Search Results - "Dundar, İsmail"

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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Nutritional rickets in Turkish and refugee children aged 0-2: an increasing problem despite vitamin D prophylaxis by Dundar, Ismail, Buyukavci, Mehmet Akif

“…Background. Nutritional rickets (NR) is still a major problem and is exacerbated by an increasing influx of immigrants. In this study, Turkish and immigrant…”
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Frequency of Dyslipidemia and Associated Risk Factors Among Obese Children and Adolescents in Turkey by Dündar, İsmail, Akıncı, Ayşehan

“…Background: The chronic inflammatory state that occurs in obesity causes metabolic complications such as dyslipidemia, hypertension, insulin resistance,…”
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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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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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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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Evaluation of Children and Adolescent Cases Admitted to the Pediatric Emergency Department for Drug Intoxication by Dündar, İsmail, Akın, Yasemin, Yücel, Melek, Yaykıran, Dündar

“…Introduction:Drug poisoning in childhood is one of the leading preventable health problems worldwide. This study aimed to evaluate the epidemiological…”
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Chronic Disease Management of Children Followed with Type 1 Diabetes Mellitus by Baysal, Senay Guven, Ciftci, Nurdan, Dundar, Ismail, Buyukavci, Mehmet Akif, Yagin, Fatma Hilal, Camtosun, Emine, Dogan, Derya Gumus, Akinci, Aysehan

“…With the diagnosis of chronic illness in children, a stressful period is likely to begin for both the affected child and their families. The aim of this study…”
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Clinical and Laboratory Characteristics of MODY Cases, Genetic Mutation Spectrum and Phenotype-genotype Relationship by Özsu, Elif, Çetinkaya, Semra, Bolu, Semih, Hatipoğlu, Nihal, Savaş Erdeve, Şenay, Evliyaoğlu, Olcay, Baş, Firdevs, Çayır, Atilla, Dündar, İsmail, Akbaş, Emine Demet, Uçaktürk, Seyid Ahmet, Berberoğlu, Merih, Şıklar, Zeynep, Özalkak, Şervan, Muratoğlu Şahin, Nursel, Keskin, Melikşah, Şiraz, Ülkü Gül, Turan, Hande, Öztürk, Ayşe Pınar, Mengen, Eda, Sağsak, Elif, Dursun, Fatma, Akyürek, Nesibe, Odabaşı Güneş, Sevinç, Aycan, Zehra

“…Maturity onset diabetes of the young (MODY) occurs due to mutations in genes involved in pancreatic beta cell function and insulin secretion, has heterogeneous…”
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Trend in initial presenting features of type 1 diabetes mellitus over a 24 year period in Turkey: a retrospective analysis of 814 cases by Dündar, İsmail, Akıncı, Ayşehan, Camtosun, Emine, Çiftçi, Nurdan, Kayas, Leman, Nalbantoğlu, Özlem

“…The study aim was to examine changes in trends of presenting features during the diagnosis of patients followed up with newly diagnosed Type 1 diabetes…”
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Type 1 Diabetes Incidence Trends in a Cohort of Turkish Children and Youth by Dündar, İsmail, Akıncı, Ayşehan, Çamtosun, Emine, Kayaş, Leman, Çiftçi, Nurdan, Özçetin, Erdener

“…OBJECTIVEThe aim was to analyze the incidence trend and annual average incidence change of type 1 diabetes (T1DM) in the population <18 years of age in Malatya…”
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17α Hydroxylase/17,20 lyase deficiency: clinical features and genetic insights from a large Turkey cohort by Siklar, Zeynep, Camtosun, Emine, Bolu, Semih, Yildiz, Melek, Akinci, Aysehan, Bas, Firdevs, Dündar, İsmail, Bestas, Asli, Ünal, Edip, Kocaay, Pinar, Guran, Tulay, Buyukyilmaz, Gonul, Ugurlu, Aylin Kilinc, Tosun, Buşra Gurpinar, Turan, Ihsan, Kurnaz, Erdal, Yuksel, Bilgin, Turkkahraman, Doga, Cayir, Atilla, Celmeli, Gamze, Gonc, E. Nazli, Eklioğlu, Beray Selver, Cetinkaya, Semra, Yilmaz, Seniha Kiremitci, Atabek, Mehmet Emre, Buyukinan, Muammer, Arslan, Emrullah, Mengen, Eda, Cakir, Esra Deniz Papatya, Karaoglan, Murat, Hatipoglu, Nihal, Orbak, Zerrin, Ucar, Ahmet, Akyurek, Nesibe, Akbas, Emine Demet, Isik, Emregül, Kaygusuz, Sare Betul, Sutcu, Zumrut Kocabey, Seymen, Gulcan, Berberoglu, Merih

