Browsing by Author "Baş, Firdevs"
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A homozygous TPO gene duplication (c. 1184_1187dup4) causes congenital hypothyroidism in three siblings born to a consanguineous family
Cangül, Hakan; Aydın, Banu; Baş, Firdevs (Georg Thieme Verlag, 2015)Congenital hypothyroidism (CH) is the most common neonatal endocrine disease, and germ-line mutations in the TPO gene cause the inherited form of the disease. Our aim in this study was to determine the genetic basis of ... -
Incidence of type 1 diabetes in children aged below 18 years during 2013-2015 in northwest Turkey
Poyrazoğlu, Şükran; Bundak, Rüveyde; Yavaş Abalı, Zehra; Önal, Hasan; Sarıkaya, Sevil; Akgün, Abdurrahman; Baş, Serpil; Abalı, Saygın; Bereket, Abdullah; Eren, Erdal; Tarım, Ömer; Güven, Ayla; Yıldız, Metin; Karaman Aksakal, Derya; Yüksel, Ayşegül; Seymen Karabulut, Gülcan; Hatun, Şükrü; Özgen, Tolga; Cesur, Yaşar; Azizoğlu, Mehmet; Dilek, Emine; Tütüncüler, Filiz; Çakır, Esra Papatya; Özcabı, Bahar; Evliyaoğlu, Olcay; Karadeniz, Songül; Dursun, Fatma; Bolu, Semih; Arslanoğlu, İlknur; Yeşiltepe Mutlu, Gül; Kırmızıbekmez, Heves; İşgüven, Pınar; Üstyol, Ala; Adal, Erdal; Uçar, Ahmet; Cebeci, Nurcan; Bezen, Didem; Binay, Çiğdem; Semiz, Serap; Korkmaz, Hüseyin Anıl; Memioğlu, Nihal; Sağsak, Elif; Peltek, Havva Nur; Yıldız, Melek; Akçay, Teoman; Turan, Serap; Güran, Tülay; Atay, Zeynep; Akcan, Neşe; Çizmecioğlu, Filiz; Ercan, Oya; Dağdeviren, Aydilek; Baş, Firdevs; İşsever, Halim; Darendeliler, Feyza (Galenos Yayıncılık, 2018)Objective: To assess the incidence of type I diabetes mellitus (T1DM) in children under 18 years of age in the northwest region of Turkey during 2013-2015. Methods: All newly diagnosed T1DM cases were recorded prospectively ... -
The investigation of genetic etiology in familial cases with congenital hypothyroidism
Kardelen Al, Aslı Derya; Işık, Fatma Büşra; Karakılıç Özturan, Esin; Sözügüzel, Mavi Deniz; Öztürk, Ayşe Pınar; Poyrazoğlu, Şükran; Parlayan, Cüneyd; Cangül, Hakan; Baş, Firdevs; Darendeliler, Feyza (Karger, 2019)Background: Congenital hypothyroidism(CH) is the most common neonatal endocrinological disorder in the world. Although most of the CH is sporadic, some genetic defects are responsible from the etiology. The aim of this ... -
Long term side effects of childhood acute lymphoblastic leukemia therapy on bone mineral metabolism
Gedik Çalışkan, Sümeyra; Karaman, Serap; Baş, Firdevs; Ünüvar, Ayşegül; Aydoğdu, Selime; Özkan Karagenç, Ayşe; Tuğcu, Deniz; Anak, Sema; Devecioğlu, Ömer; Öztürk, Gülyüz; Ocak, Süheyla; Tuna, Rümeysa; Karakaş, Zeynep (Pergamon-Elsevier Science Ltd, 2018)… -
Response to growth hormone treatment in very young patients with growth hormone deficiencies and mini-puberty
Çetinkaya, Semra; Poyrazoğlu, Şükran; Baş, Firdevs; Ercan, Oya; Yıldız, Metin; Adal, Erdal; Bereket, Abdullah; Abalı, Saygın; Aycan, Zehra; Erdeve, Senay Savaş; Berberoğlu, Merih; Şıklar, Zeynep; Tayfun, Meltem; Darcan, Şükran; Mengen, Eda; Bircan, İffet; Jones, Filiz Mine Çizmecioğlu; Şimşek, Enver; Papatya, Esra Deniz; Özbek, Mehmet Nuri; Bolu, Semih; Abacı, Ayhan; Büyükinan, Muammer; Darendeliler, Feyza (Walter de Gruyter Gmbh, 2018)Background: The aim of the study was to assess the response to growth hormone (GH) treatment in very young patients with GH deficiency (GHD) through a national, multi-center study. Possible factors affecting growth response ...
