Zobrazeno 1 - 10
of 121
pro vyhledávání: '"Uriel, Katz"'
Autor:
David Yogev, Shai Tejman-Yarden, Omer Feinberg, Yisrael Parmet, Tomer Goldberg, Shay Illouz, Netanel Nagar, Dor Freidin, Oliana Vazgovsky, Sumit Chatterji, Yishay Salem, Uriel Katz, Orly Goitein
Publikováno v:
Heliyon, Vol 8, Iss 11, Pp e11250- (2022)
Introduction: Simpson's rule is generally used to estimate cardiac volumes. By contrast, modern methods such as Virtual Reality (VR) utilize mesh modeling to present the object's surface spatial structure, thus enabling intricate volumetric calculati
Externí odkaz:
https://doaj.org/article/684184c894a24f59baa9f7b1f6d08c54
Autor:
Odelia Chorin, Yoel Hirsch, Rachel Rock, Liat Salzer Sheelo, Yael Goldberg, Hanna Mandel, Tova Hershkovitz, Nicole Fleischer, Lior Greenbaum, Uriel Katz, Ortal Barel, Nasrin Hamed, Bruria Ben-Zeev, Shoshana Greenberger, Nadra Nasser Samra, Michal Stern Zimmer, Annick Raas-Rothschild, Ben Pode-Shakked
Publikováno v:
Frontiers in Genetics, Vol 13 (2022)
Introduction: Vici Syndrome is a rare, severe, neurodevelopmental/neurodegenerative disorder with multi-systemic manifestations presenting in infancy. It is mainly characterized by global developmental delay, seizures, agenesis of the corpus callosum
Externí odkaz:
https://doaj.org/article/8e8a48b5d2af47e29c4d8e95ea739427
Publikováno v:
Frontiers in Pediatrics, Vol 10 (2022)
BackgroundNoonan syndrome (NS) is a genetic syndrome, characterized by various dysmorphic features, cardiac anomalies, short stature, and developmental delay. NS is a leading cause of cardiovascular anomalies. The syndrome results from dysregulation
Externí odkaz:
https://doaj.org/article/65d174f25257415b9352e675865b786b
Autor:
Evyatar Hubara, Irena Serencev, Or Kriger, Shatzman Steuerman Rachel, Eitan Keizman, Marianne E. Nellis, David Mishali, Reut Kassif Lerner, Uriel Katz, Yelena Skorchin, Galia Barkai, Itai Pessach
Publikováno v:
Journal of Pediatric Infectious Diseases.
Objective Delayed sternal closure (DSC) is a frequent strategy for optimizing hemodynamics for patients after complicated cardiac surgery. However, this practice is associated with increased risk for infection and mortality. Despite the importance of
Publikováno v:
The Laryngoscope. 132:1184-1188
To study the applicability of transnasal echography for the internal carotid artery (ICA) imaging during endoscopic procedures, primarily nasopharyngectomy.Non-randomized controlled cohort.The tip of a pediatric transducer for transesophageal echogra
Autor:
Uriel, Katz, Ron, Maymon, Anna, Tsviban, Adi, Sharabi-Nov, Ramzia, Abu Hamid, Hamutal, Meiri, Yifat, Wiener
Publikováno v:
Harefuah. 161(11)
Preeclampsia (PE) is a major pregnancy complication, posing considerable morbidity and mortality. The maternal serum angiogenic factors - PlGF and sFlt-1, and their ratio appear to be promising markers to predict PE. Aims: To assess whether the evalu
Autor:
Yarden Sarouf, Amir Vardi, Ben Pode-Shakked, Yishay Ben Moshe, Alvit Veber, Gideon Rechavi, Yair Anikster, Dina Marek-Yagel, Odelia Chorin, Annick Raas-Rothschild, Shrikant Mane, Yoav Bolkier, Yishay Salem, Danit Atias-Varon, Omer Shlomovitz, Elisheva Javasky, Tal Tirosh-Wagner, Uriel Katz, Jeffrey M. Jacobson, Orna Staretz-Chacham, Nechama Shalva, Ortal Barel, David Mishali, Maayan Kagan, Asaf Vivante, Aviva Eliyahu
Publikováno v:
Journal of Medical Genetics. 59:691-696
BackgroundThe molecular basis of heterotaxy and congenital heart malformations associated with disruption of left–right asymmetry is broad and heterogenous, with over 25 genes implicated in its pathogenesis thus far.ObjectiveWe sought to elucidate
Autor:
Uriel Katz, Raz Somech, Yu Nee Lee, David Mishali, Atar Lev, Shira Rabinowicz, Diti Machnes-Maayan, Amir Vardi
Publikováno v:
Pediatric Research. 89:102-109
Patients with Down syndrome (DS) are at increased risk for infections and autoimmune disorders. Although several immunological abnormalities were previously found, differences in T cell receptor repertoire have never been shown. Thus we compared the
Autor:
David Mishali, Annick Raas-Rothschild, Yishay Salem, Amir Vardi, Shachar Abudi, Ben Pode-Shakked, Uriel Katz, Yair Anikster, Dina Marek-Yagel, Gideon Rechavi, Nitzan Kol, Omri Nayshool, Yoav Bolkier, Ortal Barel
Publikováno v:
American Journal of Medical Genetics Part A. 182:987-993
The genetic basis of congenital heart malformations associated with disruption of left-right (L-R) asymmetry is broad and heterogenous, with variants in over 25 genes implicated thus far. Of these, deleterious variants in the Growth/Differentiation F
Autor:
Michalle Soudack, Michael Kinori, Eve Stern, Shani Caspi, Gadi Abebe Campino, Michal Lurye, Dalit Modan-Moses, Shoshana Greenberger, Amos Toren, Michal Yalon, Talya Finke, Ariel Hirchorn, Michal Golan, Sharon Armarnik, Uriel Katz, Michal Ben-Ami, Renana Gross
Background The MAPK pathway, is a signal transduction pathway involved in the oncogenesis of a variety of pediatric tumors. The clinical use of BRAF inhibitors and MEK inhibitors is increasingly used in oncology practice. The toxicity profile of thes
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::954da995638a9046b3fb01f8e5d1d2f6
https://doi.org/10.22541/au.160225762.21068105/v1
https://doi.org/10.22541/au.160225762.21068105/v1