Search Results - "Akinci, Ayşehan"

The Etiology and Clinical Features of Non-CAH Gonadotropin-Independent Precocious Puberty: A Multicenter Study by Atay, Zeynep, Yesilkaya, Ediz, Erdeve, Senay Savas, Turan, Serap, Akin, Leyla, Eren, Erdal, Doger, Esra, Aycan, Zehra, Abali, Zehra Yavas, Akinci, Aysşehan, Siklar, Zeynep, Ozen, Samim, Kara, Cengiz, Tayfun, Meltem, Sari, Erkan, Tutunculer, Filiz, Karabulut, Gulcan Seymen, Karaguzel, Gulay, Cetinkaya, Semra, Saglam, Halil, Bideci, Aysun, Kurtoglu, Selim, Guran, Tulay, Bereket, Abdullah

“…Aim: The causes of gonadotropin-independent precocious puberty are diverse, and often have overlapping clinical and biochemical features. With the exception of…”
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Plasma kisspeptin levels in girls with premature thelarche by Akinci, Ayşehan, Cetin, Dilek, Ilhan, Nevin

“…Premature thelarche (PT) is defined as isolated breast development without secondary sex characteristics in girls below the age of eight. We aimed to determine…”
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The Role of Ghrelin in Weight Gain and Growth in Epileptic Children Using Valproate by Gungor, Serdal, Yücel, Gül, Akinci, Ayşehan, Tabel, Yilmaz, Ozerol, Ibrahim Halil, Yologlu, Saim

“…Ghrelin is a major hormone, regulating the energy balance of the body. Weight gain is a significant side effect of valproic acid, which has not been clearly…”
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Prevalence of type 2 diabetes mellitus, metabolic syndrome, and related morbidities in overweight and obese children by Dündar, İsmail, Akıncı, Ayşehan

“…The aim of the study was to determine the prevalence of metabolic syndrome (MetS), type 2 diabetes mellitus (T2DM), and other comorbidities in overweight and…”
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The effect of gonadotropin-releasing hormone analog treatment (leuprolide) on body fat distribution in idiopathic central precocious puberty by Taşcilar, Mehmet Emre, Bilir, Pelin, Akinci, Ayşehan, Köse, Kenan, Akçora, Dilek, Inceoğlu, Deniz, Fitöz, Suat Omer

“…Gonadotropin-releasing hormone analog (GnRHa) therapy is used in idiopathic central precocious puberty (ICPP) worldwide. It has also been shown that during…”
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Prevalence and Predictive Clinical Characteristics of Metabolically Healthy Obesity in Obese Children and Adolescents by Dundar, Ismail, Akinci, Aysehan

“…The increasing prevalence of childhood obesity and accompanying comorbidities all over the world constitutes one of the most important public health problems…”
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The Frequency of Subclinical Hypothyroidism in Obese Children and Adolescents and Its Relationship with Metabolic Parameters and Atherogenic Index by Dündar, İsmail, Akıncı, Ayşehan

“…OBJECTIVEThe effect of subclinical hypothyroidism on glucose and lipid metabolism in obese children is controversial. This study aims to compare cardiovascular…”
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Liraglutide Treatment in a Morbidly Obese Adolescent with a MC4R Gene Variant: Side Effects Reduce Success by Camtosun, Emine, Akinci, Aysehan, Kayas, Leman, Ciftci, Nurdan, Tekedereli, Ibrahim

“…Variants of the melanocortin-4 receptor ( ) gene are the most common cause of monogenic obesity. It has been shown that, while obesity cannot be controlled…”
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Rare Causes of Primary Adrenal Insufficiency: Genetic and Clinical Characterization of a Large Nationwide Cohort by Guran, Tulay, Buonocore, Federica, Saka, Nurcin, Ozbek, Mehmet Nuri, Aycan, Zehra, Bereket, Abdullah, Bas, Firdevs, Darcan, Sukran, Bideci, Aysun, Guven, Ayla, Demir, Korcan, Akinci, Aysehan, Buyukinan, Muammer, Aydin, Banu Kucukemre, Turan, Serap, Agladioglu, Sebahat Yilmaz, Atay, Zeynep, Abali, Zehra Yavas, Tarim, Omer, Catli, Gonul, Yuksel, Bilgin, Akcay, Teoman, Yildiz, Metin, Ozen, Samim, Doger, Esra, Demirbilek, Huseyin, Ucar, Ahmet, Isik, Emregul, Ozhan, Bayram, Bolu, Semih, Ozgen, Ilker Tolga, Suntharalingham, Jenifer P, Achermann, John C

“…Context: Primary adrenal insufficiency (PAI) is a life-threatening condition that is often due to monogenic causes in children. Although congenital adrenal…”
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Clinical Characteristics and Genetic Analyses of Patients with Idiopathic Hypogonadotropic Hypogonadism by Çiftci, Nurdan, Akıncı, Ayşehan, Akbulut, Ekrem, Çamtosun, Emine, Dündar, İsmail, Doğan, Mustafa, Kayaş, Leman

