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	1.	[On the use and the results of cortisone in the treatment of allergic rhinitis]. [electronic resource] by TEZEL, E B KONUK, E S Producer: 20030501 In: Tip Fakultesi mecmuasi vol. 16 Availability: No items available. Save to lists Add to cart (remove)
	2.	Rubinstein-Taybi syndrome with normal FISH result and CREBBP gene analysis: a case report. [electronic resource] by Balci, Sevim Ergün, Mehmet Ali Yüksel-Konuk, E Berrin Bartsch, Oliver Producer: 20081024 In: The Turkish journal of pediatrics vol. 50 Availability: No items available. Save to lists Add to cart (remove)
	3.	Expression of cyclooxygenase-2 in orbital fibroadipose connective tissues of Graves' ophthalmopathy patients. [electronic resource] by Konuk, E Berrin Yuksel Konuk, Onur Misirlioglu, Muge Menevse, Adnan Unal, Mehmet Producer: 20070108 In: European journal of endocrinology vol. 155 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	The efficacy of eye movement desensitization and reprocessing for post-traumatic stress disorder and depression among Syrian refugees: results of a randomized controlled trial. [electronic resource] by Acarturk, C Konuk, E Cetinkaya, M Senay, I Sijbrandij, M Gulen, B Cuijpers, P Producer: 20171117 In: Psychological medicine vol. 46 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Effect of tauroursodeoxycholic acid on PUFA levels and inflammation in an animal and cell model of hepatic endoplasmic reticulum stress. [electronic resource] by Aslan, M Kıraç, E Yılmaz, Ö Ünal, B Konuk, E K Özcan, F Tuzcu, H Producer: 20181018 In: Human & experimental toxicology vol. 37 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Homozygous mutations in fibroblast growth factor 3 are associated with a new form of syndromic deafness characterized by inner ear agenesis, microtia, and microdontia. [electronic resource] by Tekin, Mustafa Hişmi, Burcu Oztürk Fitoz, Suat Ozdağ, Hilal Cengiz, Filiz Başak Sirmaci, Asli Aslan, Idil Inceoğlu, Bora Yüksel-Konuk, E Berrin Yilmaz, Seda Taşir Yasun, Oztan Akar, Nejat Producer: 20070313 In: American journal of human genetics vol. 80 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Homozygous FGF3 mutations result in congenital deafness with inner ear agenesis, microtia, and microdontia. [electronic resource] by Tekin, M Oztürkmen Akay, H Fitoz, S Birnbaum, S Cengiz, F B Sennaroğlu, L Incesulu, A Yüksel Konuk, E B Hasanefendioğlu Bayrak, A Sentürk, S Cebeci, I Utine, G E Tunçbilek, E Nance, W E Duman, D Producer: 20080723 In: Clinical genetics vol. 73 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Mutations in TMC1 contribute significantly to nonsyndromic autosomal recessive sensorineural hearing loss: a report of five novel mutations. [electronic resource] by Sirmaci, Asli Duman, Duygu Oztürkmen-Akay, Hatice Erbek, Seyra Incesulu, Armağan Oztürk-Hişmi, Burcu Arici, Z Serap Yüksel-Konuk, E Berrin Taşir-Yilmaz, Seda Tokgöz-Yilmaz, Suna Cengiz, Filiz Başak Aslan, Idil Yildirim, Müzeyyen Hasanefendioğlu-Bayrak, Aylin Ayçiçek, Abdullah Yilmaz, Ismail Fitoz, Suat Altin, Fazilet Ozdağ, Hilal Tekin, Mustafa Producer: 20090814 In: International journal of pediatric otorhinolaryngology vol. 73 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)