Zobrazeno 1 - 7
of 7
pro vyhledávání: '"İhsan Üstün"'
Autor:
İhsan Üstün, Mustafa Arı, Cumali Gökçe, Vefik Arıca, Mesut Coşkun, Murat Çelik, Kamil Cezgin, Burak Akçay
Publikováno v:
Volume: 1, Issue: 1 47-49
The Medical Journal of Mustafa Kemal University
Mustafa Kemal Üniversitesi Tıp Dergisi, Vol 1, Iss 1, Pp 47-49 (2015)
The Medical Journal of Mustafa Kemal University
Mustafa Kemal Üniversitesi Tıp Dergisi, Vol 1, Iss 1, Pp 47-49 (2015)
Bardet Biedle Syndrome is a pleiotropic disorder with variable expressivity. Up to date fourteen BBS gene mutations have been reported. Primary cilia are microtubule-based membrane projections located at the surface of many cells and defects in prima
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::ec89993ce80569ff83889b99ed450415
https://hdl.handle.net/20.500.12483/439
https://hdl.handle.net/20.500.12483/439
Autor:
Cumali Gökçe, Sema Asilyörük, Gamze Serarslan, İhsan Üstün, Murat Çelik, Nigar Yılmaz, Edip Uçar, Mehmet Demir, Hasan Kaya, Şerefettin Canda
Publikováno v:
Volume: 1, Issue: 1 15-22
The Medical Journal of Mustafa Kemal University
Mustafa Kemal Üniversitesi Tıp Dergisi, Vol 1, Iss 1, Pp 15-22 (2015)
The Medical Journal of Mustafa Kemal University
Mustafa Kemal Üniversitesi Tıp Dergisi, Vol 1, Iss 1, Pp 15-22 (2015)
Amaç: Vitiligo, herhangi bir yaşta ortaya çıkabilen, değişik büyüklükte ve sayıda, iyi sınırlı, süt beyazı renkte yamalar şeklinde görülen, melanosit yıkımı ile karakterize kazanılmış, ilerleyici, deri ve saç folikülünü tu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::22f47b3aeb56305806ea2c8634f9fe95
https://dergipark.org.tr/tr/pub/mkutfd/issue/19583/209429
https://dergipark.org.tr/tr/pub/mkutfd/issue/19583/209429
Autor:
Serdar Çukur, Hanifi Kurtaran, Oguz Tekin, Cem Uraldi, Ferhat Çatal, Adem Özkara, Ihsan Üstün, Bunyamin Isik
Publikováno v:
European Neurology. 52:156-161
Background: The relationship between hypertension and cognitive impairment has been investigated in the literature; several clinical studies suggested a relationship between hypertension and retinopathy. Methods: We examined the relationship between
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7eaca26e49cfbb1344d286cda2a5bfbf
https://doi.org/10.1159/000081855
https://doi.org/10.1159/000081855
Autor:
Yusuf Aydın, Dilek Berker, Sercan Bulut, Yasemin Ateş Tütüncü, Serhat Işık, İhsan Üstün, Tuncay Delibaşı, Serdar Güler
Publikováno v:
Turkish Journal of Endocrinology and Metabolism, Vol 13, Iss 1, Pp 13-15 (2009)
McCune-Albright syndrome (MAS) is characterized by a triad of poly/monostotic fibrous dysplasia, café-au-lait macules, and hyperfunctioning endocrinopathies, including growth hormone (GH) excess. Acromegaly, as a manifestation of endocrine hyperfunc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doajarticles::a19cd10dd21086d0015fdea980276431
http://www.turkjem.org/eng/yazilar.asp?yaziid=596&sayiid=
http://www.turkjem.org/eng/yazilar.asp?yaziid=596&sayiid=
Autor:
Merve Yilmaz, Erdal Eskioglu, Bilal Ergül, Firdes Topal, İhsan Üstün, Seyfettin Köklü, Selma Karaahmetoglu, Baris Kosan, Osman Yüksel, Emin Altiparmak
Publikováno v:
Clinical Biochemistry. 41:917-919
Background and aims Helicobacter pylori infects the gastric mucosa and can lead to chronic gastritis, gastric ulcer and gastric cancer. Colonization of H. pylori in the gastric mucosa is influenced by a variety of host, bacterial and environmental fa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bf12e5f8acfadff710987d4425d7fd0d
https://doi.org/10.1016/j.clinbiochem.2008.03.004
https://doi.org/10.1016/j.clinbiochem.2008.03.004
Publikováno v:
Turkish Journal of Medical Sciences.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9597acfe53c1bdd06b28bb7b2cc60227
https://doi.org/10.3906/sag-0806-28
https://doi.org/10.3906/sag-0806-28
Autor:
Ayşegül Ozantürk, Jan D Marshall, Gayle B Collin, Selma Düzenli, Robert P Marshall, Şükrü Candan, Tülay Tos, İhsan Esen, Mustafa Taşkesen, Atilla Çayır, Şükrü Öztürk, İhsan Üstün, Esra Ataman, Emin Karaca, Taha Reşid Özdemir, İlknur Erol, Fehime Kara Eroğlu, Deniz Torun, Erhan Parıltay, Elif Yılmaz-Güleç, Ender Karaca, M Emre Atabek, Nursel Elçioğlu, İlhan Satman, Claes Möller, Jean Muller, Jürgen K Naggert, Rıza Köksal Özgül
Publikováno v:
Journal of Human Genetics. 60:51-51
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::792f21acfc6290ea05ea191dd8d866a6
https://doi.org/10.1038/jhg.2014.101
https://doi.org/10.1038/jhg.2014.101