The middle interhemispheric variant of holoprosencephaly.

Holoprosencephaly. Orphanet J Rare Dis (2007) 2.63

Pathogenesis of holoprosencephaly. J Clin Invest (2009) 1.12

Diffusion tensor imaging and fiber tractography in brain malformations. Pediatr Radiol (2013) 1.07

New findings for phenotype-genotype correlations in a large European series of holoprosencephaly cases. J Med Genet (2011) 1.04

Ttc21b is required to restrict sonic hedgehog activity in the developing mouse forebrain. Dev Biol (2009) 0.98

The unfolding clinical spectrum of holoprosencephaly due to mutations in SHH, ZIC2, SIX3 and TGIF genes. Eur J Hum Genet (2010) 0.95

Does asymptomatic septal agenesis exist? A review of 34 cases. Pediatr Radiol (2005) 0.90

Holoprosencephaly: two case reports. Maedica (Buchar) (2012) 0.84

Balanced Shh signaling is required for proper formation and maintenance of dorsal telencephalic midline structures. BMC Dev Biol (2010) 0.84

Clinical image. Middle interhemispheric variant of holoprosencephaly. Pediatr Radiol (2009) 0.81

Links between abnormal brain structure and cognition in holoprosencephaly. Pediatr Neurol (2006) 0.80

Dorsal third ventricular cysts revisited. Childs Nerv Syst (2013) 0.78

The middle interhemispheric variant of holoprosencephaly: magnetic resonance and diffusion tensor imaging findings. Br J Radiol (2016) 0.75

Molecular analysis of holoprosencephaly in South America. Genet Mol Biol (2014) 0.75

Syntelencephaly: postnatal sonographic detection of a subtle case. Pediatr Radiol (2010) 0.75

Absent cavum septum pellucidum: a review with emphasis on associated commissural abnormalities. Pediatr Radiol (2015) 0.75

Pax6, Tbr2, and Tbr1 are expressed sequentially by radial glia, intermediate progenitor cells, and postmitotic neurons in developing neocortex. J Neurosci (2005) 6.95

The clinicopathologic spectrum of focal cortical dysplasias: a consensus classification proposed by an ad hoc Task Force of the ILAE Diagnostic Methods Commission. Epilepsia (2010) 6.23

Abnormal brain development in newborns with congenital heart disease. N Engl J Med (2007) 4.55

G protein-coupled receptor-dependent development of human frontal cortex. Science (2004) 4.42

ACR guidance document for safe MR practices: 2007. AJR Am J Roentgenol (2007) 4.12

Molar tooth sign of the midbrain-hindbrain junction: occurrence in multiple distinct syndromes. Am J Med Genet A (2004) 3.75

Somatic mutations in cerebral cortical malformations. N Engl J Med (2014) 3.13

Analysis and classification of cerebellar malformations. AJNR Am J Neuroradiol (2002) 3.00

Clinical Neonatal Seizures are Independently Associated with Outcome in Infants at Risk for Hypoxic-Ischemic Brain Injury. J Pediatr (2009) 2.96

American College of Radiology White Paper on MR Safety. AJR Am J Roentgenol (2002) 2.87

Patterns of brain injury in term neonatal encephalopathy. J Pediatr (2005) 2.86

Acute disseminated encephalomyelitis. Neurology (2007) 2.84

Somatic activation of AKT3 causes hemispheric developmental brain malformations. Neuron (2012) 2.84

Mutations in PNKP cause microcephaly, seizures and defects in DNA repair. Nat Genet (2010) 2.74

Role of intermediate progenitor cells in cerebral cortex development. Dev Neurosci (2008) 2.66

Balloon atrial septostomy is associated with preoperative stroke in neonates with transposition of the great arteries. Circulation (2006) 2.65

Early brain injury in premature newborns detected with magnetic resonance imaging is associated with adverse early neurodevelopmental outcome. J Pediatr (2005) 2.63

Adult generation of glutamatergic olfactory bulb interneurons. Nat Neurosci (2009) 2.63

Diffusion tensor imaging: serial quantitation of white matter tract maturity in premature newborns. Neuroimage (2004) 2.58

Intermediate neuronal progenitors (basal progenitors) produce pyramidal-projection neurons for all layers of cerebral cortex. Cereb Cortex (2009) 2.51

Tbr1 regulates regional and laminar identity of postmitotic neurons in developing neocortex. Proc Natl Acad Sci U S A (2010) 2.45

Mutations in WDR62, encoding a centrosome-associated protein, cause microcephaly with simplified gyri and abnormal cortical architecture. Nat Genet (2010) 2.44

SLC25A22 is a novel gene for migrating partial seizures in infancy. Ann Neurol (2013) 2.28

Abnormal development of the human cerebral cortex: genetics, functional consequences and treatment options. Trends Neurosci (2008) 2.28

Quantitative diffusion tensor MRI fiber tractography of sensorimotor white matter development in premature infants. Neuroimage (2005) 2.13

