Zobrazeno 1 - 10
of 44
pro vyhledávání: '"Endokrin ve Otonom Sistemler"'
Autor:
Uta Neumann, Annelieke van der Linde, Ruth E Krone, Nils P Krone, Ayla Güven, Tülay Güran, Heba Elsedfy, Sukran Poyrazoglu, Feyza Darendeliler, Tania A S S Bachega, Antonio Balsamo, Sabine E Hannema, Niels Birkebaek, Ana Vieites, Ajay Thankamony, Martine Cools, Tatjana Milenkovic, Walter Bonfig, Eduardo Correa Costa, Navoda Atapattu, Liat de Vries, Guilherme Guaragna-Filho, Marta Korbonits, Klaus Mohnike, Jillian Bryce, S Faisal Ahmed, Bernard Voet, Oliver Blankenstein, Hedi L Claahsen-van der Grinten
Publikováno v:
Neumann, U, van der Linde, A, Krone, R E, Krone, N P, Güven, A, Güran, T, Elsedfy, H, Poyrazoglu, S, Darendeliler, F, Bachega, T A, Balsamo, A, Hannema, S E, Birkebæk, N, Vieites, A, Thankamony, A, Cools, M, Milenkovic, T, Bonfig, W, Costa, E C, Atapattu, N, de Vries, L, Guaragna-Filho, G, Korbonits, M, Mohnike, K, Bryce, J, Ahmed, S F, Voet, B, Blankenstein, O & Claahsen-van der Grinten, H L 2022, ' Treatment of congenital adrenal hyperplasia in children aged 0-3 years : A retrospective multicenter analysis of salt supplementation, glucocorticoid and mineralocorticoid medication, growth and blood pressure ', European Journal of Endocrinology, vol. 187, no. 2, pp. 587-596 . https://doi.org/10.1530/EJE-21-1085
European Journal of Endocrinology, 187(2), 587-596. BioScientifica Ltd.
Neumann, U, van der Linde, A, Krone, R E, Krone, N P, Güven, A, Güran, T, Elsedfy, H, Poyrazoglu, S, Darendeliler, F, Bachega, T A S S, Balsamo, A, Hannema, S E, Birkebaek, N, Vieites, A, Thankamony, A, Cools, M, Milenkovic, T, Bonfig, W, Costa, E C, Atapattu, N, de Vries, L, Guaragna-Filho, G, Korbonits, M, Mohnike, K, Bryce, J, Ahmed, S F, Voet, B, Blankenstein, O & Claahsen-van der Grinten, H L 2022, ' Treatment of congenital adrenal hyperplasia in children aged 0-3 years : a retrospective multicenter analysis of salt supplementation, glucocorticoid and mineralocorticoid medication, growth and blood pressure ', European Journal of Endocrinology, vol. 186, no. 5, pp. 587-596 . https://doi.org/10.1530/EJE-21-1085
EUROPEAN JOURNAL OF ENDOCRINOLOGY
European Journal of Endocrinology, 186(5), 587-596. Bioscientifica Ltd
European Journal of Endocrinology, 186, 587-596
European Journal of Endocrinology, 186, 5, pp. 587-596
European Journal of Endocrinology, 187(2), 587-596. BioScientifica Ltd.
Neumann, U, van der Linde, A, Krone, R E, Krone, N P, Güven, A, Güran, T, Elsedfy, H, Poyrazoglu, S, Darendeliler, F, Bachega, T A S S, Balsamo, A, Hannema, S E, Birkebaek, N, Vieites, A, Thankamony, A, Cools, M, Milenkovic, T, Bonfig, W, Costa, E C, Atapattu, N, de Vries, L, Guaragna-Filho, G, Korbonits, M, Mohnike, K, Bryce, J, Ahmed, S F, Voet, B, Blankenstein, O & Claahsen-van der Grinten, H L 2022, ' Treatment of congenital adrenal hyperplasia in children aged 0-3 years : a retrospective multicenter analysis of salt supplementation, glucocorticoid and mineralocorticoid medication, growth and blood pressure ', European Journal of Endocrinology, vol. 186, no. 5, pp. 587-596 . https://doi.org/10.1530/EJE-21-1085
EUROPEAN JOURNAL OF ENDOCRINOLOGY
European Journal of Endocrinology, 186(5), 587-596. Bioscientifica Ltd
European Journal of Endocrinology, 186, 587-596
European Journal of Endocrinology, 186, 5, pp. 587-596
Objectives International guidelines recommend additional salt supplementation during infancy in classic congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency. The influence of corticoid medication and growth has not been assessed. Aim
Autor:
Diğdem Bezen, Orkide Kutlu, Stephane Mouilleron, Karine Rizzoti, Mehul Dattani, Tulay Guran, Gözde Yeşil
Publikováno v:
American Journal of Medical Genetics Part A. 188:2701-2706
Biallelic RNPC3 variants have been reported in a few patients with growth hormone deficiency, either in isolation or in association with central hypothyroidism, congenital cataract, neuropathy, developmental delay/intellectual disability, hypogonadis
Autor:
Çetinkalp, Şevki, Şahin, İbrahim, Tuzcu, Alparaslan, Dağlıoğlu, Gülçin, Haklar, Goncagül, Bayraktaroğlu, Taner, Anaforoğlu, İnan, Turan, Elif, Ağbaht, Kemal, Arpacı, Dilek, Elbüken, Gülşah, Karaca, Züleyha, Ertörer, Eda, Deniz, Ferhat, Gül, Kamile, Özdemir, Nilüfer, Dikbaş, Oğuz, Atmaca, Ayşegül, Pekkolay, Zafer, İyidir, Özlem Turhan, Toplaoğlu, Ömercan, Sezer, Kerem, Unubol, Mustafa, Yaşar, Mehmet, İplikçi, Süleyman, Üç, Ziynet Alphan, Cantürk, Zeynep, Hekimsoy, Zeliha, Şimşir, Ilgın Yıldırım, Sert, Murat, AKALIN, AYSEN, Mert, Meral, Altuntaş, Hasan, Temizkan, Şule, Apaydın, Tuğçe, Pamuk, Barış, Bilen, Habip, Altuntaş, Yüksel, ERSOY, REYHAN, YAVUZ, DİLEK
Publikováno v:
Turkish Journal of Endocrinology and Metabolism. 26:79-84
© Author(s).Objective: Vitamin D deficiency is a common health problem around the world. This study aimed to evaluate the nationwide prevalence of vitamin D status in tertiary care hospitals in Turkey. Methods: Retrospectively, the data on vitamin D
Autor:
YAVUZ, DİLEK
Introduction Obesity is a component of eating disorders grouped under several eating disturbances due to emotional problems. Eating habits are directly influenced by eating disorders. Eating disorder rates in obese patients are reported to be 15-50%
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3098::c66ed4bbbe099432bb0e64dfc40c59ac
https://hdl.handle.net/11424/289529
https://hdl.handle.net/11424/289529
Autor:
YAVUZ, DİLEK
Objective Neurofibromatosis type 1 is an autosomal dominant inherited neurocutaneous condition characterized with multipl cafe-au-lait spots, neurofibromas, predisposition to malignancies, and the incidence of disease is 1:3000. Patients are diagnose
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3098::0b5f18c902c7b854a22a3be2de9d9161
https://hdl.handle.net/11424/289528
https://hdl.handle.net/11424/289528
Autor:
YAVUZ, DİLEK
Introduction Various rates were reported regarding diabetes remission and improvement in hyperglycemia in many studies from different populations. Determinants of diabetes remission have not been definitively established so far. In this study, we aim
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3098::ac8c2de2d61c44e04422201b2e66c0d1
https://hdl.handle.net/11424/289530
https://hdl.handle.net/11424/289530
Autor:
YAVUZ, DİLEK
Objective: The aim of this study was to investigate the role of vitamin D replacement therapy on advanced glycation end-products in prediabetes and type 2 diabetes mellitus patients with vitamin D deficiency. Methods: One hundred twenty subjects with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3098::91d9e6a33b3ee56c0a547aca77fe8c77
https://hdl.handle.net/11424/289672
https://hdl.handle.net/11424/289672
Publikováno v:
Hormone Research in Paediatrics.
Introduction: Endogenous Cushing’s syndrome (CS) is a rare, severe disease that can cause multiple systemic involvement and behavioral problems due to excessive cortisol production. Structural changes can be noted in the brain magnetic resonance im
Autor:
Iliriana Alloqi Tahirbegolli, Bernard Tahirbegolli, Selçuk Şen, Betül Sayın, Mert Kaşkal, Ali Yağız Üresin
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism.
Context Stress triggers a cascade of reactions that alter the organism's dynamic steady state. There is a scarcity of interventional studies that show cortisol variability upon stress over time in groups of patients with chronic noncommunicable disea
Autor:
KIRKGÖZ, TARIK, KAYGUSUZ, SARE BETÜL, ALAVANDA, CEREN, GÜRPINAR TOSUN, BUŞRA, ELTAN, MEHMET, SEVEN MENEVŞE, TUBA, GÜRAN, TÜLAY, ARMAN, AHMET, DEMİRCİOĞLU, SERAP, BEREKET, ABDULLAH
Objectives: Central precocious puberty (CPP) develops as a result of early stimulation of the hypothalamic-pituitary-gonadal (HPG) axis. The loss-of-function mutations in the Makorin-ring-finger3 (MKRN3) gene appear to be the most common molecular ca
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3098::ebe1258835368e6805a0c718e62ec061
https://hdl.handle.net/11424/287839
https://hdl.handle.net/11424/287839