The experience of canakinumab in renal amyloidosis secondary to Familial Mediterranean fever

por Sozeri, Betul, Gulez, Nesrin, Ergin, Malik, Serdaroglu, Erkin
Publicado 2016

A child with subcorneal pustular dermatosis responded to IVIG treatment (Sneddon-Wilkinson disease)

por Kundak, Selcen, Bağ, Özlem, Gülez, Nesrin, Ergin, Malik
Publicado 2017

Coexistence of hereditary angioedema in a case of familial Mediterranean fever with partial response to colchicine

por Bahceci, Semiha Erdem, Genel, Ferah, Gulez, Nesrin, Nacaroglu, Hikmet T.
Publicado 2015

Granulomatous pyoderma preceding chronic recurrent multifocal osteomyelitis triggered by vaccinations in a two-year-old boy: a case report

por Karaca, Neslihan, Aksu, Guzide, Ozturk, Can, Gulez, Nesrin, Kutukculer, Necil
Publicado 2010

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 2012

Characteristics of the patients followed with the diagnosis of common variable immunodeficiency and the complications

por Erdem, Semiha Bahceci, Gulez, Nesrin, Genel, Ferah, Karaman, Sait, Nacaroglu, Hikmet T.
Publicado 2019

Do microdeletions lead to immune deficiency?

por KARAMAN, SAIT, HAZAN, FILIZ, ERDEM, SEMIHA BAHÇECI, GÜLEZ, NESRIN, GENEL, FERAH
Publicado 2020

Asplenia in children with congenital heart disease as a cause of poor outcome

por Erdem, Semiha Bahceci, Genel, Ferah, Erdur, Baris, Ozbek, Erhan, Gulez, Nesrin, Mese, Timur
Publicado 2015

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 2011

Familial inheritance and screening of first-degree relatives in common variable immunodeficiency and immunoglobulin A deficiency patients

por Karaca, Neslihan Edeer, Severcan, Ezgi Ulusoy, Bilgin, Burcu Guven, Azarsiz, Elif, Akarcan, Sanem, Gunaydın, Nursen Cigerci, Gulez, Nesrin, Genel, Ferah, Aksu, Guzide, Kutukculer, Necil
Publicado 2018

Early Diagnosis and Hematopoietic Stem Cell Transplantation for IL10R Deficiency Leading to Very Early-Onset Inflammatory Bowel Disease Are Essential in Familial Cases

por Karaca, Neslihan Edeer, Aksu, Guzide, Ulusoy, Ezgi, Aksoylar, Serap, Gozmen, Salih, Genel, Ferah, Akarcan, Sanem, Gulez, Nesrin, Hirschmugl, Tatjana, Kansoy, Savas, Boztug, Kaan, Kutukculer, Necil
Publicado 2016

Comparison of the efficacy of once- and twice-daily colchicine dosage in pediatric patients with familial Mediterranean fever – a randomized controlled noninferiority trial

por Polat, Adem, Acikel, Cengizhan, Sozeri, Betul, Dursun, Ismail, Kasapcopur, Ozgur, Gulez, Nesrin, Simsek, Dogan, Saldir, Mehmet, Dokurel, Ipek, Poyrazoglu, Hakan, Bakkaloglu, Sevcan, Delibas, Ali, Ekinci, Zelal, Ayaz, Nuray A., Kandur, Yasar, Peru, Harun, Kurt, Yasemin G., Polat, Safiye R., Unsal, Erbil, Makay, Balahan, Gok, Faysal, Ozen, Seza, Demirkaya, Erkan
Publicado 2016

Consensus Middle East and North Africa Registry on Inborn Errors of Immunity

por Aghamohammadi, Asghar, Rezaei, Nima, Yazdani, Reza, Delavari, Samaneh, Kutukculer, Necil, Topyildiz, Ezgi, Ozen, Ahmet, Baris, Safa, Karakoc-Aydiner, Elif, Kilic, Sara Sebnem, Kose, Hulya, Gulez, Nesrin, Genel, Ferah, Reisli, Ismail, Djenouhat, Kamel, Tahiat, Azzeddine, Boukari, Rachida, Ladj, Samir, Belbouab, Reda, Ferhani, Yacine, Belaid, Brahim, Djidjik, Reda, Kechout, Nadia, Attal, Nabila, Saidani, Khalissa, Barbouche, Ridha, Bousfiha, Aziz, Sobh, Ali, Rizk, Ragheed, Elnagdy, Marwa H., Al-Ahmed, Mona, Al-Tamemi, Salem, Nasrullayeva, Gulnara, Adeli, Mehdi, Al-Nesf, Maryam, Hassen, Amel, Mehawej, Cybel, Irani, Carla, Megarbane, Andre, Quinn, Jessica, Maródi, László, Modell, Vicki, Modell, Fred, Al-Herz, Waleed, Geha, Raif S., Abolhassani, Hassan
Publicado 2021