Evaluation of Clinical and Immunological Characteristics of Children with Common Variable Immunodeficiency

por Alkan, Gülsüm, Keles, Sevgi, Reisli, İsmail
Publicado 2018

Editorial: Advances in Primary Immunodeficiency in Central-Eastern Europe

por Pac, Malgorzata, Casanova, Jean-Laurent, Reisli, Ismail, Maródi, László
Publicado 2021

A Novel Mutation in the Complement Component 3 Gene in a Patient with Selective IgA Deficiency

por Santos-Valente, Elisangela, Reisli, Ismail, Artaç, Hasibe, Ott, Raphael, Sanal, Özden, Boztug, Kaan
Publicado 2012

Evaluation of the 10 Warning Signs in Primary and Secondary Immunodeficient Patients

por Eldeniz, Fadime Ceyda, Gul, Yahya, Yorulmaz, Alaaddin, Guner, Sukru Nail, Keles, Sevgi, Reisli, Ismail
Publicado 2022

Clinical Spectrum of LIG4 Deficiency Is Broadened with Severe Dysmaturity, Primordial Dwarfism, and Neurological Abnormalities

por IJspeert, Hanna, Warris, Adilia, Flier, Michiel, Reisli, Ismail, Keles, Sevgi, Chishimba, Sandra, Dongen, Jacques JM, Gent, Dik C, Burg, Mirjam
Publicado 2013

Evaluation of immunological abnormalities in patients with rare syndromes

por Gul, Yahya, Kapaklı, Hasan, Aytekin, Selma Erol, Guner, Şukru Nail, Keles, Sevgi, Zamani, Ayşe Gül, Yıldırım, Mahmut Selman, Reisli, Ïsmail
Publicado 2023

(Un)Awareness of Allergy

por Kalpaklioglu, A. Fusun, Kalkan, Ilkay Koca, Akcay, Ahmet, Reisli, Ismail, Can, Demet, Uzuner, Nevin, Yuksel, Hasan, Kirmaz, Cengiz, Gulen, Figen, Ediger, Dane
Publicado 2011

Molecular dissection of human b-cell tolerance - insights from primary immunodeficiencies

por Morbach, Henner, Meyers, Greta, Ng, Yen-Shing, Schickel, Jean-Nicolas, Menard, Laurence, Rudchenko, Sergei, Rojas, Jessica, Cunningham-Rundles, Charlotte, Conley, Mary, Reisli, Ismail, Franco, Jose, Meffre, Eric
Publicado 2014

Molecular dissection of human B-cell tolerance – insights from patients with rare genetic diseases

por Morbach, Henner, Meyers, Greta, Ng, Yen-Shing, Schickel, Jean-Nicolas, Menard, Laurence, Rudchenko, Sergei, Rojas, Jessica L, Cunningham-Rundles, Charlotte, Conley, Mary Ellen, Reisli, Ismail, Franco, Jose Luis, Meffre, Eric
Publicado 2014

Intraoral and maxillofacial abnormalities in patients with autosomal dominant hyper-IgE syndrome

por Tar, Ildikó, Szegedi, Márta, Krasuska-Sławińska, Ewa, Heropolitańska-Pliszka, Edyta, Bernatowska, Ewa A., Öncü, Elif, Keles, Sevgi, Guner, Sukru N., Reisli, Ismail, Gesheva, Nevena, Naumova, Elissaveta, Izakovicova-Holla, Lydie, Litzman, Jiri, Savchak, Igor, Kostyuchenko, Larysa, Erdõs, Melinda
Publicado 2023

Effectiveness of Mesenchymal Stem Cell Therapy for COVID-19 Patients in the Intensive Care Unit: A Case-Control Study

por Canbaz, Hayri, İdiz, Ufuk Oğuz, Cankar Dal, Hayriye, Kaçıroğlu, Fatih, Taş, Seher, Çubukçu, Hikmet Can, Beştemir, Attila, Gülşen, Murat, Polat, İstemi Taha, Laloğlu, Abubekir, Tör, İbrahim Hakkı, Akkurt, Halik Ekrem, Ateş, Utku, Reisli, İsmail, Koç, Esin, İnkaya, Ahmet Çağkan, Karakükçü, Musa, Ceylan, Mustafa, Haznedaroğlu, İbrahim Celalettin, Akın, Haluk
Publicado 2022

