Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Ivana Bodova"'
Autor:
Annalisa Ruggeri, Nicole Santoro, Jacques-Emmanuel Galimard, Krzysztof Kalwak, Mattia Algeri, Ludmila Zubarovskaya, Krzysztof Czyzewski, Elena Skorobogatova, Petr Sedlacek, Caroline Besley, Adriana Balduzzi, Yves Bertrand, Julia Peristeri, Franca Fagioli, Mariane Ifversen, Jolanta Gozdzik, Christina Peters, Birgitta Versluijs, Alessandra Biffi, Arcangelo Prete, Maura Faraci, Ibrahim Ghemlas, Ivana Bodova, Olga Aleinikova, Arnaud Dalissier, Vanderson Rocha, Selim Corbacioglu
Publikováno v:
Haematologica, Vol 999, Iss 1 (2024)
In children with acute myeloid leukemia (AML) who lack an HLA identical sibling, the donor can be replaced with an HLA matched unrelated donor (MUD) or a haploidentical donor (haplo). We compared outcomes of patients
Externí odkaz:
https://doaj.org/article/0cbd8179ddf14c39a5bebdf419f8d1ed
Autor:
Ayami Yoshimi, Miriam Erlacher, Peter Noellke, Senthilkumar Ramamoorthy, Gudrun Göhring, Shlomit Barzilai – Birenboim, Ivana Bodova, Jochen Buechner, Albert Catala, Valérie De Haas, Barbara De Moerloose, Michael Dworzak, Henrik Hasle, Kirsi Jahnukainen, Krisztian Kallay, Marko Kavcic, Paula Kjollerstrom, Franco Locatelli, Riccardo Masetti, Sophia Polychronopoulou, Markus Schmugge, Owen Smith, Jan Stary, Dominik Turkiewicz, Marek Ussowicz, Natalia Rotari, Marcin Wlodarski, Brigitte Strahm, Charlotte Niemeyer
Publikováno v:
EJC Paediatric Oncology, Vol 2, Iss , Pp 100071- (2023)
Externí odkaz:
https://doaj.org/article/cf18133fdb9d41dabaf3d41295f0b02d
Autor:
Dominika Tanuskova, Julia Horakova, Peter Svec, Ivana Bodova, Martina Lengerova, Matej Bezdicek, Miroslava Poczova, Jozef Koppl, Alexandra Kolenova
Publikováno v:
Medical Mycology Case Reports, Vol 16, Iss C, Pp 12-15 (2017)
Magnusiomyces capitatus (previously known as Geotrichum capitatum or Blastoschizomyces capitatus or Trichosporon capitatum) is a rare cause of fungal infection in immunocompromised patients. Most of these cases (87%) have been reported from the Medit
Externí odkaz:
https://doaj.org/article/37fc14ec02c341c488c3d59ef41483f7
Autor:
Michael H. Albert, Tiarlan Sirait, Dirk-Jan Eikema, Katerina Bakunina, Claudia Wehr, Felipe Suarez, Maria Laura Fox, Nizar Mahlaoui, Andrew R. Gennery, Arjan C. Lankester, Rita Beier, Maria Ester Bernardo, Venetia Bigley, Caroline A. Lindemans, Siobhan O. Burns, Ben Carpenter, Jaroslaw Dybko, Tayfun Güngör, Fabian Hauck, Su Han Lum, Dmitry Balashov, Roland Meisel, Despina Moshous, Ansgar Schulz, Carsten Speckmann, Mary A. Slatter, Brigitte Strahm, Duygu Uckan-Cetinkaya, Isabelle Meyts, Tanja C. Vallée, Robert Wynn, Bénédicte Neven, Emma C. Morris, Alessandro Aiuti, Alexei Maschan, Mahmoud Aljurf, Tobias Gedde-Dahl, Gunhan Gurman, Victoria Bordon, Gergely Kriván, Franco Locatelli, Fulvio Porta, David Valcárcel, Yves Beguin, Maura Faraci, Nicolaus Kröger, Aleksandr Kulagin, Peter J. Shaw, Joan Hendrik Veelken, Cristina Diaz de Heredia, Franca Fagioli, Matthias Felber, Bernd Gruhn, Wolfgang Holter, Claudia Rössig, Petr Sedlacek, Jane Apperley, Mouhab Ayas, Ivana Bodova, Goda Choi, J.J. Cornelissen, Anne Sirvent, Anjum Khan, Alphan Kupesiz, Stig Lenhoff, Hakan Ozdogu, Nicolas von der Weid, Montserrat Rovira, Rik Schots, Donald C. Vinh
Publikováno v:
Blood. 140:1635-1649
Allogeneic hematopoietic stem cell transplantation (HSCT) is the gold standard curative therapy for infants and children with many inborn errors of immunity (IEI), but adolescents and adults with IEI are rarely referred for transplant. Lack of publis
