Zobrazeno 1 - 10
of 80
pro vyhledávání: '"G. Purkalne"'
Autor:
J. Maksimenko, A. Irmejs, G. Trofimovičs, D. Bērziņa, E. Skuja, G. Purkalne, E. Miklaševičs, J. Gardovskis
Publikováno v:
Hereditary Cancer in Clinical Practice, Vol 16, Iss 1, Pp 1-7 (2018)
Abstract Background Pathogenic BRCA1 founder mutations (c.4035delA, c.5266dupC) contribute to 3.77% of all consecutive primary breast cancers and 9.9% of all consecutive primary ovarian cancers. Identifying germline pathogenic gene variants in patien
Externí odkaz:
https://doaj.org/article/860d89ac87074c95859c4153b0c9d9c4
Autor:
null Espen Thiis‐Evensen, null Magnus Kjellman, null Ulrich Knigge, null Henning Gronbaek, null Camilla Schalin‐Jäntti, null Staffan Welin, null Halfdan Sorbye, null Maria del Pilar Schneider, null Roger Belusa, null E. Thiis‐Evensen, null M. Kjellman, null U. Knigge, null S. Welin, null H. Gronbaek, null H. Sorbye, null M. T. Joergensen, null A. K. Elf, null R. Belusa, null C. Schalin‐Jäntti, null M. T. Jørgensen, null H. Waldum, null J. A. Søreide, null S. Metso, null T. Ebeling, null F. Lindberg, null K. Landerholm, null G. Wallin, null F. Salem, null G. Purkalne, null I. Kudaba, null R. Janciauskiene, null T. Suuroja, null Edita Baltruškevičienė, null The Nordic NET Biomarker Group
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5d9be146367a673fd30681b02784de84
https://doi.org/10.1111/jne.13176/v2/response1
https://doi.org/10.1111/jne.13176/v2/response1
Akademický článek
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Autor:
G. Purkalne, R. Ferrarotto, I. Anderson, B. Medgyasszay, M.R. García-Campelo, W. Edenfield, T. Feinstein, J. Johnson, S. Kalmadi, P. Lammers, A.S. Hernandez, Y. Pritchett, R.K. Malik, S.R. Morris, T. Csőszi
Publikováno v:
Journal of Thoracic Oncology. 16:S4
Autor:
J, Maksimenko, A, Irmejs, G, Trofimovičs, D, Bērziņa, E, Skuja, G, Purkalne, E, Miklaševičs, J, Gardovskis
Publikováno v:
Hereditary cancer in clinical practice. 16
PathogenicFifteen female probands and 1 male proband that met National Comprehensive Cancer Network (NCCN) criteria forIn 44% (7 out of 16) of tested probands, pathogenic mutations were identified. Six probands carried pathogenic mutations inA relati
Autor:
S. Ramalingam, J. Crawford, A. Chang, C. Manegold, R. Perez-Soler, J.-Y. Douillard, N. Thatcher, F. Barlesi, T. Owonikoko, Y. Wang, P. Pultar, J. Zhu, R. Malik, G. Giaccone, S. Della-Fiorentina, S. Begbie, R. Jennens, J. Dass, K. Pittman, N. Ivanova, T. Koynova, P. Petrov, A. Tomova, V. Tzekova, F. Couture, V. Hirsh, R. Burkes, R. Sangha, M. Ambrus, T. Janaskova, J. Musil, J. Novotny, P. Zatloukal, J. Jakesova, K. Klenha, J. Roubec, J. Vanasek, J. Fayette, J. Bennouna-Louridi, C. Chouaid, J. Mazières, H. Vallerand, G. Robinet, P.-J. Souquet, D. Spaeth, R. Schott, H. Lena, Y. Martinet, C. El Kouri, N. Baize, A. Scherpereel, O. Molinier, F. Fuchs, K.M. Josten, N. Marschner, F. Schneller, T. Overbeck, M. Thomas, J. von Pawel, M. Reck, W. Schuette, V. Hagen, C.-P. Schneider, V. Georgoulias, I. Varthalitis, K. Zarogoulidis, K. Syrigos, C. Papandreou, C. Bocskei, E. Csanky, E. Juhasz, G. Losonczy, Z. Mark, I. Molnar, Z. Papai-Szekely, S. Tehenes, I. Vinkler, S. Almel, A. Bakshi, S. Bondarde, A. Maru, A. Pathak, R.M. Pedapenki, K. Prasad, S.V.S.S. Prasad, N. Kilara, D. Gorijavolu, C.D. Deshmukh, S. John, L.M. Sharma, D. Amoroso, E. Bajetta, P. Bidoli, A. Bonetti, F. De Marinis, M. Maio, R. Passalacqua, S. Cascinu, A. Bearz, M. Bitina, A. Brize, G. Purkalne, M. Skrodele, A.A. Baba, K. Ratnavelu, M.H. Saw, M.C. Samson-Fernando, G.E. Ladrera, J. Jassem, P. Koralewski, P. Serwatowski, M. Krzakowski, C. Cebotaru, D. Filip, D.E. Ganea-Motan, C.H. Ianuli, I.G. Manolescu, A. Udrea, O. Burdaeva, M. Byakhov, A. Filippov, S. Lazarev, I. Mosin, S. Orlov, D. Udovitsa, A. Khorinko, S. Protsenko, H.L. Lim, Y.O. Tan, E.H. Tan, R. Bastus Piulats, J. Garcia-Foncillas, J. Valdivia, J. de Castro, M. Domine Gomez, S.W. Kim, J.