The transcription factor gene Nfib is essential for both lung maturation and brain development. Mol Cell Biol (2005) 2.09

Temporal and anatomic risk profile of brain injury with neonatal repair of congenital heart defects. Stroke (2007) 2.06

Intermediate progenitors in adult hippocampal neurogenesis: Tbr2 expression and coordinate regulation of neuronal output. J Neurosci (2008) 2.05

Comparing the diagnosis of white matter injury in premature newborns with serial MR imaging and transfontanel ultrasonography findings. AJNR Am J Neuroradiol (2003) 2.01

Neural stem cell engraftment and myelination in the human brain. Sci Transl Med (2012) 1.96

Serial quantitative diffusion tensor MRI of the premature brain: development in newborns with and without injury. J Magn Reson Imaging (2002) 1.96

Evolutionarily dynamic alternative splicing of GPR56 regulates regional cerebral cortical patterning. Science (2014) 1.85

Pax6 controls cerebral cortical cell number by regulating exit from the cell cycle and specifies cortical cell identity by a cell autonomous mechanism. Dev Biol (2006) 1.84

Decrease in hospital-wide mortality rate after implementation of a commercially sold computerized physician order entry system. Pediatrics (2010) 1.79

Influenza-associated encephalitis/encephalopathy with a reversible lesion in the splenium of the corpus callosum: a case report and literature review. AJNR Am J Neuroradiol (2004) 1.78

A stream of cells migrating from the caudal telencephalon reveals a link between the amygdala and neocortex. Nat Neurosci (2007) 1.76

Development of the deep cerebellar nuclei: transcription factors and cell migration from the rhombic lip. J Neurosci (2006) 1.64

Chiari type I malformation in a pediatric population. Pediatr Neurol (2009) 1.62

Brain injury and development in newborns with critical congenital heart disease. Neurology (2013) 1.61

Recurrent postnatal infections are associated with progressive white matter injury in premature infants. Pediatrics (2008) 1.60

Anomalies of the corpus callosum: an MR analysis of the phenotypic spectrum of associated malformations. AJR Am J Roentgenol (2006) 1.58

Identification of mutations in TRAPPC9, which encodes the NIK- and IKK-beta-binding protein, in nonsyndromic autosomal-recessive mental retardation. Am J Hum Genet (2009) 1.58

Midbrain-hindbrain involvement in lissencephalies. Neurology (2008) 1.58

Reversible white matter lesion in methionine adenosyltransferase I/III deficiency. AJNR Am J Neuroradiol (2004) 1.55

Neurocutaneous melanosis presenting with hydrocephalus. Case report and review of the literature. J Neurosurg (2005) 1.54

Brain involvement in muscular dystrophies with defective dystroglycan glycosylation. Ann Neurol (2008) 1.52

A spatiotemporal atlas of MR intensity, tissue probability and shape of the fetal brain with application to segmentation. Neuroimage (2010) 1.51

Childhood status epilepticus and excitotoxic neuronal injury. Pediatr Neurol (2007) 1.48

Prospective open-label clinical trial of trihexyphenidyl in children with secondary dystonia due to cerebral palsy. J Child Neurol (2007) 1.48

Peritrigonal and temporo-occipital heterotopia with corpus callosum and cerebellar dysgenesis. Neurology (2012) 1.48

Onabotulinum toxinA injection as an adjunct in the treatment of posterior shoulder subluxation in neonatal brachial plexus palsy. J Bone Joint Surg Am (2010) 1.47

Clinical signs predict 30-month neurodevelopmental outcome after neonatal encephalopathy. Am J Obstet Gynecol (2004) 1.46

Tractography-based quantitation of diffusion tensor imaging parameters in white matter tracts of preterm newborns. J Magn Reson Imaging (2005) 1.46

Neuronal migration disorders in microcephalic osteodysplastic primordial dwarfism type I/III. Acta Neuropathol (2010) 1.45

Unipolar brush cells of the cerebellum are produced in the rhombic lip and migrate through developing white matter. J Neurosci (2006) 1.43

Central roles of the roof plate in telencephalic development and holoprosencephaly. J Neurosci (2006) 1.42

DTI-based three-dimensional tractography detects differences in the pyramidal tracts of infants and children with congenital hemiparesis. J Magn Reson Imaging (2003) 1.41

Candidate gene sequencing of LHX2, HESX1, and SOX2 in a large schizencephaly cohort. Am J Med Genet A (2010) 1.40

Standardized MR terminology and reporting of implants and devices as recommended by the American College of Radiology Subcommittee on MR Safety. Radiology (2014) 1.40

Brain MR imaging in acute hyperammonemic encephalopathy arising from late-onset ornithine transcarbamylase deficiency. AJNR Am J Neuroradiol (2003) 1.40

Nucleated red blood cell counts: not associated with brain injury or outcome. Pediatr Neurol (2003) 1.39

Perinatal events and early magnetic resonance imaging in therapeutic hypothermia. J Pediatr (2010) 1.38

