Zobrazeno 1 - 10
of 26
pro vyhledávání: '"Karina Tozatto-Maio"'
Autor:
Karina Tozatto-Maio, Robert Girot, Indou Deme Ly, Ana Cristina Silva Pinto, Vanderson Rocha, Francisco Fernandes, Ibrahima Diagne, Yahia Benzerara, Carla L. Dinardo, Julia Pavan Soler, Simone Kashima, Itauá Leston Araujo, Chantal Kenzey, Guilherme H. H. Fonseca, Evandra S. Rodrigues, Fernanda Volt, Luciana Jarduli, Annalisa Ruggeri, Christina Mariaselvam, Sandra F. M. Gualandro, Hanadi Rafii, Barbara Cappelli, Felipe Melo Nogueira, Graziana Maria Scigliuolo, Renato Luiz Guerino-Cunha, Kelen Cristina Ribeiro Malmegrim, Belinda P. Simões, Eliane Gluckman, Ryad Tamouza
Publikováno v:
Frontiers in Immunology, Vol 11 (2020)
Sickle cell disease (SCD), the most common monogenic disease worldwide, is marked by a phenotypic variability that is, to date, only partially understood. Because inflammation plays a major role in SCD pathophysiology, we hypothesized that single nuc
Externí odkaz:
https://doaj.org/article/67cb8a7ed9504d0aaebc582eaf5a2b7d
Autor:
Barbara Cappelli, Fernanda Volt, Karina Tozatto-Maio, Graziana Maria Scigliuolo, Alina Ferster, Sophie Dupont, Belinda Pinto Simões, Amal Al-Seraihy, Mahmoud D. Aljurf, Fahad Almohareb, Cristina Belendez, Susanne Matthes, Nathalie Dhedin, Corinne Pondarre, Jean-Hugues Dalle, Yves Bertrand, Jean Pierre Vannier, Mathieu Kuentz, Patrick Lutz, Gérard Michel, Hanadi Rafii, Benedicte Neven, Marco Zecca, Peter Bader, Marina Cavazzana, Myriam Labopin, Franco Locatelli, Alessandra Magnani, Annalisa Ruggeri, Vanderson Rocha, Françoise Bernaudin, Josu de La Fuente, Selim Corbacioglu, Eliane Gluckman
Publikováno v:
Haematologica, Vol 104, Iss 12 (2019)
Externí odkaz:
https://doaj.org/article/37740344a46448c0bc25c6ada08b8d41
Autor:
Seiko Kato, Karina Tozatto-Maio, Arnon Nagler, Jorge Sierra, Yoshiko Atsuta, Takahiro Fukuda, Junya Kanda, Takanori Ohta, Emanuele Angelucci, Eliane Gluckman, Takafumi Kimura, Riccardo Saccardi, Masatsugu Tanaka, Hiromi Hayashi, Tatsuo Ichinohe, Satoshi Takahashi, Fumihiko Kimura, Naoyuki Uchida, Shinichi Kako, Fernanda Volt, Mohamad Mohty, Masamitsu Yanada, Guillermo Sanz, Vanderson Rocha, Annalisa Ruggeri, Shinichiro Okamoto, Edouard Forcade
Publikováno v:
BONE MARROW TRANSPLANTATION
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instname
r-IIS La Fe. Repositorio Institucional de Producción Científica del Instituto de Investigación Sanitaria La Fe
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instname
r-IIS La Fe. Repositorio Institucional de Producción Científica del Instituto de Investigación Sanitaria La Fe
The impact of GVHD and graft-versus-leukemia effect in unrelated cord blood transplantation (UCBT) is controversial. In the Eurocord/ALWP EBMT and JSTCT/JDCHCT collaborative study, we evaluated the impact of GVHD on UCBT outcomes in Japanese and Euro
Autor:
Kasys Meira Gervatauskas, Felipe Augusto Ros, Guilherme Henrique Hencklain Fonseca, Pedro Victor de Castro e Silva, Felipe Melo Nogueira, Liliana Suganuma Otsuka, Afonso Celso Almeida Cardoso, Sandra Fatima Menosi Gualandro, Vanderson Rocha, Karina Tozatto-Maio
Publikováno v:
Blood. 140:11091-11092
Autor:
Neifi Hassan Saloum Degaide, Margareth Torres, Danielli C. M. Oliveira, Eliane Gluckman, Simone Kashima, Ana Cristina Silva Pinto, Graziana Maria Scigliuolo, Ryad Tamouza, Annalisa Ruggeri, Vanderson Rocha, Juliana Fernandes Cardoso, Barbara Cappelli, Pascale Loiseau, Hendrik Veelken, Evandra Strazza Rodrigues, Hanadi Elayoubi, Chantal Kenzey, Alina Ferster, Belinda Pinto Simões, Karina Tozatto-Maio, Fernanda Volt
Publikováno v:
Biology of Blood and Marrow Transplantation, 26(11), 2034-2039. ELSEVIER SCIENCE INC
Biology of blood and marrow transplantation
Biology of blood and marrow transplantation
Sickle cell disease (SCD) is the most common inherited hemoglobinopathy. Hematopoietic stem cell transplantation (HCT) is the sole curative therapy for SCD, but few patients will have a matched sibling donor. Patients with SCD are mostly of African o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c2cb6b9d5f241a2fb95cba4f3aea50bc
