Gotowe bibliografie tematyczne / Gliomes Chordoides

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  1. Artykuły w czasopismach
  2. Rozprawy doktorskie
  3. Książki
  4. Części książek

Gotowa bibliografia na temat „Gliomes Chordoides”

Autor: Grafiati
Data publikacji: 16 listopada 2024
Data aktualizacji: 31 lipca 2025

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Artykuły w czasopismach na temat "Gliomes Chordoides"

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Leeds, Norman E., Frederick F. Lang, Teresa Ribalta, Raymond Sawaya, and Gregory N. Fuller. "Origin of Chordoid Glioma of the Third Ventricle." Archives of Pathology & Laboratory Medicine 130, no. 4 (2006): 460–64. http://dx.doi.org/10.5858/2006-130-460-oocgot.

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Abstract Context.—Chordoid glioma is a relatively recently described unique glial neoplasm that has been formally codified by the World Health Organization in Pathology and Genetics of Tumours of the Nervous System, in which it is included along with astroblastoma and gliomatosis cerebri under the rubric “Tumors of Uncertain Origin.” Many examples of chordoid glioma come to clinical attention only at a relatively large size and occupy a large portion of the third ventricle. Accordingly, the anatomic origin of chordoid glioma has been unclear and debated. Objective.—To examine the regional anat
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Thavaratnam, LK, ST Loy, A. Gupta, I. Ng, and JF Cullen. "Chordoid glioma." Singapore Medical Journal 56, no. 11 (2015): 641–43. http://dx.doi.org/10.11622/smedj.2015175.

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Liu, Wei-ping, Jin-xiang Cheng, Xi-cai Yi, et al. "Chordoid Glioma." Neurologist 17, no. 1 (2011): 52–56. http://dx.doi.org/10.1097/nrl.0b013e3181e7db67.

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Ricoy, J. R., R. D. Lobato, B. Báez, A. Cabello, M. A. Martínez, and G. Rodríguez. "Suprasellar chordoid glioma." Acta Neuropathologica 99, no. 6 (2000): 699–703. http://dx.doi.org/10.1007/s004010051183.

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Konovalov, A. N., I. V. Chernov, M. V. Ryzhova, et al. "Chordoid gliomas of the third ventricle." Voprosy neirokhirurgii imeni N.N. Burdenko 87, no. 6 (2023): 14. http://dx.doi.org/10.17116/neiro20238706114.

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Brat, D. J., B. W. Scheithauer, S. C. Cortez, K. Brecher, and P. C. Burger. "THIRD VENTRICULAR “CHORDOID GLIOMA”." Journal of Neuropathology and Experimental Neurology 56, no. 5 (1997): 586. http://dx.doi.org/10.1097/00005072-199705000-00072.

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Brat, Daniel J. "Chordoid glioma further defined." Advances in Anatomic Pathology 9, no. 1 (2002): 77. http://dx.doi.org/10.1097/00125480-200201000-00016.

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Suetens, Kristin, Jeroen Swinnen, Linde Stessens, Sofie Van Cauter, and Geert Gelin. "Chordoid Glioma as a Differential Diagnosis of Anterior Third Ventricle Tumours: A Rare Case Report and Five-Year Follow-Up." Case Reports in Radiology 2019 (December 4, 2019): 1–6. http://dx.doi.org/10.1155/2019/3584837.

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Chordoid glioma is a rare and relatively recently defined tumour entity. Worldwide there have only been around 90 cases described until now. A chordoid glioma comprises a low-grade suprasellar neuroepithelial neoplasm originating in the anterior part of the third ventricle, with consistent radiological features on MRI. This lesion should be considered as a differential of third ventricle tumours. The patient described in this paper is quite unique in the sense that despite only partial tumour resection was obtained, the residual tumour was not progressive during several years of follow-up. Pre
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Bellamy, Charlotte, Hannah Tovell, Florent Dingli, et al. "Abstract 4370: Functional characterisation of a novel mutation in PRKCA, a major driver of chordoid gliomas." Cancer Research 84, no. 6_Supplement (2024): 4370. http://dx.doi.org/10.1158/1538-7445.am2024-4370.

