• 'Choroid bar': easy-to-seek marker of normal posterior fossa at 12-14 weeks' gestation
• "Is my baby all right?" Commentary on "The importance of first trimester screening of cranial posterior fossa in predicting posterior fossa malformations which may be identified in the following weeks of gestation" by Ozdemir et al. Da
• A de novo partial trisomy 9p with Dandy-Walker malformation and ventriculomegaly
• A founder PPIL1 variant underlies a recognizable form of microlissencephaly with pontocerebellar hypoplasia
• A genotype-first analysis in a cohort of Mullerian anomaly
• A large growing occipital meningocele with Dandy-Walker syndrome: A case report and review of the literature
• A myriad of posterior fossa cysts: A single center experience
• A novel AP1S2 variant causing leaky splicing in X-linked intellectual disability: Further delineation and intrafamilial variability
• A rare association of Down syndrome with Dandy -Walker variant, pulmonary hypertension and childhood interstitial lung disease: A case report of a prognostic dilemma
• A Rare Case of Dandy-Walker Syndrome
• Adult-onset Dandy-Walker syndrome with atypical ocular manifestations
• Alternative Genetic Diagnoses in Axenfeld-Rieger Syndrome Spectrum
• Asymptomatic Dandy Walker Malformation In An Elderly Male With Acute Haemorrhagic Stroke - A Case Report
• Axenfeld-Rieger syndrome: A systematic review examining genetic, neurological, and neurovascular associations to inform screening
• Case Report: 5 Cases of Variant Hypoplastic Left Heart Syndrome Diagnosed on Prenatal Fetal Ultrasound
• Case Report: Prenatal diagnosis of fetal tetrasomy 9p initially identified by non-invasive prenatal testing
• Clinical diversity and molecular mechanism of VPS35L-associated Ritscher-Schinzel syndrome
• Clinical features and genetic analysis of Dandy-Walker syndrome
• Congenital melanocytic naevus syndrome and Dandy-Walker malformation - a mistaken association: case report and literature review
• Congenital Melanocytic Nevi Syndrome With Leptomeningeal Melanoma
• Corpus callosum disorders and associated malformations in paediatric epilepsy: MRI analytic study
• Dandy-Walker Malformation
• Dandy-Walker Malformation
• Dandy-Walker malformation and variants: clinical features and associated anomalies in 28 affected children-a single retrospective study and a review of the literature
• Dandy-Walker malformation associated with extracranial abnormalities in a newborn
• Dandy-Walker malformation in methylmalonic acidemia: a rare case report
• Dandy-Walker Malformation with Neonatal Meningitis: A Case Report
• Dandy-Walker Phenotype with Brainstem Involvement: 2 Distinct Subgroups with Different Prognosis
• Dandy-Walker syndrome associated with a giant occipital meningocele: A case report and a literature review
• Dandy-Walker syndrome with bilateral choanal atresia: A case report
• Dandy-Walker Syndrome: Delayed Acute Presentation With Unusual Symptoms
• Dandy-Walker Variant Associated with Bilateral Congenital Cataract
• Death of female infant with Dandy-Walker syndrome after head injury due to abuse: A case report
• Delineating the CCDC22-related Ritscher-Schinzel syndrome phenotype in the original family
• Detection of digynic triploidy in a second-trimester fetus presenting syndactyly, relative macrocephaly, intrauterine growth restriction, cardiomegaly, pericardial effusion, Dandy-Walker malformation, double bubble sign and single umbilical artery on pren
• Diagnosis and Treatment of Dandy-Walker Syndrome With Two Types of Ventriculoperitoneal (VP) Shunts: A Case Report
• Double Aneuploidy of Down Syndrome (Trisomy 21) and Jacobs Syndrome (Trisomy XYY) with Complete Tracheal Rings Deformity: Case Report and Literature Review
• Endoscopic ultrasonic aspiration of posterior fossa abscess in Dandy-Walker malformation: case report
• Evidence of disrupted rhombic lip development in the pathogenesis of Dandy-Walker malformation
• Expanding the phenotypic spectrum and clinical severity associated with WLS gene
• Expanding the phenotypic spectrum of MPDZ gene variants: A case report with prenatally detected Dandy-Walker malformation and single ventricle heart
• Expanding the pre- and postnatal phenotype of WASHC5 and CCDC22 -related Ritscher-Schinzel syndromes
• Family-base rare variant association analysis in Saudi Arabian hydrocephalus subjects using whole exome sequencing
• Fetal and neonatal outcomes of posterior fossa anomalies: a retrospective cohort study
• Fetal brain arrest broadens the spectrum of WDR81-related developmental brain malformations
• Further Evidence of a Continuum in the Clinical Spectrum of Dominant <em>PIEZO2</em>-Related Disorders and Implications in Cerebellar Anomalies
• G9a inactivation in progenitor cells with Isl1-Cre with reduced recombinase activity models aspects of Dandy-Walker complex
• Generalized Verrucosis on a Background of 3C Syndrome Treated With Subcutaneous IgG Supplementation
• Genetics and Molecular Pathogenesis of Human Hydrocephalus
• GWASs and polygenic scores inherit all the old problems of heritability estimates
• Homozygosity for a novel missense variant of RPGRIP1L causing Joubert syndrome with renal defects in a family of Chinese descent
