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Dynamic Thiol/Disulphide Homeostasis in Children and Adolescents with Non-Autoimmune Subclinical Hypothyroidism.
Published in:
2018
By:
- Uçaktürk, Seyit Ahmet;
- Alışık, Murat;
- Uğur, Çağatay;
- Elmaoğulları, Selin;
- Mengen, Eda;
- Erel, Özcan
Publication type:
journal article
Pediatrik Obezitede Otizm Benzeri Belirtilerin Duygu Düzenleme, Yeme Davranışı ve İnternet Bağımlılığı ile İlişkisinin Araştırılması.
Published in:
Turkish Journal of Child & Adolescent Mental Health / Çocuk ve Gençlik Ruh Sagligi Dergisi, 2024, v. 31, n. 2, p. 141, doi. 10.4274/tjcamh.galenos.2023.30316
By:
- Kafalı, Helin Yılmaz;
- Mengen, Eda;
- Ayvalık Baydur, Ümran Gül;
- Balcı, Özge;
- Bulut, İsmail;
- Uçaktürk, Seyit Ahmet
Publication type:
Article
Tip 1 Diabetes Mellitus'lu Çocuk ve Adolesan Hastaların Retrospektif Olarak Değerlendirilmesi: Tek Merkez Deneyimi.
Published in:
Journal of Pediatric Disease / Türkiye Çocuk Hastalıkları Dergisi, 2021, v. 15, n. 2, p. 142, doi. 10.12956/tchd.845703
By:
- ARMAN BİLİR, Özlem;
- MENGEN, Eda;
- KOCAAY, Pınar;
- VİDİNLİSAN, Sadi Mehmet
Publication type:
Article
Obez Çocuklarda D Vitamini Düzeylerinin İnsülin Direnci ve Hepatosteatoz ile İlişkisi.
Published in:
Journal of Pediatric Disease / Türkiye Çocuk Hastalıkları Dergisi, 2020, v. 14, n. 1, p. 36, doi. 10.12956/tjpd.2018.390
By:
- MENGEN, Eda;
- KOCAAY, Pınar
Publication type:
Article
Toplum Kökenli Çocukluk Çağı Pnömoni Olgularımızda Mycoplasma pneumoniae ve Chlamydia pneumoniae'nın Seropozitiflik Oranları.
Published in:
Journal of Pediatric Disease / Türkiye Çocuk Hastalıkları Dergisi, 2019, v. 13, n. 6, p. 406, doi. 10.12956/tjpd.2018.377
By:
- MENGEN, Eda;
- TURGUT, Mehmet
Publication type:
Article
Neonatal Diyabetes Mellitus Tanısıyla Takip Edilen Hastaların Retrospektif Olarak Değerlendirilmesi.
Published in:
Journal of Pediatric Disease / Türkiye Çocuk Hastalıkları Dergisi, 2019, v. 13, n. 1, p. 25, doi. 10.12956/tjpd.2018.349
By:
- GÜNGÖR, Ali;
- KARAGÖL, Cüneyt;
- GÖNÜLAL, Deniz;
- MENGEN, Eda;
- SİYAH BİLGİN, Betül;
- ÜNAL, Sevim;
- YAKUT, Halil İbrahim
Publication type:
Article
Clinical and Laboratory Characteristics of MODY Cases, Genetic Mutation Spectrum and Phenotype-genotype Relationship.
Published in:
Journal of Clinical Research in Pediatric Endocrinology, 2024, v. 16, n. 3, p. 297, doi. 10.4274/jcrpe.galenos.2024.2023-10-16
By:
- Özsu, Elif;
- Çetinkaya, Semra;
- Bolu, Semih;
- Hatipoğlu, Nihal;
- Erdeve, Şenay Savaş;
- Evliyaoğlu, Olcay;
- Baş, Firdevs;
- Çayır, Atilla;
- Dündar, İsmail;
- Akbaş, Emine Demet;
- Uçaktürk, Seyid Ahmet;
- Berberoğlu, Merih;
- Şıklar, Zeynep;
- Özalkak, Şervan;
- Şahin, Nursel Muratoğlu;
- Keskin, Melikşah;
- Şiraz, Ülkü Gül;
- Turan, Hande;
- Öztürk, Ayşe Pınar;
- Mengen, Eda
Publication type:
Article
A Duplication Upstream of SOX9 Associated with SRY Negative 46,XX Ovotesticular Disorder of Sex Development: A Case Report.
