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收藏分享 收藏 分享 收藏 Impact of the Transition Council in Type 1 Diabetes: Bridging the Gap to Adult Care1型糖尿病中过渡委员会的影响：弥合通往成人护理的差距
Hocaoglu, Erhan; Nursoy, Hatice; Saridas, Filiz Mercan; Yasar, Muge; Karatoprak, Kadircan; Ongen, Yasemin Denkboy; Gul, Ozen Oz; Ersoy, Canan; Eren, Erdal; Cander, Soner 分享 收藏 分享 收藏 分享 收藏 分享 收藏 High frequency of transient congenital hypothyroidism among infants referred for suspected congenital hypothyroidism from the Turkish National screening program: thyroxine dose may guide the prediction of transientsOzer, Y.; Anik, A.; Sayili, U.; Tercan, U.; Sevim, R. Deveci; Gunes, S.; Pirimoglu, M. Buhur; Elmaogullari, S.; Dundar, I.; Okdemir, D.; Besci, O.; Jalilova, A.; Cicek, D.; Singin, B.; Ulu, S. E.; Turan, H.; Albayrak, S.; Sutcu, Z. Kocabey; Eklioglu, B. S.; Eren, E.; Cetinkaya, S.; Savas-Erdeve, S.; Esen, I.; Demir, K.; Darcan, S.; Hatipoglu, N.; Parlak, M.; Dursun, F.; Siklar, Z.; Berberoglu, M.; Keskin, M.; Orbak, Z.; Tezel, B.; Yuruker, E.; Keskinkilic, B.; Kara, F.; Erginoz, E.; Darendeliler, F.; Evliyaoglu, O. 分享 收藏 Clinical features, diagnosis and treatment outcomes of Cushing's disease in children: A multicenter studyTarcin, Gurkan; Catli, Gonul; Cetinkaya, Semra; Eren, Erdal; Kardelen, Asli Derya; Akinci, Aysehan; Bober, Ece; Kara, Cengiz; Yildirim, Ruken; Er, Eren; Polat, Recep; Ozhan, Bayram; Yildiz, Melek; Kor, Yilmaz; Evliyaoglu, Olcay; Dundar, Bumin; Ercan, Oya 分享 收藏 Clinical features of generalized lipodystrophy in Turkey: A cohort analysisYildirim Simsir, Ilgin; Tuysuz, Beyhan; Ozbek, Mehmet Nuri; Tanrikulu, Seher; Celik Guler, Merve; Karhan, Asuman Nur; Denkboy Ongen, Yasemin; Gunes, Nilay; Soyaltin, Utku Erdem; Altay, Canan; Nur, Banu; Ozalkak, Servan; Akgun Dogan, Ozlem; Dursun, Fatma; Pekkolay, Zafer; Eren, Mehmet Ali; Usta, Yusuf; Ozisik, Secil; Ozgen Saydam, Basak; Adiyaman, Suleyman Cem; Unal, Mehmet Cagri; Gungor Semiz, Gokcen; Turan, Ihsan; Eren, Erdal; Kayserili, Hulya; Jeru, Isabelle; Vigouroux, Corinne; Atik, Tahir; Onay, Huseyin; Ozen, Samim; Arioglu Oral, Elif; Akinci, Baris 分享 收藏 分享 收藏 Homozygous loss-of-function mutations in SLC26A7 cause goitrous congenital hypothyroidismCangul, 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; Jaaskelainen, Jarmo; Patyra, Konrad; Lof, Christoffer; Williams, E. Dillwyn; Consortium, Ukk; Soleimani, Manoocher; Barrett, Timothy; Maher, Eamonn R.; Chatterjee, V. Krishna; Refetoff, Samuel; Schoenmakers, Nadia 分享 收藏 Genotype-phenotype correlation, gonadal malignancy