• <em>PAFAH1B1</em> Gene Deletion-Associated Classic Lissencephaly and Infantile Spasms
• 17p13.3 microdeletion including YWHAE and CRK genes: towards a clinical characterization
• 17p13.3 microduplication including CRK leads to overgrowth and elevated growth factors: A case report
• 17p13.3 quadruplication: a prenatal and postpartum clinical characterization of a copy number variant
• A Case of Class I 17p13.3 Microduplication Syndrome with Unilateral Hearing Loss
• A deletion in Eml1 leads to bilateral subcortical heterotopia in the tish rat
• A novel DCX missense mutation in a family with X-linked lissencephaly and subcortical band heterotopia syndrome inherited from a low-level somatic mosaic mother: Genetic and functional studies
• Aberrant sorting of hippocampal complex pyramidal cells in type I lissencephaly alters topological innervation
• Acquired dysgraphia in a girl with subcortical band heterotopia
• Acute Bowel Ischemia in a Premature Neonate with Miller-Dieker Syndrome and Anomalous Right Coronary Artery From the Pulmonary Artery
• An action-concept processing advantage in a patient with a double motor cortex
• An Organoid-Based Model of Cortical Development Identifies Non-Cell-Autonomous Defects in Wnt Signaling Contributing to Miller-Dieker Syndrome
• Analysis of 17 genes detects mutations in 81% of 811 patients with lissencephaly
• Analysis of ARX gene variant in a child with X-linked lissencephaly with abnormal genitalia
• Apples and Potatoes
• Array comparative genomic hybridization characterization of a 3.3-Mb 17p13.3-p13.2 deletion encompassing YWHAE, CRK, HIC1 and PAFAH1B1 in an 8-year-old girl with Miller-Dieker lissencephaly syndrome, congenital heart defects, growth restriction and develo
• Bi-allelic CAMSAP1 variants cause a clinically recognizable neuronal migration disorder
• Bi-allelic Loss of Human APC2, Encoding Adenomatous Polyposis Coli Protein 2, Leads to Lissencephaly, Subcortical Heterotopia, and Global Developmental Delay
• Biomechanical comparison of three fixation strategies for radial head fractures: a biomechanical study
• Clinical and neuroimaging findings in patients with lissencephaly/subcortical band heterotopia spectrum: a magnetic resonance conventional and diffusion tensor study
• Clinical findings and genetic analysis of patients with copy number variants involving 17p13.3 using a single nucleotide polymorphism array: a single-center experience
• Combinatory use of central venous catheter and ethanol lock for a patient with X-linked lissencephaly with ambiguous genitalia (XLAG) syndrome
• Crk Haploinsufficiency Is Associated with Intrauterine Growth Retardation and Severe Postnatal Growth Failure
• De novo heterozygous mutation in the MBD5 gene associated with bilateral band heterotopia and polymicrogyria
• Direct and Collateral Alterations of Functional Cortical Circuits in a Rat Model of Subcortical Band Heterotopia
• Disruption of YWHAE gene at 17p13.3 causes learning disabilities and brain abnormalities
• Double Cortex Syndrome (Subcortical Band Heterotopia)
• Double cortex syndrome in a male patient without lissencephaly
• Double inversion recovery MRI of subcortical band heterotopia and its variations
• Early detection and evolution of hypsarrhythmia in a patient with subcortical band heterotopia
• Early suppression of excitability in subcortical band heterotopia modifies epileptogenesis in rats
• Electrographic pattern recognition: A simple tool to predict clinical outcome in children with lissencephaly
• Emergence of non-canonical parvalbumin-containing interneurons in hippocampus of a murine model of type I lissencephaly
• Eml1 loss impairs apical progenitor spindle length and soma shape in the developing cerebral cortex
• Extended Glasgow Outcome Scale to Evaluate the Functional Impairment of Patients With Subcortical Band Heterotopia: A Multicentric Cross-sectional Study
• Familial posterior predominant subcortical band heterotopia caused by a CEP85L missense mutation
• Frequent Awakenings and Fits With Aerobics
• Functional Connectivity and Genetic Profile of a "Double-Cortex"-Like Malformation
• Further characterization of CEP85L-associated lissencephaly type 10: Report of a three-generation family and review of the literature
• Further expansion and confirmation of phenotype in rare loss of YWHAE gene distinct from Miller-Dieker syndrome
• Generation of an induced pluripotent stem cell line (SDQLCHi067-A) from a patient with subcortical band heterotopia harboring a heterozygous mutation in DCX gene
• Genetic causes underlying grey matter heterotopia
• Hepatic loss of <em>Lissencephaly 1</em> (<em>Lis1</em>) induces fatty liver and accelerates liver tumorigenesis in mice
• Human iPSC-Derived Cerebral Organoids Model Cellular Features of Lissencephaly and Reveal Prolonged Mitosis of Outer Radial Glia
• ILAE neuroimaging task force highlight: Subcortical laminar heterotopia
• Leveraging multiple approaches for the detection of pathogenic deep intronic variants in developmental and epileptic encephalopathies: A case report
• LIS1 interacts with CLIP170 to promote tumor growth and metastasis via the Cdc42 signaling pathway in salivary gland adenoid cystic carcinoma
• Lis1 relieves cytoplasmic dynein-1 autoinhibition by acting as a molecular wedge
• LIS1-associated classic lissencephaly: A retrospective, multicenter survey of the epileptogenic phenotype and response to antiepileptic drugs
