Copertina

Neuroimaging Findings and Risk Factors for Brain Injury in Foetuses Treated for Anaemia

Fuente: Wiley Open Access

Salvato in:

Dettagli Bibliografici
Autori principali:	Laurence Sophie Carmant, Carlos Robles, Seungwoo Lee, Prakesh S. Shah, Greg Ryan, Elka Miller, Shiri Shinar
Natura:	Artículo Open Access
Pubblicazione:	Wiley 2026
Soggetti:	Prenatal Diagnosis
Accesso online:	Acceder al recurso
Tags:	Aggiungi Tag Nessun Tag, puoi essere il primo ad aggiungerne!!

Documenti analoghi

Brain Abnormalities in Prenatally Diagnosed Rubinstein‐Taybi Syndrome
di: Laurence S. Carmant, et al.
Pubblicazione: (2025)

Occipital Cephalocele, Polymicrogyria, Ocular Anomaly and Vermian Dysplasia: Prenatal Markers for Knobloch Syndrome
di: Laurence Sophie Carmant, et al.
Pubblicazione: (2025)

Prenatal and Perinatal Outcomes in Fetuses With Macrocystic Congenital Pulmonary Airway Malformations: Thoracoamniotic Shunting Versus Expectant Management
di: Laurence Sophie Carmant, et al.
Pubblicazione: (2026)

Fetal Endoscopic Tracheal Occlusion (FETO) for Left and Right Congenital Diaphragmatic Hernia in Canada
di: Yada Kunpalin, et al.
Pubblicazione: (2025)

KIDINS220 Variant Associated With Hypoplasia of the Corpus Callosum and Aqueduct Stenosis
di: Kimia Ghannad‐Zadeh, et al.
Pubblicazione: (2025)

Associations and outcomes of prenatally detected rhombencephalosynapsis
di: Yada Kunpalin, et al.
Pubblicazione: (2024)

Prenatal Diagnosis to Postnatal Outcomes of Saccular Forms of Closed Spina Dysraphism: A Single Center Retrospective Study
di: Yada Kunpalin, et al.
Pubblicazione: (2025)

Deep‐learning computer vision can identify increased nuchal translucency in the first trimester of pregnancy
di: Bhavya Kasera, et al.
Pubblicazione: (2024)

Fetal Macrocephaly: Prenatal Findings and Follow‐Up in Cases With High Risk for Abnormal Outcome
di: Hadas Miremberg, et al.
Pubblicazione: (2025)

Risk Factors for Adverse Outcome in Fetuses With Heterotaxy Syndrome and Congenital Heart Disease
di: Anita Szwast, et al.
Pubblicazione: (2026)

Diagnostic Yield of Serial PR Interval Screening for Fetal Heart Block in Anti‐SSA/SSB Pregnancies
di: Alyssa Yeung, et al.
Pubblicazione: (2026)

Response to Commentary on “Virtual Reality Simulation in Teaching Fetoscopic Laser Placental Photocoagulation in Twin‐To‐Twin Transfusion Syndrome”
di: Catherine Windrim, et al.
Pubblicazione: (2026)

Early‐Onset Macrosomia, Advanced Brain Maturation, and Gonadoblastoid Testicular Dysplasia in a Fetus With a PTEN Variant
di: Danielle C. Lynch, et al.
Pubblicazione: (2025)

Lung Growth and Intrapulmonary Circulation in Fetuses With Anhydramnios Due to Severe Renal Anomalies Treated With Serial Amnioinfusions
di: Edgar Hernandez‐Andrade, et al.
Pubblicazione: (2025)

Placental and Fetal Brain Volumes in Congenital Heart Disease Are Smallest Among Fetuses With Genetic Abnormalities
di: Sonali Ajwani, et al.
Pubblicazione: (2025)

Parental Management Choices and Discordant Ultrasound Findings in Referrals for Fetal Spina Bifida
di: Emma Van den Eede, et al.
Pubblicazione: (2024)

Foetal Persistent Left Superior Vena Cava—Not Always a Benign Finding?
di: Nadezhda Dzhelepova, et al.
Pubblicazione: (2026)

Postnatal Outcome After Ultrasound Findings of an Abnormal Fetal Gallbladder: A Systematic Review and Meta‐Analysis
di: Desislava Markova, et al.
Pubblicazione: (2024)

Parental or Trio Magnetic Resonance Imaging to Improve Prenatal Counseling in Brain Anomalies
di: Carlota Rodó, et al.
Pubblicazione: (2024)

