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

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Higher body fat and lower fat-free mass in girls with premature adrenarche von Cebeci, Ayşe Nurcan, Taş, Ayşegül

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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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Clinical and Genetic Characteristics, Management and Long-Term Follow-Up of Turkish Patients with Congenital Hyperinsulinism von Güven, Ayla, Cebeci, Ayşe Nurcan, Ellard, Sian, Flanagan, Sarah E

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Isolation and characterization of Aeromonas hydrophila-specific lytic bacteriophages von Ture, Mustafa, Cebeci, Ayse, Altinok, Ilhan, Aygur, Elif, Caliskan, Nihal

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Delirium in diabetic ketoacidosis: a case report von Cebeci, Ayşe Nurcan, Güven, Ayla

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3M syndrome: a report of four cases in two families von Güven, Ayla, Cebeci, Ayşe Nurcan

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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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Erratum to: 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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Developmental defects of the thyroid gland: relationship with advanced maternal age von Kirmızibekmez, Heves, Güven, Ayla, Yildiz, Metin, Cebeci, Ayşe Nurcan, Dursun, Fatma

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Characterization of novel bacteriophage HP‐T19 that targets Hafnia alvei von Ture, Mustafa, Altinok, Ilhan, Cebeci, Ayse, Caliskan, Nihal

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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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