Search Results - "Atabek, M. Emre"

Homeostasis Model Assessment Is More Reliable Than the Fasting Glucose/Insulin Ratio and Quantitative Insulin Sensitivity Check Index for Assessing Insulin Resistance Among Obese Children and Adolescents by Keskin, Mehmet, Kurtoglu, Selim, Kendirci, Mustafa, Atabek, M. Emre, Yazici, Cevat

“…Simple fasting methods to measure insulin resistance, such as the homeostasis model assessment (HOMA), fasting glucose/insulin ratio (FGIR), and quantitative…”
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The phenotypic and molecular genetic spectrum of Alström syndrome in 44 Turkish kindreds and a literature review of Alström syndrome in Turkey by Ozantürk, Ayşegül, Marshall, Jan D, Collin, Gayle B, Düzenli, Selma, Marshall, Robert P, Candan, Şükrü, Tos, Tülay, Esen, İhsan, Taşkesen, Mustafa, Çayır, Atilla, Öztürk, Şükrü, Üstün, İhsan, Ataman, Esra, Karaca, Emin, Özdemir, Taha Reşid, Erol, İlknur, Eroğlu, Fehime Kara, Torun, Deniz, Parıltay, Erhan, Yılmaz-Güleç, Elif, Karaca, Ender, Atabek, M Emre, Elçioğlu, Nursel, Satman, İlhan, Möller, Claes, Muller, Jean, Naggert, Jürgen K, Özgül, Rıza Köksal

“…Alström syndrome (ALMS) is an autosomal recessive disease characterized by multiple organ involvement, including neurosensory vision and hearing loss,…”
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Protein oxidation in obesity and insulin resistance by EMRE ATABEK, M, KESKIN, Mehmet, YAZICI, Cevat, KENDIRCI, Mustafa, HATIPOGLU, Nihal, KOKLU, Esat, KURTOGLU, Selim

“…Advanced oxidation protein products (AOPP) are considered reliable markers to estimate the degree of oxidant-mediated protein damage. Data on oxidative stress…”
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Diabetes mellitus type 1: association with Rett syndrome by Kurtoglu, Selim, Atabek, M. Emre, Kumandas, Sefer, Keskin, Mehmet

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Rhabdomyosarcoma with coexistent diabetes insipidus and cerebral salt wasting as postoperative complication by KURTOĞLU, SELIM, ATABEK, M. EMRE, KESKIN, MEHMET, PATIROGLU, TÜRKAN, KUMANDAS, SEFER, TOPALOGLU, NACI

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The phenotypic and molecular genetic spectrum of Alström syndrome in 44 Turkish kindreds and a literature review of Alström syndrome in Turkey by Ozantürk, Ayşegül, Marshall, Jan D, Collin, Gayle B, Düzenli, Selma, Marshall, Robert P, Candan, Şükrü, Tos, Tülay, Esen, İhsan, Taşkesen, Mustafa, Çayır, Atilla, Öztürk, Şükrü, Üstün, İhsan, Ataman, Esra, Karaca, Emin, Özdemir, Taha Reşid, Erol, İlknur, Eroğlu, Fehime Kara, Torun, Deniz, Parıltay, Erhan, Yılmaz-Güleç, Elif, Karaca, Ender, Atabek, M Emre, Elçioğlu, Nursel, Satman, İlhan, Möller, Claes, Muller, Jean, Naggert, Jürgen K, Özgül, Rıza Köksal

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Proton Magnetic Resonance Spectroscopy Findings and Clinical Effects of Montelukast Sodium in a Case With Sjögren-Larsson Syndrome by Pirgon, Ozgur, Aydin, Kursad, Atabek, M. Emre

“…Sjögren-Larsson syndrome is a rare hereditary metabolic disorder characterized by congenital ichthyosis, mental retardation, and spastic diplegia or…”
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Erratum: The phenotypic and molecular genetic spectrum of Alström syndrome in 44 Turkish kindreds and a literature review of Alström syndrome in Turkey by Ozantürk, Ayşegül, Marshall, Jan D, Collin, Gayle B, Düzenli, Selma, Marshall, Robert P, Candan, Şükrü, Tos, Tülay, Esen, İhsan, Taşkesen, Mustafa, Çayır, Atilla, Öztürk, Şükrü, Üstün, İhsan, Ataman, Esra, Karaca, Emin, Özdemir, Taha Reşid, Erol, İlknur, Eroğlu, Fehime Kara, Torun, Deniz, Parıltay, Erhan, Yılmaz-Güleç, Elif, Karaca, Ender, Atabek, M Emre, Elçioğlu, Nursel, Satman, İlhan, Möller, Claes, Muller, Jean, Naggert, Jürgen K, Özgül, Rıza Köksal