DOCK8 functions as an adaptor that links Toll-like receptor–MyD88 signaling to B cell activation

por Jabara, Haifa H., McDonald, Douglas R., Janssen, Erin, Massaad, Michel J., Ramesh, Narayanaswamy, Borzutzky, Arturo, Rauter, Ingrid, Benson, Halli, Schneider, Lynda, Baxi, Sachin, Recher, Mike, Notarangelo, Luigi, Wakim, Rima, Dbaibo, Ghassan, Dasouki, Majed, Al-Herz, Waleed, Barlan, Isil, Baris, Safa, Kutukculer, Necil, Ochs, Hans, Plebani, Alessandro, Kanariou, Maria, Lefranc, Gerard, Reisli, Ismail, Fitzgerald, Kate, Golenbock, Douglas, Manis, John, Keles, Sevgi, Ceja, Reuben, Chatila, Talal, Geha, Raif S.
Publicado 2012

Mutations in CDCA7 and HELLS cause immunodeficiency–centromeric instability–facial anomalies syndrome

por Thijssen, Peter E., Ito, Yuya, Grillo, Giacomo, Wang, Jun, Velasco, Guillaume, Nitta, Hirohisa, Unoki, Motoko, Yoshihara, Minako, Suyama, Mikita, Sun, Yu, Lemmers, Richard J. L. F., de Greef, Jessica C., Gennery, Andrew, Picco, Paolo, Kloeckener-Gruissem, Barbara, Güngör, Tayfun, Reisli, Ismail, Picard, Capucine, Kebaili, Kamila, Roquelaure, Bertrand, Iwai, Tsuyako, Kondo, Ikuko, Kubota, Takeo, van Ostaijen-Ten Dam, Monique M., van Tol, Maarten J. D., Weemaes, Corry, Francastel, Claire, van der Maarel, Silvère M., Sasaki, Hiroyuki
Publicado 2015

Corrigendum: Mutations in CDCA7 and HELLS cause immunodeficiency–centromeric instability–facial anomalies syndrome

por Thijssen, Peter E., Ito, Yuya, Grillo, Giacomo, Wang, Jun, Velasco, Guillaume, Nitta, Hirohisa, Unoki, Motoko, Yoshihara, Minako, Suyama, Mikita, Sun, Yu, Lemmers, Richard J. L. F., de Greef, Jessica C., Gennery, Andrew, Picco, Paolo, Kloeckener-Gruissem, Barbara, Güngör, Tayfun, Reisli, Ismail, Picard, Capucine, Kebaili, Kamila, Roquelaure, Bertrand, Iwai, Tsuyako, Kondo, Ikuko, Kubota, Takeo, van Ostaijen-Ten Dam, Monique M., van Tol, Maarten J. D., Weemaes, Corry, Francastel, Claire, van der Maarel, Silvère M., Sasaki, Hiroyuki
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

Natural Killer Cells from Patients with Recombinase-Activating Gene and Non-Homologous End Joining Gene Defects Comprise a Higher Frequency of CD56(bright) NKG2A(+++) Cells, and Ye...

por Dobbs, Kerry, Tabellini, Giovanna, Calzoni, Enrica, Patrizi, Ornella, Martinez, Paula, Giliani, Silvia Clara, Moratto, Daniele, Al-Herz, Waleed, Cancrini, Caterina, Cowan, Morton, Bleesing, Jacob, Booth, Claire, Buchbinder, David, Burns, Siobhan O., Chatila, Talal A., Chou, Janet, Daza-Cajigal, Vanessa, Ott de Bruin, Lisa M., de la Morena, Maite Teresa, Di Matteo, Gigliola, Finocchi, Andrea, Geha, Raif, Goyal, Rakesh K., Hayward, Anthony, Holland, Steven, Huang, Chiung-Hui, Kanariou, Maria G., King, Alejandra, Kaplan, Blanka, Kleva, Anastasiya, Kuijpers, Taco W., Lee, Bee Wah, Lougaris, Vassilios, Massaad, Michel, Meyts, Isabelle, Morsheimer, Megan, Neven, Benedicte, Pai, Sung-Yun, Parvaneh, Nima, Plebani, Alessandro, Prockop, Susan, Reisli, Ismail, Soh, Jian Yi, Somech, Raz, Torgerson, Troy R., Kim, Yae-Jaen, Walter, Jolan E., Gennery, Andrew R., Keles, Sevgi, Manis, John P., Marcenaro, Emanuela, Moretta, Alessandro, Parolini, Silvia, Notarangelo, Luigi D.
Publicado 2017

