Genotype and Phenotype Heterogeneity in Neonatal Diabetes: A Single Centre Experience in Turkey von Denkboy Öngen, Yasemin, Eren, Erdal, Demirbaş, Özgecan, Sobu, Elif, Ellard, Sian, De Franco, Elisa, Tarım, Ömer

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Nationwide Turkish Cohort Study of Hypophosphatemic Rickets von 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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Clinical and Laboratory Characteristics of Hyperprolactinemia in Children and Adolescents: National Survey von Eren, Erdal, Törel Ergür, Ayça, İşgüven, Şükriye Pınar, Çelebi Bitkin, Eda, Berberoğlu, Merih, Şıklar, Zeynep, Baş, Firdevs, Yel, Servet, Baş, Serpil, Söbü, Elif, Bereket, Abdullah, Turan, Serap, Sağlam, Halil, Atay, Zeynep, Ercan, Oya, Güran, Tülay, Atabek, Mehmet Emre, Korkmaz, Hüseyin Anıl, Kılınç Uğurlu, Aylin, Akıncı, Ayşehan, Döğer, Esra, Şimşek, Enver, Akbaş, Emine Demet, Abacı, Ayhan, Gül, Ülkü, Acar, Sezer, Mengen Uçaktürk, Eda, Yıldız, Melek, Ünal, Edip, Tarım, Ömer

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Thyroid Hormones and Growth in Health and Disease - Review von Tarım, Ömer

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Revised one-bag IV fluid protocol for pediatric DKA: a feasible approach and retrospective comparative study von Doğan, Durmuş, Gökalp, Hatice D C, Eren, Erdal, Sağlam, Halil, Tarım, Ömer

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Compound Heterozygous Variants in FAM111A Cause Autosomal Recessive Kenny-Caffey Syndrome Type 2 von Eren, Erdal, Tezcan Ünlü, Havva, Ceylaner, Serdar, Tarım, Ömer

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Resolution of autoimmune oophoritis after thymectomy in a myasthenia gravis patient von Çakır, Esra Deniz Papatya, Özdemir, Özlem, Eren, Erdal, Sağlam, Halil, Okan, Mehmet, Tarım, Ömer Faruk

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A Rare Cause of Insulin-Dependent Diabetes: Two Siblings with Walcott-Rallison Syndrome von Söbü, Elif, Eren, Erdal, Demirbaş, Özgecan, Sağlam, Halil, Tarım, Ömer

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Thyroid hormones and growth in health and disease von Tarım, Ömer

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Height predictions by Bayley-Pinneau method may misguide pediatric endocrinologists von Tarım, Omer

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Mutational analysis of PHEX, FGF23 and CLCN5 in patients with hypophosphataemic rickets von Guven, Ayla, Al‐Rijjal, Roua A., BinEssa, Huda A., Dogan, Durmuş, Kor, Yılmaz, Zou, Minjing, Kaya, Namik, Alenezi, Anwar F., Hancili, Suna, Tarım, Ömer, Baitei, Essa Y., Kattan, Walaa E, Meyer, Brian F., Shi, Yufei

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Rare Causes of Primary Adrenal Insufficiency: Genetic and Clinical Characterization of a Large Nationwide Cohort von Guran, Tulay, Buonocore, Federica, Saka, Nurcin, Ozbek, Mehmet Nuri, Aycan, Zehra, Bereket, Abdullah, Bas, Firdevs, Darcan, Sukran, Bideci, Aysun, Guven, Ayla, Demir, Korcan, Akinci, Aysehan, Buyukinan, Muammer, Aydin, Banu Kucukemre, Turan, Serap, Agladioglu, Sebahat Yilmaz, Atay, Zeynep, Abali, Zehra Yavas, Tarim, Omer, Catli, Gonul, Yuksel, Bilgin, Akcay, Teoman, Yildiz, Metin, Ozen, Samim, Doger, Esra, Demirbilek, Huseyin, Ucar, Ahmet, Isik, Emregul, Ozhan, Bayram, Bolu, Semih, Ozgen, Ilker Tolga, Suntharalingham, Jenifer P, Achermann, John C

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Turner syndrome and associated problems in Turkish children: a multicenter study von Yeşilkaya, Ediz, Bereket, Abdullah, Darendeliler, Feyza, Baş, Firdevs, Poyrazoğlu, Şükran, Küçükemre Aydın, Banu, Darcan, Şükran, Dündar, Bumin, Büyükinan, Muammer, Kara, Cengiz, Sarı, Erkan, Adal, Erdal, Akıncı, Ayşehan, Atabek, Mehmet Emre, Demirel, Fatma, Çelik, Nurullah, Özkan, Behzat, Özhan, Bayram, Orbak, Zerrin, Ersoy, Betül, Doğan, Murat, Ataş, Ali, Turan, Serap, Gökşen, Damla, Tarım, Ömer, Yüksel, Bilgin, Ercan, Oya, Hatun, Şükrü, Şimşek, Enver, Ökten, Ayşenur, Abacı, Ayhan, Döneray, Hakan, Özbek, Mehmet Nuri, Keskin, Mehmet, Önal, Hasan, Akyürek, Nesibe, Bulan, Kezban, Tepe, Derya, Emeksiz, Hamdi Cihan, Demir, Korcan, Kızılay, Deniz, Topaloğlu, Ali Kemal, Eren, Erdal, Özen, Samim, Abalı, Saygın, Akın, Leyla, Selver Eklioğlu, Beray, Kaba, Sultan, Anık, Ahmet, Baş, Serpil, Ünüvar, Tolga, Sağlam, Halil, Bolu, Semih, Özgen, Tolga, Doğan, Durmuş, Deniz Çakır, Esra, Şen, Yaşar, Andıran, Nesibe, Çizmecioğlu, Filiz, Evliyaoğlu, Olcay, Karagüzel, Gülay, Pirgon, Özgür, Çatlı, Gönül, Can, Hatice Dilek, Gürbüz, Fatih, Binay, Çiğdem, Baş, Veysel Nijat, Fidancı, Kürşat, Polat, Adem, Gül, Davut, Açıkel, Cengizhan, Demirbilek, Hüseyin, Cinaz, Peyami, Bondy, Carolyn

