Zobrazeno 1 - 10
of 28
pro vyhledávání: '"Daniel, Alderete"'
Autor:
Lorena V. Baroni, Nicolas Fernández Ponce, Candela Freytes, Francisco R. Maldonado, Natalia Pinto, Javier González Ramos, Fabiana Lubieniecki, Pedro Zubizarreta, Daniel Alderete
Publikováno v:
Frontiers in Oncology, Vol 13 (2023)
Externí odkaz:
https://doaj.org/article/f0b853c9aaf14068bbb2e69df8e81e0f
Autor:
Lorena V, Baroni, Tamara, Muñoz Cassina, Nicolás, Fernández Ponce, Natalia, Pinto, Valeria, Vázquez, Fabiana, Lubieniecki, Daniel, Alderete
Publikováno v:
Journal of Pediatric Hematology/Oncology. 44:415-418
Medulloblastoma has a reduced incidence in Down syndrome (DS). This protective characteristic has not been clarified yet. Here, we report the second case of SHH medulloblastoma and DS documented in the literature. A complete surgery was performed fol
Autor:
Natalia Pinto, Nicolas Fernandez Ponce, Carlos Rugilo, Adriana Gonzalez, Fabiana Lubieniecki, Claudia Sampor, Daniel Alderete, Lorena V Baroni, Francisco R Maldonado, Candela Freytes, Agustina Oller
Publikováno v:
Journal of Neuro-Oncology. 155:53-61
Background Many studies have demonstrated in the last years that once medulloblastoma has recurred, the probability of regaining tumor control is poor despite salvage therapy. Although re-irradiation has an emerging role in other relapsed brain tumor
Autor:
Gabriela Villanueva, Claudia Sampor, Florencia Moreno, Daniel Alderete, Angelica Moresco, Natalia Pinto, Irene Szijan, Paula Schaiquevich, María Sara Felice, Adriana Rose, Pedro Zubizarreta, Mariana Sgroi, Adriana Fandiño, Guillermo Chantada
Publikováno v:
Pediatric Blood & Cancer. 69
Retinoblastoma survivors in low- and middle-income countries are exposed to high-intensity treatments that potentially place them at higher risk of early subsequent malignant neoplasms (SMNs).We followed 714 (403 [56.4%] nonhereditary and 311 [43.5%]
Autor:
Fabiana Lubieniecki, Valeria Vazquez, Gabriela S. Lamas, Sandra Camarero, Felipe J. Nuñez, Lorena Baroni, Ulrich Schüller, Daniel Alderete
Publikováno v:
Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery.
Central nervous system high-grade neuroepithelial tumor with MN1 alteration (CNS-HGNET-MN1) is a rare entity defined by its DNA methylation pattern and pathologically considered to be high-grade with mixed patterns, stromal hyalinization, and with as
Autor:
Eric, Warriner, Nicolás, Fernández Ponce, Candela, Freytes, Claudia, Sampor, Agustina, Oller, Carlos, Rugilo, Fabiana, Lubieniecki, Valeria, Vazquez, Daniel, Alderete, Lorena V, Baroni
Publikováno v:
Medicina. 81(5)
The BRAFV600E point mutation plays a key role in the tumorigenesis of many gliomas. Inhibiting its product is part of the innovative therapies emerging in recent years. Knowing the role of these treatments is essential. The aim of this experience was
Autor:
Natalia Pinto, Lorena V Baroni, Claudia Sampor, Carlos Rugilo, Agustina Oller, Nicolas Ponce Fernandez, Pedro Zubizarreta, Daniel Alderete, Fabiana Lubieniecki, Candela Freytes
Background: Intracranial germ cell tumor (iGCT) represents a rare and heterogeneous group, with variable incidence and diverse treatment strategies. Although multiagent chemotherapy with reduced radiotherapy strategy has been applied by several coope
