Regulatory T Cells and Vitamin D Status in Children with Chronic Autoimmune Thyroiditis

Por Şıklar, Zeynep, Karataş, Deniz, Doğu, Figen, Hacıhamdioğlu, Bülent, İkincioğulları, Aydan, Berberoğlu, Merih
Publicado no J Clin Res Pediatr Endocrinol (2016)

Neutrophilic Alveolitis and High Serum Pro-Brain Natriuretic Peptide Level may be Indicators of Pulmonary Functional Impairment in Connective Tissue Disorders

Por UNCULU, Serap, DİKEN, Özlem Erçen, ÇİLEDAĞ, Aydın, İKİNCİOĞULLARI, Aydan, KARNAK, Demet, KAYACAN, Oya, TURGAY, Murat
Publicado no Arch Rheumatol (2015)

Case Report: Two Patients with Partial DiGeorge Syndrome Presenting with Attention Disorder and Learning Difficulties

Por Hacıhamdioğlu, Bülent, Berberoğlu, Merih, Şıklar, Zeynep, Doğu, Figen, Bilir, Pelin, Erdeve, Şenay Savaş, İkincioğulları, Aydan, Öçal, Gönül
Publicado em 2011

c.761C>T Mutation Linked Hyper IgM Syndrome Presenting with Hypertransaminasemia and Arthritis

Por Celiksoy, Mehmet Halil, Borte, Stephan, İkincioğulları, Aydan, Bilgici, Meltem Ceyhan, Karagöz, Filiz, Kalaycı, Ayhan Gazi, Yıldıran, Alişan
Publicado no Turk J Haematol (2014)

The seroprevalence of Kaposi's sarcoma associated herpes virus and human herpes virus-6 in pediatric patients with cancer and healthy children in a Turkish pediatric oncology cente...

Por Tacyildiz, Nurdan, Dincaslan, Handan Ugur, Ozdemir, Halil, Yavuz, Gulsan, Unal, Emel, Ikinciogullari, Aydan, Dogu, Figen, Guloglu, Deniz, Suskan, Emine, Kose, Kenan
Publicado em 2014

BCG Lymphadenitis and Recurrent Oral Candidiasis in an Infant with a New Mutation Leading to Interleukin-12 Receptor Beta-1 Deficiency

Por Aytekin, Caner, Dogu, Figen, Tuygun, Nilden, Tanir, Gonul, Guloglu, Deniz, Boisson-Dupuis, Stephanie, Bustamante, Jacinta, Feinberg, Jacqueline, Casanova, Jean-Laurent, Ikinciogullari, Aydan
Publicado em 2011

A Successful HSCT in a Girl with Novel LRBA Mutation with Refractory Celiac Disease

Por Sari, Sinan, Dogu, Figen, Hwa, Vivian, Haskologlu, Sule, Dauber, Andrew, Rosenfeld, Ron, Polat, Meltem, Kuloglu, Zarife, Kansu, Aydan, Dalgic, Buket, Ikinciogullari, Aydan
Publicado no J Clin Immunol (2015)

Clinical Features and Outcomes of 23 Patients with Wiskott-Aldrich Syndrome: A Single-Center Experience

Por Haskoloğlu, Şule, Öztürk, Ayşenur, Öztürk, Gökcan, Kostel Bal, Sevgi, İslamoğlu, Candan, Baskın, Kübra, Ceylaner, Serdar, Tufan Satıroğlu, Lale, Doğu, Figen, İkincioğulları, Aydan
Publicado no Turk J Haematol (2020)

Clinical, immunological features and follow up of 20 patients with dedicator of cytokinesis 8 (DOCK8) deficiency

Por Haskologlu, Sule, Kostel Bal, Sevgi, Islamoglu, Candan, Aytekin, Caner, Guner, Sukru, Sevinc, Selin, Keles, Sevgi, Kendirli, Tanil, Ceylaner, Serdar, Dogu, Figen, Ikinciogullari, Aydan
Publicado no Pediatr Allergy Immunol (2020)

Selenium in the Prevention of Anthracycline-Induced Cardiac Toxicity in Children with Cancer

Por Tacyildiz, Nurdan, Ozyoruk, Derya, Ozelci Kavas, Guzin, Yavuz, Gulsan, Unal, Emel, Dincaslan, Handan, Atalay, Semra, Ucar, Tayfun, Ikinciogullari, Aydan, Doganay, Beyza, Oktay, Gulsah, Cavdar, Ayhan, Kucuk, Omer
Publicado em 2012

Both Granulocytic and Non-Granulocytic Blood Cells Are Affected in Patients with Severe Congenital Neutropenia and Their Non-Neutropenic Family Members: An Evaluation of Morphology...

