Complement-4 Deficiency in a Child with Systemic Lupus Erythematosus Presenting with Standard Treatment-Resistant Severe Skin Lesion

Por Sozeri, Betul, Mir, Sevgi, Berdeli, Afig
Publicado em 2011

NOD2/CARD15 gene mutations in patients with gouty arthritis

Por Karaarslan, Ahmet, Kobak, Senol, Berdeli, Afig
Publicado no Bosn J Basic Med Sci (2016)

Association of FAS -670A/G and FASL –843C/T Gene Polymorphisms on Allograft Nephropathy in Pediatric Renal Transplant Patients

Por Ertan, Pelin, Mir, Sevgi, Ozkayin, Nese, Berdeli, Afig
Publicado em 2010

X-Linked Agammaglobulinemia Presenting with Secondary Hemophagocytic Syndrome: A Case Report

Por Ozturk, Can, Sutcuoglu, Sumer, Atabay, Berna, Berdeli, Afig
Publicado em 2013

4G/5G Polymorphism of PAI-1 gene and Alu-repeat I/D polymorphism of TPA gene in Turkish patients with polycystic ovary syndrome

Por Karadeniz, Muammer, Erdogan, Mehmet, Berdeli, Afig, Saygili, Fusun, Yilmaz, Candeger
Publicado em 2007

Association between RAS Gene Polymorphisms (ACE I/D, AGT M235T) and Henoch-Schönlein Purpura in a Turkish Population

Por Nalbantoglu, Sinem, Tabel, Yılmaz, Mir, Sevgi, Serdaroğlu, Erkin, Berdeli, Afig
Publicado em 2013

The clinical and genetic features of patients with hyper-immunoglobulin D syndrome (HIDS)

Por Sozeri, Betul, Cam, Ozlem, Delebe, Metin, Mir, Sevgi, Berdeli, Afig
Publicado em 2014

Novel mutatıons and diverse clinical phenotypes in recombınase-activating gene 1 deficiency

Por Kutukculer, Necil, Gulez, Nesrin, Karaca, Neslihan Edeer, Aksu, Guzide, Berdeli, Afig
Publicado em 2012

The progesterone receptor PROGINS polymorphism is not related to oxidative stress factors in women with polycystic ovary syndrome

Por Karadeniz, Muammer, Erdogan, Mehmet, Berdeli, Afig, Tamsel, Sadik, Saygili, Fusun, Yilmaz, Candeger
Publicado em 2007

Diagnosis of early-onset sarcoidosis with non–classical symptoms

Por Gündüz, Zübeyde, Kısaarslan, Ayşenur Paç, Düşünsel, Ruhan, Berdeli, Afig, Sözeri, Betül, Poyrazoğlu, Hakan
Publicado em 2014

Recombinase Activating Gene 1 Deficiencies Without Omenn Syndrome May Also Present With Eosinophilia and Bone Marrow Fibrosis

Por Ulusoy, Ezgi, Karaca, Neslihan Edeer, Azarsiz, Elif, Berdeli, Afig, Aksu, Guzide, Kutukculer, Necil
Publicado no J Clin Med Res (2016)

X-Linked Lymphoproliferative Syndrome and Common Variable Immunodeficiency May Not Be Differentiated by SH2D1A and XIAP/BIRC4 Genes Sequence Analysis

Por Gulez, Nesrin, Aksu, Guzide, Berdeli, Afig, Karaca, Neslihan, Tanrıverdi, Sema, Kutukculer, Necil, Azarsiz, Elif
Publicado em 2011

Role of Toll-Like Receptors in Tuberculosis Infection

Por Biyikli, Oguz Oben, Baysak, Aysegul, Ece, Gulfem, Oz, Adnan Tolga, Ozhan, Mustafa Hikmet, Berdeli, Afig
Publicado no Jundishapur J Microbiol (2016)

FAS/FASL gene polymorphisms in Turkish patients with chronic myeloproliferative disorders

Por Ozdemirkiran, Fusun Gediz, Nalbantoglu, Sinem, Gokgoz, Zafer, Payzin, Bahriye Kadriye, Vural, Filiz, Cagirgan, Seckin, Berdeli, Afig
Publicado no Arch Med Sci (2016)

