Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Essam Imseis"'
Publikováno v:
Genetics in Medicine Open, Vol 1, Iss 1, Pp 100027- (2023)
Externí odkaz:
https://doaj.org/article/63f19b99682c4e90a2cf57242b3cbf7e
Autor:
Essam Imseis, Rohit Josyabhatla
Publikováno v:
Seminars in perinatology. 45(6)
Neonatal intestinal failure is a complex medical condition that is associated with the need for long term parenteral nutrition and its associated complications. The microbiome in this diseased state is different from what is now understood to be a he
Autor:
Ashish N. DebRoy, Chad Thornhill, J. Marc Rhoads, Essam Imseis, Fernando Navarro, S. Shahrukh Hashmi
Publikováno v:
Journal of pediatric gastroenterology and nutrition. 72(4)
Autor:
Kevin P. Lally, Robert F. Martin, KuoJen Tsao, Essam Imseis, Marisa A. Bartz-Kurycki, Kathryn T. Anderson, Mary T. Austin, Allison L. Speer
Publikováno v:
The Journal of surgical research. 231
BACKGROUND Parenteral nutrition for intestinal failure (IF) often requires a tunneled central venous catheter (CVC). The purpose of this study was to characterize complications after CVC placement and contributors to line loss in pediatric IF patient
Autor:
Essam Imseis, Chad Thornhill, Fernando Navarro, Baraa Alabd Alrazzak, Ashish N. DebRoy, S. Shahrukh Hashmi, Jon Marc Rhoads
Publikováno v:
Journal of clinical gastroenterology. 52(8)
GOALS To determine if carbon dioxide (CO2) insufflation in children would improve postprocedure pain following colonoscopy in children. BACKGROUND CO2 insufflation during colonoscopy has been found to reduce postcolonoscopy pain in the adult populati
Publikováno v:
Glutamine ISBN: 9781315373164
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::543248fc6d0f73b7b4955fab68fbc7b9
https://doi.org/10.1201/9781315373164-11
https://doi.org/10.1201/9781315373164-11
Autor:
Eba Hathout, Essam Imseis, Joyce K. Johnston, Estella M. Alonso, Karen Martz, Suzanne V. McDiarmid, Richard E. Chinnock, James Lopez, Ravinder Anand
Publikováno v:
Pediatric Transplantation. 13:599-605
To determine the characteristics of pediatric liver transplant recipients who develop GI and/or PTDM, data on children undergoing their first liver transplant from the SPLIT database were analyzed (n = 1611). Recipient and donor characteristics that
Publikováno v:
World Journal of Hepatology
Hereditary tyrosinemia type 1 (HT-1) is a metabolic disorder caused by a defect in tyrosine degradation. Without treatment, symptoms of hepatomegaly, renal tubular dysfunction, growth failure, neurologic crises resembling porphyrias, rickets and poss
Publikováno v:
The Journal of surgical research. 195(1)
Background Intestinal dysfunction and feeding intolerance are comorbidities associated with the abdominal wall birth defect of gastroschisis (GS). These factors contribute to prolonged hospitalization in this population of patients. The purpose of th