Published in:
Journal of Clinical Research in Pediatric Endocrinology, 2020, v. 12, n. 3, p. 308, doi. 10.4274/jcrpe.galenos.2019.2019.0101
By:
- Mengen, Eda;
- Kayhan, Gülsüm;
- Kocaay, Pınar;
- Uçaktürk, Seyit Ahmet
Publication type:
Article
Mutations Within the Transcription Factor PROP1 in a Cohort of Turkish Patients with Combined Pituitary Hormone Deficiency.
Published in:
Journal of Clinical Research in Pediatric Endocrinology, 2020, v. 12, n. 3, p. 261, doi. 10.4274/jcrpe.galenos.2020.2019.0191
By:
- Bulut, Fatma Derya;
- Dilek, Semine Özdemir;
- Kotan, Damla;
- Mengen, Eda;
- Gürbüz, Fatih;
- Yüksel, Bilgin
Publication type:
Article
The Effects of Risk Behaviors and Orthorexic Behavior on Glycemic Control in Adolescents with Type 1 Diabetes.
Published in:
Journal of Clinical Research in Pediatric Endocrinology, 2020, v. 12, n. 3, p. 233, doi. 10.4274/jcrpe.galenos.2019.2019.0128
By:
- Taş, Demet;
- Mengen, Eda;
- Kocaay, Pınar;
- Uçaktürk, Seyit Ahmet
Publication type:
Article
A Rare Etiology of 46,XY Disorder of Sex Development and Adrenal Insufficiency: A Case of MIRAGE Syndrome Caused by Mutations in the SAMD9 Gene.
Published in:
Journal of Clinical Research in Pediatric Endocrinology, 2020, v. 12, n. 2, p. 206, doi. 10.4274/jcrpe.galenos.2019.2019.0053
By:
- Mengen, Eda;
- Yavaş, Aynur Küçükçongar;
- Uçaktürk, S. Ahmet
Publication type:
Article
The Significance of Thiol/Disulfide Homeostasis and Ischemia-modified Albumin Levels in Assessing Oxidative Stress in Obese Children and Adolescents.
Published in:
Journal of Clinical Research in Pediatric Endocrinology, 2020, v. 12, n. 1, p. 45, doi. 10.4274/jcrpe.galenos.2019.2019.0039
By:
- Mengen, Eda;
- Uçaktürk, Seyit Ahmet;
- Kocaay, Pınar;
- Kaymaz, Özlem;
- Neşelioğlu, Salim;
- Erel, Özcan
Publication type:
Article
Catecholamine-induced Myocarditis in a Child with Pheochromocytoma.
Published in:
Journal of Clinical Research in Pediatric Endocrinology, 2020, v. 12, n. 2, p. 202, doi. 10.4274/jcrpe.galenos.2019.2019.0045
By:
- Uçaktürk, S. Ahmet;
- Mengen, Eda;
- Azak, Emine;
- Çetin, İbrahim İlker;
- Kocaay, Pınar;
- Şenel, Emrah
Publication type:
Article
Subclinical Myocardial Dysfunction Demonstrated by Speckle Tracking Echocardiography in Children with Euthyroid Hashimoto's Thyroiditis.
Published in:
Journal of Clinical Research in Pediatric Endocrinology, 2019, v. 11, n. 4, p. 410, doi. 10.4274/jcrpe.galenos.2019.2018.0273
By:
- Azak, Emine;
- Uçaktürk, Seyit Ahmet;
- Çetin, İbrahim İlker;
- Gürsu, Hazım Alper;
- Mengen, Eda;
- Pamuk, Utku
Publication type:
Article
Hypogonadotropic Hypogonadism due to Novel FGFR1 Mutations.