Corrigendum: Natural Killer Cells from Patients with Recombinase-Activating Gene and Non-Homologous End Joining Gene Defects Comprise a Higher Frequency of CD56(bright) NKG2A(+++)...

por Dobbs, Kerry, Tabellini, Giovanna, Calzoni, Enrica, Patrizi, Ornella, Martinez, Paula, Giliani, Silvia Clara, Moratto, Daniele, Al-Herz, Waleed, Cancrini, Caterina, Cowan, Morton, Bleesing, Jacob, Booth, Claire, Buchbinder, David, Burns, Siobhan O., Chatila, Talal A., Chou, Janet, Daza-Cajigal, Vanessa, Ott de Bruin, Lisa M., de la Morena, Maite Teresa, Di Matteo, Gigliola, Finocchi, Andrea, Geha, Raif, Goyal, Rakesh K., Hayward, Anthony, Holland, Steven, Huang, Chiung-Hui, Kanariou, Maria G., King, Alejandra, Kaplan, Blanka, Kleva, Anastasiya, Kuijpers, Taco W., Lee, Bee Wah, Lougaris, Vassilios, Massaad, Michel, Meyts, Isabelle, Morsheimer, Megan, Neven, Benedicte, Pai, Sung-Yun, Parvaneh, Nima, Plebani, Alessandro, Prockop, Susan, Reisli, Ismail, Soh, Jian Yi, Somech, Raz, Torgerson, Troy R., Kim, Yae-Jean, Walter, Jolan E., Gennery, Andrew R., Keles, Sevgi, Manis, John P., Marcenaro, Emanuela, Moretta, Alessandro, Parolini, Silvia, Notarangelo, Luigi D.
Publicado 2017

Inherited IFNAR1 deficiency in otherwise healthy patients with adverse reaction to measles and yellow fever live vaccines

por Hernandez, Nicholas, Bucciol, Giorgia, Moens, Leen, Le Pen, Jérémie, Shahrooei, Mohammad, Goudouris, Ekaterini, Shirkani, Afshin, Changi-Ashtiani, Majid, Rokni-Zadeh, Hassan, Sayar, Esra Hazar, Reisli, Ismail, Lefevre-Utile, Alain, Zijlmans, Dick, Jurado, Andrea, Pholien, Ruben, Drutman, Scott, Belkaya, Serkan, Cobat, Aurelie, Boudewijns, Robbert, Jochmans, Dirk, Neyts, Johan, Seeleuthner, Yoann, Lorenzo-Diaz, Lazaro, Enemchukwu, Chibuzo, Tietjen, Ian, Hoffmann, Hans-Heinrich, Momenilandi, Mana, Pöyhönen, Laura, Siqueira, Marilda M., de Lima, Sheila M. Barbosa, de Souza Matos, Denise C., Homma, Akira, Maia, Maria de Lourdes S., da Costa Barros, Tamiris Azamor, de Oliveira, Patricia Mouta Nunes, Mesquita, Emersom Ciclini, Gijsbers, Rik, Zhang, Shen-Ying, Seligman, Stephen J., Abel, Laurent, Hertzog, Paul, Marr, Nico, Martins, Reinaldo de Menezes, Meyts, Isabelle, Zhang, Qian, MacDonald, Margaret R., Rice, Charles M., Casanova, Jean-Laurent, Jouanguy, Emmanuelle, Bossuyt, Xavier
Publicado 2019

