Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Gulnara Nasrullayeva"'
Autor:
Hassan Abolhassani, Tadej Avcin, Nerin Bahceciler, Dmitry Balashov, Zsuzsanna Bata, Mihaela Bataneant, Mikhail Belevtsev, Ewa Bernatowska, Judit Bidló, Péter Blazsó, Bertrand Boisson, Mikhail Bolkov, Anastasia Bondarenko, Oksana Boyarchuk, Anna Bundschu, Jean-Laurent Casanova, Liudmyla Chernishova, Peter Ciznar, Ildikó Csürke, Melinda Erdős, Henriette Farkas, Daria S. Fomina, Nermeen Galal, Vera Goda, Sukru Nail Guner, Péter Hauser, Natalya I. Ilyina, Teona Iremadze, Sevan Iritsyan, Vlora Ismaili-Jaha, Milos Jesenak, Jadranka Kelecic, Sevgi Keles, Gerhard Kindle, Irina V. Kondratenko, Larysa Kostyuchenko, Elena Kovzel, Gergely Kriván, Georgina Kuli-Lito, Gábor Kumánovics, Natalja Kurjane, Elena A. Latysheva, Tatiana V. Latysheva, István Lázár, Gasper Markelj, Maja Markovic, László Maródi, Vafa Mammadova, Márta Medvecz, Noémi Miltner, Kristina Mironska, Fred Modell, Vicki Modell, Bernadett Mosdósi, Anna A. Mukhina, Marianna Murdjeva, Györgyi Műzes, Umida Nabieva, Gulnara Nasrullayeva, Elissaveta Naumova, Kálmán Nagy, Beáta Onozó, Bubusaira Orozbekova, Malgorzata Pac, Karaman Pagava, Alexander N. Pampura, Srdjan Pasic, Mery Petrosyan, Gordana Petrovic, Lidija Pocek, Andrei P. Prodeus, Ismail Reisli, Krista Ress, Nima Rezaei, Yulia A. Rodina, Alexander G. Rumyantsev, Svetlana Sciuca, Anna Sediva, Margit Serban, Svetlana Sharapova, Anna Shcherbina, Brigita Sitkauskiene, Irina Snimshchikova, Shqipe Spahiu-Konjusha, Miklós Szolnoky, Gabriella Szűcs, Natasa Toplak, Beáta Tóth, Galina Tsyvkina, Irina Tuzankina, Elena Vlasova, Alla Volokha
Publikováno v:
Frontiers in Immunology, Vol 13 (2022)
IntroductionThe J Project (JP) physician education and clinical research collaboration program was started in 2004 and includes by now 32 countries mostly in Eastern and Central Europe (ECE). Until the end of 2021, 344 inborn errors of immunity (IEI)
Externí odkaz:
https://doaj.org/article/1e2baf3d28f7485d8e4a9157d356a4b0
Autor:
Mahnaz Jamee, Gholamreza Azizi, Safa Baris, Elif Karakoc-Aydiner, Ahmet Ozen, Sara Ş. Kiliç, Hulya Kose, Zahra Chavoshzadeh, Seyed Alireza Mahdaviani, Tooba Momen, Bibi Shahin Shamsian, Mazdak Fallahi, Samin Sharafian, Nesrin Gülez, Ayşe Aygun, Neslihan Edeer Karaca, Necil Kutukculer, Nashat Al Sukait, Tariq Al Farsi, Salem Al-Tamemi, Nisreen Khalifa, Reda Shereen, Dalia El-Ghoneimy, Rasha El-Owaidy, Nesrine Radwan, Raed Alzyoud, Mohamed-Ridha Barbouche, Imen Ben-Mustapha, Najla Mekki, Afef Rais, Rachida Boukari, Reda Belbouab, Kamel Djenouhat, Azzeddine Tahiat, Souad Touri, Gehad Elghazali, Suleiman Al-Hammadi, Hiba Mohammed Shendi, Amna Alkuwaiti, Brahim Belaid, Reda Djidjik, Hasibe Artac, Mehdi Adeli, Ali Sobh, Marwa H. Elnagdy, Sara A. Bahgat, Gulnara Nasrullayeva, Janet Chou, Nima Rezaei, Waleed Al-Herz, Raif S. Geha, Hassan Abolhassani, Seyed Erfan Rasouli, Marzie Esmaeili, Reza Yazdani, Samaneh Delavari, Marzieh Tavakol, Homa Sadri, Abdollah Karimi, Reza Shiari, Samin Alavi, Delara Babaie, Peyman Eshghi, Shahnaz Armin, Ahmad Vosughimotlagh, Sevgi Bilgic Eltan, Royala Babayeva, Asena Pinar Sefer, Burcu Kolukisa, Ezgi Yalcin Gungoren, Melek Yorgun Altunbas, Vafa Mammadova
Publikováno v:
Clinical Immunology. 244:109131
Monogenic immune dysregulation diseases (MIDD) are caused by defective immunotolerance. This study was designed to increase knowledge on the prevalence and spectrum of MIDDs, genetic patterns, and outcomes in Middle East and North Africa (MENA). MIDD
Autor:
