Defects
- 3D/4D based spatio: temporal image correlation during routine fetal anomaly scan  
- A case of acondrodysplasia punctata  
- A case of Antley-Bixler syndrome  
- A case of appendiceal perforation in a fetus with trisomy 21  
- A case of Apple-peel atresia with familial duodenal atresia  
- A case of central nervous system anomaly: syntelencephaly  
- A case of complex cardiac anomaly in a case of 22q11.2 deletion syndrome  
- A case of congenital pulmonary airway malformation  
- A case of fetal brain tumor in a dichorionic twin pregnancy  
- A case of fetal cardiac rhabdomyoma and tuberous sclerosis complex  
- A case of fetal goiter: prenatal diagnosis, intrauterine treatment and follow up  
- A case of fetal ovarian cyst  
- A case of first trimester diagnosis of Meckel–Gruber syndrome  
- A case of horseshoe kidney: ultrasound findings and difficulties in diagnosis  
- A case of intracranial mass  
- A case of isolated bladder exstrophy  
- A case of Joubert syndrome with occipital encephalocele: phenotypic and genotypic correlation  
- A case of left ventricular diverticulum  
- A case of microlissencephaly  
- A case of non-immune hydrops with an underlying AARS2 gene mutation  
- A case of oculo-auriculo-vertebral spectrum or Goldenhar syndrome  
- A case of Osteogenesis imperfecta with overalap of Ehlers-Danlos syndrome  
- A case of periventricular nodular heterotopia  
- A case of reversal of heart failure after use of sirolimus in a fetal rhabdomyoma  
- A case of right aortic arch with aberrant left subclavian artery  
- A case of severe left atrium dilatation with left atrium appendage aneurysm  
- A case of spontaneously resolved cystic hygroma  
- A case of syndromic bladder exstrophy  
- A case of term anencephaly: ethical dilemma  
- A case of thanatophore dwarfism  
- A case of umbilical cord hemangioma: association with chorioamnionitis  
- A case of univentricular heart  
- A case of vein of Galen malformation: evaluation and management  
- Abdominal wall defects: prenatal diagnosis, management and perinatal outcomes  
- Aberrant right subclavian artery: chromosomal aberrations and the cell-free DNA  
- Adverse obstetric outcomes in pregnancies with major fetal congenital heart defects  
- Analysis of optimal three-port workspace for in-utero robotic fetoscopic repair of open spina bifida  
- Antenatal microcoil embolisation of giant chorioangioma: exploring the prospects  
- Antenatal Parallel Planning in Fetal Medicine: Hoping for the best but planning for the worst  
- Arachnoid cysts: does the location predicts postnatal outcomes?  
- Association of placental umbilical cord insertion site and perinatal outcomes  
- Case reports of congenital heart block associated with maternal anti-SSA/SSB antibodies  
- Case reports of cystic hygroma  
- Case series of aneurysmal malformation of the vein of Galen  
- Case series of first trimester fetal micrognathia  
- Cerebellar vermis at 12–22 weeks of gestation: why is traditional assessment incorrect?  
- Chorioangioma: challenges in clinical management  
- Choroid plexus of the fourth ventricle in first- and second-trimester fetuses  
- Clinical Implementation of first trimester screening for congenital heart defects  
- Comparison of sonographic findings and postnatal phenotype in upper limb anomalies  
- Congenital diaphragmatic hernia treated by fetal endoscopic tracheal occlusion  
- Congenital diaphragmatic hernia: prenatal diagnosis and neonatal outcomes in South America  
- Congenital pulmonary airway malformation: prenatal diagnosis, management, and perinatal outcomes  
- Congenital small bowel obstruction: accuracy of prenatal detection and postnatal outcome  
- Contribution of fetal autopsy after termination of pregnancy  
- Cord blood cardiovascular biomarkers in tetralogy of Fallot and D-transposition of great arteries  
- D-Transposition of the great arteries with restrictive foramen ovale in the fetus  
- Detection of fetal structural defects in the first trimester: protocol and new markers  
- Determination of fetal cardiac situs  
- Development of a LUTO training model for vesicoamnial shunting using 3D printing technology  
- Diastematomyelia: antenatal associations and postnatal outcomes  
- Diffusion tensor imaging of the fetal spinal cord  
- Dimensions of hysterotomy for fetal spina bifida repair determines prematurity risk  
- Early detection of major congenital heart diseases  
- Early neurosonography: diagnosis of holoprosencephaly before 10 weeks using 3D HDlive Silhouette  
- Echogenic bowel: a retrospective evaluation of associated findings  
- Effect of premature placental aging: maternal and fetal outcomes  
- Enhanced recovery after fetal spina bifida surgery: what is our global practice?  