risk, gender preference, and testosterone/dihydrotestosterone ratio in steroid 5-alpha-reductase type 2 deficiency: a multicenter study from TurkeyAbaci, A.; Catli, G.; Kirbiyik, O.; Sahin, N. M.; Abali, Z. Y.; Unal, E.; Siklar, Z.; Mengen, E.; Ozen, S.; Guran, T.; Kara, C.; Yildiz, M.; Eren, E.; Nalbantoglu, O.; Guven, A.; Cayir, A.; Akbas, E. D.; Kor, Y.; Curek, Y.; Aycan, Z.; Bas, F.; Darcan, S.; Berberoglu, M. 分享 收藏 Renal complications of lipodystrophy: A closer look at the natural history of kidney disease脂肪营养不良的肾脏并发症: 仔细观察肾脏疾病的自然史Akinci, Baris; Unlu, Sadiye Mehtat; Celik, Ali; Simsir, Ilgin Yildirim; Sen, Sait; Nur, Banu; Keskin, Fatma Ela; Saydam, Basak Ozgen; Ozdemir, Nilufer Kutbay; Yurekli, Banu Sarer; Ergur, Bekir Ugur; Sonmez, Melda; Atik, Tahir; Arslan, Atakan; Demir, Tevfik; Altay, Canan; Tunc, Ulku Aybuke; Arkan, Tugba; Gen, Ramazan; Eren, Erdal; Akinci, Gulcin; Yilmaz, Aslihan Arasli; Bilen, Habib; Ozen, Samim; Celtik, Aygul; Erdeve, Senay Savas; Cetinkaya, Semra; Onay, Huseyin; Sarioglu, Sulen; Oral, Elif Arioglu 分享 收藏 分享 收藏 The Etiology and Clinical Features of Non-CAH Gonadotropin-Independent Precocious Puberty: A Multicenter StudyAtay, Zeynep; Yesilkaya, Ediz; Erdeve, Senay Savas; Turan, Serap; Akin, Leyla; Eren, Erdal; Doger, Esra; Aycan, Zehra; Abali, Zehra Yavas; Akinci, Aysehan; Siklar, Zeynep; Ozen, Samim; Kara, Cengiz; Tayfun, Meltem; Sari, Erkan; Tutunculer, Filiz; Karabulut, Gulcan Seymen; Karaguzel, Gulay; Cetinkaya, Semra; Saglam, Halil; Bideci, Aysun; Kurtoglu, Selim; Guran, Tulay; Bereket, Abdullah 分享 收藏 Loss-of-Function Mutations in PNPLA6 Encoding Neuropathy Target Esterase Underlie Pubertal Failure and Neurological Deficits in Gordon Holmes SyndromeTopaloglu, A. Kemal; Lomniczi, Alejandro; Kretzschmar, Doris; Dissen, Gregory A.; Kotan, L. Damla; McArdle, Craig A.; Koc, A. Filiz; Hamel, Ben C.; Guclu, Metin; Papatya, Esra D.; Eren, Erdal; Mengen, Eda; Gurbuz, Fatih; Cook, Mandy; Castellano, Juan M.; Kekil, M. Burcu; Mungan, Neslihan O.; Yuksel, Bilgin; Ojeda, Sergio R. 分享 收藏 Novel TSHR mutations in consanguineous families with congenital nongoitrous hypothyroidismCangul, Hakan; Morgan, Neil V.; Forman, Julia R.; Saglam, Halil; Aycan, Zehra; Yakut, Tahsin; Gulten, Tuna; Tarim, Omer; Bober, Ece; Cesur, Yasar; Kirby, Gail A.; Pasha, Shanaz; Karkucak, Mutlu; Eren, Erdal; Cetinkaya, Semra; Bas, Veysel; Demir, Korcan; Yuca, Sevil A.; Meyer, Esther; Kendall, Michaela; Hogler, Wolfgang; Barrett, Timothy G.; Maher, Eamonn R. 分享 收藏 分享 收藏 
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