Aberrant Fetal Brain Sulcus Formation: A Clue to the Diagnosis of Sotos Syndrome
di: Caiqun Luo, et al.
Pubblicazione: (2024)

Prenatal Diagnosis of Conotruncal Anomalies Before 16 Weeks: Longitudinal Evolution, Genetic Findings and Early Prognostic Markers
di: Paolo Volpe, et al.
Pubblicazione: (2026)

Incidental Findings Identified by Prenatal Microarray Analysis and Consensus Reporting Criteria of the Catalan Public Health Network XIGENICS
di: Irene Mademont‐Soler, et al.
Pubblicazione: (2025)

Persistent Uninterpretable or Failed Prenatal Cell‐Free DNA Screening Indicates a High‐Risk Pregnancy and is Associated With Biological Factors Interfering With cfDNA‐Analysis: A Prospective Cohort Study
di: L. Lannoo, et al.
Pubblicazione: (2025)

Contemporary Outcomes of a National Fetal Spina Bifida Surgery Service
di: Charlotte C. Kik, et al.
Pubblicazione: (2024)

Prenatal Diagnosis of Arthrogryposis Multiplex Congenita (AMC): Ultrasound and Genetic Findings in 69 Fetuses From 67 Unrelated Families
di: Tingting Yao, et al.
Pubblicazione: (2026)

A de novo WBP11 Pathogenic Variant in a Fetus With Cystic Brain Malformation and Growth Restriction
di: Gulvir Gill, et al.
Pubblicazione: (2025)

The Association of Prenatal Alcohol Exposure With Brain Development During the First 1000 Days of Life: A Systematic Review
di: Marin Pielage, et al.
Pubblicazione: (2024)

Hypertrophic Cardiomyopathy as a Key Feature of MRAS‐Related Noonan Syndrome: New Case and Comprehensive Literature Review
di: Romain Martineau, et al.
Pubblicazione: (2026)

Acute fetal leukemia: When should it be suspected? What assessment should be performed? A case series and review of literature
di: Pierre‐Louis Forey, et al.
Pubblicazione: (2024)

Follow‐Up of Infants With Congenital Cytomegalovirus Following Maternal Primary Infection in the First Trimester and Normal Fetal Brain Imaging at Midgestation
di: Anna Seidenari, et al.
Pubblicazione: (2024)

Women's attitudes towards disclosure of genetic information in pregnancy with varying levels of penetrance
di: Vitalia Libman, et al.
Pubblicazione: (2024)

Risk of Genetic Abnormality in Fetuses With Unilateral Versus Bilateral Pleural Effusions
di: Brian Burnett, et al.
Pubblicazione: (2024)

Theoretical Performance of Comprehensive Non‐Invasive Prenatal Screening in Congenital Heart Defects
di: Emily Yang, et al.
Pubblicazione: (2026)

Fetal Sylvian Fissure Maturation in Congenital Heart Disease and Its Relation to Expected Brain Arterial Oxygen Saturation: A Longitudinal Study
di: Xiaowei Xiong, et al.
Pubblicazione: (2026)

A Prenatal Case of Focal Dermal Hypoplasia With Split Hand/Foot Malformation, Lack of Characteristic Skin Findings, Renal Agenesis, and Coloboma Due To a Novel PORCN Variant
di: Molly Jackson, et al.
Pubblicazione: (2025)

Fetal Pancreas in Growth Restriction: A Prenatal Window Into Metabolic and Genetic Risk
di: Hadas Miremberg, et al.
Pubblicazione: (2025)

A Novel Homozygous Frameshift Variant in the FLVCR1 Gene Is Associated With Prenatal Microcephaly, Multiple Brain Structural Anomalies, and Abnormal Foot Posture
di: Jing Chen, et al.
Pubblicazione: (2025)

Very elevated hCGβ (≥10 multiple of the median) in maternal marker screening for Down syndrome: Frequency, etiologies, outcomes, and guidelines
di: Sophie Dreux, et al.
Pubblicazione: (2024)

Prenatal Phenotypic Expansion: A Fetus With Neurodegeneration With Developmental Delay, Early Respiratory Failure, Myoclonic Seizures, and Brain Abnormalities (NDDRSB) and MED11 Variants
di: Cong Zhou, et al.
Pubblicazione: (2024)

Amniocentesis and Risk of Fetal Loss in Dichorionic‐Diamniotic Twin Pregnancy: A Case‐Control Study
di: Sofia Roero, et al.
Pubblicazione: (2025)