-S. Lee, H.K. Kim, J.S. Lee, S.W. Shin, D.-W. Kim, Y.-C. Kim, K.C. Park, C.-S. Chang, G.-C. Chang, Y.-G. Goan, W.-C. Su, C.-M. Tsai, H.-P. Kuo, M. Benekli, G. Demir, E. Gokmen, A. Sevinc, M. Haigentz, M. Agarwal, S. Pandit, R. Araujo, N. Vrindavanam, P. Bonomi, A. Berg, J. Wade, R. Bloom, B. Amin, R. Camidge, D. Hill, M. Rarick, P. Flynn, L. Klein, K. Lo Russo, M. Neubauer, P. Richards, R. Ruxer, M. Savin, D. Weckstein, R. Rosenberg, T. Whittaker, D. Richards, W. Berry, C. Ottensmeier, A. Dangoor, N. Steele, Y. Summers, E. Rankin, K. Rowley, S. Giridharan, H. Kristeleit, C. Humber, P. Taylor
Publikováno v:
Annals of Oncology. 24:2875-2880
Background Talactoferrin alfa is an oral dendritic cell (DC)-mediated immunotherapy (DCMI). We tested whether talactoferrin was superior to placebo in advanced non-small-cell lung cancer (NSCLC). Patients and methods An FORTIS-M trial was an internat
Autor:
C. Dittrich, M. Kosty, S. Jezdic, D. Pyle, R. Berardi, J. Bergh, N. El Saghir, J.-P. Lotz, P. Österlund, N. Pavlidis, G. Purkalne, Hetty Carraway, Julia Lee Close, Jill Gilbert, Carsten Bokemeyer, Andrés Cervantes, Yuichiro Ohe, Miklos Pless, Keith McGregor, Katharine Fumassoli, Roberta Candiani, Gracemarie Bricalli, Tanya Kenny, Nicola Latino, Marina Cogo, Vanessa Pavinato, Vanessa Marchesi, Ahmad Awada, Susana Banerjee, Smita Bhatia, Jan Bogaerts, Jan Buckner, Fatima Cardoso, Paolo Casali, Edward Chu, Bertrand Coiffier, Roisin Connolly, Sarah Coupland, Luigi De Petris, Maria De Santis, Elisabeth G.E. de Vries, Don S. Dizon, Jennifer Duff, Linda R. Duska, Alexandru Eniu, Marc Ernstoff, Enriqueta Felip, Martin F. Fey, Nicolas Girard, Andor W.J.M. Glaudemans, Priya K. Gopalan, Axel Grothey, Stephen M. Hahn, Diana Hanna, Christian Herold, Jørn Herrstedt, Krisztian Homicsko, Dennie V. Jones, Lorenz Jost, Ulrich Keilholz, Saad Khan, Alexander Kiss, Claus-Henning Köhne, Rainer Kunstfeld, Heinz-Josef Lenz, Stuart Lichtman, Lisa Licitra, Thomas Lion, Saskia Litière, Lifang Liu, Patrick J. Loehrer, Merry Jennifer Markham, Ben Markman, Marius Mayerhoefer, Johannes G. Meran, Olivier Michielin, Elizabeth Charlotte Moser, Giannis Mountzios, Timothy Moynihan, Torsten Nielsen, Kjell Öberg, Antonio Palumbo, Fedro Alessandro Peccatori, Michael Pfeilstöcker, Chandrajit Raut, Scot C. Remick, Mark Robson, Piotr Rutkowski, Roberto Salgado, Lidia Schapira, Eva Schernhammer, Martin Schlumberger, Hans-Joachim Schmoll, Lowell Schnipper, Cristiana Sessa, Charles L. Shapiro, Julie Steele, Cora N. Sternberg, Friedrich Stiefel, Florian Strasser, Roger Stupp, Richard Sullivan, Josep Tabernero, Luzia Travado, Marcel Verheij, Emile Voest, Everett Vokes, Jamie Von Roenn, Jeffrey S. Weber, Hans Wildiers, Yosef Yarden
Publikováno v:
Annals of Oncology
Annals of oncology, vol. 27, no. 8, pp. 1378-1381
Annals of Oncology, 27(8), 1378-1381. Oxford University Press
Annals of oncology, vol. 27, no. 8, pp. 1378-1381
Annals of Oncology, 27(8), 1378-1381. Oxford University Press
Non
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dbbf93eb74f8190a23e0f656b0db62df
https://gnosis.library.ucy.ac.cy/handle/7/41570
https://gnosis.library.ucy.ac.cy/handle/7/41570
Akademický článek
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K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Publikováno v:
Annals of Oncology. 16:i66-i68
Autor:
Robert Huddart, G. Purkalne
Publikováno v:
Annals of Oncology. 16:i37-i39