Genotype-phenotype analysis of human frontoparietal polymicrogyria syndromes. Ann Neurol (2005) 1.37

Local tissue growth patterns underlying normal fetal human brain gyrification quantified in utero. J Neurosci (2011) 1.37

Preterm cerebellar growth impairment after postnatal exposure to glucocorticoids. Sci Transl Med (2011) 1.36

Comparing microstructural and macrostructural development of the cerebral cortex in premature newborns: diffusion tensor imaging versus cortical gyration. Neuroimage (2005) 1.36

Encephalopathy with a reversible splenial lesion is associated with hyponatremia. Brain Dev (2008) 1.35

ACR guidance document on MR safe practices: 2013. J Magn Reson Imaging (2013) 1.35

Early laminar organization of the human cerebrum demonstrated with diffusion tensor imaging in extremely premature infants. Neuroimage (2004) 1.34

Extrahippocampal gray matter loss and hippocampal deafferentation in patients with temporal lobe epilepsy. Epilepsia (2010) 1.33

Bilateral frontoparietal polymicrogyria: clinical and radiological features in 10 families with linkage to chromosome 16. Ann Neurol (2003) 1.33

Imaging, anatomical, and molecular analysis of callosal formation in the developing human fetal brain. Anat Rec A Discov Mol Cell Evol Biol (2006) 1.32

Autism susceptibility candidate 2 (Auts2) encodes a nuclear protein expressed in developing brain regions implicated in autism neuropathology. Gene Expr Patterns (2009) 1.30

Pyramidal tract maturation after brain injury in newborns with heart disease. Ann Neurol (2006) 1.28

The transcription factor encyclopedia. Genome Biol (2012) 1.28

Preoperative brain injury in newborns with transposition of the great arteries. Ann Thorac Surg (2004) 1.27

Cerebellar hemorrhage on magnetic resonance imaging in preterm newborns associated with abnormal neurologic outcome. J Pediatr (2010) 1.27

Atlas-based segmentation of developing tissues in the human brain with quantitative validation in young fetuses. Hum Brain Mapp (2010) 1.25

A patient with Huntington's disease and long-surviving fetal neural transplants that developed mass lesions. Acta Neuropathol (2008) 1.25

Imaging of malformations of cortical development. Epileptic Disord (2009) 1.24

Mammalian target of rapamycin pathway mutations cause hemimegalencephaly and focal cortical dysplasia. Ann Neurol (2015) 1.24

The vascular effects of infection in Pediatric Stroke (VIPS) Study. J Child Neurol (2011) 1.23

Comprehensive EMX2 genotyping of a large schizencephaly case series. Am J Med Genet A (2007) 1.22

Early folding patterns and asymmetries of the normal human brain detected from in utero MRI. Cereb Cortex (2011) 1.21

Seizures and magnetic resonance imaging-detected brain injury in newborns cooled for hypoxic-ischemic encephalopathy. J Pediatr (2011) 1.20

Differential effects of intraventricular hemorrhage and white matter injury on preterm cerebellar growth. J Pediatr (2010) 1.17

Fibroblast growth factor signaling in development of the cerebral cortex. Dev Growth Differ (2009) 1.17

Risk factors for epilepsy in children with neonatal encephalopathy. Pediatr Res (2011) 1.14

T1 hyperintensity in the pulvinar: key imaging feature for diagnosis of Fabry disease. AJNR Am J Neuroradiol (2003) 1.14

Hypoglycemia is associated with increased risk for brain injury and adverse neurodevelopmental outcome in neonates at risk for encephalopathy. J Pediatr (2012) 1.13

Predictors of 30-month outcome after perinatal depression: role of proton MRS and socioeconomic factors. Pediatr Res (2002) 1.12

Intraventricular hemorrhage in term neonates caused by sinovenous thrombosis. Ann Neurol (2003) 1.12

American College of Radiology White Paper on MR Safety: 2004 update and revisions. AJR Am J Roentgenol (2004) 1.12

Prolonged indomethacin exposure is associated with decreased white matter injury detected with magnetic resonance imaging in premature newborns at 24 to 28 weeks' gestation at birth. Pediatrics (2006) 1.12

Neonatal watershed brain injury on magnetic resonance imaging correlates with verbal IQ at 4 years. Pediatrics (2009) 1.11

Neonatal encephalopathy: association of cytokines with MR spectroscopy and outcome. Pediatr Res (2004) 1.10

Mutations in ZIC2 in human holoprosencephaly: description of a novel ZIC2 specific phenotype and comprehensive analysis of 157 individuals. J Med Genet (2009) 1.10

Long-term outcome of transcatheter embolization of renal angiomyolipomas due to tuberous sclerosis complex. J Urol (2005) 1.10

Cerebellar development in the preterm neonate: effect of supratentorial brain injury. Pediatr Res (2009) 1.09

Human induced pluripotent stem cell-derived cortical neurons integrate in stroke-injured cortex and improve functional recovery. Brain (2013) 1.09