Results 51 to 60 of about 6,631 (169)

Postoperative and Functional Outcomes of Oropharyngectomy in Irradiated Neck for Recurrent or Metachronous Squamous Cell Carcinoma

Head &Neck, Volume 48, Issue 7, Page 1885-1895, July 2026.
ABSTRACT Objective To evaluate predictors of postoperative and functional outcomes following salvage oropharyngectomy. Methods In this single‐center retrospective study, we included all patients who underwent an oropharyngectomy in an irradiated neck for recurrent or metachronous cancer between 2014 and 2023. Results We included 94 patients.
Jade Saykaly, Agnès Dupret‐Bories, Sébastien Vergez, Virginie Woisard, Benjamin Vairel, Jérôme Sarini, Ana Cavillon, Emilien Chabrillac   +7 more
wiley   +1 more source

From Multiple Congenital Anomalies to Pituitary Gland Malformation: Wide Spectrum of Clinical Features in a Family With FOXA2 Variant

American Journal of Medical Genetics Part A, Volume 200, Issue 6, Page 1452-1457, June 2026.
ABSTRACT FOXA2 (hepatocyte nuclear factor‐3β, HNF‐3β) encodes a transcriptional activator involved in early embryogenesis, particularly in the patterning and differentiation of midline structures such as the neural tube, foregut, and pituitary gland. Its role in human pathogenesis was first suspected when patients with deletion of chromosome 20p11.2 ...
Christopher Connolly, Hemant A. Parmar, Lauren Hipp, Tomoyasu Higashimoto   +3 more
wiley   +1 more source

Anesthesia‐free transoral endoscopy using a novel modified pacifier in early infancy

Journal of Pediatric Gastroenterology and Nutrition, Volume 83, Issue 2, Page 331-334, August 2026.
Jonathan A. Berken, Zoe Rosoff‐Verbit, Tyler Babinski, Matthew J. Ryan, the Transpacifier Endoscopy Research Group, Elizabeth Silvestro, Michael A. Manfredi   +6 more
wiley   +1 more source

Facilitating Genetic Testing for Perinatal Demise: Development of a Multidisciplinary Workflow

American Journal of Medical Genetics Part A, Volume 200, Issue 6, Page 1273-1285, June 2026.
ABSTRACT Genetic contributors to perinatal demise are common but frequently undiagnosed due to clinical and logistical barriers. We aimed to improve access to genetic for intrauterine fetal demise (IUFD), stillbirth, and early neonatal death by developing a multidisciplinary workflow.
Mackenzie Mosera, Samantha Stover, Elise Boos, Molly Casey, Joseph Fanning, Chelsea Fechter, Matthew Grace, L. Dupree Hatch, Michaela Ibach, Carla Jackson, Jiancong Liang, Caitlin Mann, Emily A. Morris, Jessica Turnbull, Marie Williams, Bryce A. Schuler   +15 more
wiley   +1 more source

Determinants of Healthcare Costs in Individuals With Down Syndrome: A Systematic Review

Health Science Reports, Volume 9, Issue 6, June 2026.
ABSTRACT Background Individuals with Down syndrome (DS) require specialized medical follow‐up and services more frequently than the general population, resulting in substantial healthcare costs for families and health systems. This systematic review aimed to synthesize evidence on the magnitude and determinants of direct healthcare and indirect costs ...
Shiva Tolouei Rakhshan, Sarah Byford, Mahya Razimoghadam, Fardin Moradi, Shahin Soltani   +4 more
wiley   +1 more source

A congenital proximal tracheoesophageal fistula 14 years after surgical repair of esophageal atresia with distal tracheoesophageal fistula

The Turkish Journal of Pediatrics, 2008
Congenital esophageal atresia with proximal and distal tracheoesophageal fistula occurs very rarely. This report describes late diagnosis of a congenital proximal fistula in a 14-year-old girl who underwent surgical repair of a congenital ...
Zeynep Tamay, Nermin Güler, Gürkan Kiliç, Feryal Gün, Aleaddin Celik, Ensar Yekeler   +5 more
doaj  

Neurodevelopmental assessment at 24 months in infants with esophageal atresia: A prospective cohort study

Journal of Pediatric Gastroenterology and Nutrition, Volume 82, Issue 6, Page 1386-1393, June 2026.
Abstract Objective To evaluate neurodevelopment at 24 months in infants surgically treated for esophageal atresia (EA), using the ages and stages questionnaire (ASQ), and identify perinatal and early‐life factors associated with developmental delay. Methods Infants with EA were prospectively enrolled in a structured multidisciplinary follow‐up program.
Julia Tagmouti, Manon Midavaine, Victor Sartorius, Nicolas Vinit, Elise Leroy‐Terquem, Sylvie Beaudoin, Elsa Kermorvant‐Duchemin, Véronique Rousseau, Alexandre Lapillonne   +8 more
wiley   +1 more source

Single-stage surgical repair of a preterm neonate with congenital triple atresia: a case report

Journal of Pediatric Surgery Case Reports
Introduction: Congenital triple atresia involving esophageal atresia/tracheoesophageal fistula, duodenal atresia and anorectal malformation is an exceptionally rare association, with limited evidence guiding optimal surgical timing and staging.
Kevin Teerovengadum, Subha Shita Devi Gaya, Kenigen Manikion, Jethishka Motee, Faeza Bibi Soobadar   +4 more
doaj   +1 more source

Esophageal Microperforation due to Calcified Mediastinal Lymph Node Leading to Tracheoesophageal Fistula

Case Reports in Gastrointestinal Medicine, 2016
A 42-year-old male presented with worsening gastroesophageal reflux disease symptoms and cough. The clinical symptoms during the early course of illness were striking for aspiration pneumonia.
Sankalp Dwivedi, E. Brooke Schrickel, Fayez Siddiqui, John O’Brien, James Kruer   +4 more
doaj   +1 more source

Tracheoesophageal Fistula Caused by Tracheostomy in a Patient with Myasthenia Gravis after a Myasthenic Crisis

Frontiers in Neurology, 2017
A 57-year-old woman with myasthenia gravis (MG), who had experienced a myasthenic crisis, complained of coughing while drinking. At first, this appeared to be a sequela of the myasthenic crisis.
Chen Jiaxin, Chen Jiaxin, Li Jingjing, Li Jingjing, Zhu Kai, Zhu Kai, Zhou Zhou, Zhou Zhou, Liu Weibin, Liu Weibin, Wang Haiyan, Wang Haiyan, Feng Huiyu, Feng Huiyu   +13 more
doaj   +1 more source