Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Sandra Basic Kinda"'
Autor:
Maria Gavriatopoulou, Andrew Spencer, Daniel Coriu, Fernando Escalante Barrigón, Roman Hájek, Fernanda Seguro, Norma C. Gutiérrez, Sandra Basic Kinda, Massimo Offidani, Dorotea Beatriz Eugenia Fantl, Rosane Bittencourt, Anna Lysén, Vladimir Maisnar, Elham Askari, Joaquín Martinez-Lopez, Olivia Hughes, Rebekah Taylor, Kristin Lehn, Roby Joehanes, Jeremy Ross, Carlos Hader
Publikováno v:
HemaSphere, Vol 7, p e9381810 (2023)
Externí odkaz:
https://doaj.org/article/b5ab678bac0d4bd9be6641ea15db9cae
Autor:
Zdravko Mitrovic, Dino Dujmovic, Ozren Jaksic, Sandra Basic Kinda, Petar Gacina, Vlatka Perisa, Zeljko Prka, Barbara Dreta, Davor Galusic, Hrvoje Holik, Vlatko Pejsa, Igor Aurer
Publikováno v:
European Journal of Haematology. 110:725-731
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::af9aecbb9502240e1b7a68c9aafa2577
https://doi.org/10.1111/ejh.13957
https://doi.org/10.1111/ejh.13957
Autor:
Lea Galunic Bilic, Fedor Santek, Josip J. Grah, Sandra Basic-Kinda, Inga Mandac Smoljanovic, Slobodanka Ostojic Kolonic, Zdravko Mitrovic, Marijo Vodanovic, Dino Dujmovic, Igor Aurer
Publikováno v:
La radiologia medica. 128:492-500
Purpose Data on efficacy and toxicity of infradiaphragmal radiotherapy fields in lymphoma patients are scarce. We therefore performed this retrospective study to analyse our experience with radiotherapy exclusively to infradiaphragmal fields. Materia
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::56b1f9f03fd22b4c9088fd1c1a7aab1e
https://doi.org/10.1007/s11547-023-01615-8
https://doi.org/10.1007/s11547-023-01615-8
Autor:
Sandeep S. Davé, David B. Dunson, Jyotishka Datta, Yuan Zhuang, Shawn Levy, Cassandra Love, Anupama Reddy, Deepthi Rajagopalan, Jenny Zhang, Guojie Li, Nicholas S. Davis, Randy D. Gascoyne, Sandra Basic-Kinda, Igor Aurer, John R. Goodlad, William W. L. Choi, Gopesh Srivastava, Rex K.H. Au-Yeung, Amy Chadburn, Andrew M. Evens, Monika Pilichowska, Pierre Sujobert, Anne Moreau, Marie Parrens, Lucile Baseggio, Mayur Parihar, Anne W. Beaven, Christopher R. Flowers, Leon Bernal-Mizrachi, Steven Horwitz, Neha Mehta-Shah, Wing C. Chan, Dennis Weisenburger, Lawrence Low, Eric D. Hsi, Sarah L. Ondrejka, Yuri Fedoriw, Kristy L. Richards, Jennifer R. Chapman-Fredricks, Izidore S. Lossos, Magdalena B. Czader, Virginie Fataccioli, Marie Helene Delfau-Larue, Karim Belhadj, Javeed Iqbal, Tayla Heavican, Liqiang Xi, Stefania Pittaluga, Elaine S. Jaffe, Mark Raffeld, Alina Nicolae, Laurence De Leval, Marion Travert, Philippe Gaulard, Andrea B. Moffitt, Matthew McKinney
Supplementary Table S1. Sanger validated variants. Supplementary Table S2. Mutations in HSTL driver genes. Supplementary Table S3. Other mutations identified by exome sequencing. Supplementary Table S4. Copy number of HSTL patients and cell lines. Su
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b2977857d8e39de8241655319c2cafef
https://doi.org/10.1158/2159-8290.22532180
https://doi.org/10.1158/2159-8290.22532180
Autor:
Sandeep S. Davé, David B. Dunson, Jyotishka Datta, Yuan Zhuang, Shawn Levy, Cassandra Love, Anupama Reddy, Deepthi Rajagopalan, Jenny Zhang, Guojie Li, Nicholas S. Davis, Randy D. Gascoyne, Sandra Basic-Kinda, Igor Aurer, John R. Goodlad, William W. L. Choi, Gopesh Srivastava, Rex K.H. Au-Yeung, Amy Chadburn, Andrew M. Evens, Monika Pilichowska, Pierre Sujobert, Anne Moreau, Marie Parrens, Lucile Baseggio, Mayur Parihar, Anne W. Beaven, Christopher R. Flowers, Leon Bernal-Mizrachi, Steven Horwitz, Neha Mehta-Shah, Wing C. Chan, Dennis Weisenburger, Lawrence Low, Eric D. Hsi, Sarah L. Ondrejka, Yuri Fedoriw, Kristy L. Richards, Jennifer R. Chapman-Fredricks, Izidore S. Lossos, Magdalena B. Czader, Virginie Fataccioli, Marie Helene Delfau-Larue, Karim Belhadj, Javeed Iqbal, Tayla Heavican, Liqiang Xi, Stefania Pittaluga, Elaine S. Jaffe, Mark Raffeld, Alina Nicolae, Laurence De Leval, Marion Travert, Philippe Gaulard, Andrea B. Moffitt, Matthew McKinney