Por Olcay, Lale, Ünal, Şule, Onay, Hüseyin, Erdemli, Esra, Öztürk, Ayşenur, Billur, Deniz, Metin, Ayşe, Okur, Hamza, Yıldırmak, Yıldız, Büyükaşık, Yahya, İkincioğulları, Aydan, Falay, Mesude, Özet, Gülsüm, Yetgin, Sevgi
Publicado no Turk J Haematol (2018)

Multiple Presentations of LRBA Deficiency: a Single-Center Experience

Por Kostel Bal, Sevgi, Haskologlu, Sule, Serwas, Nina K., Islamoglu, Candan, Aytekin, Caner, Kendirli, Tanil, Kuloglu, Zarife, Yavuz, Gulsan, Dalgic, Buket, Siklar, Zeynep, Kansu, Aydan, Ensari, Arzu, Boztug, Kaan, Dogu, Figen, Ikinciogullari, Aydan
Publicado no J Clin Immunol (2017)

Extended clinical and genetic spectrum associated with biallelic RTEL1 mutations

Por Touzot, Fabien, Kermasson, Laetitia, Jullien, Laurent, Moshous, Despina, Ménard, Christelle, Ikincioğullari, Aydan, Doğu, Figen, Sari, Sinan, Giacobbi-Milet, Vannina, Etzioni, Amos, Soulier, Jean, Londono-Vallejo, Arturo, Fischer, Alain, Callebaut, Isabelle, de Villartay, Jean-Pierre, Leblanc, Thierry, Kannengiesser, Caroline, Revy, Patrick
Publicado no Blood Adv (2016)

Inherited IL-17RC deficiency in patients with chronic mucocutaneous candidiasis

Por Ling, Yun, Cypowyj, Sophie, Aytekin, Caner, Galicchio, Miguel, Camcioglu, Yildiz, Nepesov, Serdar, Ikinciogullari, Aydan, Dogu, Figen, Belkadi, Aziz, Levy, Romain, Migaud, Mélanie, Boisson, Bertrand, Bolze, Alexandre, Itan, Yuval, Goudin, Nicolas, Cottineau, Julien, Picard, Capucine, Abel, Laurent, Bustamante, Jacinta, Casanova, Jean-Laurent, Puel, Anne
Publicado no J Exp Med (2015)

Defects Along the Th17 Differentiation Pathway Underlie Genetically Distinct Forms of the Hyper IgE Syndrome

Por Khatib, Shadi Al, Keles, Sevgi, Garcia-Lloret, Maria, Karakoc-Aydiner, Elif, Reisli, Ismail, Artac, Hasibe, Camcioglu, Yildiz, Cokugras, Haluk, Somer, Ayper, Kutukculer, Necil, Yilmaz, Mustafa, Ikinciogullari, Aydan, Yegin, Olcay, Yüksek, Mutlu, Genel, Ferah, Kucukosmanoglu, Ercan, Baki, Ali, Bahceciler, Nerin N, Rambhatla, Anupama, Nickerson, Derek W., McGhee, Sean, Barlan, Isil B, Chatila, Talal
Publicado em 2009

Biallelic loss-of-function mutation in NIK causes a primary immunodeficiency with multifaceted aberrant lymphoid immunity

Por Willmann, Katharina L., Klaver, Stefanie, Doğu, Figen, Santos-Valente, Elisangela, Garncarz, Wojciech, Bilic, Ivan, Mace, Emily, Salzer, Elisabeth, Domínguez Conde, Cecilia, Sic, Heiko, Májek, Peter, Banerjee, Pinaki P., Vladimer, Gregory I., Haskoloğlu, Şule, Gökalp Bolkent, Musa, Küpesiz, Alphan, Condino-Neto, Antonio, Colinge, Jacques, Superti-Furga, Giulio, Pickl, Winfried F., van Zelm, Menno C., Eibel, Hermann, Orange, Jordan S., Ikincioğulları, Aydan, Boztuğ, Kaan
Publicado no Nat Commun (2014)