Published in:
Journal of Clinical Research in Pediatric Endocrinology, 2017, v. 9, n. 2, p. 95, doi. 10.4274/jcrpe.3908
By:
- Akkuş, Gamze;
- Kotan, Leman Damla;
- Durmaz, Erdem;
- Mengen, Eda;
- Turan, İhsan;
- Ulubay, Ayça;
- Gürbüz, Fatih;
- Yüksel, Bilgin;
- Tetiker, Tamer;
- Topaloğlu, A. Kemal
Publication type:
Article
Idiopathic Hypogonadotropic Hypogonadism Caused by Inactivating Mutations in SRA1.
Published in:
Journal of Clinical Research in Pediatric Endocrinology, 2016, v. 8, n. 2, p. 125, doi. 10.4274/jcrpe.3248
By:
- Kotan, Leman Damla;
- Cooper, Charlton;
- Darcan, Şükran;
- Carr, Ian M.;
- Özen, Samim;
- Yi Yan;
- Hamedani, Mohammad K.;
- Gürbüz, Fatih;
- Mengen, Eda;
- Turan, İhsan;
- Ulubay, Ayça;
- Akkuş, Gamze;
- Yüksel, Bilgin;
- Kemal Topaloğlu, A.;
- Leygue, Etienne
Publication type:
Article
Idiopathic Hypogonadotrophic Hypogonadism Caused by Inactivating Mutations in SRA1.
Published in:
Journal of Clinical Research in Pediatric Endocrinology, 2016, v. 8, p. 17
By:
- Ulubay, Ayça;
- Kotan, L. Damla;
- Cooper, Charlton;
- Darcan, Şükran;
- Carr, Ian M.;
- Özen, Samim;
- Yi Yan;
- Hamedani, Mohammad K.;
- Gürbüz, Fatih;
- Mengen, Eda;
- Turan, İhsan;
- Akkuş, Gamze;
- Yüksel, Bilgin;
- Leygue, Etienne;
- Topaloğlu, A. Kemal
Publication type:
Article
A Novel GH1 Functional Mutation in a Family with Isolated Growth Hormone Deficiency.
Published in:
Journal of Clinical Research in Pediatric Endocrinology, 2015, v. 7, p. 13
By:
- Gürbüz, Fatih;
- Yüksel, Bilgin;
- Bişgin, Atıl;
- Mengen, Eda;
- Topalo287;lu, Ali Kemal
Publication type:
Article
Is there a relationship between hyperchloremia status and the risk of developing acute kidney injury in pediatric patients with diabetic ketoacidosis?
Published in:
European Journal of Pediatrics, 2024, v. 183, n. 10, p. 4319, doi. 10.1007/s00431-024-05697-y
By:
- Tas, Nesrin;
- Mengen, Eda;
- Alacakır, Nuri;
- Goncu, Sultan;
- Boluk, Oguz;
- Ucakturk, Ahmet
Publication type:
Article
Enzyme Replacement Therapy in Hypophosphatasia.
Published in:
Journal of the College of Physicians & Surgeons Pakistan, 2018, v. 28, p. S198, doi. 10.29271/jcpsp.2018.09.S198
By:
- Uçaktürk, S. Ahmet;
- Elmaogullari, Selin;
- Ünal, Sevim;
- Gönülal, Deniz;
- Mengen, Eda
Publication type:
Article
A Novel Frameshift Mutation in ESCO2 Gene in Roberts Syndrome.
Published in:
Journal of the College of Physicians & Surgeons Pakistan, 2018, v. 28, n. 5, p. 403, doi. 10.29271/jcpsp.2018.05.403
By:
- Mengen, Eda;
- Kotan, Leman Damla;
- Ucakturk, Seyit Ahmet;
- Topaloglu, Ali Kemal;
- Yuksel, Bilgin
Publication type:
Article
CCDC141 Mutations in Idiopathic Hypogonadotropic Hypogonadism.
