Clinical significance of hypouricemia in children and adolescents von Köksoy, Adem Yasin, Görükmez, Özlem, Dorum, Sevil

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NOTCH3 variants in patients with suspected CADASIL von Gorukmez, Orhan, Gorukmez, Ozlem, Topak, Ali, Seferoglu, Meral, Sivaci, Ali, Ali, Asuman, Tepe, Nermin, Kabay, Sibel, Taskapilioglu, Ozlem

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Approaches for diagnosis and treatment in neurotransmitter disorders of childhood von Havalı, Cengiz, Dorum, Sevil, Ekici, Arzu, Görükmez, Özlem

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Two patients with glutaric aciduria type 3: a novel mutation and brain magnetic resonance imaging findings von Dorum, Sevil, Havalı, Cengiz, Görükmez, Özlem, Görükmez, Orhan

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A Novel Homozygous Mutation in the MYO5B Gene Associated With Normal-Gamma-Glutamyl Transferase Progressive Familial Intrahepatic Cholestasis von Uyar Aksu, Nihal, Görükmez, Orhan, Görükmez, Özlem, Uncuoğlu, Ayşen

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Clinical features of pediatric renal glucosuria cases due to SLC5A2 gene variants von Dorum, Sevil, Erdoğan, Hakan, Köksoy, Adem Yasin, Topak, Ali, Görükmez, Özlem

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Expanding the clinical spectrum in trichohepatoenteric syndrome von Dorum, Sevil, Gorukmez, Ozlem

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Association of GSTM1, GSTT1, GSTP1-ILE105VAL and ACE I/D polymorphisms with ankylosing spondylitis von İnal, Esra Erkol, Görükmez, Orhan, Eroğlu, Selma, Görükmez, Özlem, Solak, Özlem, Topak, Ali, Yakut, Tahsin

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Clinical exome sequencing findings in 1589 patients von Gorukmez, Ozlem, Gorukmez, Orhan, Topak, Ali

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First Infertile Case with CSTF2T Gene Mutation von Gorukmez, Ozlem, Gorukmez, Orhan

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First Infertile Case with CSTF2TGene Mutation von Gorukmez, Ozlem, Gorukmez, Orhan

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Associations analysis of GSTM1, T1 and P1 Ile105Val polymorphisms with carpal tunnel syndrome von Eroğlu, Pınar, Erkol İnal, Esra, Sağ, Şebnem Özemri, Görükmez, Özlem, Topak, Ali, Yakut, Tahsin

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Association of the ACE I/D gene polymorphisms with JAK2V617F-positive polycythemia vera and essential thrombocythemia von Gorukmez, Orhan, Sag, Şebnem Ozemri, Gorukmez, Özlem, Ture, Mehmet, Topak, Ali, Sahinturk, Serdar, Ozkaya, Güven, Gulten, Tuna, Ali, Rıdvan, Yakut, Tahsin

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Alkaptonuria in Turkey: Clinical and molecular characteristics of 66 patients von Kisa, Pelin Teke, Gunduz, Mehmet, Dorum, Sevil, Uzun, Ozlem Unal, Cakar, Nafiye Emel, Yildirim, Gonca Kilic, Erdol, Sahin, Hismi, Burcu Ozturk, Tugsal, Handan Yarkan, Ucar, Ulku, Gorukmez, Ozlem, Gulten, Zumrut Arslan, Kucukcongar, Aynur, Bulbul, Selda, Sari, Ismail, Arslan, Nur

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Distribution of KRAS and BRAF Mutations in Metastatic Colorectal Cancers in Turkish Patients von Gorukmez, Orhan, Yakut, Tahsin, Gorukmez, Ozlem, Sag, Sebnem Ozemri, Karkucak, Mutlu, Kanat, Ozkan

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THE EFFECT OF NIVOLUMAB IN PEDIATRIC MALIGNANT TUMORS: A SINGLE CENTER EXPERIENCE WITH EIGHT PATIENTS von Veysel GOK, Firdevs AYDIN, Alper OZCAN, Ebru YILMAZ, Ekrem UNAL, Musa KARAKUKCU, Türkan PATIROGLU, Mehmet Akif OZDEMIR, Filiz KARAMAN, Orhan GORUKMEZ, Ozlem GORUKMEZ, Atil BISGIN

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WITHDRAWN: THE EFFECT OF NIVOLUMAB IN PEDIATRIC MALIGNANT TUMORS: A SINGLE CENTER EXPERIENCE WITH EIGHT PATIENTS von Gok, Veysel, Aydin, Firdevs, Ozcan, Alper, Yilmaz, Ebru, Unal, Ekrem, Karakukcu, Musa, Patiroglu, Türkan, Ozdemir, Mehmet Akif, Karaman, Filiz, Gorukmez, Orhan, Gorukmez, Ozlem, Bisgin, Atil

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The Influence of Polymorphisms of Interleukin-17A and -17F Genes on Susceptibility and Activity of Rheumatoid Arthritis von Erkol İnal, Esra, Görükmez, Orhan, Dündar, Ümit, Görükmez, Özlem, Yener, Mahmut, Özemri Sağ, Şebnem, Yakut, Tahsin

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Qualitative and quantitative evaluation of the BCR-ABL fusion gene in chronic myelogenous leukemia by flourescence in situ hybridization and molecular genetic methods von Ozemri Sag, Sebnem, Yakut, Tahsin, Gorukmez, Ozlem, Gorukmez, Orhan, Ture, Mehmet, Karkucak, Mutlu, Gulten, Tuna, Ali, Ridvan

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MMP2 Gene-735 C/T and MMP9 gene -1562 C/T Polymorphisms in JAK2V617F Positive Myeloproliferative Disorders von Sag, Sebnem Ozemri, Gorukmez, Ozlem, Ture, Mehmet, Gorukmez, Orhan, Topak, Ali, Sahinturk, Serdar, Ocakoglu, Gokhan, Gulten, Tuna, Ali, Ridvan, Yakut, Tahsin

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