Autor:
Luca Vinci, Christian Flotho, Peter Noellke, Dirk Lebrecht, Riccardo Masetti, Valerie de Haas, Barbara De Moerloose, Michael Dworzak, Henrik Hasle, Tayfun Güngör, Jan Starý, Dominik Turkiewicz, Marek Ussowicz, Cristina Diaz de Heredia, Jochen Buechner, Kirsi Jahnukainen, Krisztian Kallay, Ivana Bodova, Owen P. Smith, Marco Zecca, Dorine Bresters, Peter Lang, Tania Nicole Masmas, Roland Meisel, Herbert Pichler, Miriam Erlacher, Gudrun Göhring, Franco Locatelli, Brigitte Strahm, Charlotte M. Niemeyer, Ayami Yoshimi
Publikováno v:
Scientia
Vinci, L, Flotho, C, Noellke, P, Lebrecht, D, Masetti, R, de Haas, V, De Moerloose, B, Dworzak, M, Hasle, H, Güngör, T, Starý, J, Turkiewicz, D, Ussowicz, M, de Heredia, C D, Buechner, J, Jahnukainen, K, Kallay, K, Bodova, I, Smith, O P, Zecca, M, Bresters, D, Lang, P, Masmas, T N, Meisel, R, Pichler, H, Erlacher, M, Göhring, G, Locatelli, F, Strahm, B, Niemeyer, C M & Yoshimi, A 2023, ' Second allogeneic stem cell transplantation can rescue a significant proportion of patients with JMML relapsing after first allograft ', Bone Marrow Transplantation, vol. 58, no. 5, pp. 607-609 . https://doi.org/10.1038/s41409-023-01942-4
Vinci, L, Flotho, C, Noellke, P, Lebrecht, D, Masetti, R, de Haas, V, De Moerloose, B, Dworzak, M, Hasle, H, Güngör, T, Starý, J, Turkiewicz, D, Ussowicz, M, de Heredia, C D, Buechner, J, Jahnukainen, K, Kallay, K, Bodova, I, Smith, O P, Zecca, M, Bresters, D, Lang, P, Masmas, T N, Meisel, R, Pichler, H, Erlacher, M, Göhring, G, Locatelli, F, Strahm, B, Niemeyer, C M & Yoshimi, A 2023, ' Second allogeneic stem cell transplantation can rescue a significant proportion of patients with JMML relapsing after first allograft ', Bone Marrow Transplantation, vol. 58, no. 5, pp. 607-609 . https://doi.org/10.1038/s41409-023-01942-4
Myeloproliferative disease; Paediatrics Enfermedad mieloproliferativa; Pediatría Malaltia mieloproliferativa; Pediatria Open Access funding enabled and organized by Projekt DEAL.
Autor:
Akshay Sharma, Jacques-Emmanuel Galimard, Angharad Pryce, Senthil Bhoopalan, Arnaud Dalissier, Jean-Hugues Dalle, Franco Locatelli, Charlotte Jubert, Oana Mirci-Danicar, Vassiliki Kitra-Roussou, Yves Bertrand, Franca Fagioli, Fanny Rialland, Alessandra Biffi, Robert F Wynn, Gerard Michel, Francesco Paolo P Tambaro, Ali Abdallah Ahmari, Abdelghani Tbakhi, Caroline Furness, Miguel Ángel Díaz Pérez, Petr Sedlacek, Ivana Bodova, Maura Faraci, Kanchan Rao, Marie Thérèse Rubio, Brenda Gibson, Neel S. Bhatt, Selim Corbacioglu
Publikováno v:
Blood. 140:1882-1884
Autor:
Peter Bader, Ardeshir Ghavamzadeh, Bénédicte Bruno, Akif Yeşilipek, Josu de la Fuente, Charlotte M. Niemeyer, Tatiana A Bykova, Stefano Giardino, Roland Meisel, Yasmina Mozo, Antonio M. Risitano, Jolanta Gozdzik, Ivana Bodova, Jean Hugues Dalle, Wolfgang Holter, Anne Sirvent, Henrik Sengeløv, Yves Beguin, Gergely Kriván, Miguel Pérez, Jelena Rascon, Dirk-Jan Eikema, Régis Peffault de Latour, Yves Bertrand, Maura Faraci, Marc Ansari, Vanderson Rocha, Renata Formankova, Daniela Onofrillo, Carlo Dufour, Sonia Bonanomi, Karin Mellgren, Safiatou Diallo, Matthias Wölfl, Frans J. Smiers, Andrzej Lange, Maurizio Miano, Tariq Mahmood Satti, Paul Bosman
Publikováno v:
TRANSPLANTATION AND CELLULAR THERAPY, 27(3). ELSEVIER SCIENCE INC