http://hdl.handle.net/1887/3185161
http://hdl.handle.net/1887/3185161
Autor:
Karina Tozatto-Maio, V. Mariano a Rocha, Bruna D. G. C. Moraes, M. F. D. D. Santos, A. A. G. S. Brandão, António Ferreira, Erica Okazaki, M. C. Farias, Guilherme Henrique Hencklain Fonseca
Publikováno v:
Hematology, Transfusion and Cell Therapy
Hematology, Transfusion and Cell Therapy, Vol 42, Iss, Pp 522-(2020)
Hematology, Transfusion and Cell Therapy, Vol 42, Iss, Pp 522-(2020)
Autor:
Marco Zecca, Annalisa Ruggeri, Graziana Maria Scigliuolo, Vanderson Rocha, Karina Tozatto-Maio, Elisabetta Calore, Arjan C. Lankester, Fernanda Volt, Farah O'Boyle, Anna Paisiou, Eliane Gluckman, Selim Corbacioglu, Frans J. Smiers, Claudia Bettoni Da Cunha-Riehm, Mina Tommaso, Michael H. Albert, Sonia Bonanomi, Josu de la Fuente, Barbara Cappelli, Stelios Graphakos
Publikováno v:
Bone Marrow Transplantation. NATURE PUBLISHING GROUP
Bone Marrow Transplantation
Bone Marrow Transplantation
We report the results of an analysis of unrelated allogeneic hematopoietic stem cell transplantations (HSCT) in 71 patients with sickle cell disease (SCD) transplanted in EBMT centers between 2005 and 2017. Median age was 9.3 years; graft type was bo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::971b427ffef1bfe79d767de8aecb3fe1
https://hdl.handle.net/1887/3181395
https://hdl.handle.net/1887/3181395
Autor:
Vanderson Rocha, Myriam Labopin, Seiko Kato, Mohamad Mohty, Maria Teresa Van Lint, Guillermo Sanz, Yoshiko Atsuta, Eliane Gluckman, Heiwa Kanamori, Karina Tozatto-Maio, Shinichi Kako, Takahiro Fukuda, Naoyuki Uchida, Yuju Ohno, Annalisa Ruggeri, Satoshi Takahashi, Edouard Forcade, Shinichiro Okamoto, Jorge Sierra, Minoko Takanashi, Riccardo Saccardi, Junya Kanda, Fumihiko Kimura, Tatsuo Ichinohe, Hiromi Hayashi, Fernanda Volt, Shingo Yano, Arnon Nagler
Publikováno v:
Leukemia
r-IIS La Fe. Repositorio Institucional de Producción Científica del Instituto de Investigación Sanitaria La Fe
instname
LEUKEMIA
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
r-IIS La Fe. Repositorio Institucional de Producción Científica del Instituto de Investigación Sanitaria La Fe
instname
LEUKEMIA
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
Large differences in patient and transplant backgrounds make it difficult to identify consistent prognostic factors of unrelated cord blood transplantation (UCBT) among different populations. Thus, we performed a collaborative study between Eurocord/
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::84dae6430875d697e34f888913af1e20
https://fundanet.iislafe.san.gva.es/publicaciones/ProdCientif/PublicacionFrw.aspx?id=11057
https://fundanet.iislafe.san.gva.es/publicaciones/ProdCientif/PublicacionFrw.aspx?id=11057
Autor:
Eliane, Gluckman, Josu de la, Fuente, Barbara, Cappelli, Graziana M, Scigliuolo, Fernanda, Volt, Karina, Tozatto-Maio, Vanderson, Rocha, Mina, Tommaso, Farah, O'Boyle, Frans, Smiers, Claudia Bettoni Da, Cunha-Riehm, Elisabetta, Calore, Sonia, Bonanomi, Stelios, Graphakos, Anna, Paisiou, Michael H, Albert, Annalisa, Ruggeri, Marco, Zecca, Arjan C, Lankester, Selim, Corbacioglu
Publikováno v:
Bone marrow transplantation. 55(10)
We report the results of an analysis of unrelated allogeneic hematopoietic stem cell transplantations (HSCT) in 71 patients with sickle cell disease (SCD) transplanted in EBMT centers between 2005 and 2017. Median age was 9.3 years; graft type was bo
Autor:
Lucas Assis Pereira, Karina Griesi-Oliveira, Karina Tozatto-Maio, Barbara Ferri Moraschi, Andréa L. Sertié, Luiz Vicente Rizzo, Ricardo Weinlich, Davi Coe Coe Torres, Mariana Tereza Lira Benício, Priscila Keiko Matsumoto Martin, Mariana Morato Marques
Publikováno v:
Blood. 138:1857-1857
Background: Although gene editing by CRISPR/Cas9 is a promising curative strategy for inherited and acquired diseases, potential off-targets remain a major concern. Most computational and biochemical methods for off-target search have focused on sing