Disease: Malformations in neuronal migration
- <em>DCX</em> variants in two unrelated Chinese families with subcortical band heterotopia: Two case reports and review of literature
- <em>DOCK3</em>-Associated Neurodevelopmental Disorder-Clinical Features and Molecular Basis
- 4E-BP1 expression in embryonic postmitotic neurons mitigates mTORC1-induced cortical malformations and behavioral seizure severity but does not prevent epilepsy in mice
- A <em>de novo</em> Mutation (p.Gln277X) of <em>Cyclin D2</em> is Responsible for a Child with Megalencephaly-Polymicrogyria-Polydactyly-Hydrocephalus Syndrome
- A lissencephaly-associated BAIAP2 variant causes defects in neuronal migration during brain development
- A recurrent missense variant in the E3 ubiquitin ligase substrate recognition subunit FEM1B causes a rare syndromic neurodevelopmental disorder
- Altered hippocampal doublecortin expression in Parkinson's disease
- An adhesion signaling axis involving Dystroglycan, β1-Integrin, and Cas adaptor proteins regulates the establishment of the cortical glial scaffold
- An unusual presentation of de novo RAC3 variation in prenatal diagnosis
- Antisense oligonucleotide therapeutic approach for Timothy syndrome
- Assessing the Safety and Therapeutic Efficacy of Cannabidiol Lipid Nanoparticles in Alleviating Metabolic and Memory Impairments and Hippocampal Histopathological Changes in Diabetic Parkinson's Rats
- Bi-allelic truncating variants in CASP2 underlie a neurodevelopmental disorder with lissencephaly
- Brain Pathways in LIS1-Associated Lissencephaly Revealed by Diffusion MRI Tractography
- Case Report: Novel biallelic moderately damaging variants in <em>RTTN</em> in a patient with cerebellar dysplasia
- Cell type specificity of mosaic chromosome 1q gain resolved by snRNA-seq in a case of epilepsy with hyaline protoplasmic astrocytopathy
- Cell-Type Specificity of Mosaic Chromosome 1q Gain Resolved by snRNA-seq in a Case of Epilepsy With Hyaline Protoplasmic Astrocytopathy
- Cilostazol treats transient heart failure caused by ATP1A3 variant-associated polymicrogyria
- Clustered de novo start-loss variants in GLUL result in a developmental and epileptic encephalopathy via stabilization of glutamine synthetase
- CMV-induced Hearing Loss
- Coactosin-like protein 1 regulates integrity and repair of model intestinal epithelial barriers via actin binding dependent and independent mechanisms
- Comparison of accidental findings of brain magnetic resonance imaging of patients with obsessive-compulsive disorder and healthy controls
- Congenital cranial dysinnervation disorder with homozygous KIF26A variant
- Connecting neurodevelopment to neurodegeneration: a spotlight on the role of kinesin superfamily protein 2A (KIF2A)
- Contribution of the serotonergic system to developmental brain abnormalities in autism spectrum disorder
- Cortical malformation adjacent to a large pial arteriovenous fistula
- CT Scan Data Analysis in Malformations of Cortical Development
- De novo monoallelic Reelin missense variants act in a dominant-negative manner causing neuronal migration disorders
- De novo monoallelic Reelin missense variants cause dominant neuronal migration disorders via a dominant-negative mechanism
- Deficits in olfactory system neurogenesis in neurodevelopmental disorders
- Dorsal visual stream and LIMK1: hemideletion, haplotype, and enduring effects in children with Williams syndrome
- Double Cortex Syndrome: An Unusual Cause of Seizures
- Downregulation of miR-144 blocked the proliferation and invasion of nerve cells in Hirschsprung disease by regulating Transcription Factor AP 4 (TFAP4)
- Dysregulation of mTOR signaling mediates common neurite and migration defects in both idiopathic and 16p11.2 deletion autism neural precursor cells
- Early developmental changes in a rat model of malformations of cortical development: Abnormal neuronal migration and altered response to NMDA-induced excitotoxic injury
- Establishment of human cerebral organoid systems to model early neural development and assess the central neurotoxicity of environmental toxins
- Excess cerebellar granule neurons induced by the absence of p75NTR during development elicit social behavior deficits in mice
- Exploring unsolved cases of lissencephaly spectrum: integrating exome and genome sequencing for higher diagnostic yield
- Expression patterns of Piezo1 in the developing mouse forebrain
- Features of Remyelination after Transplantation of Olfactory Ensheathing Cells with Neurotrophic Factors into Spinal Cord Cysts
- FEZ1 participates in human embryonic brain development by modulating neuronal progenitor subpopulation specification and migrations
- FGF9 is required for Purkinje cell development and function in the cerebellum
- FMRP regulates postnatal neuronal migration via MAP1B
- Focal cortical dysplasia II caused by brain somatic mutation of IRS-1 is associated with ERK signaling pathway activation
- Further characterization of CEP85L-associated lissencephaly type 10: Report of a three-generation family and review of the literature
- Gamma-Tubulin 1 (TUBG1) Mutation-Associated Lissencephaly and Microcephaly in an Indian Child: A Rare Case
- 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 background of dyslexia and dysgraphy in children
- Genetic Variability of <em>SOX10</em>-Related Disorders within an Italian Family: Straddling the Line between Kallmann and Waardenburg Syndrome
- Heterozygous truncating variant of TAOK1 in a boy with periventricular nodular heterotopia: a case report and literature review of TAOK1-related neurodevelopmental disorders
- HiPSC-derived 3D neural models reveal neurodevelopmental pathomechanisms of the Cockayne Syndrome B
- HNRNPC haploinsufficiency affects alternative splicing of intellectual disability-associated genes and causes a neurodevelopmental disorder
- Human cytomegalovirus infection impairs neural differentiation via repressing sterol regulatory element binding protein 2-mediated cholesterol biosynthesis
- Human enteric nervous system progenitor transplantation improves functional responses in Hirschsprung disease patient-derived tissue
- Illuminating the terminal nerve: Uncovering the link between GnRH-1 neuron and olfactory development
- Ion channels in neurodevelopment: lessons from the Integrin-KCNB1 channel complex
- Is periventricular heterotopia a useful endpoint for developmental thyroid hormone system disruption in mouse toxicity studies?