• How to differentiate PHACES syndrome from Blake's pouch cyst in first half of pregnancy
• Identification of a 5 bp duplicate in the AP1S2 gene of an individual with X-linked intellectual disability
• Incidental Presentation of Dandy Walker Variant in 66 Year Male Patient
• Indirect causes of maternal deaths (except stroke, cardiovascular diseases and infections) in France 2016-2018
• Indirects causes of maternal deaths (except stroke, cardiovascular diseases and infections) in France 2016-2018
• Intrauterine ultrasound phenotyping, molecular characteristics, and postnatal follow-up of fetuses with the 15q11.2 BP1-BP2 microdeletion syndrome: a single-center, retrospective clinical study
• Joubert-Plus syndrome with an atretic cephalocele: a case report
• Keratitis-ichthyosis-deafness syndrome: A comprehensive review of cutaneous and systemic manifestations
• Lateral ventricle pleomorphic xanthoastrocytoma concurrent with Dandy-Walker complex: A case report
• Magnetic resonance imaging of Joubert syndrome associated with Dandy-Walker malformation: pathognomonic imaging
• Meckel-Gruber syndrome together with Dandy-Walker malformation: an atypical case report of a 2nd recurrence in a consanguine marriage
• Meticulous and Early Understanding of Congenital Cranial Defects Can Save Lives
• Nanopore long-read sequencing analysis reveals ZIC1 dysregulation caused by a de novo 3q inversion with a breakpoint located 7 kb downstream of ZIC1
• Neurosurgical intervention for the Meckel-Gruber Syndrome: A systematic review
• NID1-related autosomal dominant Dandy-Walker malformation with occipital cephalocele in three generations
• Not Dandy Walker variant: a review of prominent retrocerebellar CSF space in children
• Novel association of Dandy-Walker malformation with CAPN15 variants expands the phenotype of oculogastrointestinal neurodevelopmental syndrome
• Occipital encephalocele associated with Dandy-Walker malformation: a case-based review
• Ocular manifestations in a patient with Dandy-Walker malformation: A case report
• Pathogenic/likely pathogenic copy number variations and regions of homozygosity in fetal central nervous system malformations
• PHACE syndrome: not always 'tilting telephones' and Dandy-Walker malformations
• PHACE syndrome: not always 'tilting telephones' and Dandy-Walker malformations…
• PHACE(S) SYNDROME - EARLY DIAGNOSTICS IN THE MAXILLOFACIAL AREA
• Prenatal diagnosis of distal 13q deletion syndrome in a fetus with esophageal atresia: a case report and review of the literature
• Prenatal diagnosis of Emanuel syndrome - case series and review of the literature
• Prenatal diagnosis of fetuses with Emanuel syndrome: Results of ultrasound examination and invasive genetic testing
• Prenatal diagnosis of the Dandy-Walker malformation associated with partial trisomy 12p and distal 15q deletion
• Prenatal diagnosis of vermian cyst: a new type of posterior fossa cyst
• Propranolol for the Treatment of Hemangioma in PHACE Syndrome: A Case Report
• Propranolol Treatment for Facial Hemangioma in a Patient with Dandy-Walker Malformation and PHACE Syndrome: A Case Report
• Refining the Neuroimaging Definition of the Dandy-Walker Phenotype
• Refractory psychiatric symptoms and seizure associated with Dandy-Walker syndrome: A case report and literature review
• Regional brain development in fetuses with Dandy-Walker malformation: A volumetric fetal brain magnetic resonance imaging study
• Relative prevalence and outcome of fetal posterior fossa abnormality
• Revisiting Dandy-Walker Malformation with Associated Neurofibromatosis
• Severe cerebellar malformations in mutant mice demonstrate a role for PDGF-C/PDGFRα signalling in cerebellar development
• Severe coarctation of the aorta, developmental delay, and multiple dysmorphic features in a child with SMAD6 and SMARCA4 variants
• Short Report: Clinical Features and Epilepsy Monitoring in an Adult With 22q11.2 Deletion Syndrome
• Short- and Long-Term Outcomes of Prenatally Diagnosed Dandy-Walker Malformation, Vermian Hypoplasia, and Blake Pouch Cyst
• Somatic variation as an incidental finding in the pediatric next-generation sequencing era
• Speech and Language Delays Associated With New-Onset Seizures Revealing Dandy-Walker Variant
• The First 50 Years of Postnatal Neurogenesis in the Cerebellum: a Long Journey Across Phenomena, Mechanisms, and Human Disease
• The Management of Hydrocephalus in Midline Posterior Fossa Cystic Collections: Surgical Outcome From a Retrospective Single-Center Case Series of 54 Consecutive Pediatric Patients
• The RRAS2 pathogenic variant p.Q72L produces severe Noonan syndrome with hydrocephalus: A case report
• Trigeminal neuralgia caused by Dandy-walker malformation: A case report and systematic review of the literature
• Trigeminal Neuralgia in a Case of Dandy Walker Malformation: An Unusual Association
• Two case reports of KBG syndrome with Dandy-Walker variant
• Undifferentiated psychosis or schizophrenia associated with vermis-predominant cerebellar hypoplasia
• Unveiling Dandy-Walker syndrome: A surprising twist in the tale of acute hydrocephalus and Down syndrome child