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ÖZGEN, İLKER TOLGA

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İLKER TOLGA
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ÖZGEN
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Now showing 1 - 10 of 114
  • PublicationMetadata only
    Ürik asit düşüklüğünden hareket edilerek tanı konulan geç başlangıçlı bir molibden kofaktör eksikliği vakası
    (2013-05-04) CESUR, YAŞAR; ÖZGEN, İLKER TOLGA; PEMBEGÜL YILDIZ, EDİBE; NURSOY, MUSTAFA ATİLLA; CESUR, YAŞAR; ÖZGEN, İLKER TOLGA; ÖZBEK, NUR; NURSOY, MUSTAFA ATİLLA
  • PublicationMetadata only
    Turner sendromlu çocukların başvuru özellıklerı ve eşlık eden patolojıler: 842 vakanın ulusal veri tabanında değerlendirme sonuçları
    (2014-11-08) Yeşilkaya, E; Bereket, A; Darendeliler, F; Baş, F; Poyrazoğlu, Ş; Küçükemre Aydın, B; Darcan, Ş; Dündar, B; Büyükinan, M; Kara, C; Sarı, E; Akıncı, A; Adal, E; Atabek, M E; Demirel, F; Çelik, N; Özken, B; Ozhan, B; Orbak, Z; Ersoy, B; Doğan, M; Ataş, A; Turan, S; Gökşen, D; Tarım, Ö; Yüksel, B; Ercan, O; Hatun, Ş; Şimşek, E; ABACI, Ayhan; Döneray, H; Özbek, M N; Keskin, M; Önal, H; Akyürek, N; Bulan, K; Tepe, D; Kızılay, D; Topaloğlu, A K; Eren, E; Ozen, S; Akın, L; Emeksiz, H C; Kaba, S; Demir, K; Baş, S; Unuvar, T; Sağlam, H; Bolu, S; ÖZGEN, İLKER TOLGA; Doğan, D; Çakır, E D; Eklioğlu, B S; Andıran, N; Çizmecioğlu, F; Evliyaoğlu, O; Karagüzel, G; Pirgon, Ö; Çatlı, G; Can, H D; Gürbüz, F; Binay, Ç; Binay, V N; Fidancı, K; Polat, AYTEN; Gül, D; Açıkel, C; Demirbilek, H; Cinaz, P; ÖZGEN, İLKER TOLGA; POLAT, AYTEN
  • PublicationMetadata only
    Is there any association between the variants of receptor for advanced glycation end products (RAGEs) and obesity?
    (2013-07-01T00:00:00Z) Yaylim, I.; Kucukhuseyin, O.; Karagedik, E. Hande; Torun, E.; Ozgen, T.; Yilmaz-Aydogan, H.; Ergen, H. Arzu; ÖZGEN, İLKER TOLGA
  • PublicationMetadata only
    The Core Strength, Endurance and Flexibility in Adolescents with Type 1 Diabetes Mellitus: A Pilot Study
    (2019-11-17T00:00:00Z) BİRİNCİ, TANSU; KAYA MUTLU, EBRU; ÖZGEN, İLKER TOLGA; ÖZGEN, İLKER TOLGA
  • PublicationMetadata only
    Yeni mutasyon saptanan hipofosfatemik raşitizm olgusu
    (2017-04-30) KUTLU, ESRA; ÖZGEN, İLKER TOLGA; CESUR, YAŞAR; DUMAN, NİLGÜN; KUTLU, ESRA; ÖZGEN, İLKER TOLGA; CESUR, YAŞAR; DUMAN, NİLGÜN
  • PublicationMetadata only
    SIRT1 gene variants are related to risk of childhood obesity
    (2015-04-01) Kilic, Ulkan; GOK, Ozlem; ELIBOL-CAN, BİRSEN; Ozgen, Ilker Tolga; Erenberk, UFUK; Uysal, Omer; DUNDAROZ, Mehmet Rusen; ELİBOL, BİRSEN; ÖZGEN, İLKER TOLGA; ERENBERK, UFUK; UYSAL, ÖMER
    Obesity is a multifactorial disorder resulting from the interaction between genetic, psychological, physical, environmental, and socioeconomic factors. SIRT1 gene has important effects on the regulation of adiponectin, caloric restriction, insulin sensitivity, coronary atherosclerosis, and cardiovascular diseases. The aim of this study was to investigate the association between childhood obesity and SIRT1 gene polymorphisms regarding rs7895833 A > G in the promoter region, rs7069102 C > G in intron 4, and rs2273773 C > T in exon 5 using PCR-CTPP method in 120 obese and 120 normal weight children. In this study, BMI, systolic and diastolic blood pressure, LDL cholesterol, triglyceride, and insulin levels were significantly higher and HDL-cholesterol levels were significantly lower in obese children compared to normal weight children. For rs7895833 A > G, the rate of having AG genotype and G allele was significantly higher in obese children compared to non-obese group (p T. There was no significant difference for rs7069102 C > G gene polymorphism between groups.