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::349fa1af4a09a26164bdc758f8822692
https://doi.org/10.21203/rs.3.rs-157912/v1
https://doi.org/10.21203/rs.3.rs-157912/v1
Autor:
Katja von Hoff, Christine Haberler, Felix Schmitt-Hoffner, Elizabeth Schepke, Teresa de Rojas, Sandra Jacobs, Michal Zapotocky, David Sumerauer, Marta Perek-Polnik, Christelle Dufour, Dannis von Vuurden, Irene Slavc, Johannes Gojo, Jessica C. Pickles, Nicolas U. Gerber, Maura Massimino, Maria Joao Gil-da-Costa, Miklos Garami, Ella Kumirova, Astrid Sehested, David Scheie, Ofelia Cruz, Lucas Moreno, Jaeho Cho, Bernward Zeller, Niels Bovenschen, Michael Grotzer, Daniel Alderete, Matija Snuderl, Olga Zheludkova, Andrey Golanov, Konstantin Okonechnikov, Martin Mynarek, B. Ole Juhnke, Stefan Rutkowski, Ulrich Schüller, Barry Pizer, Barbara von Zezschwitz, Robert Kwiecien, Maximilian Wechsung, Frank Konietschke, Eugene I. Hwang, Dominik Sturm, Stefan M. Pfister, Andreas von Deimling, Elisabeth J. Rushing, Marina Ryzhova, Peter Hauser, Maria Lastowska, Pieter Wesseling, Felice Giangaspero, Cynthia Hawkins, Dominique Figarella-Branger, Charles Eberhardt, Peter Burger, Marco Gessi, Andrey Korshunov, Tom S. Jacques, David Capper, Torsten Pietsch, Marcel Kool
Publikováno v:
SSRN Electronic Journal.
Autor:
Christelle Dufour, Johannes Gojo, Sandra Jacobs, Barry Pizer, Dominik Sturm, Torsten Pietsch, Stefan Rutkowski, Christine Haberler, Nicolas U. Gerber, Teresa de Rojas, Peter Hauser, Ulrich Schüller, Peter C. Burger, Marta Perek-Polnik, Martin Mynarek, Jaeho Cho, Matija Snuderl, Bernward Zeller, Michal Zapotocky, Maura Massimino, Robert Kwiecien, Dominique Figarella-Branger, Andrey Golanov, Charles G. Eberhart, Stefan M. Pfister, Daniel Alderete, Thomas S. Jacques, Ella Kumirova, Konstantin Okonechnikov, Astrid Sehested, Ofelia Cruz, Andrey Korshunov, Björn Ole Juhnke, Niels Bovenschen, Jessica C Pickles, David Sumerauer, Cynthia Hawkins, David Scheie, Eugene Hwang, Pieter Wesseling, Barbara von Zezschwitz, Felice Giangaspero, Marcel Kool, Elizabeth Schepke, Andreas von Deimling, Marco Gessi, Dannis G. van Vuurden, Maximilian Wechsung, Miklós Garami, David Capper, Katja von Hoff, Maria Joao Gil-da-Costa, Maria Łastowska, Felix Schmitt-Hoffner, Olga Zheludkova, Lucas Moreno, Michael A. Grotzer, Frank Konietschke, Marina Ryzhova, Elisabeth J. Rushing, Irene Slavc
Publikováno v:
Neuro-Oncology 23(9), 1597-1611 (2021). doi:10.1093/neuonc/noab136
Neuro-Oncology
r-FSJD: Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
Fundació Sant Joan de Déu
Neuro-Oncology, Oxford University Press (OUP), 2021, ⟨10.1093/neuonc/noab136⟩
Neuro-Oncology, 23(9), 1597-1611. Oxford University Press
