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Molecular Biology Reports|April 22, 2019
The molecular basis and genotype-phenotype correlations of congenital adrenal hyperplasia (CAH) in Anatolian populationAyca Dundar, Ruslan Bayramov, Muge G Onal, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|October 2, 2008
Evaluation of diagnosis and treatment results in children with Graves' disease with emphasis on the pubertal status of patientsSükran Poyrazoğlu, Nurcin Saka, Firdevs Bas, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|January 22, 2018
Response to growth hormone treatment in very young patients with growth hormone deficiencies and mini-pubertySemra Çetinkaya, Şükran Poyrazoğlu, Firdevs Baş, et al.
The Turkish Journal of Pediatrics|December 24, 2008
Adult height in Turkish patients with Turner syndrome without growth hormone treatmentAbdullah Bereket, Serap Turan, Nursel Elçioğlu, et al.
The New England Journal of Medicine|January 19, 2007
Clinical and molecular genetic spectrum of congenital deficiency of the leptin receptorI Sadaf Farooqi, Teresia Wangensteen, Stephan Collins, et al.
Journal of Clinical Research in Pediatric Endocrinology|November 7, 2018
Clinical and Laboratory Characteristics of Hyperprolactinemia in Children and Adolescents: National SurveyErdal Eren, Ayça Törel Ergür, Şükriye Pınar İşgüven, et al.
Journal of Clinical Research in Pediatric Endocrinology|May 24, 2018
Incidence of Type 1 Diabetes in Children Aged Below 18 Years during 2013-2015 in Northwest TurkeyŞükran Poyrazoğlu, Rüveyde Bundak, Zehra Yavaş Abalı, et al.
Endocrine|August 11, 2025
Central precocious puberty in boys; diagnosis, treatment and follow-up: a nation-wide studySevinc Odabasi Gunes, Merve Sakar, Nursel Muratoglu Sahin, et al.
American Journal of Medical Genetics. Part A|January 21, 2016
Anthropometric findings from birth to adulthood and their relation with karyotpye distribution in Turkish girls with Turner syndromeErkan Sari, Abdullah Bereket, Ediz Yeşilkaya, et al.
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