• <em>TUBA1A</em> tubulinopathy mutants disrupt neuron morphogenesis and override XMAP215/Stu2 regulation of microtubule dynamics
• Abnormal course of the corticospinal tracts in KIF5C-related encephalopathy
• Automatic Quantification of Normal Brain Gyrification Patterns and Changes in Fetuses with Polymicrogyria and Lissencephaly Based on MRI
• Autosomal Recessive Primary Microcephaly (MCPH) and Novel Pathogenic Variants in <em>ASPM</em> and <em>WDR62</em> Genes
• Brain MRI Abnormalities, Epilepsy and Intellectual Disability in LAMA2 Related Dystrophy - a Genotype/Phenotype Correlation
• Broadening the phenotypic spectrum of TUBA1A tubulinopathy to syndromic arthrogryposis multiplex congenita
• De novo monoallelic Reelin missense variants cause dominant neuronal migration disorders via a dominant-negative mechanism
• Diagnosis of fetal cortical abnormalities by new reference charts for assessment of sylvian fissure biometry
• Diagnostic utility of exome sequencing followed by research reanalysis in human brain malformations
• Diagnostic work-up in malformations of cortical development
• Embryology, Central Nervous System, Malformations
• Embryology, Central Nervous System, Malformations
• Fetal Brain Development: Regulating Processes and Related Malformations
• Homozygous MFN2 variants causing severe antenatal encephalopathy with clumped mitochondria
• Imaging of Congenital Malformations of the Brain
• Insights on the Role of α- and β-Tubulin Isotypes in Early Brain Development
• Long-term Outcome of Epilepsy and Cortical Malformations Due to Abnormal Migration and Postmigrational Development: A Cohort Study
• MAPping tubulin mutations
• Neurodevelopmental Findings and Epilepsy in Malformations of Cortical Development
• Novel compound heterozygous <em>GPR56</em> gene mutation in a twin with lissencephaly: A case report
• Novel LAMC3 pathogenic variant enriched in Finnish population causes malformations of cortical development and severe epilepsy
• PAEDIATRIC SYMPTOMATIC SEIZURES IN INDIA: UNRAVELLING VARIED ETIOLOGIES AND NEUROIMAGING PATTERNS - A MULTICENTRIC STUDY
• Prenatal diagnosis of microcephaly with simplified gyral pattern: series of 8 cases
• Prenatal diagnosis of microcephaly with simplified gyral pattern: series of eight cases
• Quantitative Structural Brain Magnetic Resonance Imaging Analyses: Methodological Overview and Application to Rett Syndrome
• X-linked neuronal migration disorders: Gender differences and insights for genetic screening