  • PublicationOpen Access
    Pseudohypoparathyroidism Type Ia with Normocalcemia
    (2019-04-01T00:00:00Z) Kutlu, Esra; CESUR, Yaşar; ÖZGEN, İLKER TOLGA; Yesil, Gozde; KUTLU, ESRA; ÖZGEN, İLKER TOLGA; CESUR, YAŞAR; YEŞİL, GÖZDE
    Pseudohypoparathyroidism (PHP) is a heterogeneous group of disorder with parathormone target organ resistance, characterized by hypocalcemia, hyperphosphatemia and high blood parathormone (PTH). Typical phenotypic symptoms and additional hormonal resistance can be observed in type Ia, which is also known as Albright hereditary osteodystrophy. Our patient was an eight-year and nine-month old girl with typical Albright-s hereditary osteodystrophy phenotype including short stature, obesity, round face, low nasal bridge, shortened metacarpals, and mild mental retardation. In her biochemical examination, high PTH level and hypothyroidism is detected in spite of normal calcium and phosphor levels. As a result of clinic and laboratory tests, the findings were consistent with PHP type Ia with normocalcemia. In her guanine nucleotide binding protein (G protein), alpha stimulating activity polypeptide 1 (GNAS 1) gene serial analysis, C-308T>C (p1103T) transformation was detected, which was previously reported in a PHP type Ia patient. In this report, we-ve aimed to emphasize the fact that calcium and phosphor level in the blood of the patient with PHP type Ia can be measured normal.
  • PublicationMetadata only
    Kistik Fibrozis dısı bronsiektazi hastaların endokrinolojik açıdan degerlendirilmesi
    (2015-04-02T00:00:00Z) Özgen, İlker Tolga; Çakır, Erkan; Nursoy, Mustafa Atilla; Cesur, Yaşar; ÖZGEN, İLKER TOLGA; ÇAKIR, ERKAN; NURSOY, MUSTAFA ATİLLA; CESUR, YAŞAR
  • PublicationMetadata only
    Çocuğumun Boyu Kısa mı kalacak?
    (2022-09-29) Özgen İ. T.; ÖZGEN, İLKER TOLGA
  • PublicationMetadata only
    Primary Adrenal Insufficiency in Children without Congenital Adrenal Hyperplasia: Molecular and Clinical Characterisation of a Nationwide Cohort
    (2015-10-03) Bolu, Semih; Ozhan, Bayram; Ucar, Ahmet; Demirbilek, Huseyin; Yavas Abali, Zehra; Berberoglu, Merih; Hacihamdioglu, Bulent; Achermann, John C.; Eren, Erdal; Guran, Tulay; Buonocore, Federica; Saka, Nurcin; Ozbek, Mehmet Nuri; Aycan, Zehra; Bereket, Abdullah; Darcan, Sukran; Bideci, Aysun; Turan, Serap; Guven, Ayla; Tarim, Omer; Agladioglu, Sebahat Yilmaz; ÖZGEN, İLKER TOLGA; Atay, Zeynep; Demir, Korcan; Akinci, Aysehan; Kucukemre Aydin, Banu; Buyukinan, Muammer; Yuksel, Bilgin; Doger, Esra; Akcay, Teoman; Kara, Cengiz; Catli, Gonul; ÖZGEN, İLKER TOLGA