Thrombotic Microangiopathy with Complement Factor H Gene Mutations Unassociated with Atypical Hemolytic Uremic Syndrome

Por Oymak, Yeşim, Karapınar, Tuba Hilkay, Ay, Yılmaz, Özcan, Esin, Müminoğlu, Neryal, Aydın Köker, Sultan, Töret, Ersin, Berdeli, Afig, Serdaroğlu, Erkin, Vergin, Canan
Publicado no Turk J Haematol (2015)

Validity and reliability of medication adherence scale in FMF (adult version)

Por Fidanci, Berna Eren, Yesilkaya, Sirzat, Acikel, Cengizhan, Ozden, Aslan, Simsek, Dogan, Yildiz, Fatih, Kisacik, Bunyamin, Sayarlıoglu, Mehmet, Akar, Servet, Senel, Soner, Tunca, Mehmet, Yavuz, Sule, Tufan, Abdurrahman, Berdeli, Afig, Onat, Ahmet, Gul, Ahmet, Goker, Berna, Kasifoglu, Timucin, Direskeneli, Haner, Erten, Sukran, Ozcelik, Gul, Gok, Faysal, Ozen, Seza, Demirkaya, Erkan
Publicado em 2014

Advillin acts upstream of phospholipase C ϵ1 in steroid-resistant nephrotic syndrome

Por Rao, Jia, Ashraf, Shazia, Tan, Weizhen, van der Ven, Amelie T., Gee, Heon Yung, Braun, Daniela A., Fehér, Krisztina, George, Sudeep P., Esmaeilniakooshkghazi, Amin, Choi, Won-Il, Jobst-Schwan, Tilman, Schneider, Ronen, Schmidt, Johanna Magdalena, Widmeier, Eugen, Warejko, Jillian K., Hermle, Tobias, Schapiro, David, Lovric, Svjetlana, Shril, Shirlee, Daga, Ankana, Nayir, Ahmet, Shenoy, Mohan, Tse, Yincent, Bald, Martin, Helmchen, Udo, Mir, Sevgi, Berdeli, Afig, Kari, Jameela A., El Desoky, Sherif, Soliman, Neveen A., Bagga, Arvind, Mane, Shrikant, Jairajpuri, Mohamad A., Lifton, Richard P., Khurana, Seema, Martins, Jose C., Hildebrandt, Friedhelm
Publicado no J Clin Invest (2017)

COQ6 mutations in human patients produce nephrotic syndrome with sensorineural deafness

Por Heeringa, Saskia F., Chernin, Gil, Chaki, Moumita, Zhou, Weibin, Sloan, Alexis J., Ji, Ziming, Xie, Letian X., Salviati, Leonardo, Hurd, Toby W., Vega-Warner, Virginia, Killen, Paul D., Raphael, Yehoash, Ashraf, Shazia, Ovunc, Bugsu, Schoeb, Dominik S., McLaughlin, Heather M., Airik, Rannar, Vlangos, Christopher N., Gbadegesin, Rasheed, Hinkes, Bernward, Saisawat, Pawaree, Trevisson, Eva, Doimo, Mara, Casarin, Alberto, Pertegato, Vanessa, Giorgi, Gianpietro, Prokisch, Holger, Rötig, Agnès, Nürnberg, Gudrun, Becker, Christian, Wang, Su, Ozaltin, Fatih, Topaloglu, Rezan, Bakkaloglu, Aysin, Bakkaloglu, Sevcan A., Müller, Dominik, Beissert, Antje, Mir, Sevgi, Berdeli, Afig, ϖzen, Seza, Zenker, Martin, Matejas, Verena, Santos-Ocaña, Carlos, Navas, Placido, Kusakabe, Takehiro, Kispert, Andreas, Akman, Sema, Soliman, Neveen A., Krick, Stefanie, Mundel, Peter, Reiser, Jochen, Nürnberg, Peter, Clarke, Catherine F., Wiggins, Roger C., Faul, Christian, Hildebrandt, Friedhelm
Publicado em 2011