Zobrazeno 1 - 10
of 37
pro vyhledávání: '"Fırat, Yezdan"'
Autor:
Firat, Yezdan ∗, Engin-Ustun, Yaprak †, Kizilay, Ahmet ∗, Ustun, Yusuf †, Akarcay, Mustafa ∗, Selimoglu, Erol ∗, Kafkasli, Ayse †
Publikováno v:
In Journal of Voice 2009 23(6):716-720
Publikováno v:
In American Journal of Otolaryngology--Head and Neck Medicine and Surgery 2008 29(5):339-345
Publikováno v:
In Otolaryngology - Head and Neck Surgery 2007 137(2):218-223
Publikováno v:
In International Journal of Pediatric Otorhinolaryngology 2006 70(8):1431-1438
Akademický článek
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Publikováno v:
In European Journal of Radiology 2005 56(2):192-196
Autor:
Fırat, Ahmet Kemal, Fırat, Yezdan, Karakaş, Hakkı Muammer, Önal, Çağatay, Kahraman, Bayram, Alkan, Alpay, Altınok, Tayfun
Publikováno v:
Volume: 12, Issue: 2 139-143
Journal of Turgut Ozal Medical Center
Journal of Turgut Ozal Medical Center
The most prominent MRI finding of abcess is the peripheric enhancement following gadolinium injection. This finding usually persists despite the reduced volume of abcess and clinical improvement. In this study we presented the succeeding diffusion we
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=tubitakulakb::2fc2dbce270907b71fe1e810aa13a235
https://dergipark.org.tr/tr/pub/totm/issue/13117/158063
https://dergipark.org.tr/tr/pub/totm/issue/13117/158063
Publikováno v:
Volume: 15, Issue: 2 117-119
Journal of Turgut Ozal Medical Center
Journal of Turgut Ozal Medical Center
Growth retardation, microcephaly, hypoplasia or aplasia of thumb, renal and urinary tract anomalies, skin pigmentation and eye anomalies are well known signs of Fanconi aplastic anemia. While congenital sensorineural hearing loss is an unusual sympto
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=tubitakulakb::e74f5fc949042054b9f75475197a1bde
https://dergipark.org.tr/tr/pub/totm/issue/13105/157880
https://dergipark.org.tr/tr/pub/totm/issue/13105/157880
Autor:
Mutlu, Deniz Yakar, Fırat, Ahmet Kemal, Karakaş, Hakkı Muammer, Erdem, Gülnur, Fırat, Yezdan, Güngör, Serdal
Publikováno v:
Volume: 15, Issue: 2 103-107
Journal of Turgut Ozal Medical Center
Journal of Turgut Ozal Medical Center
Adrenoleukodystrophy is an X-linked hereditary disorder involving cerebral white matter, adrenal cortex and testis. The incidence of this disease is ranging between 1/25 000 and 1/100 000. This disease is diagnosed by demonstrating accumulation of ve
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=tubitakulakb::2da4115b0f3f248ae461fd75efbb2a33
https://dergipark.org.tr/tr/pub/totm/issue/13105/157877
https://dergipark.org.tr/tr/pub/totm/issue/13105/157877
Amaç: Rekürren sekretuar otitis mediası (SOM) olan erişkin hastalarda, göreceli yeni bir yöntem olan Phadiatop ile atopi varlığı araştırıldı; yöntemin duyarlılığı, özgüllüğü ve tarama testi olarak kullanılabilirliği incelendi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______9506::12c198c489d31b27229462351d67d7e4
https://hdl.handle.net/20.500.12587/1125
https://hdl.handle.net/20.500.12587/1125