• Lissencephaly with Congenital Hypothyroidism: A Case Report
• Lissencephaly: Expanded imaging and clinical classification
• Lissencephaly: Update on diagnostics and clinical management
• Loss of Lgl1 Disrupts the Radial Glial Fiber-guided Cortical Neuronal Migration and Causes Subcortical Band Heterotopia in Mice
• MACF1, Involved in the 1p34.2p34.3 Microdeletion Syndrome, is Essential in Cortical Progenitor Polarity and Brain Integrity
• Megalencephaly, polymicrogyria and ribbon-like band heterotopia: A new cortical malformation
• Miller-Dieker Syndrome due to a 5.5-Mb 17p Deletion in a 17;Y Pseudodicentric Chromosome
• Miller-Dieker Syndrome with unbalanced translocation 45, X, psu dic(17;Y)(p13;p11.32) detected by fluorescence in situ hybridization and G-banding analysis using high resolution banding technique
• Mutations in the Heterotopia Gene Eml1/EML1 Severely Disrupt the Formation of Primary Cilia
• Neuroanatomical characterization of the cellular and axonal architecture of subcortical band heterotopia in the BXD29-Tlr4(lps-2J)/J mouse cortex
• Neuroanatomical characterization of the cellular and axonal architecture of subcortical band heterotopia in the BXD29-Tlr4^lps-2J/J mouse cortex
• Neuronal migration genes and a familial translocation t (3;17): candidate genes implicated in the phenotype
• Non-pharmacological treatment options of drug-resistant epilepsy in subcortical band heterotopia: systematic review and illustrative case
• Novel lissencephaly-associated DCX variants in the C-terminal DCX domain affect microtubule binding and dynamics
• Novel role of the synaptic scaffold protein Dlgap4 in ventricular surface integrity and neuronal migration during cortical development
• Pathogenic Variants in CEP85L Cause Sporadic and Familial Posterior Predominant Lissencephaly
• Phenotypic Variability in Novel Doublecortin Gene Variants Associated with Subcortical Band Heterotopia
• Posterior Lissencephaly Associated with Subcortical Band Heterotopia Due to a Variation in the <em>CEP85L</em> Gene: A Case Report and Refining of the Phenotypic Spectrum
• Posterior Lissencephaly Associated with Subcortical Band Heterotopia Due to a Variation in the CEP85L Gene: A Case Report and Refining of the Phenotypic Spectrum
• Prenatal diagnosis and genetic analysis of a fetus with Miller-Dieker syndrome
• Prenatal diagnosis of a fetus with Miller-Dieker syndrome
• Prenatal diagnosis of a fetus with Miller-Dieker syndrome
• Prenatal diagnosis of fetal gray matter heteropia in one case and literature review
• Prenatal diagnosis of Miller-Dieker syndrome by chromosomal microarray
• Prenatal diagnosis of Miller-Dieker syndrome/PAFAH1B1-related lissencephaly: Ultrasonography and genetically investigative results
• Prenatal genetic analysis of a fetus with Miller-Dieker syndrome
• Prenatal genetic analysis of two fetuses with Miller-Dieker syndrome
• Quadruple Semitendinosus Graft Construct With Double Cortical Suspensory Fixation for Anterior Cruciate Ligament Reconstruction: A Biomechanical Study
• Rare Concurrence of Two Congenital Disorders: Miller-Dieker Syndrome and T-Cell Lymphopenia
• Recurrent Guillain-Barré syndrome, Miller Fisher syndrome and Bickerstaff brainstem encephalitis
• Recurrent KIF2A mutations are responsible for classic lissencephaly
• Reply to: "Susceptibility-Weighted Imaging Reveals Subcortical Iron Deposition in PLAN: The "Double Cortex Sign""
• Sensitive quantitative detection of somatic mosaic mutation in "double cortex" syndrome
• Similar return to sport between double cortical button and docking techniques for ulnar collateral ligament reconstruction in baseball players
• Spared cognitive and behavioral functions prior to epilepsy onset in a rat model of subcortical band heterotopia
• Spontaneous epileptiform activity in a rat model of bilateral subcortical band heterotopia
• Stimulation of the bilateral anterior nuclei of the thalamus in the treatment of refractory epilepsy: two cases of subcortical band heterotopia
• Structures of human dynein in complex with the lissencephaly 1 protein, LIS1
• Subcortical band heterotopia disrupting white matter tracts
• Subcortical band heterotopia in a patient with phenylketonuria: Co-Existence or consequence?
• Subcortical Band Heterotopia Shows Increased Perfusion on Arterial Spin Labeling Maps
• Subcortical laminar heterotopia 'double cortex syndrome'
• Susceptibility-Weighted Imaging Reveals Subcortical Iron Deposition in PLA2G6-associated Neurodegeneration: The "Double Cortex Sign"
• Sustained seizure freedom with transcutaneous vagal nerve stimulation in drug-resistant epilepsy caused by subcortical band heterotopias
• T2-sequence with contrast inversion: diagnostic value in the investigation of gray matter heterotopias
• Targeted re-sequencing in malformations of cortical development: genotype-phenotype correlations
• Teaching NeuroImages: Double cortex: Rare diagnosis in adulthood
• The neuroanatomy of Eml1 knockout mice, a model of subcortical heterotopia
• Thyroid hormone-dependent formation of a subcortical band heterotopia (SBH) in the neonatal brain is not exacerbated under conditions of low dietary iron (FeD)
• Unusual presentation of acute encephalopathy with biphasic seizures and late reduced diffusion in Miller-Dieker syndrome
• YWHAE loss of function causes a rare neurodevelopmental disease with brain abnormalities in human and mouse