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Anthropometric findings from birth to adulthood and their relation with karyotpye distribution in Turkish girls with Turner syndrome von Sari, Erkan, Bereket, Abdullah, Yeşilkaya, Ediz, Baş, Firdevs, Bundak, Rüveyde, Aydın, Banu Küçükemre, Darcan, Şükran, Dündar, Bumin, Büyükinan, Muammer, Kara, Cengiz, Adal, Erdal, Akıncı, Ayşehan, Atabek, Mehmet Emre, Demirel, Fatma, Çelik, Nurullah, Özkan, Behzat, Özhan, Bayram, Orbak, Zerrin, Ersoy, Betül, Doğan, Murat, Ataş, Ali, Turan, Serap, Gökşen, Damla, Tarım, Ömer, Yüksel, Bilgin, Ercan, Oya, Hatun, Şükrü, Şimşek, Enver, Ökten, Ayşenur, Abacı, Ayhan, Döneray, Hakan, Özbek, Mehmet Nuri, Keskin, Mehmet, Önal, Hasan, Akyürek, Nesibe, Bulan, Kezban, Tepe, Derya, Emeksiz, Hamdi Cihan, Demir, Korcan, Kızılay, Deniz, Topaloğlu, Ali Kemal, Eren, Erdal, Özen, Samim, Demirbilek, Hüseyin, Abalı, Saygın, Akın, Leyla, Eklioğlu, Beray Selver, Kaba, Sultan, Anık, Ahmet, Baş, Serpil, Unuvar, Tolga, Sağlam, Halil, Bolu, Semih, Özgen, Tolga, Doğan, Durmuş, Çakır, Esra Deniz, Şen, Yaşar, Andıran, Nesibe, Çizmecioğlu, Filiz, Evliyaoğlu, Olcay, Karagüzel, Gülay, Pirgon, Özgür, Çatlı, Gönül, Can, Hatice Dilek, Gürbüz, Fatih, Binay, Çiğdem, Baş, Veysel Nijat, Fidancı, Kürşat, Gül, Davut, Polat, Adem, Acıkel, Cengizhan, Cinaz, Peyami, Darendeliler, Feyza

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Clinical and Laboratory Characteristics of Hyperprolactinemia in Children and Adolescents: National Survey von Eren, Erdal, Törel Ergür, Ayça, İşgüven, Şükriye Pınar, Çelebi Bitkin, Eda, Berberoğlu, Merih, Şıklar, Zeynep, Baş, Firdevs, Yel, Servet, Baş, Serpil, Söbü, Elif, Bereket, Abdullah, Turan, Serap, Sağlam, Halil, Atay, Zeynep, Ercan, Oya, Güran, Tülay, Atabek, Mehmet Emre, Korkmaz, Hüseyin Anıl, Kılınç Uğurlu, Aylin, Akıncı, Ayşehan, Döğer, Esra, Şimşek, Enver, Akbaş, Emine Demet, Abacı, Ayhan, Gül, Ülkü, Acar, Sezer, Mengen Uçaktürk, Eda, Yıldız, Melek, Unal, Edip, Tarım, Ömer

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Increased incidence of congenital hypothyroidism due to iodine deficiency von SAG˘LAM, HALIL, BÜYÜKUYSAL, LEVENT, KÖKSAL, NILGÜN, ERCAN, I˙LKER, TARIM, ÖMER

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Pediatric patients with pheochromocytoma: Experience of a tertiary health center von Eren, Erdal, Saglam, Halil, Caliskan, Yusuf, Kiristioglu, Irfan, Tarim, Omer

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Thyroid dyshormonogenesis is mainly caused by TPO mutations in consanguineous community von Cangul, Hakan, Aycan, Zehra, Olivera-Nappa, Alvaro, Saglam, Halil, Schoenmakers, Nadia A., Boelaert, Kristien, Cetinkaya, Semra, Tarim, Omer, Bober, Ece, Darendeliler, Feyza, Bas, Veysel, Demir, Korcan, Aydin, Banu K., Kendall, Michaela, Cole, Trevor, Högler, Wolfgang, Chatterjee, V. Krishna K., Barrett, Timothy G., Maher, Eamonn R.

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Liver Involvement in Congenital Hypopituitarism von Altay, Derya, Eren, Erdal, Ozkan, Tanju Basarır, Ozgur, Taner, Tarım, Omer

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Homozygous loss-of-function mutations in SLC26A7 cause goitrous congenital hypothyroidism von Cangul, Hakan, Liao, Xiao-Hui, Schoenmakers, Erik, Kero, Jukka, Barone, Sharon, Srichomkwun, Panudda, Iwayama, Hideyuki, Serra, Eva G, Saglam, Halil, Eren, Erdal, Tarim, Omer, Nicholas, Adeline K, Zvetkova, Ilona, Anderson, Carl A, Frankl, Fiona E Karet, Boelaert, Kristien, Ojaniemi, Marja, Jääskeläinen, Jarmo, Patyra, Konrad, Löf, Christoffer, Williams, E Dillwyn, Soleimani, Manoocher, Barrett, Timothy, Maher, Eamonn R, Chatterjee, V Krishna, Refetoff, Samuel, Schoenmakers, Nadia

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