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Case Reports in Pediatrics|May 31, 2014
Troubling toys: rare-Earth magnet ingestion in children causing bowel perforationsParkash Mandhan, Muthana Alsalihi, Saleem Mammoo, et al.Case Reports in Pediatrics|April 5, 2021
A 6-Year-Old Boy with COVID-19-Positive Pleural Effusion and Kawasaki-Like FeaturesSedigheh Yousefzadegan, Ramin Zare Mahmoudabadi, Golnaz GharehbaghiCase Reports in Pediatrics|August 11, 2020
Delayed Presentation of Congenital Diaphragmatic Hernia with Acute Respiratory Distress: Challenges in Diagnosis and ManagementKam Lun Hon, Ronald C M Fung, Alexander K C LeungCase Reports in Pediatrics|October 10, 2022
Thanatophoric Dysplasia: A Report of 2 Cases with Antenatal MisdiagnosisLamidi Audu, Amina Gambo, Tokan Silas Baduku, et al.Case Reports in Pediatrics|November 4, 2022
Identification of a New Variant of the MBTPS1 Gene of the Kondo-Fu Type of Spondyloepiphyseal Dysplasia (SEDKF) in a Saudi PatientMaha Alotaibi, Ali Aldossari, Imran Khan, et al.Case Reports in Pediatrics|June 5, 2024
Airway Management for Massive Anterior Mediastinal Tumor Resection in an Infant: A Strategy Involving Spontaneous Breathing-Preserving Endotracheal Intubation under Intravenous AnesthesiaHiromi Matsuda, Ei Ito, Akiko Katsuike, et al.Case Reports in Pediatrics|October 9, 2023
Striatal Lacunar Infarction in a Late Preterm Infant Born to a Mother with Active Peripartum SARS-CoV-2 InfectionChristoph Hochmayr, Marlene Hammerl, Ira Winkler, et al.Case Reports in Pediatrics|October 27, 2023
Duodenogastric Intussusception in a 14-Week-Old Infant with Donohue Syndrome: Case StudyCorina Ramona Nicolescu, Clara Cremillieux, Jean-Louis StephanCase Reports in Pediatrics|January 2, 2019
Novel HAX1 Gene Mutation in a Vietnamese Boy with Severe Congenital NeutropeniaTham Thi Tran, Quang Van Vu, Taizo Wada, et al.Case Reports in Pediatrics|September 10, 2020
Brain and Cardiac Concomitant Localization of the Hydatid CystAmal El Ouarradi, Sara Oualim, Ilham Bensahi, et al.Pageof 115