Zobrazeno 1 - 10
of 1 655
pro vyhledávání: '"glioneuronal"'
Autor:
Vincenzo Di Nunno, Marta Aprile, Lidia Gatto, Alicia Tosoni, Lucia Ranieri, Stefania Bartolini, Enrico Franceschi
Publikováno v:
CNS Oncology, Vol 13, Iss 1 (2024)
Aim: Glioneuronal and neuronal tumors are rare primary central nervous system malignancies with heterogeneous features. Due to the rarity of these malignancies diagnosis and treatment remains a clinical challenge. Methods: Here we performed a narrati
Externí odkaz:
https://doaj.org/article/1b549ac3aff74934ad2277c2ab33be82
Autor:
Emilie Russler-Germain, Shamaita Majumdar, Theresa Nguyen, Keiko Hirose, Peter H. Yang, Ali Mian, Sonika Dahiya
Publikováno v:
Free Neuropathology, Vol 5 (2024)
Externí odkaz:
https://doaj.org/article/3af3e00006ce436b84f1c4a148633b3b
Autor:
V. S. Khalilov, A. N. Kislyakov, A. A. Kholin, U. A. Kukota, N. A. Medvedeva, A. S. Shapovalov, A. E. Druy
Publikováno v:
Русский журнал детской неврологии, Vol 19, Iss 2, Pp 64-71 (2024)
Diffuse leptomeningeal glioneuronal tumor was introduced into the World Health Organization classification of central nervous system tumors in 2016. According to the actual World Health Organization classification of central nervous system tumors eme
Externí odkaz:
https://doaj.org/article/dfea64631e4c4f06ae2c35b96c178dfb
Autor:
Margaret Shatara, Kathleen M. Schieffer, Marilena Melas, Elizabeth A. Varga, Diana Thomas, Brianna A. Bucknor, Heather M. Costello, Gregory Wheeler, Benjamin J. Kelly, Katherine E. Miller, Diana P. Rodriguez, Mariam T. Mathew, Kristy Lee, Erin Crotty, Sarah Leary, Vera A. Paulson, Bonnie Cole, Mohamed S. Abdelbaki, Jonathan L. Finlay, Margot A. Lazow, Ralph Salloum, Maryam Fouladi, Daniel R. Boué, Elaine R. Mardis, Catherine E. Cottrell
Publikováno v:
Frontiers in Oncology, Vol 14 (2024)
IntroductionIn the setting of pediatric and adolescent young adult cancer, increased access to genomic profiling has enhanced the detection of genetic variation associated with cancer predisposition, including germline syndromic conditions. Noonan sy
Externí odkaz:
https://doaj.org/article/3f7187b0ada1421ea4a77df0475dfdd6
Publikováno v:
Interdisciplinary Neurosurgery, Vol 36, Iss , Pp 101972- (2024)
A Diffuse Leptomeningeal Glioneuronal Tumor (DLGNT), a rare entity as classified in the World Health Organization’s Fifth Edition of the Classification of Tumors of the Central Nervous System (WHO CNS5), is characterized by oligodendrocyte-like cel
Externí odkaz:
https://doaj.org/article/59bb9e3da082454eb9013548b948739d
Publikováno v:
Diagnostic Pathology, Vol 19, Iss 1, Pp 1-7 (2024)
Abstract Background This study aimed to investigate the clinicopathological characteristics, diagnostic indicators, and critical factors for the differential diagnosis of rosette-forming glioneuronal tumor (RGNT). Patients and methods This retrospect
Externí odkaz:
https://doaj.org/article/6bb95a16eb93473aa5c080650fba4af3
Autor:
Nova Kristine de los Reyes-Nabhan, Stefanie Scheil-Bertram, Sangamitra Boppudi, Barbara Carl, Daniel Jussen
Publikováno v:
Case Reports in Oncology, Vol 17, Iss 1, Pp 337-343 (2024)
Introduction: Diffuse leptomeningeal glioneuronal tumor (DLGNT), a new addition to the 2016 World Health Organization (WHO) classification, is a rare childhood neoplasm presenting with disseminated leptomeningeal enhancement and an occasional intrapa
Externí odkaz:
https://doaj.org/article/3624ae01b34e4cf393bd69826aab4e60
Glial and glioneuronal tumors: Navigating the complexity of evolving concepts and new classification
Autor:
Han, Peng Cheng a, ⁎, Baker, Tiffany G. b
Publikováno v:
In Journal of the Neurological Sciences 15 June 2024 461
Akademický článek
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Autor:
Zijiang Yang, Xiaobiao Zhang
Publikováno v:
Biomedicines, Vol 12, Iss 10, p 2325 (2024)
Background: Rosette-Forming Glioneuronal Tumors (RGNTs) are rare, typically benign central nervous system tumors primarily located in the fourth ventricle and pineal region. Despite being classified as WHO grade I with generally favorable prognoses,
Externí odkaz:
https://doaj.org/article/7dedfcb541e44b27bb08c8e5e83bd39f