“…Idiopathic hypogonadotropic hypogonadism (IHH) is classified into two groups-Kalman syndrome and normosmic IHH (nIHH). Half of all cases can be explained by…”
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The relationship between serum FGF-23 concentration and insulin resistance, prediabetes and dyslipidemia in obese children and adolescents by Kutluturk, Yesim, Akinci, Aysehan, Ozerol, Ibrahim Halil, Yologlu, Saim

“…Background Obesity is known to cause metabolic disturbances including insulin resistance, dyslipidemia and alters bone mineralization. The effects of obesity…”
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Clinical features, diagnosis and treatment outcomes of Cushing's disease in children: A multicenter study by Tarçın, Gürkan, Çatlı, Gönül, Çetinkaya, Semra, Eren, Erdal, Kardelen, Aslı Derya, Akıncı, Ayşehan, Böber, Ece, Kara, Cengiz, Yıldırım, Ruken, Er, Eren, Polat, Recep, Özhan, Bayram, Yıldız, Melek, Kor, Yılmaz, Evliyaoğlu, Olcay, Dündar, Bumin, Ercan, Oya

“…Since Cushing's disease (CD) is less common in the paediatric age group than in adults, data on this subject are relatively limited in children. Herein, we aim…”
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TSHRV656F Activating Variant of the Thyroid Stimulating Hormone Receptor Gene in Neonatal Onset Hyperthyroidism: A Case Review by Kayaş, Leman, Çamtosun, Emine, Akıncı, Ayşehan, Bircan, Rıfat

“…An activating variant of the thyroid stimulating hormone receptor ( ) gene is one of the rare causes of neonatal hyperthyroidism. This disorder may occur as a…”
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Tuberculous meningitis associated with diabetic ketoacidosis by Elmas, Özlem Nalbantoğlu, Akıncı, Ayşehan, Bilir, Pelin

“…Diabetic ketoacidosis (DKA) is a life-threatening acute complication of type 1 diabetes mellitus. Infections are the leading cause of DKA, but trauma,…”
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Pediatric Primary Adrenal Insufficiency: A 21-year Single Center Experience by Camtosun, Emine, Dundar, Ismail, Akinci, Aysehan, Kayas, Leman, Ciftci, Nurdan

“…Primary adrenal insufficiency (PAI) is a rare but potentially life-threatening condition. In childhood, PAI is usually caused by monogenic diseases. Although…”
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P.352: Recombinant growth hormone treatment in two patients with progressive familial intrahepatic cholestasis by Ertaş, Nur Berna Çelik, Akinci, Ayşehan, Özçay, Figen, Haberal, Mehmet

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46,XY Sex Development Defect due to a Novel Homozygous (Splice Site) c.673_1G>C Variation in the HSD17B3 Gene: Case Report by Çiftci, Nurdan, Kayaş, Leman, Çamtosun, Emine, Akıncı, Ayşehan

“…The enzyme 17-β-hydroxysteroid dehydrogenase type 3 (17β-HSD3) catalyzes the biosynthesis of testosterone (T) from Δ4-androstenedione, and plays an important…”
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Genomic analysis to screen potential genes and mutations in children with non-syndromic early onset severe obesity: a multicentre study in Turkey by Akinci, Aysehan, Kara, Altan, Özgür, Aykut, Turkkahraman, Doga, Aksu, Soner

“…Background Obesity is a complex genetic-based pediatric disorder which triggers life-threatening conditions. Therefore, the understanding the molecular…”
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A Case of Cleidocranial Dysplasia with a Novel Mutation and Growth Velocity Gain with Growth Hormone Treatment by Çamtosun, Emine, Akıncı, Ayşehan, Demiral, Emine, Tekedereli, İbrahim, Sığırcı, Ahmet

“…Cleidocranial dysplasia (CCD) is a rare congenital autosomal dominant skeletal disorder that is characterized by hypoplasia or aplasia of clavicles, failure of…”
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Neonatal Screening for Congenital Adrenal Hyperplasia in Turkey: Outcomes of Extended Pilot Study in 241,083 Infants by Guran, Tulay, Tezel, Basak, Cakir, Meltem, Akinci, Aysehan, Orbak, Zerrin, Keskin, Mehmet, Eklioglu, Beray Selver, Ozon, Alev, Ozbek, Mehmet Nuri, Karaguzel, Gulay, Hatipoglu, Nihal, Gurbuz, Fatih, Cizmecioglu, Filiz Mine, Kara, Cengiz, Simsek, Enver, Bas, Firdevs, Aydin, Murat, Darendeliler, Feyza

“…What is already known on this topic? Classical congenital adrenal hyperplasia (CAH) occurs in 1:13,000 to 1:15,000 live births. 21-hydroxylase enzyme…”
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