von Hoff, K, Haberler, C, Schmitt-Hoffner, F, Schepke, E, de Rojas, T, Jacobs, S, Zapotocky, M, Sumerauer, D, Perek-Polnik, M, Dufour, C, van Vuurden, D, Slavc, I, Gojo, J, Pickles, J C, Gerber, N U, Massimino, M, Gil-da-Costa, M J, Garami, M, Kumirova, E, Sehested, A, Scheie, D, Cruz, O, Moreno, L, Cho, J, Zeller, B, Bovenschen, N, Grotzer, M, Alderete, D, Snuderl, M, Zheludkova, O, Golanov, A, Okonechnikov, K, Mynarek, M, Juhnke, B O, Rutkowski, S, Schüller, U, Pizer, B, von Zezschwitz, B, Kwiecien, R, Wechsung, M, Konietschke, F, Hwang, E I, Sturm, D, Pfister, S M, von Deimling, A, Rushing, E J, Ryzhova, M, Hauser, P, Łastowska, M, Wesseling, P, Giangaspero, F, Hawkins, C, Figarella-Branger, D, Eberhart, C, Burger, P, Gessi, M, Korshunov, A, Jacques, T S, Capper, D, Pietsch, T & Kool, M 2021, ' Therapeutic implications of improved molecular diagnostics for rare CNS embryonal tumor entities : Results of an international, retrospective study ', Neuro-Oncology, vol. 23, no. 9, pp. 1597-1611 . https://doi.org/10.1093/neuonc/noab136
Neuro Oncol
r-FSJD. Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
instname
Neuro-Oncology, 2021, ⟨10.1093/neuonc/noab136⟩
Neuro-Oncology
r-FSJD: Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
Fundació Sant Joan de Déu
Neuro-Oncology, Oxford University Press (OUP), 2021, ⟨10.1093/neuonc/noab136⟩
Neuro-Oncology, 23(9), 1597-1611. Oxford University Press
von Hoff, K, Haberler, C, Schmitt-Hoffner, F, Schepke, E, de Rojas, T, Jacobs, S, Zapotocky, M, Sumerauer, D, Perek-Polnik, M, Dufour, C, van Vuurden, D, Slavc, I, Gojo, J, Pickles, J C, Gerber, N U, Massimino, M, Gil-da-Costa, M J, Garami, M, Kumirova, E, Sehested, A, Scheie, D, Cruz, O, Moreno, L, Cho, J, Zeller, B, Bovenschen, N, Grotzer, M, Alderete, D, Snuderl, M, Zheludkova, O, Golanov, A, Okonechnikov, K, Mynarek, M, Juhnke, B O, Rutkowski, S, Schüller, U, Pizer, B, von Zezschwitz, B, Kwiecien, R, Wechsung, M, Konietschke, F, Hwang, E I, Sturm, D, Pfister, S M, von Deimling, A, Rushing, E J, Ryzhova, M, Hauser, P, Łastowska, M, Wesseling, P, Giangaspero, F, Hawkins, C, Figarella-Branger, D, Eberhart, C, Burger, P, Gessi, M, Korshunov, A, Jacques, T S, Capper, D, Pietsch, T & Kool, M 2021, ' Therapeutic implications of improved molecular diagnostics for rare CNS embryonal tumor entities : Results of an international, retrospective study ', Neuro-Oncology, vol. 23, no. 9, pp. 1597-1611 . https://doi.org/10.1093/neuonc/noab136
Neuro Oncol
r-FSJD. Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
instname
Neuro-Oncology, 2021, ⟨10.1093/neuonc/noab136⟩
Background Only few data are available on treatment-associated behavior of distinct rare CNS embryonal tumor entities previously treated as “CNS-primitive neuroectodermal tumors” (CNS-PNET). Respective data on specific entities, including CNS neu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0cfda65d63cf766e727aec652e64d395
Autor:
Michal Zápotocký, Carlos Rugilo, Barbora Ondrová, Vajiranee S Malalasekera, Jordan R. Hansford, Ute Bartels, Candela Freytes, Vijay Ramaswamy, Martin Kyncl, Normand Laperriere, Daniel Alderete, Derek S. Tsang, Uri Tabori, Suzanne Laughlin, Palma Solano-Paez, Eric Bouffet, Lorena V Baroni, Adriana Fonseca, David Sumerauer, Annie Huang
Publikováno v:
Neurooncol Pract
Background Radiation necrosis is a frequent complication occurring after the treatment of pediatric brain tumors; however, treatment options remain a challenge. Bevacizumab is an anti-VEGF monoclonal antibody that has been shown in small adult cohort