Zobrazeno 1 - 10
of 117
pro vyhledávání: '"Benjamin Zendejas"'
Autor:
Benjamin Zendejas
Publikováno v:
Jornal de Pediatria, Vol 100, Iss 3, Pp 227-228 (2024)
Externí odkaz:
https://doaj.org/article/a1ae2b7f2adc4c46ae609a7860fbdeb6
Autor:
The International EA-QOL Group, Michaela Dellenmark Blom, Stefanie Witt, Benjamin Zendejas, Ivana Sabolić, Juan Domingo Porras-Hernandez, Natalie Durkin, Simon Eaton, Kjersti Birketvedt, Alba Sánchez Galán, Katalin Eszter Müller, Anna Rozensztrauch, Tutku Soyer, Siqi Li, Anastasia Fourtaka, Corne de Vos, Graham Slater, Ana Špoljarić, John Bennett, Ragnhild Emblem, Zita Andrásdi, Robert Smigiel, Dariusz Patkowski, Çiğdem Ulukaya Durakbaşa, Marina Stilinović, Frederic Gottrand, Dora Škrljak Šoša, Tomislav Luetić, Sylwester Gerus, Shen Yang, Yong Zhao, Yichao Gu, Shuangshuang Li, Diego Rodriguez-Alvirde, Orsolya Kadenczki, Miram Pasini, Vuokko Wallace, Anke Widenmann, Feliciana Milagres Sikwete, Jinshi Huang, Leopoldo Martínez Martínez, Kate Abrahamsson, Shawn Izadi, Benno M Ure, Daniel Sidler, Julia H Quitmann, Jens Dingemann
Publikováno v:
Frontiers in Pediatrics, Vol 11 (2023)
BackgroundEsophageal atresia (EA) is a rare congenital anomaly characterized by a discontinuity of the esophagus. Following surgical repair, survival rates have improved dramatically the past decenniums and today exceed 90%, but the children commonly
Externí odkaz:
https://doaj.org/article/4829ecacbcbb4ffebab6b964fbec1314
Autor:
Christine Finck, Benjamin Zendejas, J. Leslie Knod, Peter J. Tramontozzi, Dana Jungbauer, Megan Anderson, William Middlesworth, Stefan Scholz, Shaun M. Kunisaki
Publikováno v:
Journal of Pediatric Surgery Open, Vol 3, Iss , Pp 100029- (2023)
Background: Less than 10% of infants born with esophageal atresia (EA) have a long gap that precludes primary anastomosis at birth. The purpose of this study was to evaluate the diagnosis, management, and outcomes of infants with long-gap esophageal
Externí odkaz:
https://doaj.org/article/d17c123563884a839b2155398e5c9de8
Autor:
Maximiliano Servin-Rojas, Antonio Olivas-Martinez, Michelle Dithurbide-Hernandez, Julio Chavez-Vela, Vera L. Petricevich, Ignacio García-Juárez, Alice Gallo de Moraes, Benjamin Zendejas
Publikováno v:
BMC Medical Education, Vol 22, Iss 1, Pp 1-8 (2022)
Abstract Background The COVID-19 pandemic has brought unprecedented changes to medical education. However, no data are available regarding the impact the pandemic may have on medical training in Mexico. The aim of our study was to evaluate and identi
Externí odkaz:
https://doaj.org/article/5eb0a5f1bff94e04b9ceaab0aabd0a9c
Autor:
Devon Michael Evanovich, Anne O'Donnell-Luria, Benjamin Zendejas, Dusica Bajic, Jue Teresa Wang
Publikováno v:
Journal of Pediatric Surgery Case Reports, Vol 87, Iss , Pp 102478- (2022)
CHARGE syndrome (Coloboma, Heart defect, Atresia of the choanae, growth Retardation, Genital abnormalities, Ear anomalies/deafness) is a rare genetic autosomal dominant disease with a prevalence of 1/10,000 live births. It is associated with pathogen
Externí odkaz:
https://doaj.org/article/d64e9c0b333e4c71b07387b2ce913fa0
Autor:
Devon Michael Evanovich, Jue Teresa Wang, Benjamin Zendejas, Russell William Jennings, Dusica Bajic
Publikováno v:
Frontiers in Surgery, Vol 9 (2022)
Esophageal atresia (EA), although a rare congenital anomaly, represents one of the most common gastrointestinal birth defects. There is a gap in our knowledge regarding the impact of perioperative critical care in infants born with EA. This study add
Externí odkaz:
https://doaj.org/article/9dab86e0aa344a76aaf24665189b8d73
Publikováno v:
Journal of Pediatric Surgery Case Reports, Vol 77, Iss , Pp 102147- (2022)
Tracheal duplication cysts are extremely uncommon, with only a few cases reported in the literature. In some cases, symptoms are ambiguous or absent, making the diagnosis challenging. Due to its rarity, there are no formal guidelines on the managemen
Externí odkaz:
https://doaj.org/article/15c597fd96b54064842b9835bf89e509
Autor:
Osama Baghdadi, Susannah Clark, Peter Ngo, Jessica Yasuda, Steven Staffa, Benjamin Zendejas, Thomas Hamilton, Russell Jennings, Michael Manfredi
Publikováno v:
Frontiers in Pediatrics, Vol 9 (2021)
Background and Aims: Children with esophageal atresia (EA) who undergo surgical repair are at risk for anastomotic stricture, which may need multiple dilations or surgical resection if the stricture proves refractory to endoscopic therapy. To date, n
Externí odkaz:
https://doaj.org/article/baa1cb04a2474e4a96e200959cb56428
Autor:
Claire M. Lawlor, Benjamin Zendejas, Christopher Baird, Carlos Munoz-San Julian, Russell W. Jennings, Sukgi S. Choi
Publikováno v:
Frontiers in Pediatrics, Vol 8 (2020)
Objective: Review techniques for intraoperative recurrent laryngeal nerve (RLN) monitoring during pediatric surgery for esophageal atresia, tracheoesophageal fistula, tracheobronchomalacia, and cardiac surgery.Summary Background Data: Literature was
Externí odkaz:
https://doaj.org/article/2b6432deb06845f28706a06eb588fafd
Publikováno v:
Journal of Pediatric Surgery Case Reports, Vol 34, Iss C, Pp 41-44 (2018)
Introduction: Gastro-jejunostomy tubes (GJT) are commonly used for enteral nutrition in patients with gastric feeding intolerance, gastroesophageal reflux, and those at high risk of aspiration. Complications are generally minor, however highly morbid
Externí odkaz:
https://doaj.org/article/99c0889b54e24922afec63a755e538d1