Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Mazhar Muslim Tuna"'
Autor:
Irfan Peksoy, Bercem Aycicek Dogan, Ufuk Ozuguz, Ayse Arduc, Mazhar Muslim Tuna, Dilek Berker, Yusuf Aydin, Serhat Isik, Serdar Güler, Ferhat Gokay, Yasemin Tutuncu
Publikováno v:
Clinical Nuclear Medicine. 39:1022-1026
Purpose: Radioactive 131Iodine therapy (RAIT) plays a major role in the treatment of hyperthyroidism. In addition to the thyroid gland, significant amounts of radioactive iodine are maintained in the stomach. The aim of this study was to determine if
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e1f16a29bad02861b4c25ae4ead15880
https://doi.org/10.1097/rlu.0000000000000519
https://doi.org/10.1097/rlu.0000000000000519
Autor:
Dilek Berker, Ayse Iriz, Mazhar Muslim Tuna, Serhat Isik, Serpil Allusoglu, Bercem Aycicek Dogan, Ayse Arduc, Serdar Güler, Celil Gocer
Sensorineural hearing loss has been reported in various autoimmune diseases. The relationship between Hashimoto's thyroiditis (HT) and the auditory system has not been previously evaluated. In this study, we investigated the effect of euthyroid HT on
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a9d53cfacadb64c4539f1df603c92723
https://avesis.gazi.edu.tr/publication/details/aaeff3a4-551e-429d-80c6-7bccaf69f23a/oai
https://avesis.gazi.edu.tr/publication/details/aaeff3a4-551e-429d-80c6-7bccaf69f23a/oai
Autor:
Bercem Aycicek Dogan, Ayse Arduc, Serpil Allusoglu, Mazhar Muslim Tuna, Dilek Berker, Ayşe İriz, Serdar Güler, Celil Göçer, Serhat Isik
Publikováno v:
Turkish Journal of Endocrinology and Metabolism, Vol 19, Iss 4, Pp 124-129 (2015)
Purpose: It is well known that congenital hypothyroidism can cause hearing loss. However, conflicting results were found in studies investigating hearing functions in acquired hypothyroidism. Therefore, we evaluated the audiometric findings in patien
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6f95b41b66acf38f1d45910c382a4d39
https://hdl.handle.net/11491/1410
https://hdl.handle.net/11491/1410
Autor:
E. Yilmaz, Yavuz Yalcin, Mehmet Resid Onen, Turkan Mete, G. Ozgen, Serdar Guler, D. Ciliz, Mazhar Muslim Tuna, Dilek Berker, Yusuf Aydin
YILMAZ, Engin/0000-0001-8873-7645 WOS: 000331638200020 PubMed: 23673869 Von Hippel Lindau (VHL) syndrome is an autosomal dominant disorder characterized by benign and malignant tumors. This study presents the clinical and genetic features of VHL synd
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::21ac5fe5d1b4e3a288faae2465241850
https://avesis.gazi.edu.tr/publication/details/0c557372-1a0f-4721-b482-412149336d29/oai
https://avesis.gazi.edu.tr/publication/details/0c557372-1a0f-4721-b482-412149336d29/oai