Zobrazeno 1 - 10
of 39
pro vyhledávání: '"Mordechai, Slae"'
Publikováno v:
BMJ Open Gastroenterology, Vol 11, Iss 1 (2024)
Familial dysautonomia (FD) is a genetic disease of the autonomous and sensory nervous systems. Severe gastro-oesophageal reflux is common and one of the major complications. Some patients with FD develop megaoesophagus. Oesophageal malfunction, accom
Externí odkaz:
https://doaj.org/article/829eda38ea11408697690595cdfaa46d
Autor:
Irina Zaidman, Ehud Even-Or, Elroee Aharoni, Dina Averbuch, Yael Dinur-Schejter, Adeeb NaserEddin, Mordechai Slae, Bella Shadur, Polina Stepensky
Publikováno v:
Frontiers in Pediatrics, Vol 11 (2023)
BackgroundHematopoietic stem cell transplantation (HSCT) is the only curative option for many nonmalignant hematopoietic-derived diseases in pediatric patients. Survival after HSCT has improved in recent years and resulted in a 90% survival rate and
Externí odkaz:
https://doaj.org/article/5686bde0f1354afe9f086434e02bf8c4
Autor:
Li, Yue, Führer, Marita, Bahrami, Ehsan, Socha, Piotr, Klaudel-Dreszler, Maja, Bouzidi, Amira, Liu, Yanshan, Lehle, Anna S., Magg, Thomas, Hollizeck, Sebastian, Rohlfs, Meino, Conca, Raffaele, Field, Michael, Warner, Neil, Mordechai, Slae, Shteyer, Eyal, Turner, Dan, Boukari, Rachida, Belbouab, Reda, Walz, Christoph, Gaidt, Moritz M., Hornung, Veit, Baumann, Bernd, Pannicke, Ulrich, Idrissi, Eman Al, Alghamdi, Hamza Ali, Sepulveda, Fernando E., Gil, Marine, de Saint Basile, Geneviève, Hönig, Manfred, Koletzko, Sibylle, Muise, Aleixo M., Snapper, Scott B., Schwarz, Klaus, Klein, Christoph, Kotlarz, Daniel
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America, 2019 Jan . 116(3), 970-975.
Externí odkaz:
https://www.jstor.org/stable/26574125
Autor:
Joel Reiter, Hiba Abuelhija, Mordechai Slae, Peri Millman, Zev Davidovics, Elinor Chaimov, Alex Gileles-Hillel, Michael Wilschanski
Publikováno v:
Journal of clinical sleep medicine : JCSM : official publication of the American Academy of Sleep Medicine.
Celiac disease (CD), an immune-mediated enteropathy, has a clinical spectrum that is remarkably wide including neuropsychiatric manifestations. While studies of adults have shown sleep disturbances, there is limited data in children. Our objectives w
Publikováno v:
European Journal of Pediatrics. 180:1733-1737
Congenital intrahepatic portosystemic shunts are rare vascular malformations in which abnormal communications are created between the portal veins and the hepatic veins or the inferior vena cava system. Diagnosis is made by prenatal or postpartum ult
Autor:
Oded Shamriz, Leon Joseph, Elie Picard, Raz Somech, P Millman, Michael Berger, Vered Molho-Pessach, Amos J. Simon, Orli Megged, Ori Toker, Mordechai Slae, Oren Ledder, Atar Lev, Yuval Tal
Publikováno v:
Clin Exp Immunol
Summary Capping protein regulator and myosin 1 linker 2 (CARMIL2) deficiency is characterized by impaired T cell activation, which is attributed to defective CD28-mediated co-signaling. Herein, we aimed to analyze the effect of exogenous interleukin
Publikováno v:
Pancreas
OBJECTIVES It is unknown to what extent coronavirus 2019 (COVID-19) may co-occur with acute pancreatitis (AP) in children and how their clinical course may differ from children with AP alone. METHODS An online survey was sent to pediatric gastroenter
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3ce5708e302885d71c0dab60243f99be
https://europepmc.org/articles/PMC8647781/
https://europepmc.org/articles/PMC8647781/
Autor:
Ehud Even Or, Polina Stepensky, Diana Pinhasov, Shimon Reif, Diana Averbuch, Irina Zaidman, Mordechai Slae, Zev Davidovics
Publikováno v:
Pediatric Blood & Cancer. 68
Background Hematopoietic stem cell transplantation (HSCT) is a curative therapy used to treat high-risk hematological malignant disorders and other life-threatening nonmalignant diseases. Gastrointestinal (GI) symptoms post-HSCT might be due to GI gr
Autor:
Michael Wilschanski, Mordechai Slae
Publikováno v:
Current Opinion in Pulmonary Medicine. 25:674-679
Malnutrition is one of the major burdens of disease in cystic fibrosis. The prevention of malnutrition remains a priority throughout the life of a patient with cystic fibrosis. Literature and guidelines on the management of nutrition in cystic fibros