Person: KUTLU, ESRA
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Publication Metadata 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, NİLGÜNPublication Open 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, GÖZDEPseudohypoparathyroidism (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.Publication Metadata only Tiroid hormone direnci olan iki olgu(2017-04-30) CESUR, YAŞAR; KUTLU, ESRA; ÖZGEN, İLKER TOLGA; YEŞİL, GÖZDE; CESUR, YAŞAR; KUTLU, ESRA; ÖZGEN, İLKER TOLGA; YEŞİL, GÖZDEPublication Metadata only Normokalsemik seyreden psödohipoparatiroidi tip 1A(2016-10-09) ÖZGEN, İLKER TOLGA; KUTLU, ESRA; YEŞİL, GÖZDE; CESUR, YAŞAR; DUMAN, NİLGÜN; ÖZGEN, İLKER TOLGA; KUTLU, ESRA; YEŞİL, GÖZDE; CESUR, YAŞAR; DUMAN, NİLGÜNPublication Metadata only The Relationship Between Precocious Puberty and Premature Thelarche with Serum Irisin Levels(2019-09-01T00:00:00Z) Özgen, İlker Tolga; Kutlu, Esra; Bulut, Huri; Temur, Hafize Otcu; Torun, Emel; Cesur, Yaşar; KUTLU, ESRA; ÖZGEN, İLKER TOLGA; BULUT, HURI; TORUN, EMEL; CESUR, YAŞARhttps://www.karger.com/?DOI=10.1159/000495021Publication Metadata only Assessment of retinal thickness as a marker of brain masculinization in children with congenital adrenal hyperplasia: a pilot study(2019-07-01T00:00:00Z) Onal, Hasan; KUTLU, Esra; Aydin, Banu; Ersen, Atilla; Topal, Neval; Adal, Erdal; Gunes, Hatice; Doktur, Hilal; Tanidir, Canan; PİRHAN, DİLARA; Sayin, Nihat; KUTLU, ESRAObjective: To investigate the relationship between brain masculinization and retinal thickness in children with congenital adrenal hyperplasia (CAH).Publication Metadata only Laron sendromu(2016-10-09) KUTLU, ESRA; ÖZGEN, İLKER TOLGA; YEŞİL, GÖZDE; OĞUR, MUSTAFA; CESUR, YAŞAR; KUTLU, ESRA; ÖZGEN, İLKER TOLGA; YEŞİL, GÖZDE; OĞUR, MUSTAFA; CESUR, YAŞARPublication Metadata only 46XY Cinsel Gelişim Bozukluğunun Nadir Nedeni: 17?-hidroksilaz Eksikliği(2017-04-30) CESUR, YAŞAR; ÖZGEN, İLKER TOLGA; KUTLU, ESRA; YEŞİL, GÖZDE; CESUR, YAŞAR; ÖZGEN, İLKER TOLGA; KUTLU, ESRA; YEŞİL, GÖZDEPublication Metadata only Tübülopati ilişkili hipomagnezemi olgu sunumu(2017-04-30) KADAKAL, NİLAY; CESUR, YAŞAR; ÖZGEN, İLKER TOLGA; KUTLU, ESRA; KADAKAL, NİLAY; CESUR, YAŞAR; ÖZGEN, İLKER TOLGA; KUTLU, ESRAPublication Metadata only Polikistik over sendromlu adölesanlarda omentin-1 düzeyleri(2016-10-09) ÖZGEN, İLKER TOLGA; ORUÇ, ŞÜERA; SELEK, ŞAHBETTİN; KUTLU, ESRA; GÜZEL, GÜLSÜM; CESUR, YAŞAR; ÖZGEN, İLKER TOLGA; DOĞAN DEMİR, AYŞEGÜL; SELEK, ŞAHABETTİN; KUTLU, ESRA; GÜZEL, GÜLSÜM; CESUR, YAŞAR