Novel MTTP Gene Mutation in a Case of Abetalipoproteinemia with Central Hypothyroidism von Acar, Sezer

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Whole-genome sequencing analysis in families with recurrent pregnancy loss: A pilot study von Workalemahu, Tsegaselassie, Avery, Cecile, Lopez, Sarah, Blue, Nathan R, Wallace, Amelia, Quinlan, Aaron R, Coon, Hilary, Warner, Derek, Varner, Michael W, Branch, D Ware, Jorde, Lynn B, Silver, Robert M

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Modelling timing and tempo of adrenarche in a prospective cohort study von Dashti, S Ghazaleh, Mundy, Lisa, Goddings, Anne-Lise, Canterford, Louise, Viner, Russell M, Carlin, John B, Patton, George, Moreno-Betancur, Margarita

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Loss of MANF Causes Childhood-Onset Syndromic Diabetes Due to Increased Endoplasmic Reticulum Stress von Montaser, Hossam, Patel, Kashyap A., Balboa, Diego, Ibrahim, Hazem, Lithovius, Vaino, Naatanen, Anna, Chandra, Vikash, Demir, Korcan, Acar, Sezer, Ben-Omran, Tawfeg, Colclough, Kevin, Locke, Jonathan M., Wakeling, Matthew, Lindahl, Maria, Hattersley, Andrew T., Saarimaki-Vire, Jonna, Otonkoski, Timo

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Oxytocin receptor gene polymorphism and low serum oxytocin level are associated with hyperphagia and obesity in adolescents von Çatli, Gönül, Acar, Sezer, Cingöz, Gülten, Rasulova, Khayala, Yarim, Ayça Kanat, Uzun, Hamide, Küme, Tuncay, Kızıldağ, Sefa, Dündar, Bumin Nuri, Abacı, Ayhan

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Systematic genetic testing for recessively inherited monogenic diabetes: a cross-sectional study in paediatric diabetes clinics von Patel, Kashyap A., Ozbek, Mehmet N., Yildiz, Melek, Guran, Tulay, Kocyigit, Cemil, Acar, Sezer, Siklar, Zeynep, Atar, Muge, Colclough, Kevin, Houghton, Jayne, Johnson, Matthew B., Ellard, Sian, Flanagan, Sarah E., Cizmecioglu, Filiz, Berberoglu, Merih, Demir, Korcan, Catli, Gonul, Bas, Serpil, Akcay, Teoman, Demirbilek, Huseyin, Weedon, Michael N., Hattersley, Andrew T.

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Genetic diagnosis of congenital hypopituitarism in Turkish patients by a target gene panel: novel pathogenic variants in GHRHR, GLI2, LHX4 and POU1F1 genes von Kırkgöz, Tarık, Gürsoy, Semra, Acar, Sezer, Nalbantoğlu, Özlem, Özkaya, Beyhan, Korkmaz, Hüseyin Anıl, Hazan, Filiz, Özkan, Behzat

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Evaluation of Liver Iron Content by Magnetic Resonance Imaging in Children with Acute Lymphoblastic Leukemia after Cessation of Treatment von Acar, Sezer, Gozmen, Salih, Bayraktaroglu, Selen, Acar, Sultan O., Tahta, Neryal, Aydinok, Yesim, Vergin, Raziye C.

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Development of propolis and essential oils containing oral/throat spray formulation against SARS-CoV-2 infection von Pelvan, Ebru, Serhatlı, Müge, Karaoğlu, Öznur, Karadeniz, Bülent, Pembeci Kodolbaş, Ceyda, Aslı Öncü, Neşe, Çakırca, Gamze, Damarlı, Emel, Başdoğan, Günay, Mergen Duymaz, Gizem, Emir Akyıldız, İsmail, Düz, Gamze, Acar, Sezer, Özhan, Yağmur, Sipahi, Hande, Charehsaz, Mohammad, Aydın, Ahmet, Yesilada, Erdem, Alasalvar, Cesarettin

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Investigating the Efficiency of Vitamin D Administration with Buccal Spray in the Treatment of Vitamin D Deficiency in Children and Adolescents von Nalbantoglu, Ozlem, Acar, Sezer, Arslan, Gulcin, Koprulu, Ozge, Ozkan, Behzat