Supplementary Figure S1. Sanger sequencing chromatograms. Supplementary Figure S2. Cancer cell fraction for driver genes. Supplementary Figure S3. Ideogram with chromosome 7 alterations. Supplementary Figure S4. Examples of Exome Copy Number. Supplem
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1096702833396e08e883c3e0ac18c2a4
https://doi.org/10.1158/2159-8290.22532186
https://doi.org/10.1158/2159-8290.22532186
Autor:
Andrew Spencer, Maria Gavriatopoulou, Daniel Coriu, Sandra Basic - Kinda, Roman Hajek, Ankit Pahwa, Rebekah Taylor, Kristin Lehn, Roby Joehanes, Jeremy A. Ross, Carlos Hader
Publikováno v:
Blood. 140:12481-12482
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4b2d6333ae30426ce01dea81335f7deb
https://doi.org/10.1182/blood-2022-159677
https://doi.org/10.1182/blood-2022-159677
Autor:
Sanja Perkovic, Sandra Basic-Kinda, Vladimir Gasparovic, Zeljko Krznaric, Jaksa Babel, Ivana Ilic, Igor Aurer, Drago Batinic
Publikováno v:
Hematology Reports, Vol 4, Iss 3, Pp e16-e16 (2012)
Aggressive natural killer-cell leukaemia (ANKL) is a rare type of disease with fulminant course and poor outcome. The disease is more prevalent among Asians than in other ethnic groups and shows strong association with Epstein-Barr virus (EBV) and P-
Externí odkaz:
https://doaj.org/article/3bb95d01adf4443b8e983f42977ea6eb
Autor:
Sandra, Basic-Kinda, Ivan, Karlak, Nadira, Durakovic, Zvonimir I, Lubina, Ivo, Livaja Radman, Snježana, Dotlic, Zinaida, Peric, Ida, Hude, Igor, Aurer
Publikováno v:
Internal medicine journal. 48(5)
Escalated BEACOPP (eBEACOPP) is an effective but fairly toxic regimen for the treatment of Hodgkin lymphoma (HL). Avascular necrosis (AVN) of femoral head was previously reported to increase in patients treated with eBEACOPP, but so far, no systemati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::8638a31b8cc34edf2eed522da9d0d583
https://pubmed.ncbi.nlm.nih.gov/29898275
https://pubmed.ncbi.nlm.nih.gov/29898275
Autor:
Matthew McKinney, Andrea B. Moffitt, Philippe Gaulard, Marion Travert, Laurence De Leval, Alina Nicolae, Mark Raffeld, Elaine S. Jaffe, Stefania Pittaluga, Liqiang Xi, Tayla Heavican, Javeed Iqbal, Karim Belhadj, Marie Helene Delfau-Larue, Virginie Fataccioli, Magdalena B. Czader, Izidore S. Lossos, Jennifer R. Chapman-Fredricks, Kristy L. Richards, Yuri Fedoriw, Sarah L. Ondrejka, Eric D. Hsi, Lawrence Low, Dennis Weisenburger, Wing C. Chan, Neha Mehta-Shah, Steven Horwitz, Leon Bernal-Mizrachi, Christopher R. Flowers, Anne W. Beaven, Mayur Parihar, Lucile Baseggio, Marie Parrens, Anne Moreau, Pierre Sujobert, Monika Pilichowska, Andrew M. Evens, Amy Chadburn, Rex K.H. Au-Yeung, Gopesh Srivastava, William W. L. Choi, John R. Goodlad, Igor Aurer, Sandra Basic-Kinda, Randy D. Gascoyne, Nicholas S. Davis, Guojie Li, Jenny Zhang, Deepthi Rajagopalan, Anupama Reddy, Cassandra Love, Shawn Levy, Yuan Zhuang, Jyotishka Datta, David B. Dunson, Sandeep S. Davé
Hepatosplenic T-cell lymphoma (HSTL) is a rare and lethal lymphoma; the genetic drivers of this disease are unknown. Through whole-exome sequencing of 68 HSTLs, we define recurrently mutated driver genes and copy-number alterations in the disease. Ch
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::df0a020f12d7fb0edabbf2fb5c025d8d
http://hdl.handle.net/10722/242321
http://hdl.handle.net/10722/242321
Autor:
Nadira Duraković, Zinaida Perić, Sandra Bašić Kinda, Lana Desnica, Dino Dujmović, Ivo Radman Livaja, Ranka Serventi Seiwerth, Igor Aurer, Radovan Vrhovac
Publikováno v:
Clinical Hematology International, Vol 3, Iss 3 (2021)
Externí odkaz:
https://doaj.org/article/cd5db7e76ca04e8f809d3a388da93dd5