- Establishment of a nomogram for ultrasound assessment of fetal thoracic dimensions  
- Evaluation of hepatobiliary system among fetuses with major congenital anomalies  
- Evaluation of non-immune hydrops fetalis diagnosed in the first trimester with postnatal follow up  
- Ex utero intrapartum treatment experience for fetal airway obstruction  
- Fetal aortic valvuloplasty for critical aortic stenosis: postnatal outcomes  
- Fetal brain biometry in isolated mega cisterna magna  
- Fetal brain dimensions in congenital diaphragmatic hernia  
- Fetal central nervous system biometry: semi-automated 5D ultrasound vs. standard 2D ultrasound  
- Fetal diffusion tensor imaging in case of short corpus callosum  
- Fetal diffusion tensor imaging to assess normal white and grey matter development  
- Fetal interatrial stent implantation  
- Fetal intraventricular hemorrhage of genetic etiology  
- Fetal megacystis: a comprehensive analysis of associated conditions and underlying causes  
- Fetal oropharyngeal tumor pathology prenatal managment and results  
- Fetal outcomes of non-visualized gallbladder  
- Fetal ovarian cysts  
- Fetal premature atrial contractions: natural course, risk factors and adverse outcomes  
- Fetal umbilical-portal anastomosis and abdominal circumference <10th percentile  
- Fetoplacental vascular reactivity is altered in fetuses with congenital diaphragmatic hernia  
- Fetoscopic endoluminal tracheal occlusion for severe congenital diaphragmatic hernia  
- First trimester shunting for fetal megacystis: initial results of an ongoing prospective trial  
- Gastroschisis outcomes  
- Genetic anomalies diagnosed in a referred series of major congenital heart defects  
- Gestational trophoblastic diseases  
- Hajdu-Cheney syndrome: could it be detected on prenatal ultrasound?  
- How can AI assist sonographers in performing fetal cardiac screening examination?  
- Hydrops fetalis and Down syndrome: ultrasound and prenatal diagnosis in the first trimester  
- Hypoplastic left heart syndrome: a challenge for cardiofetal medicine  
- Impact of diagnosis of congenital heart defects during the third trimester  
- Incidence of an underlying genetic syndromes in children with isolated cleft lip  
- Increasing maternal weight is an independent risk factor for fetal heart defects  
- Intrauterine bowel rupture in a fetus with gastroschisis  
- Is 3D Omniview ultrasound helpful for diagnosis of fetal cleft palate?  
- Is a wide fetal cavum septi pellucidi associated with DiGeorge syndrome?  