Data on stem cell transplantation (SCT) for Diamond-Blackfan Anemia (DBA) is limited. We studied patients transplanted for DBA and registered in the EBMT database. Between 1985 and 2016, 106 DBA patients (median age, 6.8 years) underwent hematopoieti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c777b4a8fbeb4bc7fac6eb8d3f5a197a
https://doi.org/10.1016/j.jtct.2020.12.024
https://doi.org/10.1016/j.jtct.2020.12.024
Autor:
Paula Kjollerstrom, Marta Derecka, Brigitte Schlegelberger, Peter Lang, Dirk Lebrecht, Manching Ku, Birgit Burkhardt, Robert Durruthy-Durruthy, Marcin W. Wlodarski, Martin Čermák, Albert Català, Kalliopi Manola, Nadine Van Roy, Ingrid Simonitsch-Kluppp, Roos Leguit, Peter Bader, Barbara Gazic, Yaniv Zohar, Kalliopi Stefanaki, Michael Dworzak, Maureen O’Sullivan, Roland Meisel, Sophia Polychronopoulou, Emilia J Kozyra, Rita De Vito, David Betts, Pritam Kumar Panda, Amina Szvetnik, Peter Noellke, Brigitte Strahm, Julius Wehrle, Helena Podgornik, Carole Gengler, Valerie de Haas, Krisztián Kállay, Zuzana Zemanova, Luis Mascarenhas de Lemos, Marena R. Niewisch, Joelle Tchinda, Ayami Yoshimi-Noellke, Margarita Llavador Ros, Charlotte M. Niemeyer, Ivana Bodova, Gunnar Cario, Charnise Goodings, Berna Beverloo, Karin Nebral, Hajnalka Andrikovics, Dominik Turkiewicz, Pascale De Paepe, Sushree S. Sahoo, Owen P. Smith, Christian Flotho, Jan Starý, Marek Ussowicz, Jadwiga Maldyk, Riccardo Masetti, Stephan Schwarz-Furlan, Gudrun Göhring, Vit Campr, Francesco Pasquali, Irith Baumann, Henrik Hasle, Michael H. Albert, Shlomit Barzilai, Oksana Fabri, Helena Alaiz, Erik Clasen-Linde, Victor B Pastor, Miriam Erlacher, Kirsi Jahnukainen, Tine Plesner, Franco Locatelli, Olga Haus, Rebecca K Voss, Marta Jeison, Lukas Plank, Markus Schmugge, Rita Beier, José Cervera, Barbara De Moerloose, Owen Smith, Martina Rudelius, Ingo Müller, Jochen Buechner, Marko Kavcic, Martin Sauer, Ansgar Schulz, Judit Csomor, Shinsuke Hirabayashi
Publikováno v:
Nature Medicine. 27:2248-2248
Autor:
Lili Kotmayer, Emilia Kozyra, Maximilian Kaiser, Michael Dworzak, Barbara De Moerloose, Jan Starý, Henrik Hasle, Kirsi Jahnukainen, Sophia Polychronopoulou, Krisztián Kállay, Owen Smith, Shlomit Barzilai, Riccardo Masetti, Jochen Buechner, Marek Ussowicz, Paula Kjollerstrom, Ivana Boďová, Marko Kavcic, Albert Catala, Dominik Turkiewicz, Markus Schmugge, Valérie De Haas, Rebecca Voss, Anna Bigas, Damia Romero, Csaba Bödör, Miriam Erlacher, Alessandra Giorgetti, Charlotte Niemeyer, Marcin Wlodarski
Publikováno v:
EJC Paediatric Oncology, Vol 2, Iss , Pp 100051- (2023)
Externí odkaz:
https://doaj.org/article/c011b85abdfb4cc3bb60ff8c8419145c
Autor:
Yves Bertrand, Akif Yeşilipek, Vanderson Rocha, Tatiana A Bykova, Paul Bosman, Tariq Mahmood Satti, Antonio M. Risitano, Jolanta Gozdzik, Miguel Pérez, Yasmina Mozo, Ardeshir Ghavamzadeh, Gergely Kriván, Carlo Dufour, Dirk-Jan Eikema, Andrzej Lange, Régis Peffault de Latour, Josu de la Fuente, Henrik Sengeløv, Edoardo Lanino, Bénédicte Bruno, Jelena Rascon, Anne Sirvent, Renata Formankova, Matthias Wölfl, Yves Beguin, Karin Mellgren, Maurizio Miano, Charlotte M. Niemeyer, Marc Ansari, Frans J. Smiers, Peter Bader, Ivana Bodova, Attilio Rovelli, Roland Meisel, Dominique Bron, Daniela Onofrillo
Publikováno v:
Blood. 134:44-44
INTRODUCTION Diamond-Blackfan Anemia (DBA) is a congenital pure red cell aplasia, secondary to ribosomal protein genetic defects that usually presents within the first year of age and can be associated with congenital abnormalities and increased risk