Search Results - "Emine Kartal Baykan"
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Differential Diagnosis of Acromegaly: Pachydermoperiostosis Two New Cases from Turkey
Published in Journal of clinical research in pediatric endocrinology (01-09-2022)“…Pachydermoperiostosis (PDP), also known as primary hypertrophic osteoarthropathy, is a rare genetic disorder characterized by pachyderma and periostosis…”
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Subacute Thyroiditis Secondary to SARS-COV-2 Infection; Case Studies From Turkey
Published in Turkish journal of endocrinology and metabolism (2021)“…Coronavirus disease-2019 (COVID-19) has infected more than 100 million people globally, with the pandemic still showing a quick increase in number. We reported…”
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Growth Hormone Level in COVID-19 Patients
Published in Northern Clinics of Istanbul (01-01-2022)“…OBJECTIVE: Coronavirus disease-2019 (COVID-19) disease can cause asymptomatic and mild flu-like symptoms as well as severe symptoms ranging from respiratory…”
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Coexistence of Primary Hyperparathyroidism and Differentiated Thyroid Carcinoma: Is It a Coincidence?
Published in Turkish journal of endocrinology and metabolism (01-09-2022)Get full text
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Aromatase deficiency, a rare syndrome: case report
Published in Journal of clinical research in pediatric endocrinology (01-01-2013)“…Aromatase deficiency (AD) is a rare autosomal recessive inheritance syndrome. Its worldwide incidence is unknown, and there are few case reports in the…”
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Characteristics and Treatment Results of 5 Patients with Fibrous Dysplasia and Review of the Literature
Published in Case reports in endocrinology (01-01-2015)“…Aim. Fibrous dysplasia is a rare bone disease caused by missense mutation leading to abnormal fibroblast and osteoblast proliferation and increased bone…”
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Prolaktinoma Tanılı Hastalarda Prediyabet Sıklığı
Published in Dicle tıp dergisi (17-06-2020)“…Amaç: Prolaktinin (PRL) çeşitli hayvan türlerinde glikoz intoleransı, hiperinsülinemi ve insülin direncini indüklediği daha önce yapılan çalışmalarda…”
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Tip 2 diyabetli bireylerde serum vitamin D düzeyleri ile mikroalbüminüri arasındaki ilişkinin değerlendirilmesi
Published in Ege tıp dergisi (15-03-2022)“…Amaç: D vitamin eksikliği, birçok çalışmada diyabet gelişimi için önemli bir risk faktörü olarak gösterilmiştir. Tip 2 diabetes mellitus’lu hastalarında, D…”
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Basal and pentagastrin-stimulated calcitonin cut-off values in diagnosis of preoperative medullary thyroid cancer
Published in Turkish journal of medical sciences (30-04-2021)Get full text
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Genotypic Sex and Severity of the Disease Determine the Time of Clinical Presentation in Steroid 17α-Hydroxylase/17,20-Lyase Deficiency
Published in Hormone research in paediatrics (01-04-2021)“…Steroid 17α-hydroxylase/17,20-lyase deficiency (17OHD) is characterized by decreased sex steroids and cortisol, and excessive mineralocorticoid action. The…”
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The Spectrum of Low-Density Lipoprotein Receptor Mutations in a Large Turkish Cohort of Patients with Familial Hypercholesterolemia
Published in Metabolic syndrome and related disorders (01-08-2021)“…Monogenic hypercholesterolemia with Mendelian inheritance is a heterogeneous group of diseases that are characterized by elevated plasma low-density…”
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A Novel Mutation in Deficiency of 11 B-Hydroxylase: A Possible Association with Disease Severity
Published in Journal of clinical research in pediatric endocrinology (01-09-2015)“…Congenital adrenal hyperplasia (CAH) is an autosomal recessive disorder caused by the loss of one of five steroidogenic enzymes affecting cortisol synthesis…”
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Aromatase Deficiency, a Rare Syndrome: Case Report
Published in Journal of clinical research in pediatric endocrinology (01-09-2013)Get full text
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