“…Purpose 17α Hydroxylase/17,20 lyase deficiency (17OHD) is a rare form of congenital adrenal hyperplasia, typically diagnosed in late adolescence with symptoms…”
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The Effectiveness of Cinacalcet as an Adjunctive Therapy for Hereditary 1,25 Dihydroxyvitamin D3-Resistant Rickets by Akıncı, Ayşehan, Dündar, İsmail, Kıvılcım, Meltem

“…High doses of oral calcium or long-term calcium infusions are recommended to correct the hypocalcemia and secondary hyperparathyroidism in patients with…”
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Comprehensive Insights Into Pediatric Craniopharyngioma: Endocrine and Metabolic Profiles, Treatment Challenges, and Long-term Outcomes from a Multicenter Study by Şıklar, Zeynep, Özsu, Elif, Kızılcan Çetin, Sirmen, Özen, Samim, Çizmecioğlu-Jones, Filiz, Balkı, Hanife Gül, Aycan, Zehra, Gökşen, Damla, Kilci, Fatih, Abseyi, Sema Nilay, Tercan, Ummahan, Gürpınar, Gözde, Poyrazoğlu, Şükran, Darendeliler, Feyza, Demir, Korcan, Besci, Özge, Özgen, İlker Tolga, Akın, Semra Bahar, Kocabey Sütçü, Zümrüt, Aykaç Kaplan, Emel Hatun, Çamtosun, Emine, Dündar, İsmail, Sağsak, Elif, Korkmaz, Hüseyin Anıl, Anık, Ahmet, Yeşiltepe Mutlu, Gül, Özcabi, Bahar, Uçar, Ahmet, Dağdeviren Çakır, Aydilek, Selver Eklioğlu, Beray, Kırel, Birgül, Berberoğlu, Merih

“…Craniopharyngiomas (CPG) have complex treatment challenges due to their proximity to vital structures, surgical and radiotherapeutic complexities, and the…”
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Laron syndrome related to homozygous growth hormone receptor c.784>C mutation in a patient with hypoplastic pulmonary arteries by Karakurt, Cemşit, Çamtosun, Emine, Dündar, İsmail, Akıncı, Ayşehan, Hwa, Vivian

“…Laron syndrome, also known as growth hormone insensitivity, is an autosomal recessive disorder characterised by short stature due to mutations or deletions in…”
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Comprehensive Insights into Pediatric Craniopharyngioma: Endocrine and Metabolic Profiles, Treatment Challenges, and Long-term Outcomes with a Multicenter Approach by Şıklar, Zeynep, Özsu, Elif, Kızılcan Çetin, Sirmen, Özen, Samim, Çizmecioğlu-Jones, Filiz, Gül Balkı, Hanife, Aycan, Zehra, Goksen, Damla, Kilci, Fatih, Abseyi, Sema Nilay, Tercan, Ummahan, Gürpınar, Gözde, Poyrazoğlu, Şükran, Darendeliler, Feyza, Demir, Korcan, Besci, Özge, Özgen, İlker Tolga, Akın, Semra Bahar, Kocabey Sütçü, Zümrüt, Aykaç Kaplan, Emel Hatun, Çamtosun, Emine, Dundar, İsmail, Sağsak, Elif, Korkmaz, Hüseyin Anıl

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Etiological, clinical, and laboratory evaluation of congenital hypothyroidism and determination of levothyroxine (LT4) dose at treatment interruption in differentiating permanent vs. transient patients by Dündar, İsmail, Büyükavcı, Mehmet Akif, Çiftçi, Nurdan

“…Congenital hypothyroidism (CH) is the most common cause of preventable but irreversible mental retardation in children, although the risk has been widely…”
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Presentation, Diagnosis, and Follow-Up Characteristics of 17α-Hydroxylase Deficiency Cases with Exon 1-6 Deletion (Founder Mutation) in the CYP17A1Gene: 20-Year Single-Center Experience by Dundar, Ismail, Akinci, Aysehan, Camtosun, Emine, Ciftci, Nurdan, Kayas, Leman

“…17α-Hydroxylase/17,20-lyase deficiency (17OHD) is characterized by decreased sex steroids and cortisol synthesis, as well as an increased mineralocorticoid…”
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Effect of Growth Hormone Treatment on Growth Rates in Patients With Growth Hormone Deficiency, Idiopathic Short Stature, and Small for Gestational Age by Guliyeva, Lale, Dundar, Ismail, Akinci, Aysehan, Gozukara Bag, Harika Gozde

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