Prospective, randomized comparison of OM-85 BV and a prophylactic antibiotic in children with recurrent infections and immunoglobulin A and/or G subclass deficiency()

Por Genel, Ferah, Kutukculer, Necil
Publicado em 2003

Development of hydrocephalus in a patient with Joubert syndrome

Por Genel Ferah, Atlihan F, Ozdemir D, Targan S
Publicado em 2004-04-01

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 no Cent Eur J Immunol (2015)

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 no Cent Eur J Immunol (2019)

Do microdeletions lead to immune deficiency?

Por KARAMAN, SAIT, HAZAN, FILIZ, ERDEM, SEMIHA BAHÇECI, GÜLEZ, NESRIN, GENEL, FERAH
Publicado no Cent Eur J Immunol (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 no Cent Eur J Immunol (2015)

Late diagnosis of leukocyte adhesion deficiency type II and Bombay blood type in a child: a rare case report

Por Yaman, Yöntem, Köker, Sultan Aydin, Ayhan, Fahri Yüce, Genel, Ferah, Acıpayam, Can, Oymak, Yeşim, Sarıbeyoğlu, Ebru Tuğrul, Vergin, Canan Raziye
Publicado no Cent Eur J Immunol (2019)

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 no Int J Immunopathol Pharmacol (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 no Case Reports Immunol (2016)

DOCK8 Regulates STAT3 Activation and Promotes Th17 Cell Differentiation

Por Keles, Sevgi, Charbonnier, Louis Marie, Kabaleeswaran, Venkataraman, Reisli, Ismail, Genel, Ferah, Gulez, Nesrin, Al-Herz, Waleed, Ramesh, Narayanaswamy, Perez-Atayde, Antonio, Eeder, Neslihan Karaca, Kutukculer, Necil, Wu, Hao, Geha, Raif S., Chatila, Talal A.
Publicado no J Allergy Clin Immunol (2016)

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

CD137 deficiency causes immune dysregulation with predisposition to lymphomagenesis

Por Somekh, Ido, Thian, Marini, Medgyesi, David, Gülez, Nesrin, Magg, Thomas, Gallón Duque, Alejandro, Stauber, Tali, Lev, Atar, Genel, Ferah, Unal, Ekrem, Simon, Amos J., Lee, Yu Nee, Kalinichenko, Artem, Dmytrus, Jasmin, Kraakman, Michael J., Schiby, Ginette, Rohlfs, Meino, Jacobson, Jeffrey M., Özer, Erdener, Akcal, Ömer, Conca, Raffaele, Patiroglu, Türkan, Karakukcu, Musa, Ozcan, Alper, Shahin, Tala, Appella, Eliana, Tatematsu, Megumi, Martinez-Jaramillo, Catalina, Chinn, Ivan K., Orange, Jordan S., Trujillo-Vargas, Claudia Milena, Franco, José Luis, Hauck, Fabian, Somech, Raz, Klein, Christoph, Boztug, Kaan
Publicado no Blood (2019)

Large Deletions and Point Mutations Involving DOCK8 in the Autosomal Recessive Form of the Hyper-IgE Syndrome

Por Engelhardt, Karin R., McGhee, Sean, Winkler, Sabine, Sassi, Atfa, Woellner, Cristina, Lopez-Herrera, Gabriela, Chen, Andrew, Kim, Hong Sook, Lloret, Maria Garcia, Schulze, Ilka, Ehl, Stephan, Thiel, Jens, Pfeifer, Dietmar, Veelken, Hendrik, Niehues, Tim, Siepermann, Kathrin, Weinspach, Sebastian, Reisli, Ismail, Keles, Sevgi, Genel, Ferah, Kütükçüler, Necil, Camcioğlu, Yildiz, Somer, Ayper, Aydiner, Elif Karakoc, Barlan, Isil, Gennery, Andrew, Metin, Ayse, Degerliyurt, Aydan, Pietrogrande, Maria C., Yeganeh, Mehdi, Baz, Zeina, Al-Tamemi, Salem, Klein, Christoph, Puck, Jennifer M., Holland, Steven M., McCabe, Edward R. B., Grimbacher, Bodo, Chatila, Talal
Publicado em 2009

Incomplete penetrance for isolated congenital asplenia in humans with mutations in translated and untranslated RPSA exons

Por Bolze, Alexandre, Boisson, Bertrand, Bosch, Barbara, Antipenko, Alexander, Bouaziz, Matthieu, Sackstein, Paul, Chaker-Margot, Malik, Barlogis, Vincent, Briggs, Tracy, Colino, Elena, Elmore, Aurora C., Fischer, Alain, Genel, Ferah, Hewlett, Angela, Jedidi, Maher, Kelecic, Jadranka, Krüger, Renate, Ku, Cheng-Lung, Kumararatne, Dinakantha, Lefevre-Utile, Alain, Loughlin, Sam, Mahlaoui, Nizar, Markus, Susanne, Garcia, Juan-Miguel, Nizon, Mathilde, Oleastro, Matias, Pac, Malgorzata, Picard, Capucine, Pollard, Andrew J., Rodriguez-Gallego, Carlos, Thomas, Caroline, Von Bernuth, Horst, Worth, Austen, Meyts, Isabelle, Risolino, Maurizio, Selleri, Licia, Puel, Anne, Klinge, Sebastian, Abel, Laurent, Casanova, Jean-Laurent
Publicado no Proc Natl Acad Sci U S A (2018)

The extended clinical phenotype of 64 patients with DOCK8 deficiency

Por Engelhardt, Karin R., Gertz, E. Michael, Keles, Sevgi, Schäffer, Alejandro A., Sigmund, Elena C., Glocker, Cristina, Saghafi, Shiva, Pourpak, Zahra, Ceja, Ruben, Sassi, Atfa, Graham, Laura E., Massaad, Michel J., Mellouli, Fethi, Ben-Mustapha, Imen, Khemiri, Monia, Kilic, Sara Sebnem, Etzioni, Amos, Freeman, Alexandra F., Thiel, Jens, Schulze, Ilka, Al-Herz, Waleed, Metin, Ayse, Sanal, Özden, Tezcan, Ilhan, Yeganeh, Mehdi, Niehues, Tim, Dueckers, Gregor, Weinspach, Sebastian, Patiroglu, Turkan, Unal, Ekrem, Dasouki, Majed, Yilmaz, Mustafa, Genel, Ferah, Aytekin, Caner, Kutukculer, Necil, Somer, Ayper, Kilic, Mehmet, Reisli, Ismail, Camcioglu, Yildiz, Gennery, Andrew R., Cant, Andrew J., Jones, Alison, Gaspar, H. Bobby, Arkwright, Peter D., Pietrogrande, Maria C., Baz, Zeina, Al-Tamemi, Salem, Lougaris, Vassilios, Lefranc, Gerard, Megarbane, Andre, Boutros, Jeannette, Galal, Nermeen, Bejaoui, Mohamed, Barbouche, Mohamed-Ridha, Geha, Raif S., Chatila, Talal A., Grimbacher, Bodo
Publicado no J Allergy Clin Immunol (2015)