Zobrazeno 1 - 10
of 38
pro vyhledávání: '"Marisa E. Schwab"'
Publikováno v:
Journal of Pediatric Surgery Case Reports, Vol 102, Iss , Pp 102767- (2024)
Introduction: Hemolytic uremic syndrome (HUS) usually presents with mild gastrointestinal symptoms, typically managed medically. We describe 3 patients with challenging clinical presentations diagnosed with colonic perforation, review the literature,
Externí odkaz:
https://doaj.org/article/41c5554b81ed4f9295ff0777b5cce251
Autor:
Marisa E. Schwab, Sophia Hernandez, Sarah Watanaskul, Hueylan Chern, Madhulika Varma, Ankit Sarin
Publikováno v:
BMC Surgery, Vol 22, Iss 1, Pp 1-6 (2022)
Abstract Background Robotic transanal minimally invasive surgery (R-TAMIS) is an appealing alternative to transanal minimally invasive surgery (TAMIS) and transanal endoscopic microsurgery (TEM) for benign and early malignant rectal lesions that are
Externí odkaz:
https://doaj.org/article/c46e1b31a9924bafac0b49d8af18391a
Publikováno v:
BMC Surgery, Vol 22, Iss 1, Pp 1-5 (2022)
Abstract Background Malrotation with bowel ischemia is classically thought of as a disease of infants. However, the true prevalence of malrotation in both the pediatric and adult population is unknown due to the unclear number of asymptomatic patient
Externí odkaz:
https://doaj.org/article/be08308814234c94b15daccfc7cf3d88
Autor:
Marisa E. Schwab, Julia E. H. Brown, Billie Lianoglou, Chengshi Jin, Patricia C. Conroy, Renata C. Gallagher, Paul Harmatz, Tippi C. MacKenzie
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 17, Iss 1, Pp 1-11 (2022)
Abstract Background Lysosomal storage diseases (LSDs) are inherited metabolic disorders that may lead to severe multi-organ disease. Current ERTs are limited by anti-drug antibodies, the blood–brain barrier, and early disease onset and progression
Externí odkaz:
https://doaj.org/article/26b2ae6f02f64042b5ae5b03889d8f10
Autor:
Marisa E. Schwab, Billie R. Lianoglou, Dawn Gano, Juan Gonzalez Velez, Isabel E. Allen, Regina Arvon, Ahmet Baschat, Diana W. Bianchi, Melissa Bitanga, Anne Bourguignon, Richard N. Brown, Bruce Chen, May Chien, Shareece Davis-Nelson, Monique W. M. de Laat, Supachai Ekwattanakit, Yvonne Gollin, Greigh Hirata, Angie Jelin, Jennifer Jolley, Paul Meyer, Jena Miller, Mary E. Norton, Keith K. Ogasawara, Tachjaree Panchalee, Erica Schindewolf, Steven W. Shaw, Tammy Stumbaugh, Alexis A. Thompson, Dena Towner, Pai-Jong Stacy Tsai, Vip Viprakasit, Emmanuel Volanakis, Li Zhang, Elliott Vichinsky, Tippi C. MacKenzie
Publikováno v:
Blood advances, vol 7, iss 2
Alpha thalassemia major (ATM) is a hemoglobinopathy that usually results in perinatal demise if in utero transfusions (IUTs) are not performed. We established an international registry (NCT04872179) to evaluate the impact of IUTs on survival to disch
Autor:
Marisa E. Schwab, Shirley Shao, Li Zhang, Billie Lianoglou, Lisa Belter, Jill Jarecki, Mary Schroth, Charlotte J. Sumner, Tippi MacKenzie
Publikováno v:
Prenat Diagn
Prenatal diagnosis, vol 42, iss 11
Prenatal diagnosis, vol 42, iss 11
ObjectiveIn utero SMA treatment could improve survival and neurologic outcomes. We investigated the attitudes of patients and parents with SMA regarding prenatal diagnosis, fetal therapies, and clinical trials.MethodsA multidisciplinary team designed
Autor:
Sarah Watanaskul, Marisa E. Schwab, Alexis Colley, Hueylan Chern, Madhulika G. Varma, William Y. Hoffman, Ankit Sarin
Publikováno v:
Surgical endoscopy, vol 37, iss 3
Background Perineal hernias can be secondarily acquired following abdominoperineal resection of the rectum. While transabdominal minimally invasive techniques have traditionally used laparoscopy, there are few studies published on the robotic platfor
Autor:
Marisa E. Schwab, Miriam Crennan, Shannon Burke, Helen Sang, Mary Kate Klarich, Roberta L. Keller, Lan T. Vu
Publikováno v:
Dysphagia. 37:1305-1313
Autor:
Stephen Sanders, Billie R. Lianoglou, Tippi C. MacKenzie, Shan Dong, Mary E. Norton, Marisa E. Schwab, Alessandra F. Aguilar Lucero, Grace Schwartz
Publikováno v:
The American Journal of Surgery. 223:182-186
Background To identify genes associated with congenital diaphragmatic hernia (CDH) to help understand the etiology and inform prognosis. Methods We performed exome sequencing on fetuses with CDH and their parents to identify rare genetic variants lik
Autor:
Mara Rosner, Barbara A. Koenig, Sandra Gilbert, Craig Butler, Roberta L. Keller, Mary E. Norton, Tippi C. MacKenzie, Wade Kyono, Billie R. Lianoglou, Alexis A. Thompson, Elliott Vichinsky, Melanie Kirby-Allen, Marisa E. Schwab, John S. Waye, Juan M. Gonzalez, Michael Angastiniotis, Ali Amid, Ashutosh Lal, Tachjaree Panchalee, Keith K. Ogasawara, Sandhya Kharbanda
Publikováno v:
Blood Advances