammation. Brain Pathol (2012) 0.91
Embryology of the neural crest: its inductive role in the neurocutaneous syndromes. J Child Neurol (2005) 0.90
Role of Cajal-Retzius and subplate neurons in cerebral cortical development. Semin Pediatr Neurol (2002) 0.85
Brain imaging findings in neonatal hypoglycemia: case report and review of 23 cases. Clin Pediatr (Phila) (2005) 0.84
Severe mitochondrial cytopathy with complete A-V block, PEO, and mtDNA deletions. Pediatr Neurol (2002) 0.81
Integrative classification of morphology and molecular genetics in central nervous system malformations. Am J Med Genet A (2004) 0.81
Cerebral palsy due to chromosomal anomalies and continuous gene syndromes. Clin Perinatol (2006) 0.80
Plasma glucose concentrations in profound neonatal hypoglycemia. Clin Pediatr (Phila) (2006) 0.80
Synaptogenesis in the fetal corpus striatum, globus pallidus, and substantia nigra: correlations with striosomes of Graybiel and dyskinesias in premature infants. J Child Neurol (2012) 0.79
Radial microcolumnar cortical architecture: maturational arrest or cortical dysplasia? Pediatr Neurol (2013) 0.79
Mitochondrial "hypermetabolic" neurons in paediatric epileptic foci. Can J Neurol Sci (2011) 0.78
Muenke syndrome with pigmentary disorder and probable hemimegalencephaly: An expansion of the phenotype. Am J Med Genet A (2011) 0.78
Hemimegalencephaly: foetal tauopathy with mTOR hyperactivation and neuronal lipidosis. Folia Neuropathol (2012) 0.78
Cajal-Retzius and subplate neurons: their role in cortical development. Eur J Paediatr Neurol (2002) 0.77
Neurologic aspects of neonatal hypoglycemia. Isr Med Assoc J (2005) 0.77
Sequence of synaptogenesis in the fetal and neonatal cerebellar system - part 1: Guillain-Mollaret triangle (dentato-rubro-olivo-cerebellar circuit). Dev Neurosci (2013) 0.76
Endothelial ultrastructural alterations of intramuscular capillaries in infantile mitochondrial cytopathies: "mitochondrial angiopathy". Neuropathology (2012) 0.76
Genetics of neural crest and neurocutaneous syndromes. Handb Clin Neurol (2013) 0.76
Congenital infiltrating lipomatosis of the face: recognition and pathogenesis. Neuropediatrics (2012) 0.75
Precocious and delayed neocortical synaptogenesis in fetal holoprosencephaly. Clin Neuropathol (2013) 0.75
Synaptophysin immunoreactivity in the human hippocampus and neocortex from 6 to 41 weeks of gestation. J Neuropathol Exp Neurol (2010) 0.75
Lobar holoprosencephaly. J Child Neurol (2002) 0.75
Etiological classification of CNS malformations: integration of molecular genetic and morphological criteria. Epileptic Disord (2003) 0.75
Fetal opercular cavernous angioma causing cerebral cleft: contralateral primitive vascular anomaly and subicular dysgenesis. J Child Neurol (2011) 0.75
Synaptogenesis in the foetal and neonatal cerebellar system. 2. Pontine nuclei and cerebellar cortex. Dev Neurosci (2013) 0.75
Neuroembryology and brain malformations: an overview. Handb Clin Neurol (2013) 0.75
Molecular genetic and morphologic integration in malformations of the nervous system for etiologic classification. Semin Pediatr Neurol (2002) 0.75