Published in:
2017
By:
- Turan, Ihsan;
- Hutchins, B. Ian;
- Hacihamdioglu, Bulent;
- Kotan, L. Damla;
- Gurbuz, Fatih;
- Ulubay, Ayca;
- Mengen, Eda;
- Yuksel, Bilgin;
- Wray, Susan;
- Topaloglu, A. Kemal
Publication type:
journal article
Loss-of-function mutations in PNPLA6 encoding neuropathy target esterase underlie pubertal failure and neurological deficits in Gordon Holmes syndrome.
Published in:
2014
By:
- Topaloglu, A Kemal;
- Lomniczi, Alejandro;
- Kretzschmar, Doris;
- Dissen, Gregory A;
- Kotan, L Damla;
- McArdle, Craig A;
- Koc, A Filiz;
- Hamel, Ben C;
- Guclu, Metin;
- Papatya, Esra D;
- Eren, Erdal;
- Mengen, Eda;
- Gurbuz, Fatih;
- Cook, Mandy;
- Castellano, Juan M;
- Kekil, M Burcu;
- Mungan, Neslihan O;
- Yuksel, Bilgin;
- Ojeda, Sergio R
Publication type:
journal article
Investigation of autism spectrum disorder and autistic symptoms in obese children and adolescents.
Published in:
Anatolian Journal of Psychiatry / Anadolu Psikiyatri Dergisi, 2018, v. 19, n. 5, p. 518, doi. 10.5455/apd.289937
By:
- UĞUR, Çağatay;
- UÇAKTÜRK, Ahmet;
- MENGEN UÇAKTÜRK, Eda
Publication type:
Article
The Relationship Between Hypothyroidism and Cardiac Findings in Children With and Without Down Syndrome.
Published in:
Archives of the Turkish Society of Cardiology / Türk Kardiyoloji Derneği Arşivi, 2023, v. 51, n. 3, p. 163, doi. 10.5543/tkda.2023.70337
By:
- Celbek, Busra Suzen;
- Gursu, Hazım Alper;
- Azak, Emine;
- Mengen, Eda;
- Kocaay, Pınar;
- Cetin, Ibrahim Ilker
Publication type:
Article
Investigation of the prevalence of cardiovascular risk factors in obese patients diagnosed with metabolic syndrome in childhood and examination of left ventricular function by echocardiography.
Published in:
Journal of Pediatric Endocrinology & Metabolism, 2021, v. 34, n. 7, p. 885, doi. 10.1515/jpem-2020-0597
By:
- Özden, Güzin;
- Kibar Gül, Ayşe Esin;
- Mengen, Eda;
- Ucaktürk, Ahmet;
- Gürsu, Hazım Alper;
- Çetin, İbrahim İlker;
- Kızılgün, Murat
Publication type:
Article
Evaluation of the relationship between the one-hour plasma glucose concentration and beta-cell functions and cardiometabolic parameters during oral glucose tolerance test in obese children and adolescents.
Published in:
Journal of Pediatric Endocrinology & Metabolism, 2020, v. 33, n. 6, p. 767, doi. 10.1515/jpem-2020-0016
By:
- Mengen, Eda;
- Uçaktürk, Seyit Ahmet
Publication type:
Article
Evaluation of the relationship between short-term glycemic control and netrin-1, a urinary proximal tubular injury marker in children with type 1 diabetes.
Published in:
Journal of Pediatric Endocrinology & Metabolism, 2019, v. 32, n. 8, p. 851, doi. 10.1515/jpem-2018-0373
By:
- Uçaktürk, Seyit Ahmet;
- Mengen, Eda;
- Elmaoğulları, Selin;
- Yücel, Çiğdem;
- A. Yılmaz, Aslıhan;
- Çifci, Atilla
Publication type:
Article
Response to growth hormone treatment in very young patients with growth hormone deficiencies and mini-puberty.
