Zobrazeno 1 - 10
of 63
pro vyhledávání: '"59"'
Publikováno v:
International Journal of Laboratory Hematology. 43:259-265
BACKGROUND FLAER-based flow cytometry assay is considered the gold standard for diagnosis of paroxysmal nocturnal hemoglobinuria (PNH). CD157 is a recently reported marker for GPI-anchored protein found both on neutrophils and monocytes. This study h
Autor:
Josy Reiffers, Philippe Bernard, Francis Lacombe, D. Dachary, Antoine Broustet, Michel R. Boisseau
Publikováno v:
Scandinavian Journal of Haematology. 32:429-440
In 71 adult acute myelogenous leukaemia (AML) cases, the relationship between well-known prognostic features and complete remission (CR) rate and survival was studied. These features were: (i) bone marrow karyotype classified NN, AN, AA according to
Autor:
R. Dall'Amico, C. Messina
Publikováno v:
Therapeutic Apheresis and Dialysis. 6:296-304
Photopheresis (extracorporeal photochemotherapy, ECP) is a new type of photochemotherapy used for the treatment of oncological and autoimmune diseases. Additionally, recent reports indicate that this therapy is promising in both pediatric and adult p
Autor:
Jukka Ollgren, Emilia Attman, Outi Lyytikäinen, Reetta Huttunen, Risto Vuento, Jaana Syrjänen, Marjatta Sinisalo, Erja Mattila
Publikováno v:
European Journal of Haematology. 107:311-317
OBJECTIVES The aim was to identify the clinical characteristics, outcome, and antimicrobial susceptibility of healthcare-associated bloodstream infections (BSIs) in hematological patients. METHODS This retrospectively collected laboratory-based surve
Autor:
Laura K. Sedig, Michelle F. Jacobs, Rajen J. Mody, Lan Q. Le, Natalie J. Bartnik, Michele C. Gornick, Bailey Anderson, Arul M. Chinnaiyan, J. Scott Roberts
Publikováno v:
Pediatric Blood & Cancer. 69
Next-generation sequencing offers opportunities for targeted cancer therapies and may identify pathogenic germline variants. Adolescents' perception of testing is not well understood. We surveyed 16 adolescents and 59 parents regarding motivations, a
Publikováno v:
Pediatric Blood & Cancer. 69
Children with β-thalassemia major and β-thalassemia intermedia frequently have low bone mass. However, studies of bone mineral density (BMD) in children with transfusion-dependent (TD) or non-transfusion-dependent (NTD) hemoglobin (Hb) E/β-thalass
Autor:
Haipeng Shao, Ling Zhang, Ning Dong, Lubomir Sokol, Qianxing Mo, Franco Castillo Tokumori, Todd C. Knepper, Yumeng Zhang, Ankita Tandon, Leidy Isenalumhe
Publikováno v:
American Journal of Hematology. 96:772-780
Large granular lymphocytic leukemia (LGLL) is a rare hematological malignancy that arises from cytotoxic T lymphocytes (T-LGLL) in 85% of cases and natural killer (NK) cells in the rest. A significant knowledge gap exists regarding the pathogenesis,
Autor:
Wonho Choe, Sung Shin, Hyungsuk Kim, Dae-Hyun Ko, Su-Kil Park, Seog-Woon Kwon, Duck Jong Han, Young Hoon Kim
Publikováno v:
Transfusion. 60:598-606
Background Recent advances in desensitization techniques and immunosuppressive therapy have led to improved outcomes after ABO-incompatible (ABO-i) kidney transplantation (KT). However, questions remain unanswered, particularly regarding which type o
Publikováno v:
Journal of Clinical Laboratory Analysis
Background Bronchial asthma (BA) was a heterogeneous disease characterized by chronic airway inflammation. Spondin 2 (SPON2) was reported to be implicated in the integrin pathway, protein metabolism, and drug‐induced lupus erythematosus. The purpos
Autor:
Uwe Platzbecker, Maria R. Baer, Benedikt Brors, Zuzana Šustková, Richard F. Schlenk, Tomáš Szotkowski, Pavel Zak, Carsten Müller-Tidow, Gregor Warsow, Francesca Guijarro, Sabine Kayser, Alan Kenneth Burnett, Angela Schulz, Mark J. Levis, Roland B. Walter, Carole Shaw, David Grimwade, Jordi Esteve, Christoph Röllig, Gerhard Ehninger, Christian Thiede, Elihu H. Estey, Petr Cetkovsky, Andrew M. Brunner, Anthony D. Ho, Robert Kerrin Hills, Ralitsa Langova, Nigel H. Russell, Zdeněk Ráčil, Michael Kramer, Jiri Mayer
In acute myeloid leukaemia (AML) t(8;16)(p11;p13)/MYST3-CREBBP is a very rare abnormality. Previous small series suggested poor outcome. We report on 59 patients with t(8;16) within an international, collaborative study. Median age was 52 (range: 16-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ff05dfb4c0cfe20e3c626f735710e68a