Výsledky vyhledávání - "Odabasi, Eylem"

Akademický článek

Stereotactic radiotherapy in acoustic neuroma cases: Tumor control and clinical results.

Autor: Soykut, Ela Delikgoz, Sahin, Nilgun, Odabasi, Eylem, Aksan, Donay, Cecen, Ayse, Tataroglu, Hatice

Publikováno v: Medicine Science; Sep2023, Vol. 12 Issue 3, p933-940, 8p

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Akademický článek

Re-irradiation with stereotactic radiotherapy for recurrent high-grade glial tumors.

Autor: Soykut, Ela Delikgoz, Odabasi, Eylem, Sahin, Nilgun, Tataroglu, Hatice, Baran, Ahmet, Guney, Yildiz

Publikováno v: Reports of Practical Oncology & Radiotherapy; 2023, Vol. 28 Issue 3, p361-369, 9p

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Pre-treatment and post-treatment neutrophil-to-lymphocyte ratio predict pathological tumor response and survival in rectal cancer patients treated with neoadjuvant chemoradiotherapy

Autor: Delikgoz Soykut, Ela, Kemal, Yasemin, Odabasi, Eylem, Sahin, Nilgun, Keskinkilic Yagiz, Betul

OBJECTIVE The aim of this study is to investigate the relationship between baseline and post-treatment neutrophil-to-lymphocyte ratio (NLR) levels and response to neoadjuvant chemoradiotherapy (CRT) in terms of good pathological response and survival

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::60c1d4556f2f65f789d3bfb380adfb8d
https://hdl.handle.net/20.500.12713/2624

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Well controlled atypical central neurocytoma by CyberKnife radiosurgery: Review of the literature with a case report

Autor: Bedir Recep, Yilmaz Rakici Sema, Koksal Vaner, Odabasi Eylem

Publikováno v: International Journal of Case Reports and Images. 11:1

Introduction: Central neurocytomas are rare primary central nervous system tumors. The main treatment method is gross total surgical resection that can only be performed in half of the patients. As the possibility of relapse is higher, post-resection

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::a530f62fa551ced5a6b9a325579dd70a
https://doi.org/10.5348/101178z01sr2020cr

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Long-Time Survival in A Patient with Turcot Syndrome Diagnosed in the Fifth Decade: Case Report

Autor: Meydan, Deniz, Gursel, Bilge, Ozbek, Nilgun, Odabasi, Eylem, Yildiz, Levent, Demirag, Guzin

GURSEL, SUKRIYE BILGE/0000-0002-3109-7146 WOS: 000288679800013 Turcot syndrome is a rare inherited disorder characterized by the association of colon and central nervous system neuroepithelial tumors. Here, we present a patient with Turcot Syndrome h

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______9773::d46b4abbc42ad55d4eea2dd478ae7c40
https://hdl.handle.net/20.500.12712/17441

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