Published in:
Journal of Pediatric Endocrinology & Metabolism, 2018, v. 31, n. 2, p. 175, doi. 10.1515/jpem-2017-0123
By:
- Çetinkaya, Semra;
- Poyrazoğlu, Şükran;
- Baş, Firdevs;
- Ercan, Oya;
- Yıldız, Metin;
- Adal, Erdal;
- Bereket, Abdullah;
- Abalı, Saygın;
- Aycan, Zehra;
- Erdeve, Şenay 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
Publication type:
Article
Effects of methylphenidate on appetite and growth in children diagnosed with attention deficit and hyperactivity disorder.
Published in:
Journal of Pediatric Endocrinology & Metabolism, 2016, v. 29, n. 1, p. 85, doi. 10.1515/jpem-2015-0171
By:
- Gurbuz, Fatih;
- Gurbuz, Berrak Bilginer;
- Celik, Gonca Gul;
- Yildirim, Veli;
- Ucakturk, Seyit Ahmet;
- Seydaoglu, Gulsah;
- Ucakturk, Eda Mengen;
- Topaloglu, Ali Kemal;
- Yuksel, Bilgin
Publication type:
Article
Emotion dysregulation and pediatric obesity: investigating the role of Internet addiction and eating behaviors on this relationship in an adolescent sample.
Published in:
Eating & Weight Disorders, 2021, v. 26, n. 6, p. 1767, doi. 10.1007/s40519-020-00999-0
By:
- Yilmaz Kafali, Helin;
- Uçaktürk, Seyit Ahmet;
- Mengen, Eda;
- Akpinar, Serap;
- Erguven Demirtas, Merve;
- Uneri, Ozden Sukran
Publication type:
Article
Hipoparatiroidizm ve Psödohipoparatiroidi Nedeni ile Çocuk Endokronoloji Polikliniğine Başvuran Hastaların Değerlendirmesi.
Published in:
Journal of Ankara University Faculty of Medicine / Ankara Üniversitesi Tip Fakültesi Mecmuasi, 2018, v. 71, n. 3, p. 212, doi. 10.4274/atfm.43043
By:
- Kocaay, Pınar;
- Mengen, Eda
Publication type:
Article
Superb Microvascular Imaging for Detecting Ovarian Vascularity in Precocious Puberty, Premature Thelarche, and Pubertal Girls.
Published in:
Cerrahpaşa Medical Journal, 2024, v. 48, n. 2, p. 172, doi. 10.5152/cjm.2024.23053
By:
- Akyel, Nazlı Gülsüm;
- Uçaktürk, Eda Mengen;
- Sivri, Mesut;
- Alımlı, Ayşe Gül;
- Ünlü, Havva Akmaz;
- Uçaktürk, Seyit Ahmet
Publication type:
Article
Prevalence and associated phenotypes of PLXNA1 variants in normosmic and anosmic idiopathic hypogonadotropic hypogonadism.
Published in:
Clinical Genetics, 2019, v. 95, n. 2, p. 320, doi. 10.1111/cge.13482
By:
- Kotan, Leman D.;
- Isik, Emregul;
- Turan, Ihsan;
- Mengen, Eda;
- Akkus, Gamze;
- Tastan, Mehmet;
- Gurbuz, Fatih;
- Yuksel, Bilgin;
- Topaloglu, A. Kemal
Publication type:
Article
A novel genetic mutation in a Turkish family with GCK-MODY.
Published in:
International Journal of Diabetes in Developing Countries, 2017, v. 37, n. 3, p. 323, doi. 10.1007/s13410-016-0539-9
By:
- Ahmet Ucakturk, S.;
- Gunindi, Figen;
- Ceylaner, Serdar;
- Mengen, Eda;
- Elmaogulları, Selin;
- Yuksel, Bilgin
Publication type:
Article
DLG2 Mutations in the Etiology of Pubertal Delay and Idiopathic Hypogonadotropic Hypogonadism.
