Zobrazeno 1 - 10
of 70
pro vyhledávání: '"Dina, Attias"'
Autor:
Tamar Tadmor, Alessia Bari, Stefano Sacchi, Luigi Marcheselli, Eliana Valentina Liardo, Irit Avivi, Noam Benyamini, Dina Attias, Samantha Pozzi, Maria Christina Cox, Luca Baldini, Maura Brugiatelli, Massimo Federico, Aaron Polliack
Publikováno v:
Haematologica, Vol 99, Iss 1 (2014)
In this study we assessed the prognostic significance of absolute monocyte count and selected the best cut-off value at diagnosis in a large cohort of patients with diffuse large B-cell lymphoma. Data were retrieved for therapy-naïve patients with d
Externí odkaz:
https://doaj.org/article/1d318177f13e4479ac8436fd14aaec54
Publikováno v:
Canadian Journal of Gastroenterology, Vol 21, Iss 6, Pp 393-395 (2007)
Malignant lymphoma of mucosa-associated lymphoid tissue (MALT) can arise in a variety of anatomical sites. The majority of these tumors arise in the stomach, with fewer than 30% arising in the small intestine. Primary duodenal MALT lymphoma is a very
Externí odkaz:
https://doaj.org/article/b037c4f8c3214d9691542ea784f5c531
Autor:
Hannah Tamary, Daniella Nishri, Joanne Yacobovich, Rama Zilber, Orly Dgany, Tanya Krasnov, Shraga Aviner, Polina Stepensky, Shoshana Ravel-Vilk, Menachem Bitan, Chaim Kaplinsky, Ayelet Ben Barak, Ronit Elhasid, Joseph Kapelusnik, Ariel Koren, Carina Levin, Dina Attias, Ruth Laor, Isaac Yaniv, Philip S. Rosenberg, Blanche P. Alter
Publikováno v:
Haematologica, Vol 95, Iss 8 (2010)
Background Inherited bone marrow failure syndromes are rare genetic disorders characterized by bone marrow failure, congenital anomalies, and cancer predisposition. Available single disease registries provide reliable information regarding natural hi
Externí odkaz:
https://doaj.org/article/bb504ea66c3c4cddb37a077242ea27d8
Autor:
Batia Stark, Dina Attias, Herzel Gabriel, Shai Izraeli, Myriam Weyl Ben-Arush, Gali Avrahami, Aya Abramov, Ronit Elhasid, Michael Wientraub, Amos Toren, Yoav Burstein, Ami Ballin, Isaac Yaniv, Joseph Kapelushnik, Sarah Elitzur, Nira Arad, Smadar Avigad, Michal Hameiri-Grossman, Bella Bielorai, Dalia Sthoeger, Ronit Nirel
Publikováno v:
Pediatric bloodcancerREFERENCES. 67(1)
BACKGROUND Therapy outcomes for childhood acute lymphoblastic leukemia (ALL) had substantially improved in the last decades, but variability across racial and ethnic groups was identified in some clinical studies. In this study, we aimed to investiga
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::99404955f28cda4f3e03bf779d4b2618
https://pubmed.ncbi.nlm.nih.gov/31595664
https://pubmed.ncbi.nlm.nih.gov/31595664
Publikováno v:
Education for health (Abingdon, England). 29(3)
Emotional intelligence (EI) is increasingly viewed as one of the important skills required for a successful career and personal life. Consequently, efforts have been made to improve personal and group performance in EI, mostly in commercial organizat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f352047a5ea4de2f4c9ffa55d114307c
https://pubmed.ncbi.nlm.nih.gov/28406101
https://pubmed.ncbi.nlm.nih.gov/28406101
Autor:
Dina Attias, Vijay G. Sankaran, Jacob C. Ulirsch, Tanya Krasnov, Orly Dgany, Ruth Laor, Sharon Noy-Lotan, Hannah Tamary, Orna Steinberg-Shemer
Publikováno v:
Cold Spring Harbor Molecular Case Studies
Whole-exome sequencing (WES) has been increasingly useful for the diagnosis of patients with rare causes of anemia, particularly when there is an atypical clinical presentation or targeted genotyping approaches are inconclusive. Here, we describe a 2
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9465260df975e39a69615f2cd67bc6b5
http://europepmc.org/articles/PMC5701307
http://europepmc.org/articles/PMC5701307
Autor:
Hannah Tamary, Dalia Shtager, Tanya Krasnov, Ariel Koren, Amir A. Kuperman, Blanche P. Alter, Orly Dgany, Dina Attias, Chaim Kaplinsky, Hagit Miskin, Neelam Giri, Jerry Stein, Carina Levin, Shoshana Ravel-Vilk, Asaf Lebel, Ayelet Ben Barak, Ruth Laor, Joanne Yacobovich
Publikováno v:
Pediatric Blood & Cancer. 62:103-108
Background The relative frequency of mutated genes among patients with severe congenital neutropenia (SCN) may differ between various ethnic groups. To date, few population-based genetic studies have been reported. This study describes the genetic an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f3d6592186535c3fd604ef1231f03f81
https://doi.org/10.1002/pbc.25251
https://doi.org/10.1002/pbc.25251
Publikováno v:
American Journal of Hematology. 88:355-358
Myeloproliferative neoplasms (MPNs) are malignant disorders originating from clonal expansion of a single neoplastic stem cell and characteristically show an increase in bone marrow reticulin fibers. Lysyl oxidases (LOXs) are copper-dependent amine o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::932d0822a0a3e0f72ba18be37f8a72ef
https://doi.org/10.1002/ajh.23409
https://doi.org/10.1002/ajh.23409
Publikováno v:
Harefuah. 155(1)
Diffuse large B-cell lymphoma (DLBCL) is the most common form of non-Hodgkin's lymphoma (NHL), and constitutes 30-40% of all cases in adults. DLBCL is heterogeneous in terms of its clinical course, and related molecular and genetic features. In the c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::4ae37bddb0fd298d85d415d2109a9b46
https://pubmed.ncbi.nlm.nih.gov/27012075
https://pubmed.ncbi.nlm.nih.gov/27012075
Publikováno v:
Leukemia & Lymphoma. 54:1547-1551
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e9b249d2bda843b8a21a915656da15a6
https://doi.org/10.3109/10428194.2012.745934
https://doi.org/10.3109/10428194.2012.745934