Zobrazeno 1 - 10 of 68 pro vyhledávání: '"Murat, Araz"'
1
Akademický článek
The relationship between EGFR mutation and metastasis pattern in lung adenocarcinoma
Autor: Ismail Beypinar, Hacer Demir, Murat Araz, Mukremin Uysal
Publikováno v: Journal of Oncological Sciences, Vol 5, Iss 2, Pp 65-69 (2019)
Aim: The metastatic pattern of non-small cell lung cancer (NSCLC) has been described in several studies. Frequent metastatic sites are lung, liver, bone, surrenal, and brain. Hypotheses were speculated to explain the tendency of specific sites. Over-
Externí odkaz: https://doaj.org/article/4b596b1cab854585867fd432790b5735
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2
Akademický článek
Reactivation risk of Hepatitis B Virus in both HBsAg negative and HBcIgG positive patients with solid malignancy. Is antiviral prophylaxis really necessary?
Autor: Murat Araz, Ismail Beypinar, Tarik Demir, Hacer Demir, Mukremin Uysal
Publikováno v: Medicine Science, Vol 8, Iss 2, Pp 418-21 (2019)
Prophylactic antiviral treatment is controversial due to a lack of studies in both HBsAg negative/HBcIgG positive patients who treated conventional chemotherapy with solid malignancy, unlike HBsAg positive. In this cross-sectional and retrospective s
Externí odkaz: https://doaj.org/article/793bdbc16f924458b3e7f2756a4bb9bd
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4
Akademický článek
Oxaliplatin induced acute immune-mediated thrombocytopenia; a case report
Autor: İsmail Beypinar, Alper Sari, Beray Coker, Murat Araz, Mukremin Uysal
Publikováno v: Journal of Oncological Sciences, Vol 3, Iss 1, Pp 18-21 (2017)
Oxaliplatin is a third-generation platinum anti-neoplastic agent, which is used in the treatment of colorectal, gastric, and biliary tract cancers with combination other chemotherapy drugs. In rare cases, thrombocytopenia may occur suddenly in approx
Externí odkaz: https://doaj.org/article/3973aed161d4463aabd15f54afa2742e
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6
Fabry disease prevalence in patients with familial Mediterranean fever: A cohort study
Autor: Sinan KAZAN, Elif DİZEN KAZAN, Onur TUNCA, Murat ARAZ, Sena ULU
Publikováno v: Journal of Surgery and Medicine. 6:601-604
Background/Aim: Fabry disease is an X-chromosome inherited disease, which constitutes a rare disease group. Fabry disease has a wide spectrum of symptoms and some of these symptoms that are seen in other diseases. Familial Mediterranean fever (FMF) i
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::74d69ba7d3a8631f0e3cda91b78ee248
https://doi.org/10.28982/josam.1004427
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Plný text Recenzováno Digitální knihovna AV ČR
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