Simple Measurement of IgA Predicts Immunity and Mortality in Ataxia-Telangiectasia

por Zielen, Stefan, Duecker, Ruth Pia, Woelke, Sandra, Donath, Helena, Bakhtiar, Sharhzad, Buecker, Aileen, Kreyenberg, Hermann, Huenecke, Sabine, Bader, Peter, Mahlaoui, Nizar, Ehl, Stephan, El-Helou, Sabine M., Pietrucha, Barbara, Plebani, Alessandro, van der Flier, Michiel, van Aerde, Koen, Kilic, Sara S., Reda, Shereen M., Kostyuchenko, Larysa, McDermott, Elizabeth, Galal, Nermeen, Pignata, Claudio, Pérez, Juan Luis Santos, Laws, Hans-Juergen, Niehues, Tim, Kutukculer, Necil, Seidel, Markus G., Marques, Laura, Ciznar, Peter, Edgar, John David M., Soler-Palacín, Pere, von Bernuth, Horst, Krueger, Renate, Meyts, Isabelle, Baumann, Ulrich, Kanariou, Maria, Grimbacher, Bodo, Hauck, Fabian, Graf, Dagmar, Granado, Luis Ignacio Gonzalez, Prader, Seraina, Reisli, Ismail, Slatter, Mary, Rodríguez-Gallego, Carlos, Arkwright, Peter D., Bethune, Claire, Deripapa, Elena, Sharapova, Svetlana O., Lehmberg, Kai, Davies, E. Graham, Schuetz, Catharina, Kindle, Gerhard, Schubert, Ralf
Publicado 2021

Care of patients with inborn errors of immunity in thirty J Project countries between 2004 and 2021

por Abolhassani, Hassan, Avcin, Tadej, Bahceciler, Nerin, Balashov, Dmitry, Bata, Zsuzsanna, Bataneant, Mihaela, Belevtsev, Mikhail, Bernatowska, Ewa, Bidló, Judit, Blazsó, Péter, Boisson, Bertrand, Bolkov, Mikhail, Bondarenko, Anastasia, Boyarchuk, Oksana, Bundschu, Anna, Casanova, Jean-Laurent, Chernishova, Liudmyla, Ciznar, Peter, Csürke, Ildikó, Erdős, Melinda, Farkas, Henriette, Fomina, Daria S., Galal, Nermeen, Goda, Vera, Guner, Sukru Nail, Hauser, Péter, Ilyina, Natalya I., Iremadze, Teona, Iritsyan, Sevan, Ismaili-Jaha, Vlora, Jesenak, Milos, Kelecic, Jadranka, Keles, Sevgi, Kindle, Gerhard, Kondratenko, Irina V., Kostyuchenko, Larysa, Kovzel, Elena, Kriván, Gergely, Kuli-Lito, Georgina, Kumánovics, Gábor, Kurjane, Natalja, Latysheva, Elena A., Latysheva, Tatiana V., Lázár, István, Markelj, Gasper, Markovic, Maja, Maródi, László, Mammadova, Vafa, Medvecz, Márta, Miltner, Noémi, Mironska, Kristina, Modell, Fred, Modell, Vicki, Mosdósi, Bernadett, Mukhina, Anna A., Murdjeva, Marianna, Műzes, Györgyi, Nabieva, Umida, Nasrullayeva, Gulnara, Naumova, Elissaveta, Nagy, Kálmán, Onozó, Beáta, Orozbekova, Bubusaira, Pac, Malgorzata, Pagava, Karaman, Pampura, Alexander N., Pasic, Srdjan, Petrosyan, Mery, Petrovic, Gordana, Pocek, Lidija, Prodeus, Andrei P., Reisli, Ismail, Ress, Krista, Rezaei, Nima, Rodina, Yulia A., Rumyantsev, Alexander G., Sciuca, Svetlana, Sediva, Anna, Serban, Margit, Sharapova, Svetlana, Shcherbina, Anna, Sitkauskiene, Brigita, Snimshchikova, Irina, Spahiu-Konjusha, Shqipe, Szolnoky, Miklós, Szűcs, Gabriella, Toplak, Natasa, Tóth, Beáta, Tsyvkina, Galina, Tuzankina, Irina, Vlasova, Elena, Volokha, Alla
Publicado 2022