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Abstract Chordoid gliomas (ChG) are a rare low-grade brain tumor, believed to be derived from tanycytes. An analysis by the team identified a novel mutation present in all ChGs: PRKCA p.D463H. This mutation involves a D463H substitution at the kinase domain of the Protein kinase C alpha (PKCα), it is not found in any other cancer, and represents the hallmark of ChG. The aim of the project is to identify novel and biologically relevant PKCαD463H signaling pathways, which will demonstrate the involvement and the role of this mutated kinase in cellular functions implicated in the development of C
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Sanda, Nicolae, Claudiu-Nicolae Mircea, Michèle Bernier, Avinoam B. Safran, and Sorin Aldea. "Chordoid Glioma Infiltrating Optic Structures." Journal of Neuro-Ophthalmology 39, no. 3 (2019): 408–10. http://dx.doi.org/10.1097/wno.0000000000000757.

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Rozprawy doktorskie na temat "Gliomes Chordoides"

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Bellamy, Charlotte. "Functional characterization of a novel mutation in PRKCA, the major driver of Chordoid glioma." Electronic Thesis or Diss., université Paris-Saclay, 2024. http://www.theses.fr/2024UPASL052.

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Le gliome chordoïde (ChG) est une tumeur cérébrale rare de bas grade, caractérisée par une nouvelle mutation ponctuelle récurrente PRKCA p.D463H, une substitution dans le domaine kinase de la protéine kinase C alpha (PKCα). Cette étude démontre le rôle de cette kinase mutée dans le développement des ChG. Ici, nous montrons l'inactivation et l'effet négatif dominant de PKCαD463H via des tests d'activité in vitro et in cellulo. Nos résultats montrent que la mutation affecte la structure tertiaire, ce qui entraîne une protéine ouverte et instable. Les données de spectrométrie de masse phosphoprot
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Książki na temat "Gliomes Chordoides"

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van den Bent, Martin J., Frederic Dhermain, and Walter Stummer. Other neuroepithelial tumours: astroblastoma, angiocentric glioma, and chordoid glioma. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780199651870.003.0007.

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This chapter contains a description of three rare entities: astroblastoma, angiocentric glioma, and chordoid glioma. Because these tumours are so rare, the evidence on how to best treat them is anecdotal and essentially consists of case series, but it is the best guidance available and the presentation of larger series with new cases remain unlikely. If one is confronted with such a case, a meticulous review of the clinical, radiological, and pathological characteristics of the case is indicated, to minimize the risk of an erroneous diagnosis. If the case does not fit in with the descriptions
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Części książek na temat "Gliomes Chordoides"

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Liu, Dongyou. "Chordoid Glioma, Angiocentric Glioma, and Diffuse Midline Glioma." In Tumors and Cancers. CRC Press, 2017. http://dx.doi.org/10.1201/9781315120522-6.

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Filbin, Mariella, Sanda Alexandrescu, Daphne Haas-Kogan, Ian F. Pollack, David A. Reardon, and Christine Haberler. "Circumscribed astrocytic gliomas." In Oxford Textbook of Neuro-Oncology, 2nd ed., edited by Tracy Batchelor and Michael Weller. Oxford University PressOxford, 2025. https://doi.org/10.1093/med/9780198869702.003.0009.

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Abstract Pilocytic astrocytoma is a slow-growing tumor occurring in children and corresponds to World Health Organization grade 1. It is characterized by MAPK pathway alterations and prognosis is very good. High-grade astrocytoma with piloid features occurs in adults, shows signs of anaplasia, MAPK pathway alterations, and distinct DNA methylation. Pleomorphic xanthoastrocytoma occurs in children and young adults with BRAF V600E mutations, homozygous CDKN2A/CDKN2B deletions, and is assigned grade 2 or 3. Chordoid glioma is a rare, slow-growing glioma occurring in adults, and is characterized b
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"Chordoid Glioma of 3rd Ventricle." In Diagnostic Pathology: Neuropathology. Elsevier, 2016. http://dx.doi.org/10.1016/b978-0-323-44592-4.50027-5.

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"Chordoid Glioma of the Third Ventricle." In Diagnostic Imaging: Brain. Elsevier, 2016. http://dx.doi.org/10.1016/b978-0-323-37754-6.50140-8.

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Gallia, Gary L., Martin G. Pomper, and Alessandro Olivi. "Chordoid Glioma of the Third Ventricle." In Textbook of Neuro-Oncology. Elsevier, 2005. http://dx.doi.org/10.1016/b978-0-7216-8148-1.50032-2.

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Brat, Daniel. "Chordoid glioma of the third ventricle." In Russell & Rubinstein's Pathology of Tumors of the Nervous System 7Ed. CRC Press, 2006. http://dx.doi.org/10.1201/b13439-17.

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