Sökresultat - Cayir, Atilla

Growth Hormone Therapy in Children with Chronic Renal Failure av Cayir, Atilla, Kosan, Celalettin

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First Report of a de novo 10q23.31q23.33 Microdeletion: Obesity, Intellectual Disability and Microcephaly av Turkyilmaz, Ayberk, Kurnaz, Erdal, Cayir, Atilla

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Evaluation of Hearing in Children with Metabolic Syndrome av Kılıç, Korhan, Sakat, Muhammed Sedat, Çayır, Atilla

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Cystinosis Presenting with Findings of Bartter Syndrome av Özkan, Behzat, Çayır, Atilla, Koşan, Celalettin, Alp, Handan

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Anogenital Distance in Turkish Newborns av Özkan, Behzat, Konak, Belkıs, Çayır, Atilla, Konak, Murat

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Bone mineral density and vitamin K status in children with celiac disease: Is there a relation? av Volkan, Burcu, Fettah, Ali, İşlek, Ali, Kara, Soner Sertan, Kurt, Nezahat, Çayır, Atilla

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The Relationship between Psychopathology, Self-esteem, Body Perception and Serum Sex Steroids in Pubertal Gynecomastia av Arslan, Semiha Comertoglu, Esin, Ibrahim Selcuk, Cayır, Atilla, Orbak, Zerrin, Dursun, Onur Burak

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An Unusual Congenital Anomaly in Fanconi Aplastic Anemia: Congenital Lobar Emphysema av Fettah, Ali, Reis, Gökçe Pınar, Kara, Soner Sertan, Aksu, Tekin, Durur Karakaya, Afak, Subaşı, Mahmut, Çayır, Atilla

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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 av 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, Riza Taner, Özbek, Mehmet Nuri, Hussain, Khalid

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Comparison of Treatment Regimens in Management of Severe Hypercalcemia Due to Vitamin D Intoxication in Children av Demir, Korcan, Döneray, Hakan, Kara, Cengiz, Atay, Zeynep, Çetinkaya, Semra, Çayır, Atilla, Anık, Ahmet, Eren, Erdal, Uçaktürk, Ahmet, Can Yılmaz, Gülay, Törel Ergür, Ayça, Kendirci, Mustafa, Aycan, Zehra, Bereket, Abdullah, Aydın, Murat, Orbak, Zerrin, Özkan, Behzat

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Novel Mutations in Obesity-related Genes in Turkish Children with Non-syndromic Early Onset Severe Obesity: A Multicentre Study av Akıncı, Ayşehan, Türkkahraman, Doğa, Tekedereli, İbrahim, Özer, Leyla, Evren, Bahri, Şahin, İbrahim, Kalkan, Tarkan, Çürek, Yusuf, Çamtosun, Emine, Döğer, Esra, Bideci, Aysun, Güven, Ayla, Eren, Erdal, Sangün, Özlem, Çayır, Atilla, Bilir, Pelin, Törel Ergür, Ayça, Ercan, Oya

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Management of Thyrotoxicosis in Children and Adolescents: A Turkish Multi-center Experience av Esen, İhsan, Bayramoğlu, Elvan, Yıldız, Melek, Aydın, Murat, Karakılıç Özturhan, Esin, Aycan, Zehra, Bolu, Semih, Önal, Hasan, Kör, Yılmaz, Ökdemir, Deniz, Ünal, Edip, Önder, Aşan, Evliyaoğlu, Olcay, Çayır, Atilla, Taştan, Mehmet, Yüksel, Ayşegül, Kılınç, Aylin, Büyükinan, Muammer, Özcabı, Bahar, Akın, Onur, Binay, Çiğdem, Kılınç, Suna, Yıldırım, Ruken, Hatun Aytaç, Emel, Sağsak, Elif

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Clinical Characteristics and Long-term Follow-up of Patients with Diabetes Due To PTF1A Enhancer Mutations av Demirbilek, Huseyin, Cayir, Atilla, Flanagan, Sarah E, Yıldırım, Ruken, Kor, Yılmaz, Gurbuz, Fatih, Haliloğlu, Belma, Yıldız, Melek, Baran, Rıza Taner, Akbas, Emine Demet, Demiral, Meliha, Ünal, Edip, Arslan, Gulcin, Vuralli, Dogus, Buyukyilmaz, Gonul, Al-Khawaga, Sara, Saeed, Amira, Al Maadheed, Maryam, Khalifa, Amel, Onal, Hasan, Yuksel, Bilgin, Ozbek, Mehmet Nuri, Bereket, Abdullah, Hattersley, Andrew T, Hussain, Khalid, De Franco, Elisa

