• A de novo partial trisomy 9p with Dandy-Walker malformation and ventriculomegaly
• A novel ACTB variant in an atypical case of Baraitser-Winter syndrome with cerebellar hypoplasia and diaphragmatic hernia
• Arnold-Chiari Malformation
• Arnold-Chiari Malformation
• Case Report: Complex Congenital Brain Anomaly in a BBxHF Calf-Clinical Signs, Magnetic Resonance Imaging, and Pathological Findings
• Challenges in the pre- and post-natal diagnosis of posterior fossa cysts: A case report and review of historical evolution of descriptive terminologies
• Chiari Malformation Type 2
• Corpus callosum disorders and associated malformations in paediatric epilepsy: MRI analytic study
• Epilepsy and EEG Abnormalities in Congenital Zika Syndrome
• Evidence of disrupted rhombic lip development in the pathogenesis of Dandy-Walker malformation
• Hydrocephalus associated with a molar tooth sign: A distinct subtype of Joubert syndrome
• Intracranial tuberculomas: review of MRI findings and clinical features
• Joubert syndrome a rare entity and role of radiology: A case report
• Joubert syndrome and hydrocephalus: Further expanding the phenotypic spectrum of a pleiotropic ciliopathy
• Late-onset cobalamin C deficiency type in adult with cognitive and behavioral disturbances and significant cortical atrophy and cerebellar damage in the MRI: a case report
• Magnetic resonance imaging of Joubert syndrome associated with Dandy-Walker malformation: pathognomonic imaging
• Nanopore long-read sequencing analysis reveals ZIC1 dysregulation caused by a de novo 3q inversion with a breakpoint located 7 kb downstream of ZIC1
• Novel association of Dandy-Walker malformation with CAPN15 variants expands the phenotype of oculogastrointestinal neurodevelopmental syndrome
• Prenatal diagnosis of a 15q24.1 microdeletion in a fetus with cerebral and urogenital abnormalities
• Prenatal Diagnosis of Gómez-López-Hernández Syndrome
• Prenatal diagnosis of vermian cyst: a new type of posterior fossa cyst
• Prenatal Magnetic Resonance Imaging helps Discover Cerebellar Dysplasia or Malformations in Foetuses
• Refining the Neuroimaging Definition of the Dandy-Walker Phenotype
• Rhombencephalosynapsis: a rare congenital malformation
• Rhomboencephalosynapsis: Review of the Literature
• Undifferentiated psychosis or schizophrenia associated with vermis-predominant cerebellar hypoplasia
• Upward gaze palsy and convergence insufficiency as a rare presentation of primary intraventricular haemorrhage
• X-linked pyruvate dehydrogenase complex deficiency due to a novel PDHA1 variant associated with structural brain abnormalities in a fetus