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Journal of Clinical Research in Pediatric Endocrinology|December 27, 2014
Is Hyperpigmentation on the First Day of Life Always Associated with IMAGe Syndrome?Elif Özsu, Rahime Gül Yeşiltepe Mutlu, Olcay Işık, et al.Journal of Clinical Research in Pediatric Endocrinology|June 8, 2012
Developmental defects of the thyroid gland: relationship with advanced maternal ageHeves Kirmızibekmez, Ayla Güven, Metin Yildiz, et al.Journal of Clinical Research in Pediatric Endocrinology|June 8, 2012
Early onset of liver steatosis in a Japanese girl with maturity-onset diabetes of the young type 3 (MODY3)Akie Nakamura, Katsura Ishidu, Toshihiro TajimaJournal of Clinical Research in Pediatric Endocrinology|November 21, 2012
Thyroid nodules in pediatrics: which ones can be left alone, which ones must be investigated, when and howAndrea Corrias, Alessandro MussaJournal of Clinical Research in Pediatric Endocrinology|February 3, 2016
The Role of Thyrotropin-Releasing Hormone Stimulation Test in Management of Hyperthyrotropinemia in InfantsAyça Altıncık, Korcan Demir, Gönül Çatlı, et al.Journal of Clinical Research in Pediatric Endocrinology|February 3, 2016
Relationship Between Functional Exercise Capacity and Lung Functions in Obese Chidrenİlker Tolga Özgen, Erkan Çakır, Emel Torun, et al.Journal of Clinical Research in Pediatric Endocrinology|February 3, 2016
Assessment of Cardiovascular Parameters in Obese Children and Adolescents with Non-Alcoholic Fatty Liver DiseaseBeray Selver Eklioğlu, Mehmet Emre Atabek, Nesibe Akyürek, et al.Journal of Clinical Research in Pediatric Endocrinology|February 3, 2016
The Missense Alteration A5T of the Thyroid Peroxidase Gene is Pathogenic and Associated with Mild Congenital HypothyroidismHakan Cangül, Korcan Demir, H Ömür Babayiğit, et al.Journal of Clinical Research in Pediatric Endocrinology|January 19, 2016
Cardiac Function in Newborns with Congenital Hypothyroidism: Association with Thyroid-Stimulating Hormone LevelsTaliha Öner, Rahmi Özdemir, Önder Doksöz, et al.Journal of Clinical Research in Pediatric Endocrinology|January 19, 2016
A Homozygous Nonsense Thyroid Peroxidase Mutation (R540X) Consistently Causes Congenital Hypothyroidism in Two Siblings Born to a Consanguineous FamilyHakan Cangül, Murat Doğan, Duran ÜstekPageof 112