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Journal of Pediatric Gastroenterology and Nutrition|October 13, 2006
Long-term lamivudine therapy for chronic hepatitis B infection in children unresponsive to interferonCorina Hartman, Drora Berkowitz, Orly Eshach-Adiv, et al.Journal of Pediatric Surgery|June 5, 2003
Trophic enteral nutrition increases hepatic glutathione and protects against peroxidative damage after exposure to endotoxinAlexander Dzakovic, Amir Kaviani, Orly Eshach-Adiv, et al.Arteriosclerosis, Thrombosis, and Vascular Biology|January 14, 2003
Oral insulin supplementation attenuates atherosclerosis progression in apolipoprotein E-deficient miceRaanan Shamir, Naim Shehadeh, Mira Rosenblat, et al.Pediatric Blood & Cancer|February 3, 2021
Hematopoietic stem cell transplantation for mitochondrial neurogastrointestinal encephalopathy: A single-center experience underscoring the multiple factors involved in the prognosisIrina Zaidman, Ronit Elhasid, Aharon Gefen, et al.The Pediatric Infectious Disease Journal|March 14, 2003
Lamivudine treatment for chronic hepatitis B infection in children unresponsive to interferonCorina Hartman, Drora Berkowitz, Daniel Shouval, et al.Journal of Pediatric Gastroenterology and Nutrition|December 2, 2004
Bone quantitative ultrasound and bone mineral density in children with celiac diseaseCorina Hartman, Bayan Hino, Aaron Lerner, et al.The Israel Medical Association Journal : IMAJ|August 30, 2008
Nutritional supplementation with polymeric diet enriched with transforming growth factor-beta 2 for children with Crohn's diseaseCorina Hartman, Drora Berkowitz, Batia Weiss, et al.Journal of Pediatric Gastroenterology and Nutrition|November 13, 2018
Eculizumab Is Safe and Effective as a Long-term Treatment for Protein-losing Enteropathy Due to CD55 DeficiencyAlina Kurolap, Orly Eshach Adiv, Tova Hershkovitz, et al.Journal of Medical Genetics|June 8, 2018
Establishing the role of <i>PLVAP</i> in protein-losing enteropathy: a homozygous missense variant leads to an attenuated phenotypeAlina Kurolap, Orly Eshach-Adiv, Claudia Gonzaga-Jauregui, et al.Orphanet Journal of Rare Diseases|February 11, 2025
The patient experience of CHAPLE disease: results from interviews conducted as part of a clinical trial for an ultra-rare conditionLeighann Litcher-Kelly, Ahmet Ozen, Sarah Ollis, et al.Pageof 3