Zobrazeno 1 - 10
of 35
pro vyhledávání: '"Ehud Even-Or"'
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:
Irina Zaidman, Tamar Shaziri, Dina Averbuch, Ehud Even-Or, Yael Dinur-Schejter, Adeeb NaserEddin, Rebecca Brooks, Bella Shadur, Aharon Gefen, Polina Stepensky
Publikováno v:
Frontiers in Pediatrics, Vol 10 (2022)
BackgroundAllogeneic hematopoietic stem cell transplantation (HSCT) is an efficient treatment for numerous malignant and nonmalignant conditions affecting children. This procedure can result in infectious and noninfectious neurological complications
Externí odkaz:
https://doaj.org/article/22b74a28384544a5aeb9e1ca75d0bbfd
Autor:
Ehud Even-Or, Yael Dinur Schejter, Adeeb NaserEddin, Irina Zaidman, Bella Shadur, Polina Stepensky
Publikováno v:
Frontiers in Immunology, Vol 13 (2022)
Autoimmune cytopenia (AIC) is a rare complication post hematopoietic stem cell transplantation (HSCT), with a higher incidence in nonmalignant diseases. The etiology of post-HSCT AIC is poorly understood, and in many cases, the cytopenia is prolonged
Externí odkaz:
https://doaj.org/article/8f0a78e716664e04a8aa1db505828ff0
Autor:
Boaz Nachmias, Svetlana Krichevsky, Dvora Filon, Ehud Even-Or, Moshe E. Gatt, Revital Saban, Batia Avni, Sigal Grisariu, Shlomzion Aumann, Vladimir Vainstein
Publikováno v:
Acta Haematologica. 145:642-649
Introduction: Mutated RUNX1 is considered a poor prognostic factor and usually is mutually exclusive with NPM1 mutations. Monitoring of molecular markers for minimal residual disease provides a powerful tool to assess remission and guide clinical dec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bc09535c2e7434b1710e22a4b32c940b
https://doi.org/10.1159/000526353
https://doi.org/10.1159/000526353
Autor:
Maria Gabelli, Polina Stepensky, Giorgio Ottaviano, Khushnuma Mullanfiroze, Arina Lazareva, Irina Zaidman, Ehud Even-Or, Giovanna Lucchini, Robert Chiesa, Juliana Silva, Stuart Adams, Susanne Kricke, Maria Finch, Annette Hill, Rachel Mead, Delphine Veys, Yael Dinur Schejter, Adeeb Naser Eddin, Austen Worth, Persis J. Amrolia, Kanchan Rao
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7d916ecab56ed5f2f35473daf471e50e
https://hdl.handle.net/11577/3473038
https://hdl.handle.net/11577/3473038
Autor:
Orly, Fink, Ehud, Even-Or, Batia, Avni, Sigal, Grisariu, Irina, Zaidman, Yael Dinur, Schejter, Adeeb, NaserEddin, Mohammad, Najajreh, Polina, Stepensky
Publikováno v:
Clinical Transplantation. 37
Allogeneic hematopoietic stem cell transplantation (HSCT) is currently the only curative treatment for the hematological complications of patients with Fanconi anemia (FA). Over the last two decades, HSCT outcomes have improved dramatically following
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::97f5cbe7ade858e10a208e4cb17fbb98
https://doi.org/10.1111/ctr.14835
https://doi.org/10.1111/ctr.14835
Autor:
Amir A. Kuperman, Jerry Stein, Ehud Even-Or, Joanne Yacobovich, Elad Jacoby, Polina Stepensky, Irina Zaidman, Yarden Greental Ness, Bella Bielorai, Neta Nevo, Amos Toren, Aharon Gefen, Bernice Oberman
Publikováno v:
Bone Marrow Transplantation. 56:2088-2096
We report the results of national retrospective study of 45 children with hemophagocytic lymphohistiocytosis (HLH) who underwent allogeneic hematopoietic stem-cell transplantation (HSCT) in Israel between the years 2000–2018. Donors were either HLA
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f0b7c3ac31836eb638cc94ecedfad079
https://doi.org/10.1038/s41409-021-01290-1
https://doi.org/10.1038/s41409-021-01290-1
Autor:
Ehud Even-Or, Bella Shadur, Adeeb NaserEddin, Irina Zaidman, Yael Dinur Schejter, Polina Stepensky
Publikováno v:
Bone Marrow Transplantation
Allogeneic hematopoietic stem cell transplantation (HSCT) is curative for a variety of nonmalignant disorders including osteopetrosis, bone marrow failures, and immune deficiencies. Haploidentical HSCT is a readily available option in the absence of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cd6ab755ef3dee592c740cfa78d23280
http://europepmc.org/articles/PMC7450679
http://europepmc.org/articles/PMC7450679
Autor:
Irina Zaidman, Hadhud Mohamad, Lidor Shalom, Myriam Ben Arush, Ehud Even‐Or, Dina Averbuch, Amir Zilkha, Jacques Braun, Asaf Mandel, David Kleid, Ori Attias, Josef Ben‐Ari, Rebecca Brooks, Aharon Gefen, Polina Stepensky
Publikováno v:
Pediatric Blood & Cancer. 69
Although hematopoietic stem cell transplantation (HSCT) is the only curative option for some children with malignant and nonmalignant disorders, the procedure itself carries a high risk of complications. A proportion of children undergoing HSCT devel
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1d8ba65ae5a09baf4547cb06593e38eb
https://doi.org/10.1002/pbc.29549
https://doi.org/10.1002/pbc.29549
Autor:
Ehud Even-Or, Adeeb NaserEddin, Hagar Mor-Shaked, Polina Stepensky, Gali Schiesel, Natalia Simanovsky, Irina Zaidman, Orly Elpeleg
Publikováno v:
Bone. 154
Malignant infantile osteopetrosis (MIOP) is the autosomal recessive, severe form of osteopetrosis. This rare genetic syndrome usually presents soon after birth and is often fatal if left untreated. Early diagnosis is key for proper management but cli
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b42c1de914c5a1d95f59f9c69f80ce4e
https://pubmed.ncbi.nlm.nih.gov/34624559
https://pubmed.ncbi.nlm.nih.gov/34624559