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The Effect of Supplementary Feeding with Different Pollens in Autumn on Colony Development under Natural Environment and In Vitro Lifespan of Honey Bees von Topal, Erkan, Mărgăoan, Rodica, Bay, Veysel, Takma, Çiğdem, Yücel, Banu, Oskay, Devrim, Düz, Gamze, Acar, Sezer, Kösoğlu, Mustafa

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Clinical and genetic characteristics of 15 families with hereditary hypophosphatemia: Novel Mutations in PHEX and SLC34A3 von Acar, Sezer, BinEssa, Huda A, Demir, Korcan, Al-Rijjal, Roua A, Zou, Minjing, Çatli, Gönül, Anık, Ahmet, Al-Enezi, Anwar F, Özışık, Seçil, Al-Faham, Manar S A, Abacı, Ayhan, Dündar, Bumin, Kattan, Walaa E, Alsagob, Maysoon, Kavukçu, Salih, Tamimi, Hamdi E, Meyer, Brian F, Böber, Ece, Shi, Yufei

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Evaluation of Thyroid Function Tests in Children with Chronic Liver Diseases von On, S. Sebnem, Acar, Sezer, Demir, Korcan, Abaci, Ayhan, Ozturk, Yesim, Celik, Sinem Kahveci, Bober, Ece

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A Null Mutation of TNFRSF11A Causes Dysosteosclerosis, Not Osteopetrosis von Kırkgöz, Tarık, Özkan, Behzat, Hazan, Filiz, Acar, Sezer, Nalbantoğlu, Özlem, Özkaya, Beyhan, Kulalı, Melike Ataseven, Gürsoy, Semra, Ikegawa, Shiro, Guo, Long

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Hyperandrogenism correlates with psychological symptoms in adolescents with polycystic ovary syndrome von Donbaloğlu, Zeynep, Tuhan, Hale, Çoban, Özge Gizli, Kızılay, Deniz Özalp, İsmailoğlu, Eren, Önder, Arif, Acar, Sezer, Bedel, Aynur, Çetiner, Ebru Barsal, Singin, Berna, Erdem, Harun, Parlak, Mesut

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The Relationship between Serum Zonulin Level and Clinical and Laboratory Parameters of Childhood Obesity von Küme, Tuncay, Acar, Sezer, Tuhan, Hale, Çatlı, Gönül, Anık, Ahmet, Gürsoy Çalan, Özlem, Böber, Ece, Abacı, Ayhan

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Clinical and Laboratory Characteristics of Hyperprolactinemia in Children and Adolescents: National Survey von Eren, Erdal, Törel Ergür, Ayça, İşgüven, Şükriye Pınar, Çelebi Bitkin, Eda, Berberoğlu, Merih, Şıklar, Zeynep, Baş, Firdevs, Yel, Servet, Baş, Serpil, Söbü, Elif, Bereket, Abdullah, Turan, Serap, Sağlam, Halil, Atay, Zeynep, Ercan, Oya, Güran, Tülay, Atabek, Mehmet Emre, Korkmaz, Hüseyin Anıl, Kılınç Uğurlu, Aylin, Akıncı, Ayşehan, Döğer, Esra, Şimşek, Enver, Akbaş, Emine Demet, Abacı, Ayhan, Gül, Ülkü, Acar, Sezer, Mengen Uçaktürk, Eda, Yıldız, Melek, Ünal, Edip, Tarım, Ömer

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A Case of Late-onset Hyperinsulinemic Hypoglycemia: HNF4A Mutation von Arslan, Gulcin, Acar, Sezer, Ozdemir, Taha Resid, Nalbantoglu, Ozlem, Kirbiyik, Ozgur, Koprulu, Ozge, Ozkaya, Beyhan, Ozkan, Behzat

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Distinctively Different Phenotypes of Two Cases with a Rare Karyotype of 45,X/47,XYY Mosaicism: Case Report and Literature Review von Koprulu, Ozge, Acar, Sezer, Erdogan, Kadri Murat, Nalbantoglu, Ozlem, Kirkgoz, Tarik, Arslan, Gulcin, Ozkaya, Beyhan, Kutbay, Yasar Bekir, Ozkan, Behzat

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Spectrum of Clinical Manifestations in Turkish Patients with Williams-Beuren Syndrome: A Monocentric Study von Gursoy, Semra, Hazan, Filiz, Zihni, Cuneyt, Acar, Sezer, Yilmazer, Murat Muhtar, Mese, Timur, Ozkan, Behzat

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