“…Correction to: Journal of Human Genetics (2015) 60, 1–9; doi:10.1038/jhg.2014.85; published online 9 October 2014 Since the advance online publication of this…”
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The exon 3-deleted/full-length growth hormone receptor polymorphism and response to growth hormone therapy in growth hormone deficiency and Turner syndrome: a multicenter study by Baş, Firdevs, Darendeliler, Feyza, Aycan, Zehra, Çetinkaya, Ergun, Berberoğlu, Merih, Sıklar, Zeynep, Öcal, Gönül, Timirci, Özlem, Çetinkaya, Semra, Darcan, Şükran, Gökşen Şimşek, Damla, Bideci, Aysun, Cinaz, Peyami, Böber, Ece, Demir, Korcan, Bereket, Abdullah, Turan, Serap, Atabek, M Emre, Tütüncüler, Filiz, Isbir, Turgay, Bozkurt, Nilüfer, Kabataş Eryılmaz, Sema, Uzunhan, Ozan, Küçükemre Aydın, Banu, Bundak, Rüveyde

“…The exon 3-deleted/full-length (d3/fl) growth hormone (GH) receptor (GHR) polymorphism has been associated with responsiveness to GH therapy in some diagnostic…”
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Prevalence of anti-HAV and anti-HEV antibodies in Konya, Turkey by Atabek, M.Emre, Fýndýk, Duygu, Gulyuz, Abdulgani, Erkul, Ibrahim

“…Objective: To determine the prevalence of antibodies to hepatitis A (HAV) and E (HEV) viruses in the different areas of Konya. Methods: Anti-HAV and anti-HEV…”
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Turner's syndrome with situs inversus totalis by Atabek, M Emre, Alp, Hayrullah, Pirgon, Ozgur

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Homeostasis model assessment is more reliable than the fasting glucose/insulin ratio and quantitative insulin sensitivity check index for assessing insulin resistance among obese children and adolescents by Keskin, Mehmet, Kurtoglu, Selim, Kendirci, Mustafa, Atabek, M. Emre, Yazici, Cevat

“…Objective. Simple fasting methods to measure insulin resistance, such as the homeostasis model assessment (HOMA), fasting glucose/insulin ratio (FGIR), and…”
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Different clinical features of amitraz poisoning in children by Atabek, M Emre, Aydin, K, Erkul, I

“…To evaluate clinical experience of amitraz poisoning in children. In this study, the clinical and laboratory features of amitraz poisoning in 14 children are…”
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Effects of 3 years of intravenous pamidronate treatment on bone markers and bone mineral density in a patient with osteoporosis-pseudoglioma syndrome (OPPG) by Bayram, Fahri, Tanriverdi, Fatih, Kurtoğlu, Selim, Atabek, M Emre, Kula, Mustafa, Kaynar, Leyla, Keleştimur, Fahrettin

“…We present a 21 year-old woman with osteoporosis-pseudoglioma syndrome (OPPG) suffering from bone pain and frequent long bone fractures (approximately 1 or 2…”
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Plasmapheresis as an adjunct treatment in severe botulism by Atabek, M Emre, Yavuz, Haluk, Oran, Bulent, Karaaslan, Sevim, Erkul, Ibrahim

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Female pseudohermaphroditism due to classical 21-hydroxylase deficiency and insulin resistance in a girl with Turner syndrome by Atabek, M Emre, Kurtoğlu, Selim, Keskin, Mehmet

“…We report five-year-old girl with female pseudohermaphroditism due to classical form of 21-hydroxylase deficiency associated with Turner's syndrome…”
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Plasma homocysteine concentrations in adolescents with subclinical hypothyroidism by Atabek, M Emre, Pirgon, Ozgur, Erkul, Ibrahim

“…Hyperhomocysteinemia is a risk factor for premature atherosclerotic vascular disease and venous thrombosis. The aim of the present study was to assess plasma…”
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Bardet-Biedl syndrome with syndrome X: a patient report by Keskin, Mehmet, Atabek, M Emre, Kurtoğlu, Selim

“…Bardet-Biedl syndrome (BBS) is an autosomal recessive condition with a wide spectrum of clinical features. The principal manifestations are rod-cone dystrophy…”
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Adrenocortical adenoma associated with inadequately treated congenital adrenal hyperplasia by Kurtoğlu, Selim, Atabek, M Emre, Keskin, Mehmet, Patiroglu, Tahir Ercan

“…We report a 6 year-old boy with the simple virilizing form of 21-hydroxylase deficiency in whom an adrenal adenoma developed following 5 years of steroid…”
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Growth hormone deficiency, situs inversus, hypertrichosis and brachydactyly by Kurtoglu, Selim, Atabek, M Emre

“…A 6 year-old female showed growth hormone deficiency, situs inversus totalis, short stature, blue sclerae, facial dismorphism, brachydactyly, developmental…”
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