Salem Al-Tamemi, Amel Hassen, Ismail Reisli, André Mégarbané, Waleed Al-Herz, Fred Modell, Gulnara Nasrullayeva, Ahmet Ozen, Jessica Quinn, Elif Karakoc-Aydiner, Nabila Attal, Safa Baris, Reda Djidjik, Nadia Kechout, Ridha Barbouche, László Maródi, Maryam Ali Al-Nesf, Necil Kutukculer, Samir Ladj, Mehdi Adeli, Khalissa Saidani, Ragheed Rizk, Yacine Ferhani, Sara Sebnem Kilic, Mona Al-Ahmed, Vicki Modell, Hassan Abolhassani, Marwa H. Elnagdy, Kamel Djenouhat, Reda Belbouab, Nima Rezaei, Asghar Aghamohammadi, Rachida Boukari, Samaneh Delavari, Carla Irani, Raif S. Geha, Hulya Kose, Nesrin Gulez, Ali Sobh, Ferah Genel, Cybel Mehawej, Ezgi Topyildiz, Azzeddine Tahiat, Aziz Bousfiha, Reza Yazdani, Brahim Belaid
Publikováno v:
Journal of Clinical Immunology
Background Inborn errors of immunity (IEIs) are a heterogeneous group of genetic defects of immunity, which cause high rates of morbidity and mortality mainly among children due to infectious and non-infectious complications. The IEI burden has been
Autor:
Gulnara Nasrullayeva, Daniela Gerent Petry Piotto, Vafa Mammadova, Zuoming Deng, Vibke Lilleby, Annet van Royen-Kerkhof, Andreas Reiff, Troy R. Torgerson, Sara Taber, Mary Beth F. Son, Laura S. Finn, Anne Marie C. Brescia, Yangfeng Hou, Philip J. Hashkes, Marco Gattorno, Alexei A. Grom, Elizabeth Stringer, Marite Rygg, Lisa G. Rider, Eric P. Hanson, Eric J. Allenspach, Ruy Carrasco, Elizabeth A. Kessler, Susan Moir, Ian Ferguson, Edward M. Behrens, Bita Arabshahi, Heinrike Schmeling, Victoria R. Dimitriades, Theresa Wampler Muskardin, Polly J. Ferguson, Rolando Cimaz, Pascal Pillet, Adriana Almeida de Jesus, Maria Teresa Terreri, Andrew J. Oler, Pui Y. Lee, Liliana Bezrodnik, Laura B Lewandowski, Rita Jerath, Stephen R. Brooks, Bernadette Marrero, Tova Ronis, Hanna Kim, Amina Ahmed, Alice Y. Chan, Yuriy Stepanovskiy, Christiaan Scott, Angelique Biancotto, Nancy Pan, Ronald M. Laxer, Adam L Reinhardt, Yan Huang, Johannes Roth, Paul Dancey, Suzanne C. Li, Lakshmi N. Moorthy, Jason Dare, Gisella Seminario, Raphaela Goldbach-Mansky, Natasha M. Ruth, Gina A. Montealegre Sanchez, Grant S. Schulert, Gerd Horneff, Min Ae Lee-Kirsch, Seza Ozen, Daniel J. Kingsbury, Louise Malle, Susanne M. Benseler, Rafael Rivas-Chacon, Laura L. Tosi, Scott W. Canna, Ronit Herzog, Angela Rösen-Wolff, Katherine R. Calvo, Sharon Bout-Tabaku, Diane E. Brown, Jon M. Burnham, Andrew I. Shulman, Karen Onel, Cynthia J. Tifft, Christian M. Hedrich, Vidya Sivaraman, Marilynn Punaro, Kathleen M. O'Neil, Marietta DeGuzman, María Soledad Caldirola
Publikováno v:
The Journal of clinical investigation, vol 130, iss 4
J Clin Invest
CONICET Digital (CONICET)
Consejo Nacional de Investigaciones Científicas y Técnicas
instacron:CONICET
J Clin Invest
CONICET Digital (CONICET)
Consejo Nacional de Investigaciones Científicas y Técnicas
instacron:CONICET
BACKGROUND. Undifferentiated systemic autoinflammatory diseases (USAIDs) present diagnostic and therapeutic challenges. Chronic interferon (IFN) signaling and cytokine dysregulation may identify diseases with available targeted treatments. METHODS. S
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::548766e234ab1c57c7cf4e03193e4e2c
https://escholarship.org/uc/item/49d2m8ws
https://escholarship.org/uc/item/49d2m8ws
Publikováno v:
The Journal of Immunology. 206:52.14-52.14
More than 350 kinds of PID (Primary Immunodeficiency disorders) related gene defects have been found, which lead to multiple clinical manifestations including repeated infection or opportunistic bacterial infections, autoimmune and malignant tumors.
