All Stories

  1. Idiopathic infantile hypercalcemia: mutations in SLC34A1 and CYP24A1 in two siblings and fathers

    Article • Journal of Pediatric Endocrinology and Metabolism, August 2020, De Gruyter

    PROF AYLA GUVEN

  2. Five novel ALMS1 gene mutations in six patients with Alström syndrome

    Article • Journal of Pediatric Endocrinology and Metabolism, May 2018, De Gruyter

    PROF AYLA GUVEN

  3. Seven cases with Williams-Beuren syndrome: endocrine evaluation and long-term follow-up

    Article • Journal of Pediatric Endocrinology and Metabolism, January 2017, De Gruyter

    PROF AYLA GUVEN

  4. Obesity and Increasing Rate of Infantile Blount Disease

    Article • Clinical Pediatrics, January 2014, SAGE Publications

    PROF AYLA GUVEN