Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Nyree Cole"'
Publikováno v:
Children, Vol 8, Iss 5, p 356 (2021)
Psychosocial and palliative care support during stem cell transplants (SCT) is known to improve outcomes. Aim: evaluate the support provided to children and families at the New Zealand National Allogeneic Stem Cell Transplant unit (NATC). Method: the
Externí odkaz:
https://doaj.org/article/c00ce9eb7bdc4a799549b2910c0d1b03
Publikováno v:
Pediatric Transplantation. 25
Background Endoscopically obtained mucosal biopsies are the gold standard for diagnosing acute graft-versus-host disease of the gastrointestinal tract (GI-GVHD). There is no consensus on the ideal endoscopic approach in children. We aimed to ascertai
Publikováno v:
Pediatric bloodcancer. 64(12)
Background The frequency of common cytogenetic abnormalities in pediatric acute lymphoblastic leukemia (ALL) is known to vary by geographic location and ethnic origin. This study aimed to determine the frequency of hypodiploidy, ETV6-RUNX1, BCR-ABL1,
Autor:
Ryuta Nishikomori, Rainer Doffinger, Beatriz Tavares Costa-Carvalho, Andrew R. Gennery, Shinya Sasaki, Erwin W. Gelfand, Shanmuganathan Chandrakasan, Tsubasa Okano, Alberto Olaya-Vargas, Paul Veys, Alfons Krol, Andrea M. Jones, Jean-Laurent Casanova, Etsuro Ito, Waseem Qasim, Thomas Vraetz, Jordan S. Orange, Estelle Colin, Marco Antonio Yamazaki-Nakashimada, Mario Abinun, Nyree Cole, Zeynep Yesim Kucuk, Tayfun Güngör, Chihaya Imai, Capucine Picard, Charline Miot, Steven M. Holland, Stéphane Blanche, Sara Espinosa Padilla, Isabelle Pellier, Despina Moshous, Benedicte Neven, Antonio Condino-Neto, Gulbu Uzel, Jana Pachlopnik Schmid, Smita Y. Patel, Kohsuke Imai, Jérémie Rosain, Jack J. Bleesing, Sophie Dupuis Girod, Stephan Ehl, Jacinta Bustamante, Anthony J. Mancini, Anne Puel, Tokomki Kawai, Stephen Jolles
Publikováno v:
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
Blood
Blood, American Society of Hematology, 2017, 130 (12), pp.1456-1467. ⟨10.1182/blood-2017-03-771600⟩
Universidade de São Paulo (USP)
instacron:USP
Blood
Blood, American Society of Hematology, 2017, 130 (12), pp.1456-1467. ⟨10.1182/blood-2017-03-771600⟩
International audience; X-linked recessive ectodermal dysplasia with immunodeficiency is a rare primary immunodeficiency caused by hypomorphic mutations of the gene encoding the nuclear factor κB essential modulator (NEMO) protein. This condition di
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2de5330d991630d1d83655fb0c9593e3
Publikováno v:
Journal of Paediatrics and Child Health. 48:921-925
Aims: The aim of this study was to review patterns of requests for heritable thrombophilia and to audit these findings against an international standard. Methods: Review of requests for antithrombin, protein C, protein S, activated protein C resistan
Publikováno v:
Integrative Molecular Medicine. 2
Publikováno v:
Journal of paediatrics and child health. 48(10)
The aim of this study was to review patterns of requests for heritable thrombophilia and to audit these findings against an international standard.Review of requests for antithrombin, protein C, protein S, activated protein C resistance, Factor V Lei
Publikováno v:
Hemoglobin. 32(3)
The 5' untranslated region (5'UTR) of beta-globin has been well characterized and is often used as a model for eukaryotic transcription/translation, but there are still questions regarding the mechanism of translational control. Mutations affecting t
Autor:
Magnus Mansouri Taleghani, Peter Bradbeer, Nyree Cole, George Chan, Monica Schaller, Bernhard Laemmle, Johanna A. Kremer Hovinga
Publikováno v:
The Journal of Immunology. 190:51.13-51.13
Autoimmune thrombotic thrombocytopenic purpura (aTTP) is a rare disease characterized by thrombocytopenia, microangiopathic hemolytic anemia and a variable degree of endorgan ischemia as well as an often relapsing course. Underlying is a severe ADAMT