Publikováno v:
The Journal of Immunology. 204:145.6-145.6
The most common type of Primary Immune Deficiencies (PID) are Antibody Deficiencies (AD) characterized by the recurrent bacterial infections. Usually the immune disbalance is observed as a decrease in B-cell function, hypogammaglobulinemia and defici
Autor:
J Marodi, Tadej Avcin, P Ciznar, Gulnara Nasrullayeva, Elisabeth Förster-Waldl, B Sitkauskiene, Anna Sediva, J Kelecic, A Blaziene, V Tenembaum, Beáta Tóth, M Belevtsev, M Serban, Fred Modell, E Naumova, K Ress, M Marković, M Bataneant, Vicki Modell
Publikováno v:
Immunologic Research. 68:71-71
Due to authors' internal mistake they have misspelled the name of one of the co-authors in this article.
Publikováno v:
The Journal of Immunology. 202:182.5-182.5
Genetic immune pathologies are common in Azerbaijan. Primary immune deficiencies (PID) include more than 300 rare congenital diseases. There are more than 250 genes known to be involved in different immune disorders, especially in PID. Around 30% of
Autor:
Dmitry Balashov, Hans D. Ochs, Eleonora Gambineri, Anna Shcherbina, Irina Kondratenko, John B. Ziegler, Isabelle Meyts, Tanja C Bittner, Gulnara Nasrullayeva, Fabian Hauck, Christoph Klein, Susanne Matthes, Uta Behrends, Sara Sebnem Kilic, Joseph H. Chewning, Anders Fasth, Theresa Cole, Peter D. Arkwright, Hirokazu Kanegane, Catharina Schuetz, Elisa Bertoni, G Dueckers, Fabio Candotti, Wojciech Czogała, David Hagin, Xuan Zhang, Michael H. Albert, Renata Formankova, Anastasiia Bondarenko, Luis Ignacio Gonzalez-Granado, Tiago N Gulmaraes, Claudio Pignata, Isabelle Pellier, Polina Stepensky, Pere Soler-Palacín, Beata Wolska-Kusnierz, Troy R. Torgerson, Tomas Freiberger, Lucia Dora Notarangelo, Michael J. Browning, Frederick D. Goldman, Robert Sokolic, Liudmyla Chernyshova, Tarja Heiskanen-Kosma, David Buchbinder, Siraj A. Misbah, Juliana Themudo Lessa Mazzucchelli, Joanne Smart, Sylwia Kołtan, Peter Ciznar, David M Edgar, Jannik S Glasmacher, Kim Vettenranta, Leena Kainulainen, Alessandro Aiuti, Hanna Juntti, Gesmar Rodrigues Silva Segundo, Srdjan Pasic, Alessandro Cattoni, Zohreh Nademi, Beatriz Tavares Costa-Carvalho, Andrew R. Gennery, Neslihan Edeer Karaca, Olga Pashchenko, Svetlana Vakhlyarskaya, Joris M. van Montfrans, Fatih Erbey, Camilla Roepstorff, Ansgar Schulz, Bernd H. Belohradsky, Xiaodong Zhao, Manfred Hoenig, Dawei Liu
Publikováno v:
Blood. 128:366-366
Background: The Wiskott-Aldrich syndrome (WAS) including X-linked thrombocytopenia (XLT) is a complex disorder with a wide range of disease severity and unique hematological and immunological manifestations. Based on this complexity, several approach