Published in:
Hormone Research in Paediatrics, 2021, v. 94, n. 9/10, p. 364, doi. 10.1159/000520409
By:
- Turan, Ihsan;
- Demir, Korcan;
- Mengen, Eda;
- Kotan, Leman Damla;
- Gürbüz, Fatih;
- Yüksel, Bilgin;
- Topaloglu, Ali Kemal
Publication type:
Article
Complete Idiopathic Hypogonadotropic Hypogonadism due to Homozygous GNRH1 Mutations in the Mutational Hot Spots in the Region Encoding the Decapeptide.
Published in:
Hormone Research in Paediatrics, 2016, v. 85, n. 2, p. 107, doi. 10.1159/000441977
By:
- Mengen, Eda;
- Tunc, Selma;
- Kotan, L. Damla;
- Nalbantoglu, Ozlem;
- Demir, Korcan;
- Gurbuz, Fatih;
- Turan, Ihsan;
- Seker, Gül;
- Yuksel, Bilgin;
- Topaloglu, a. Kemal
Publication type:
Article
The Novel Mutation p.Trp147Arg of the Steroidogenic Acute Regulatory Protein Causes Classic Lipoid Congenital Adrenal Hyperplasia with Adrenal Insufficiency and 46,XY Disorder of Sex Development.
Published in:
Hormone Research in Paediatrics, 2013, v. 80, n. 3, p. 163, doi. 10.1159/000354086
By:
- Yüksel, Bilgin;
- Kulle, alexandra E.;
- Gürbüz, Fatih;
- Welzel, Maik;
- Kotan, Damla;
- Mengen, Eda;
- Holterhus, Paul-Martin;
- Topaloğlu, ali Kemal;
- Grötzinger, Joachim;
- Riepe, Felix G.
Publication type:
Article
Diazoksit Tedavisine Bağlı Nadir Bir Yan Etki: ID Pulmoner Hipertansiyon.
Published in:
Journal of Dr. Behcet Uz Children's Hospital, 2020, v. 10, n. 3, p. 306, doi. 10.5222/buchd.2020.94547
By:
- Gürsu, Alper Hazım;
- Azak, Emine;
- Mengen, Eda;
- Ünal, Sevim;
- Çetin, İbrahim İlker
Publication type:
Article
Distribution of Gene Mutations Associated with Familial Normosmic Idiopathic Hypogonadotropic Hypogonadism.
Published in:
Journal of Clinical Research in Pediatric Endocrinology, 2012, v. 4, n. 3, p. 121, doi. 10.4274/Jcrpe.725
By:
- Gurbuz, Fatih;
- Damla Kotan, L.;
- Mengen, Eda;
- Şıklar, Zeynep;
- Berberoğlu, Merih;
- Dokmetaş, Sebila;
- Kılıclı, Mehmet Fatih;
- Güven, Ayla;
- Kirel, Birgül;
- Saka, Nurçin;
- Poyrazoğlu, Şükran;
- Cesur, Yaşar;
- Doğan, Murat;
- Özen, Samim;
- Nuri Özbek, Mehmet;
- Demirbilek, Hüseyin;
- Burcu Kekil, M.;
- Temiz, Fatih;
- Mungan, NeslihanÖnenli;
- Yüksel, Bilgin
Publication type:
Article
Normosmic idiopathic hypogonadotropic hypogonadism due to a novel homozygous nonsense c.C969A (p.Y323X) mutation in the KISS1R gene in three unrelated families.
Published in:
Clinical Endocrinology, 2015, v. 82, n. 3, p. 429, doi. 10.1111/cen.12618
By:
- Demirbilek, Huseyin;
- Ozbek, M. Nuri;
- Demir, Korcan;
- Kotan, L. Damla;
- Cesur, Yasar;
- Dogan, Murat;
- Temiz, Fatih;
- Mengen, Eda;
- Gurbuz, Fatih;
- Yuksel, Bilgin;
- Topaloglu, A. Kemal
Publication type:
Article

Found: 41