- Isolated right-sided congenital diaphragmatic hernia: prenatal MRI assessment of mediastinal shift  
- Maternal cardiovascular disease and pregnancy: a 20-year experience  
- Maternal outcomes after open spina bifida repair: a prospective cohort study of 100 women  
- Motor and urological outcomes following fetal surgery for spina bifida  
- Neonatal 3D face reconstruction using 2D images  
- Neurodevelopment in congenital diaphragmatic hernia survivors  
- Novel insights into fetal spina bifida pathogenesis and maternal gut microbiome  
- Nutrient-sensitive placental gene network dysregulation is associated with spina bifida  
- Olfactory sulci as a marker of genetic disorders  
- Open fetal surgery for myelomeningocele – the 17 years of experience  
- Optimal time of delivery in placenta accreta spectrum  
- Outcome analysis of fetuses with megacystis after intrauterine vesico‑amniotic shunting  
- Outcome of fetuses with corpus callosum or cavum septum pellucidum anomalies  
- Partial agenesis of corpus callosum: case report and review of literature  
- Perforation of the Cavum Septi Pellucidi in Open Spina Bifida: Association with Need for Hydrocephalus Treatment in the First Year of Life  
- Perinatal management of fetal oral tumors  
- Perinatal outcomes in presence the of placental massive perivillous fibrin deposition  
- Periventricular echogenicity in fetuses with haemoglobin Bart’s related hydrops fetalis  
- Placenta bilobata: incidence, risk factors and impact on perinatal outcomes  
- Placental exosome in maternal circulation for the identification of Bart’s hydrops fetalis  
- Posterior fossa malformations: diagnosis and neurodevelopmental outcome  
- Precision medicine in perinatal cardiology: single center experience  
- Prediction for emergency balloon removal after fetoscopic endoluminal tracheal occlusion for congenital diaphragmatic hernia  
- Predictive value of ultrasound in the diagnosis of hydatidiform mole  
- Pregnancy outcome in correlation with prenatal detection of congenital heart disease  
- Prenatal diagnosis and outcomes of congenital ventricular outpouching  
- Prenatal diagnosis and postnatal outcome in fetuses with congenital pulmonary airway malformation  
- Prenatal diagnosis and postnatal outcome in foetuses with ductus venosus abnormalities  
- Prenatal diagnosis of Binder phenotype and their outcomes  
- Prenatal diagnosis of congenital agenesis of portal venous system  
- Prenatal diagnosis of congenital clubfoot: role of genetic testing in isolated cases  
- Prenatal diagnosis of fetal cardiac rhabdomyoma  
- Prenatal diagnosis of rare Aicardi and Anderman syndromes and management tactics  
- Prenatal diagnosis, associations and outcomes of cleft lip and palate  
- Prenatal diagnosis, associations, and outcomes of micrognathia  
- Prenatal diagnostic accuracy of the origin of the fetal intraabdominal cysts  
- Prenatal exome sequencing for apparently isolated agenesis of the corpus callosum  
- Prenatal intracranial hemorrhage: new classification and neurodevelopmental outcome  
- Prenatal ultrasound clinical FAQ: what are the most frequent diagnostic doubts in ultrasound?  
- Pulmonary stenosis: evaluation of global longitudinal strain and mechanical dyssynchrony  
- Role of prenatal next generaition sequencing in the etiological diagnosis of fetal renal dysplasias  
- Scoring system in echogenic kidneys in prediction of outcome  
- Screening for agenesis of the corpus callosum with the use of pattern recognition software  
- Sexual dimorphism of the fetal brain biometry: magnetic resonance imaging based study  
- Short long bones: prenatal ultrasound phenotype  
- Spectrum of cardiac abnormalities in fetuses at 11+0 to 13+6 weeks of gestation  
- Subarachnoid space measurements in fetuses using magnetic resonance imaging  
- Syndromic congenital diaphragmatic hernia: current incidence and outcome  
- Thanatophoric dysplasia diagnosed by clinical exome examination  
- The 11-14 weeks interhemispheric cyst-like midline structure  
- The challenges of prenatal diagnosis – regarding a clinical case  
- The cortical bite sign: a midtrimester sonographic marker of unilateral cortical focal dysplasia  
- The impact of a biocellulose based fetal repair of open spina bifida  
- The normal fetal cavum septum pellucidum in magnetic resonance imaging  
- The third trimester anomaly scan - a hunt for evolving structural abnormalities  
- Therapy for in utero repair of the ovine fetal myelomeningocele model  
- Three-dimensional ultrasound evaluation of lung volume in fetuses with abdominal wall defect  
- Trainee management of emergency placenta accrete  
- Two cases of ductus venosus agenesis  
- Two cases of intra-abdominal arteriovenous fistula in fetuses with trisomy 21  
- Two cases of persistent right umbilical vein  
- Two cases of prenatal diagnosis in fetuses with brain anomalies  
- Ultrasonography and magnetic resonance imaging in the measurements of the fetal brain structures  
- Ultrasound characteristics and postnatal outcomes of congenital pulmonary airway malformations  
- Umbilical cord hernia - a misleading diagnosis  
- Use of exome sequencing in fetuses with complex central nervous system anomalies  
- Utility of 3-dimensional modeling in prenatally diagnosed large fetal neck mass  
- Value of fetopathological examination following therapeutic termination of pregnancy  
- Widening of the femoral proximal diaphysis–metaphysis angle in fetuses with achondroplasia  