Patients with Primary Immunodeficiencies Are a Reservoir of Poliovirus and a Risk to Polio Eradication

Por Aghamohammadi, Asghar, Abolhassani, Hassan, Kutukculer, Necil, Wassilak, Steve G., Pallansch, Mark A., Kluglein, Samantha, Quinn, Jessica, Sutter, Roland W., Wang, Xiaochuan, Sanal, Ozden, Latysheva, Tatiana, Ikinciogullari, Aydan, Bernatowska, Ewa, Tuzankina, Irina A., Costa-Carvalho, Beatriz T., Franco, Jose Luis, Somech, Raz, Karakoc-Aydiner, Elif, Singh, Surjit, Bezrodnik, Liliana, Espinosa-Rosales, Francisco J., Shcherbina, Anna, Lau, Yu-Lung, Nonoyama, Shigeaki, Modell, Fred, Modell, Vicki, Barbouche, Mohamed-Ridha, McKinlay, Mark A.
Publicado no Front Immunol (2017)

Expanding the Nude SCID/CID Phenotype Associated with FOXN1 Homozygous, Compound Heterozygous, or Heterozygous Mutations

Por Giardino, Giuliana, Sharapova, Svetlana O., Ciznar, Peter, Dhalla, Fatima, Maragliano, Luca, Radha Rama Devi, Akella, Islamoglu, Candan, Ikinciogullari, Aydan, Haskologlu, Sule, Dogu, Figen, Hanna-Wakim, Rima, Dbaibo, Ghassan, Chou, Janet, Cirillo, Emilia, Borzacchiello, Carla, Kreins, Alexandra Y., Worth, Austen, Rota, Ioanna A., Marques, José G., Sayitoglu, Muge, Firtina, Sinem, Mahdi, Moaffaq, Geha, Raif, Neven, Bénédicte, Sousa, Ana E., Benfenati, Fabio, Hollander, Georg A., Davies, E. Graham, Pignata, Claudio
Publicado no J Clin Immunol (2021)

Impaired respiratory burst contributes to infections in PKCδ-deficient patients

Por Neehus, Anna-Lena, Moriya, Kunihiko, Nieto-Patlán, Alejandro, Le Voyer, Tom, Lévy, Romain, Özen, Ahmet, Karakoc-Aydiner, Elif, Baris, Safa, Yildiran, Alisan, Altundag, Engin, Roynard, Manon, Haake, Kathrin, Migaud, Mélanie, Dorgham, Karim, Gorochov, Guy, Abel, Laurent, Lachmann, Nico, Dogu, Figen, Haskologlu, Sule, İnce, Erdal, El-Benna, Jamel, Uzel, Gulbu, Kiykim, Ayca, Boztug, Kaan, Roderick, Marion R., Shahrooei, Mohammad, Brogan, Paul A., Abolhassani, Hassan, Hancioglu, Gonca, Parvaneh, Nima, Belot, Alexandre, Ikinciogullari, Aydan, Casanova, Jean-Laurent, Puel, Anne, Bustamante, Jacinta
Publicado no J Exp Med (2021)

Combined immunodeficiency and Epstein-Barr virus–induced B cell malignancy in humans with inherited CD70 deficiency

Por Abolhassani, Hassan, Edwards, Emily S.J., Ikinciogullari, Aydan, Jing, Huie, Borte, Stephan, Buggert, Marcus, Du, Likun, Matsuda-Lennikov, Mami, Romano, Rosa, Caridha, Rozina, Bade, Sangeeta, Zhang, Yu, Frederiksen, Juliet, Fang, Mingyan, Bal, Sevgi Kostel, Haskologlu, Sule, Dogu, Figen, Tacyildiz, Nurdan, Matthews, Helen F., McElwee, Joshua J., Gostick, Emma, Price, David A., Palendira, Umaimainthan, Aghamohammadi, Asghar, Boisson, Bertrand, Rezaei, Nima, Karlsson, Annika C., Lenardo, Michael J., Casanova, Jean-Laurent, Hammarström, Lennart, Tangye, Stuart G., Su, Helen C., Pan-Hammarström, Qiang
Publicado no J Exp Med (2017)