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