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The Growth Characteristics of Patients with Noonan Syndrome: Results of Three Years of Growth Hormone Treatment: A Nationwide Multicenter Study av Şıklar, Zeynep, Genens, Mikayir, Poyrazoğlu, Şükran, Baş, Firdevs, Darendeliler, Feyza, Bundak, Rüveyde, Aycan, Zehra, Savaş Erdeve, Şenay, Çetinkaya, Semra, Güven, Ayla, Abalı, Saygın, Atay, Zeynep, Turan, Serap, Kara, Cengiz, Can Yılmaz, Gülay, Akyürek, Nesibe, Abacı, Ayhan, Çelmeli, Gamze, Sarı, Erkan, Bolu, Semih, Korkmaz, Hüseyin Anıl, Şimşek, Enver, Çatlı, Gönül, Büyükinan, Muammer, Çayır, Atilla, Evliyaoğlu, Olcay, İşgüven, Pınar, Özgen, Tolga, Hatipoğlu, Nihal, Elhan, Atilla Halil, Berberoğlu, Merih

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The phenotypic and molecular genetic spectrum of Alström Syndrome in 44 Turkish kindreds and a literature review of Alström Syndrome in Turkey av Ozantürk, Ayşegül, Marshall, Jan D, Collin, Gayle B, Düzenli, Selma, Marshall, Robert P, Candan, Şükrü, Tos, Tülay, Esen, İhsan, Taşkesen, Mustafa, Çayır, Atilla, Öztürk, Şükrü, Üstün, İhsan, Ataman, Esra, Karaca, Emin, Özdemir, Taha Reşid, Erol, İlknur, Eroğlu, Fehime Kara, Torun, Deniz, Parıltay, Erhan, Yılmaz-Güleç, Elif, Karaca, Ender, Atabek, M. Emre, Elçioğlu, Nursel, Satman, İlhan, Möller, Claes, Müller, Jean, Naggert, Jürgen K, Özgül, Rıza Köksal

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Nationwide Turkish Cohort Study of Hypophosphatemic Rickets av Şıklar, Zeynep, Turan, Serap, Bereket, Abdullah, Baş, Firdevs, Güran, Tülay, Akberzade, Azad, Abacı, Ayhan, Demir, Korcan, Böber, Ece, Özbek, Mehmet Nuri, Kara, Cengiz, Poyrazoğlu, Şükran, Aydın, Murat, Kardelen, Aslı, Tarım, Ömer, Eren, Erdal, Hatipoğlu, Nihal, Büyükinan, Muammer, Akyürek, Nesibe, Çetinkaya, Semra, Bayramoğlu, Elvan, Selver Eklioğlu, Beray, Uçaktürk, Ahmet, Abalı, Saygın, Gökşen, Damla, Kor, Yılmaz, Ünal, Edip, Esen, İhsan, Yıldırım, Ruken, Akın, Onur, Çayır, Atilla, Dilek, Emine, Kırel, Birgül, Anık, Ahmet, Çatlı, Gönül, Berberoğlu, Merih

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WNT Signaling Perturbations Underlie the Genetic Heterogeneity of Robinow Syndrome av White, Janson J., Mazzeu, Juliana F., Coban-Akdemir, Zeynep, Bayram, Yavuz, Bahrambeigi, Vahid, Hoischen, Alexander, van Bon, Bregje W.M., Gezdirici, Alper, Gulec, Elif Yilmaz, Ramond, Francis, Touraine, Renaud, Thevenon, Julien, Shinawi, Marwan, Beaver, Erin, Heeley, Jennifer, Hoover-Fong, Julie, Durmaz, Ceren D., Karabulut, Halil Gurhan, Marzioglu-Ozdemir, Ebru, Cayir, Atilla, Duz, Mehmet B., Seven, Mehmet, Price, Susan, Ferreira, Barbara Merfort, Vianna-Morgante, Angela M., Ellard, Sian, Parrish, Andrew, Stals, Karen, Flores-Daboub, Josue, Jhangiani, Shalini N., Gibbs, Richard A., Brunner, Han G., Sutton, V. Reid, Lupski, James R., Carvalho, Claudia M.B.

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