Zobrazeno 1 - 10
of 10
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:
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:
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
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
Publikováno v:
Transfusion
Background With coronavirus disease 2019 (COVID‐19) convalescent plasma (CCP) offering an early treatment option for COVID‐19, blood collectors needed to quickly overcome obstacles to recruiting and qualifying eligible donors. We provide attribut
Autor:
Ryosuke Ogawa, Shouhei Yokota, Koichi Akashi, Tomoaki Fujisaki, Noriaki Kawano, Yasuhiko Miyazaki, Toshiro Kurokawa, Ken Takase, Hirokazu Okumura, Koji Nagafuji, Toshihiro Miyamoto, Atsushi Wake, Yasushi Takamatsu, Tomohiko Kamimura, Yuju Ohno, Tetsuya Eto
Publikováno v:
European Journal of Haematology. 103:164-171
Objective We investigated whether minimal residual disease (MRD) status in adult patients with Philadelphia chromosome (Ph)-negative acute lymphoblastic leukemia (ALL) is useful for decision on clinical indications for allogeneic hematopoietic stem c
Autor:
Edward Vincent S. Faustino, Joana A. Tala, Theia Study Investigators, Shira J. Gertz, Lee A. Polikoff, Simon Li, Erin Trakas, Michael Miksa, Matthew Pinto
Publikováno v:
Pediatric Blood & Cancer. 67
Background There are no tests to identify critically ill children at high risk of deep venous thrombosis (DVT). In this exploratory study, we aimed to identify proteins that are associated with incident DVT in critically ill adolescents. Procedure Pl
Autor:
Jane S Chen, Portia Kamthunzi, J. Brett Heimlich, Irving F. Hoffman, Khadija Paseli, Satish Gopal, Nigel S. Key, Kenneth I. Ataga, Wiza Kumwenda, Hillary M. Topazian, Isobel Kambalame, Tisungane Mvalo, Noel Mumba, Graham Ellis, Katherine D. Westmoreland, Gerald Tegha, Pilirani Mafunga, Msandeni Chiume
Publikováno v:
Pediatr Blood Cancer
INTRODUCTION Sickle cell disease (SCD) is among the most common inherited hematologic diseases in sub-Saharan Africa (SSA). Historically, hydroxyurea administration in SSA has been restricted due to limited region-specific evidence for safety and eff
Autor:
Laura Magnano, Natalia Espinosa-Lara, Jose Luis Bello, Alejandro Martín, Lourdes Lopez, Silvana Novelli, Emilia Pardal, Ana Jiménez-Ubieto, Marcos González, Itziar Carro, Ana Isabel Teruel, Maria Stefania Infante, Juan M. Sancho, Santiago Mercadal, Julio Delgado, Armando López-Guillermo, Jimena Cannata, Guillermo Rodríguez, Antonio Salar, Sonia González de Villambrosia, María Teresa García-Álvarez, Reyes Arranz, Antonia Rodriguez, Francesc Garcia-Pallarols, Erik de Cabo, Maria Dolores Caballero, Sara Alonso-Álvarez, Silvia Monsalvo, Miriam Moreno, Miguel Alcoceba, Marcio Andrade-Campos, María José Terol
Publikováno v:
BRITISH JOURNAL OF HAEMATOLOGY
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
Universitat Pompeu Fabra
r-INCLIVA. Repositorio Institucional de Producción Científica de INCLIVA
instname
British Journal of Haematology
r-IGTP. Repositorio Institucional de Producción Científica del Instituto de Investigación Germans Trias i Pujol
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
Universitat Pompeu Fabra
r-INCLIVA. Repositorio Institucional de Producción Científica de INCLIVA
instname
British Journal of Haematology
r-IGTP. Repositorio Institucional de Producción Científica del Instituto de Investigación Germans Trias i Pujol
Summary The diagnostic criteria for follicular lymphoma (FL) transformation vary among the largest series, which commonly exclude histologically-documented transformation (HT) mandatorily. The aims of this retrospective observational multicentre stud
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3fe13fbc2dfd09cb3dd0dabba7f3eea2
https://iibsantpau.fundanetsuite.com/Publicaciones/ProdCientif/PublicacionFrw.aspx?id=14118
https://iibsantpau.fundanetsuite.com/Publicaciones/ProdCientif/PublicacionFrw.aspx?id=14118
Autor:
Arja Harila-Saari, Thomas Frandsen, Outi Mäkitie, Kjeld Schmiegelow, Kadri Saks, Nina Toft, Anne Vestli, Signe Sloth Mogensen, Ida Hed Myrberg, Louise Rold Helt, Riitta Niinimäki, Laimonas Griskevicius, Jens Retpen, Solveig Hafsteinsdottir, Helene Hallböök
Publikováno v:
Pediatric Blood & Cancer. 65:e27300
BACKGROUND Treatment-related osteonecrosis (ON) is a serious complication of treatment of acute lymphoblastic leukemia (ALL). PROCEDURE This study included 1,489 patients with ALL, aged 1-45 years, treated according to the Nordic Society of Paediatri