• 3'UTR Deletion of <em>NONO</em> Leads to Corpus Callosum Anomaly, Left Ventricular Non-Compaction and Ebstein's Anomaly in a Male Fetus
• A case of closedlip schizencephaly with absent septum pellucidum in an adult presenting with seizure disorder
• A case report of severe panhypopituitarism in a newborn delivered by a women with Turner syndrome
• A rare case of trisomy 15pter-q21.2 due to a de novo marker chromosome
• Abnormalities Associated With the Cavum Septi Pellucidi on Fetal MRI: What Radiologists Need to Know
• Absence of septum pellucidum
• Absent cavum septum pellucidum: a review with emphasis on associated commissural abnormalities
• Acquired hump of the corpus callosum: a rare morphologic complication after CSF shunting
• Adhesio interthalamica and cavum septum pellucidum in mesial temporal lobe epilepsy
• Adult Radiographic Presentation of Corpus Callosal Agenesis With a Single Interhemispheric Cyst and Dandy-Walker Malformation: A Case Report
• Agenesis of the fetal corpus callosum: sonographic signs change with advancing gestational age
• Alobar holoprosencephaly with cebocephaly in a neonate: A rare case report from Northern Tanzania
• An exome sequencing study of Moebius syndrome including atypical cases reveals an individual with CFEOM3A and a <em>TUBB3</em> mutation
• AN UNEXPECTED COMBINATION OF PROLACTINOMA AND SEPTO-OPTIC DYSPLASIA
• An unusual case of neonatal cholestasis
• Analysis of 270 fetuses with non-visualization of cavum septi pellucidi and vergae on in-utero magnetic resonance imaging
• Antenatal diagnosis of absence of septum pellucidum
• Atypical presentation of primary central nervous system non-Hodgkin lymphoma in immunocompetent young adults
• Automated Midline Estimation for Symmetry Analysis of Cerebral Hemispheres in FLAIR MRI
• Bedside Percutaneous Twist Drill Craniostomy of Chronic Subdural Hematoma-A Single-Center Study
• Benefits of examination by post mortem performed magnetic resonance imaging of foetus: haemorrhage in germinal matrix
• Bilateral subependymal pseudocysts as a pitfall in diagnosis of absence of the cavum septum pellucidum
• Body mass index and hypothalamic morphology on MRI in children with congenital midline cerebral abnormalities
• Brain imaging studies in Leber's congenital amaurosis: new radiologic findings associated with the complex trait
• Can Absence of Cavum Septum Pellucidum in Early Pregnancy Predict Fetal Brain Abnormality Later?
• Case Report: Novel <em>CSF1R</em> Variant in a Patient With Behavioral Variant Frontotemporal Dementia Syndrome With Prodromal Repetitive Scratching Behavior
• Caval variations in neurologically diseased patients
• Cavum Septi Pellucidi in Symptomatic Former Professional Football Players
• Cerebral abnormalities in infants with myelomeningocele
• Chronic schizophrenia with the absence of the septum pellucidum: A case report
• Clinical correlates of enlarged cavum septum pellucidum in schizophrenia: A revisit through computed tomography
• Comparative Study of Single Burr-Hole Craniostomy versus Twist-Drill Craniostomy in Patients with Chronic Subdural Hematoma
• Conservative treatment of cysts of the cavum septum pellucidum presenting in childhood: report of 3 cases
• Diagnostic accuracy and clinical outcomes associated with prenatal diagnosis of fetal absent cavum septi pellucidi
• Dilated cavum septi pellucidi as sole prenatal ultrasound defect: Case-base analysis of fetal outcomes
• Dyke-Davidoff-Masson Syndrome: Time to Revisit Case Series
• Examining for Cavum Septum Pellucidum and Ventricular Enlargement in Retired Elite-Level Rugby League Players
• Extra-Pituitary Birth Defects May Predict Diagnosis of Congenital Hypopituitarism in a Short Child
• Factors Contributing to Risk of Persistence of Positive and Negative Symptoms in Schizophrenia during Hospitalization
• Fetal neurosonography: extended examination of the CNS in the fetus
• Fetal Ultrasound and Magnetic Resonance Imaging Findings in Suspected Septo-Optic Dysplasia: A Diagnostic Dilemma
• Holoprosencephaly or severe hydrocephalus: T1 sequence tells the story
• Increased Intraocular Pressure in a Patient With Septooptic Dysplasia: A Case Report
• Interhypothalamic adhesions in endoscopic third ventriculostomy
• Interrelationships Among Neuroimaging Biomarkers, Neuropsychological Test Data, and Symptom Reporting in a Cohort of Retired National Football League Players
• Isolated absence of septum pellucidum: prenatal diagnosis and outcome
• Isolated absence of the cavum septum pellucidum
• Isolated Absent Septum Pellucidum: A Retrospective Study of Fetal Diagnosis and Postnatal Outcomes
• Isolated Agenesis of Septum Pellucidum and Adult-Onset Seizure Tendency With Eye Closure Sensitivity
• It does Exist! Traumatic Hemorrhage in Septum Pellucidum
• Long-term postnatal outcome of fetuses with prenatally suspected septo-optic dysplasia
