Gonad Development of Black Sea European Flounder, Platichthys flesus, Under Culture Conditions von AYDIN, İlhan, FİRİDİN, Şirin, CEBECİ, Ayşe, ÖZTÜRK, Rafet Çağrı, TERZİ, Yahya, POLAT, Hamza, KÜÇÜK, Ercan

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Population abundance and growth parameters of an exotic bivalve species, Anadara kagoshimensis, in the Southwestern Black Sea von DAĞTEKİN, MURAT, DALGIÇ, GÖKTUĞ, ERBAY, MURAT, AKPINAR, İLKAY ÖZCAN, AYDIN, MEHMET, ÖZDEMİR, SÜLEYMAN, CEBECİ, AYŞE, KARAYÜCEL, SEDAT

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Kapitalist Toplumsal İlişkilerde Dönüşüm – Dönüşümün Katalizörü Olarak Salgın von CEBECİ-, Ayşe

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Gonadotropin releasing hormone analog treatment in children with congenital adrenal hyperplasia complicated by central precocious puberty von Güven, Ayla, Cebeci, Ayşe Nurcan, Hancili, Suna

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Identification of Three Novel and One Known Mutation in the WFS1 Gene in Four Unrelated Turkish Families: The Role of Homozygosity Mapping in the Early Diagnosis von Sherif, Maha, Demirbilek, Hüseyin, Çayır, Atilla, Tahir, Sophia, Çavdarlı, Büşra, Demiral, Meliha, Cebeci, Ayşe Nurcan, Vurallı, Doğuş, Rahman, Sofia Asim, Unal, Edip, Büyükyılmaz, Gönül, Baran, Rıza Taner, Özbek, Mehmet Nuri, Hussain, Khalid

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A rare etiology of tetralogy of Fallot with pulmonary atresia: Renpenning syndrome von Kaymakçalan, Hande, Ercan-Şençiçek, A Gülhan, Cebeci, Ayşe Nurcan, Dong, Weilai, Yalım Yalçın, Ali Seyfi

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Profile of hypothyroidism in Down's syndrome von Cebeci, Ayşe Nurcan, Güven, Ayla, Yıldız, Metin

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Impact of eating habits and nutritional status on children with autism spectrum disorder von Şengüzel, Seda, Cebeci, Ayşe N., Ekici, Barış, Gönen, İsmail, Tatlı, Burak

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A rare cause of autistic regression in a boy with Down syndrome: Hashimoto encephalopathy von Cebeci, Ayse, Kutlu, Feyza, Ekici, Baris

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The first outbreak of citrobacteriosis caused by Citrobacter gillenii in reared Russian sturgeon (Acipenser gueldenstaedtii) in Turkiye von Türe, Mustafa, Cebeci, Ayşe, Özcelep, Tuna

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Whole Genome Sequence of a Novel Bacteriophage APT65 Infecting Aeromonas hydrophila von Cebeci, Ayşe, Türe, Mustafa, Alemdağ, Melike, Altinok, Ilhan

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Mutation of SGK3, a Novel Regulator of Renal Phosphate Transport, Causes Autosomal Dominant Hypophosphatemic Rickets von Cebeci, Ayşe Nurcan, Zou, Minjing, BinEssa, Huda A, Alzahrani, Ali S, Al-Rijjal, Roua A, Al-Enezi, Anwar F, Al-Mohanna, Futwan A, Cavalier, Etienne, Meyer, Brian F, Shi, Yufei

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Remission with cabergoline in adolescent boys with Cushing's disease von Güven, Ayla, Baltacıoğlu, Feyyaz, Dursun, Fatma, Cebeci, Ayşe Nurcan, Kırmızıbekmez, Heves

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Graves' disease in children with Down syndrome von Nurcan Cebeci, Ayse, Schempp, Vera, Förtsch, Katharina, Gohlke, Bettina, Marx, Michaela, Dörr, Helmuth-Guenther, Woelfle, Joachim

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SERMAYENİN ULUSLARARASILAŞMASI VE SUUDİ ARABİSTAN'DA TOPLUMSAL DÖNÜŞÜM von CEBECİ, Ayşe

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Characterization of SP-T1 Phage for Potential Biological Control of Salmonella Enteritidis von ALTINOK, Melih Enes, TURE, Mustafa, CEBECİ, Ayse, ALTINOK, Ilhan

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Spondyloenchondrodysplasia Due to Mutations in ACP5: A Comprehensive Survey von Briggs, Tracy A., Rice, Gillian I., Adib, Navid, Ades, Lesley, Barete, Stephane, Baskar, Kannan, Baudouin, Veronique, Cebeci, Ayse N., Clapuyt, Philippe, Coman, David, De Somer, Lien, Finezilber, Yael, Frydman, Moshe, Guven, Ayla, Heritier, Sébastien, Karall, Daniela, Kulkarni, Muralidhar L., Lebon, Pierre, Levitt, David, Le Merrer, Martine, Linglart, Agnes, Livingston, John H., Navarro, Vincent, Okenfuss, Ericka, Puel, Anne, Revencu, Nicole, Scholl-Bürgi, Sabine, Vivarelli, Marina, Wouters, Carine, Bader-Meunier, Brigitte, Crow, Yanick J.

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The debate on the link between subclinical hypothyroidism and childhood migraine: is initial endocrinological evaluation necessary for children with migraine? von Ekici, Bariş, Cebeci, Ayşe Nurcan

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EVALUATION OF THE ALTERNATIVES FOR GOLD ORE GRINDING CIRCUITS BY USING OF LABORATORY STUDIES RESULTS AND SIMULATION METHOD; CASE STUDY: IRANIAN GOLD CO von HOSSEINZADEH GHAREHGHESHLAGH, Hojjat, CEBECİ, Ayşe Tuğba, ERGÜN, Şevket Levent

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Hyperkeratosis as a clue to diagnosis in a patient with myopathy von Cebeci, Ayşe Nurcan, Ekici, Barış

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