- Lhermitte-Duclos Disease: A Case Series
- Lissencephaly caused by a <em>de novo</em> mutation in tubulin <em>TUBA1A</em>: a case report and literature review
- Lissencephaly-associated BAIAP2 variant causes defects in neuronal migration during brain development
- Loss of <em>Slc35a2</em> alters development of the mouse cerebral cortex
- Loss of Slc35a2 alters development of the mouse cerebral cortex
- LTK and ALK promote neuronal polarity and cortical migration by inhibiting IGF1R activity
- Lymphocytic choriomeningitis virus injures the developing brain: effects and mechanisms
- Metformin rescues migratory deficits of cells derived from patients with periventricular heterotopia
- Mice Mutated in the First Fibronectin Domain of Adhesion Molecule L1 Show Brain Malformations and Behavioral Abnormalities
- Mice Mutated in the Third Fibronectin Domain of L1 Show Enhanced Hippocampal Neuronal Cell Death, Astrogliosis and Alterations in Behavior
- Neocortical and cerebellar malformations affect flurothyl-induced seizures in female C57BL/6J mice
- Neuroanatomical Alterations in the CNTNAP2 Mouse Model of Autism Spectrum Disorder
- Neurodevelopmental disorders: 2023 update
- Neuroimaging Features in Children with Optic Nerve Hypoplasia and Septo-Optic-Pituitary Dysplasia
- Neuronal migration abnormalities in patients with normal development and without seizures
- New cases of recently described Thauvin-Robinet-Faivre syndrome with a novel homozygous FIBP gene variant
- Nidogen in development and disease
- Non-cell-autonomous regulation of interneuron specification mediated by extracellular vesicles
- Novel lissencephaly-associated NDEL1 variant reveals distinct roles of NDE1 and NDEL1 in nucleokinesis and human cortical malformations
- Novel loss of function mutation in <em>TUBA1A</em> gene compromises tubulin stability and proteostasis causing spastic paraplegia and ataxia
- Olfactory bulb anomalies in KBG syndrome mouse model and patients
- Oro-facial-digital syndrome type 1 and neuronal migration disorders
- Patient-specific mutation of Dync1h1 in mice causes brain and behavioral deficits
- Phenotypic Variability in Novel Doublecortin Gene Variants Associated with Subcortical Band Heterotopia
- Physiopathologic Bases of Moebius Syndrome: Combining Genetic, Vascular, and Teratogenic Theories
- Pin1 Downregulation Is Involved in Excess Retinoic Acid-Induced Failure of Neural Tube Closure
- Prenatal diagnosis of microcephaly with simplified gyral pattern: series of 8 cases
- Purinosomes and Purine Metabolism in Mammalian Neural Development: A Review
- Rapamycin improves social and stereotypic behavior abnormalities induced by pre-mitotic neuronal subset specific Pten deletion
- Reelin Signaling and Synaptic Plasticity in Schizophrenia
- SASH1 contributes to glial cell migration in the early development of the central nervous system
- Septic encephalopathy in the elderly - biomarkers of potential clinical utility
- Shaping the brain: The emergence of cortical structure and folding
- Spatial omics reveals molecular changes in focal cortical dysplasia type II
- TFEB overexpression through GFAP promoter disrupts neuronal lamination by dysregulating neurogenesis during embryonic development
- The GTPase Rab21 is required for neuronal development and migration in the cerebral cortex
- The impact of the recipient intestinal site on the differentiation of transplanted enteric neural crest cells
- The role of microRNAs in neurobiology and pathophysiology of the hippocampus
- Thrombospondin-1 Regulates Trophoblast Necroptosis via NEDD4-Mediated Ubiquitination of TAK1 in Preeclampsia
- Transcriptional correlates of frequency-dependent brain functional activity associated with symptom severity in degenerative cervical myelopathy
- Visual Deficits and Diagnostic and Therapeutic Strategies for Neurofibromatosis Type 1: Bridging Science and Patient-Centered Care
- VRK1 variants at the cross road of Cajal body neuropathogenic mechanisms in distal neuropathies and motor neuron diseases
- X-linked neuronal migration disorders: Gender differences and insights for genetic screening
- Zika virus infection histories in brain development