Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Bella Shadur"'
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
Autor:
Bella Shadur, Irina Zaidman, Yael Dinur Schejter, Adeeb NaserEddin, Ehud Even-Or, Polina Stepensky
Publikováno v:
Journal of clinical immunology. 40(1)
Purine nucleoside phosphorylase (PNP) is a known yet rare cause of combined immunodeficiency with a heterogeneous clinical presentation. We aim to add to the expanding clinical spectrum of disease, and to summarize the available data on bone marrow t
Autor:
Klaus-Michael Debatin, Ingrid Furlan, Orly Elpeleg, Donald Bunjes, Meinrad Beer, Catharina Schuetz, Stephanie von Harsdorf, Batia Avni, Sigal Grisariu, Polina Stepensky, Bella Shadur, Ansgar Schulz, Irina Zaidman, Manfred Hoenig, Mehtap Sirin
Osteopetrosis (OP) is a rare disease caused by defective osteoclast differentiation or function. Hematopoietic stem cell transplantation (HSCT) is the only curative treatment available in the infantile “malignant” form of OP. Improved clinical an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dc4833fa953f1355081b779ead2182f1
https://europepmc.org/articles/PMC6436016/
https://europepmc.org/articles/PMC6436016/
Publikováno v:
Pediatric bloodcancer. 66(1)
Mutations in the VPS45 gene lead to a severe primary immune deficiency characterized by severe congenital neutropenia and primary myelofibrosis, leading to overwhelming infection and early death. This condition is exceedingly rare with only 16 patien
Autor:
Hodaya Cohen Oron, Fatma Hussein, Irina Zaidman, Batia Avni, Sigal Grisariu, Polina Stepensky, Bella Shadur, Elana Lokshin, Adeeb NaserEddin
Publikováno v:
Pediatric Blood & Cancer. 65:e27010
Background Infantile malignant osteopetrosis (IMO) is an autosomal recessive condition characterized by defective osteoclast activity, with hematopoietic bone marrow transplant being the only available cure. Over the past several years, new condition