congenital-anomalies

Documents about congenital-anomalies

• Co‐Occurring Non‐Cardiac Congenital Anomalies Among Cases With Congenital Heart Defects#218177HAL (France)
• Ultrasound Localization Microscopy in Patient With Congenital Anomalies of the Kidney and Urinary Tract (CAKUT)#912739ClinicalTrials.gov
• The Alberta Congenital Anomalies Surveillance System: a 40-year review with prevalence and trends for selected congenital anomalies, 1997–2019#20100DOAJ
• Sex differences in global burden of Congenital Heart Anomalies in children under five from 1990 to 2021#158310PLOS
• Tramadol During Pregnancy: Risk of Adverse Pregnancy Outcome and Major Congenital Anomalies. A Comparative Study in the EFEMERIS Database#137522HAL (France)
• A Study of a Renal Autologous Cell Therapy (REACT) in Patients With Chronic Kidney Disease (CKD) From Congenital Anomalies of the Kidney and Urinary Tract (CAKUT).#208336ClinicalTrials.gov
• Congenital Uterine Anomalies: Identifying Cancer Associations and Genetic and Environmental Factors to Improve Clinical Care#841647ClinicalTrials.gov
• Teratogenicity of antiepileptic drugs#954917Koc University Digital Collections
• Risk of major congenital anomalies and beta‐blockers: A comparative study from the EFEMERIS database#129376HAL (France)
• A Prospective Registry of Patients With Congenital Penile Anomalies#848210ClinicalTrials.gov
• Genetic Modifiers for 22q11.2 Syndrome#802405ClinicalTrials.gov
• Experiences of family caregivers regarding the health of children with congenital craniofacial anomalies in Colombia#201585bioRxiv / medRxiv
• Disrupted endosomal trafficking of the Vangl-Celsr polarity complex underlies congenital anomalies in Xenopus trachea-esophageal morphogenesis.#221028NCBI PubMed Central
• Weaning From Mechanical Ventilation After Pediatric Cardiac Surgery#862841ClinicalTrials.gov
• Genetic Studies of Strabismus, Congenital Cranial Dysinnervation Disorders (CCDDs), and Their Associated Anomalies#840889ClinicalTrials.gov
• Impact of cannabis and cannabis legalization on US atrial septal defect rates#270322Research Online
• Sex differences in global burden of Congenital Heart Anomalies in children under five from 1990 to 2021#161661Unpaywall
• Congenital central nervous system malformations in piedmontese calves—part 1. structural brain disorders#284513IRIS
• Ultrasonography in Children With First Febrile Urinary Tract Infection#883588ClinicalTrials.gov
• Evaluating Prenatal Exome Sequencing Study#891605ClinicalTrials.gov
• Beyond associations: Navigating the safety of non-steroidal anti-inflammatory drugs (NSAIDs) in early pregnancy#258685PLOS
• Evaluating a family-centered care intervention for reducing post-traumatic stress and aggression among parents of infants with congenital anomalies: a randomized controlled trial.#13815NCBI PubMed Central
• Survival disparities and competing mortality risks in offspring of consanguineous marriages in Yemen: A 26-year retrospective cohort analysis#240414PLOS
• PUF60-related developmental disorder: A case series and phenotypic analysis of 10 additional patients with monoallelic PUF60 variants#647520Repositorio Universidad del Desarrollo
• Genetic Analysis of PHACE Syndrome (Hemangioma With Other Congenital Anomalies)#850991ClinicalTrials.gov
• Variants in ZFX are associated with an X-linked neurodevelopmental disorder with recurrent facial gestalt#301127HAL (France)
• A Study of the Value of Trio Genome Sequencing in the Etiological Evaluation of Early-Onset and/or Atypical Psychiatric Disorders Without Intellectual Disability or Congenital Anomalies#861921ClinicalTrials.gov
• Expanding congenital abnormalities of the kidney and urinary tract (CAKUT) genetics: basonuclin 2 (BNC2) and lower urinary tract obstruction#955707Koc University Digital Collections
• Endoglin Deficiency Impairs Stroke Recovery#634742eScholarship
• Association between phenotype and deletion size in 22q11.2 microdeletion syndrome: Systematic review and meta-analysis#947739Repositorio de Universidad Autónoma de Chile.
• Management and outcomes of gastrointestinal congenital anomalies in low, middle and high income countries: protocol for a multicentre, international, prospective cohort study#955843Koc University Digital Collections
• Genetic analysis of non‐syndromic craniosynostosis#970656eScholarship
• PTH treatment is effective in the Aga2/+ mouse model of moderate to severe osteogenesis imperfecta#922240eScholarship
• Dental, Oral, and Craniofacial Regenerative Medicine: Transforming Biotechnologies for Innovating Patient Care#780509eScholarship
• A novel DPH5-related diphthamide-deficiency syndrome causing embryonic lethality or profound neurodevelopmental disorder#784289eScholarship
• Intratracheal Umbilical Cord-derived Mesenchymal Stem Cells for Severe Bronchopulmonary Dysplasia#857185ClinicalTrials.gov
• Basal Dendritic Morphology of Cortical Pyramidal Neurons in Williams Syndrome: Prefrontal Cortex and Beyond#492102eScholarship
• National Analysis of Secular Trends and Racial Disparities in Age at Kasai Hepatoportoenterostomy for Infants with Biliary Atresia, 2005-2025#634650eScholarship