IL-23R gene polymorphisms in rheumatoid arthritis von Soysal, Ergün, Ulutaş, Firdevs, Tepeli, Emre, Kaymaz, Serdar, Çobankara, Veli

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The Relationship Between Sexual Dysfunctions With Disease Prolactin and Genetic Polymorphisms in Schizophrenia and Bipolar Disorder Patients Receiving Pharmacotherapy von Öztürk Atkaya, Neşe, Özdel, İsmail Osman, Türel, Samet, Tepeli, Emre

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Interleukin-1 gene (IL-1) polymorphism in patients with Behçet’s Disease, and its relationship with disease manifestations von Özkan, Ümit, Ulutaş, Firdevs, Tepeli, Emre, Çobankara, Veli

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A Case of the Perinatal Form Hypophosphatasia Caused by a Novel Large Duplication of the ALPL Gene and Report of One Year Follow-up with Enzyme Replacement Therapy von Hacıhamdioğlu, Bülent, Özgürhan, Gamze, Pereira, Catarina, Tepeli, Emre, Acar, Gülşen, Cömert, Serdar

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Neonatal Bartter syndrome with cholelithiasis and hydrocephalus: Rare association von Özdemir, Özmert MA, Çıralı, Ceren, Yılmaz Ağladıoğlu, Sebahat, Evrengül, Havva, Tepeli, Emre, Ergin, Hacer

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Possible Role of GADD45γ Methylation in Diffuse Large B-Cell Lymphoma: Does It Affect the Progression and Tissue Involvement? von Barış, İkbal Cansu, Caner, Vildan, Şen Türk, Nilay, Sarı, İsmail, Hacıoğlu, Sibel, Doğu, Mehmet Hilmi, Çetin, Ozan, Tepeli, Emre, Can, Özge, Bağcı, Gülseren, Keskin, Ali

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Detection of deletions and/or amplifications of genes related with lung cancer by multiplex ligation-dependent probe amplification (MLPA) technique von Tepeli, Emre, Muslumanoglu, Muhammed Hamza, Uludag, Ahmet, Buyukpinarbasili, Nur, Ozdemir, Muhsin, Oznur, Murat, Aslan, Huseyin, Artan, Sevilhan

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Altered microRNA 5692b and microRNA let-7d expression levels in children and adolescents with attention deficit hyperactivity disorder von Aydin, Sezai Ustun, Kabukcu Basay, Burge, Cetin, Gokhan Ozan, Gungor Aydin, Aysegul, Tepeli, Emre

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Association of synaptosomal-associated protein 25 (SNAP-25) gene polymorphism with temperament and character traits in women with fibromyalgia syndrome von Dogru, Atalay, Balkarli, Ayse, Tepeli, Emre, Aydin, Emel, Cobankara, Veli

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Relationship of Plasminogen Activator Inhibitor 1 4G/5G Gene Polymorphism and Nontraumatic Lunatum Avascular Necrosis von Gönen, Metin, Yörükoğlu, Ali Çağdaş, Aydemir, A. Nadir, Gönen, Gizem Akıncı, Tepeli, Emre, Demirkan, A. Fahir

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The miRNA content of circulating exosomes in DLBCL patients and in vitro influence of DLBCL-derived exosomes on miRNA expression of healthy B-cells from peripheral blood von Caner, Vildan, Cetin, Gokhan Ozan, Hacioglu, Sibel, Baris, Ikbal Cansu, Tepeli, Emre, Turk, Nilay Sen, Bagci, Gulseren, Yararbas, Kanay, Cagliyan, Gulsum

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Synaptosomal-associated protein 25 (Snap-25) gene polymorphism frequency in fibromyalgia syndrome and relationship with clinical symptoms von Balkarli, Ayse, Sengül, Cem, Tepeli, Emre, Balkarli, Huseyin, Cobankara, Veli

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A variant allele of the Mediterranean‐fever gene increases the severity of gout von Balkarli, Ayse, Tepeli, Emre, Balkarli, Huseyin, Kaya, Arif, Cobankara, Veli

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Perinatal form hypophosphatasia caused by a novel large duplication of ALPL gene and one year follow-up under enzyme replacement therapy; a case report von Hacıhamdioğlu, Bülent, Özgürhan, Gamze, Pereira, Catarina, Tepeli, Emre, Acar, Gülşah, Cömert, Serdar

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Vitamin D receptor gene polymorphisms and haplotypes (Apa I, Bsm I, Fok I, Taq I) in Turkish psoriasis patients von Acikbas, Ibrahim, Sanlı, Berna, Tepeli, Emre, Ergin, Seniz, Aktan, Sebnem, Bagci, Huseyin

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HIF1A as a major vascular endothelial growth factor regulator: do its polymorphisms have an association with age-related macular degeneration? von Okur, Volkan, Cetin, Ozan, Cetin, Ebru, Tepeli, Emre, Bulgu, Yunus, Yildirim, Cem

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Could serum pentraxin 3 levels and IgM deposition in skin biopsies predict subsequent renal involvement in children with Henoch–Schönlein purpura? von Yüksel, Selçuk, Çağlar, Murat, Evrengül, Havva, Becerir, Tülay, Tepeli, Emre, Ergin, Ahmet, Çiçek, Esin Avcı, Aybek, Hülya, Yalçın, Nagihan, Demirkan, Neşe Çallı

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MYD88 expression and L265P mutation in mature B-cell non-Hodgkin lymphomas von Caner, Vildan, Sen Turk, Nilay, Baris, Ikbal Cansu, Cetin, Gokhan Ozan, Tepeli, Emre, Hacioglu, Sibel, Sari, Ismail, Zencir, Sevil, Dogu, Mehmet Hilmi, Bagci, Gulseren, Keskin, Ali

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Familial mutation in Caffey disease with reduced penetrance: A case report von Özdemir, Özmert M A, Tancer-Elçi, Hazal, Polat, Aziz, Güçtürk, İnci, Tepeli, Emre, Zeybek, Selcan, Ayaz, Akif

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Quantitative comparison of immunohistochemical and PCR analysis of midkine expression in breast cancer types and serum midkine level von Çetin Sorkun, Hülya, Akbulut, Metin, Enli, Yaşar, Tepeli, Emre, Özkan, Sevgi, Erdem, Ergün

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