• Maternal tetrahydrobiopterin deficiency: the course of two pregnancies and follow-up of two children in a mother with 6-pyruvoyl-tetrahydropterin synthase deficiency
• Midline Brain Abnormalities Across Psychotic and Mood Disorders
• MRI of lobar holoprosencephaly in a cat with hypodipsic hypernatraemia
• NANS-CDG: Delineation of the Genetic, Biochemical, and Clinical Spectrum
• Neuroradiologic Evaluation of MRI in High-Contact Sports
• New insights into septo-optic dysplasia
• Outcome of Isolated Absent Septum Pellucidum Diagnosed by Fetal Magnetic Resonance Imaging (MRI) Scan
• Posterior ocular malformations in children: somatic, neuroradiological and cognitive aspects
• Prenatal abnormal width of the cavum septum pellucidum - MRI features and neurodevelopmental outcome
• Prenatal detection of Peters plus-like syndrome
• Prenatal diagnosis and outcome of fetuses with isolated agenesis of septum pellucidum: cohort study and meta-analysis
• Prenatal phenotyping of fetal tubulinopathies: A multicenter retrospective case series
• Prenatal ultrasound phenotypic and genetic etiology of the 17q12 microduplication syndrome
• Progeny in an Inhospitable Milieu-Solitary Intraventricular Metastasis From a Triple-Negative Breast Cancer Mimicking Central Neurocytoma: Case Report and Review of Diagnostic Pitfalls and Management Strategies
• Quantitative pupillometry and radiographic markers of intracranial midline shift: A pilot study
• Re-assigned diagnosis of D4ST1-deficient Ehlers-Danlos syndrome (adducted thumb-clubfoot syndrome) after initial diagnosis of Marden-Walker syndrome
• Restoration of peripheral V2 receptor vasopressin signaling fails to correct behavioral changes in Brattleboro rats
• Review of the MRI brain findings of septo-optic dysplasia
• Rhombencephalosynapsis With Obstructive Hydrocephalus: A Rare Presentation of the Cerebellar Anomaly on MRI Findings
• Rhombencephalosynapsis: a hindbrain malformation associated with incomplete separation of midbrain and forebrain, hydrocephalus and a broad spectrum of severity
• Rhomboencephalosynapsis: Review of the Literature
• Risk Factors and Preoperative Risk Scoring System for Shunt-Dependent Hydrocephalus Following Aneurysmal Subarachnoid Hemorrhage
• Role of three-dimensional ultrasound measurement of the optic tract in fetuses with agenesis of the septum pellucidum
• Semilobar Holoprosencephaly Caused by a Novel and De Novo <em>ZIC2</em> Pathogenic Variant
• Septo-optic Dysplasia : Assessment of Associated Findings with Special Attention to the Olfactory Sulci and Tracts
• Septo-optic dysplasia (De Morsier's syndrome). About one case discovered during the pregnancy
• Septo-optic dysplasia (Morsier's syndrome): a case report
• Septo-optic dysplasia associated with congenital persistent fetal vasculature, retinal detachment, and gastroschisis
• Septo-optic dysplasia caused by a novel FLNA splice site mutation: a case report
• Septo-optic Dysplasia Complex with Omphalocele, Pre-maxillary Agenesis and Encephalocele
• Septo-optic dysplasia complex: Clinical and radiological manifestations in Omani children
• Septo-Optic Dysplasia Diagnosed in a Newborn Infant with Normoglycemia: The Importance of Thorough Physical Examination
• Septo-optic dysplasia presenting with nystagmus, pseudo-disc edema, and fovea hypoplasia
• Septo-optic dysplasia with amniotic band syndrome sequence: a case report
• Septo-optic dysplasia with fovea plana: A case report
• Septo-optic dysplasia-plus and dyskinetic cerebral palsy in a child
• Successful treatment of hypodipsic/adipsic hypernatremia in a cat with lobar holoprosencephaly using oral desmopressin
• Thalamic Massa Intermedia in Children with and without Midline Brain Malformations
• The association of sphenoidal encephalocele and right anophthalmia with septo-optic dysplasia: a case report
• The middle interhemispheric variant of holoprosencephaly: magnetic resonance and diffusion tensor imaging findings
• The relationship between cavum septum pellucidum and psychopathic traits in female offenders
• The role of routine first-trimester ultrasound screening for central nervous system abnormalities: a longitudinal single-center study using an unselected cohort with 3-year experience
• The split notochord syndrome with dorsal enteric fistula
• The wide spectrum of ultrasound diagnosis of holoprosencephaly
• Transcranial Doppler ultrasonography identifies symptomatic cavum septum pellucidum cyst: case report
• Ultrasound diagnosis of isolated aplasia of the septum pellucidum
• Unilateral closed lip schizencephaly with septo-optic dysplasia
• Utility of Measuring Fetal Cavum Septum Pellucidum (CSP) Width During Routine Obstetrical Ultrasound for Improving Diagnosis of 22q11.2 Deletion Syndrome: A Case-Control Study
• Xq27.1 Duplication Encompassing SOX3: Variable Phenotype and Smallest Duplication Associated with Hypopituitarism to Date - A Large Case Series of Unrelated Patients and a Literature Review