Could immune cells be associated with nephropathy in Fabry disease patients?
Turkmen, K., Karaselek, M. A., Celik, S. C., Esen, H. H., Ozer, H., Baloglu, I., Ozturk, Y., Guner, S. N., Reisli, I., Keles, S.
Published in International urology and nephrology (01.06.2023)
Published in International urology and nephrology (01.06.2023)
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Anaphylaxis in Turkish children: a multi-centre, retrospective, case study
Orhan, F., Canitez, Y., Bakirtas, A., Yilmaz, O., Boz, A. B., Can, D., Kuyucu, S., Harmanci, K., Tahan, F., Reisli, I., Karakas, T., Baki, A., Cokugras, H., Cakir, M., Yuksel, H.
Published in Clinical and experimental allergy (01.12.2011)
Published in Clinical and experimental allergy (01.12.2011)
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Journal Article
A Novel Homozygous Mutation With Different Clinical Presentations in 2 IRAK-4-Deficient Siblings: First Case With Recurrent Salmonellosis and Non-Hodgkin Lymphoma
Gokturk, B, Casanova, J L, Picard, C, Cagdas Ayvaz, D, Erman, B, Tezcan, I, Ozdemir, H, Ozel, A, Reisli, I
Published in Journal of investigational allergology & clinical immunology (01.08.2018)
Published in Journal of investigational allergology & clinical immunology (01.08.2018)
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Journal Article
CD3G Gene Defects in Familial Autoimmune Thyroiditis
Gokturk, B., Keles, S., Kirac, M., Artac, H., Tokgoz, H., Guner, S. N., Caliskan, U., Caliskaner, Z., Burg, M., Dongen, J., Morgan, N. V., Reisli, I.
Published in Scandinavian journal of immunology (01.11.2014)
Published in Scandinavian journal of immunology (01.11.2014)
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Journal Article
Clinical spectrum of immunodeficiency, centromeric instability and facial dysmorphism (ICF syndrome)
Hagleitner, M M, Lankester, A, Maraschio, P, Hultén, M, Fryns, J P, Schuetz, C, Gimelli, G, Davies, E G, Gennery, A, Belohradsky, B H, de Groot, R, Gerritsen, E J A, Mattina, T, Howard, P J, Fasth, A, Reisli, I, Furthner, D, Slatter, M A, Cant, A J, Cazzola, G, van Dijken, P J, van Deuren, M, de Greef, J C, van der Maarel, S M, Weemaes, C M R
Published in Journal of medical genetics (01.02.2008)
Published in Journal of medical genetics (01.02.2008)
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Journal Article
The PedPAD study: boys predominate in the hypogammaglobulinaemia registry of the ESID online database
Schatorjé, E. J. H., Gathmann, B., Hout, R. W. N. M., Vries, E., Alsina, L, Baumann, U, Belohradsky, BH, Bienemann, K, Boardman, B, Borte, M, Bredius, RG, Brodszki, N, Caracseghi, F, Ciznar, P, Vries, E, Driessen, GJ, Dückers, G, Duppenthaler, A, Farmaki, E, Galal, N, Gennery, A, Gonzalez‐Granado, LI, Hlavackova, E, Hoernes, M, Kilic, SS, Krüger, R, Kuijpers, TW, Kütükcüler, N, Llobet, P, Marques, L, Montfrans, JM, Papadopoulou‐Alataki, E, Paschenko, O, Pasic, S, Pietrogrande, MC, Pignata, C, Reda, SM, Reisli, I, Roesler, J, Santos, JL, Schölvinck, EH, Schulze, Ilka, Seidel, MG, Shcherbina, A, Sundin, M, Szaflarska, A, Velbri, S, Warnatz, K, Warris, A
Published in Clinical and experimental immunology (01.06.2014)
Published in Clinical and experimental immunology (01.06.2014)
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Journal Article
B-cell maturation and antibody responses in individuals carrying a mutated CD19 allele
Artac, H, Reisli, I, Kara, R, Pico-Knijnenburg, I, Adin-Çinar, S, Pekcan, S, Jol-van der Zijde, C M, van Tol, M J D, Bakker-Jonges, L E, van Dongen, J J M, van der Burg, M, van Zelm, M C
Published in Genes and immunity (01.10.2010)
Published in Genes and immunity (01.10.2010)
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Journal Article
DOCK8 Deletions and Mutations Are Associated With The Autosomal Recessive Hyper-IgE Phenotype
McGhee, S.A, Engelhardt, K, Winkler, S, Sassi, A, Woellner, C, Lopez-Herrera, G, Chen, A, Kim, H, Lloret, M. Garcia, Schulze, I, Ehl, S, Thiel, J, Pfeifer, D, Veelken, H, Niehues, T, Siepermann, K, Weinspach, S, Reisli, I, Keles, S, Genel, F, Kütükçüler, N, Camcioglu, Y, Somer, A, Karakoc-Aydiner, E, Barlan, I
Published in Journal of allergy and clinical immunology (01.02.2010)
Published in Journal of allergy and clinical immunology (01.02.2010)
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Journal Article
An intensive approach to the treatment of disseminated BCG infection in a SCID patient
IKINCIOGULLARI, A, DOGU, F, CIFTCI, E, ÜNAL, E, ERTEM, M, REISLI, I, ADIYAMAN, S, YILDIRAN, S. T, EREKUL, S, BABACAN, E
Published in Bone marrow transplantation (Basingstoke) (01.07.2002)
Published in Bone marrow transplantation (Basingstoke) (01.07.2002)
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Journal Article
Esophageal cyst applied with asthma clinic
Pekcan, S, Aslan, E, Keles, S, Artac, H, Reisli, I, Odev, K, Arıbas, O
Published in Paediatric respiratory reviews (2010)
Published in Paediatric respiratory reviews (2010)
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Journal Article
DCLRE1C (ARTEMIS) mutations causing phenotypes ranging from atypical severe combined immunodeficiency to mere antibody deficiency
Volk, Timo, Pannicke, Ulrich, Reisli, Ismail, Bulashevska, Alla, Ritter, Julia, Björkman, Andrea, Schäffer, Alejandro A, Fliegauf, Manfred, Sayar, Esra H, Salzer, Ulrich, Fisch, Paul, Pfeifer, Dietmar, Di Virgilio, Michela, Cao, Hongzhi, Yang, Fang, Zimmermann, Karin, Keles, Sevgi, Caliskaner, Zafer, Güner, S Ükrü, Schindler, Detlev, Hammarström, Lennart, Rizzi, Marta, Hummel, Michael, Pan-Hammarström, Qiang, Schwarz, Klaus, Grimbacher, Bodo
Published in Human molecular genetics (20.12.2015)
Published in Human molecular genetics (20.12.2015)
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The Middle East and North Africa Diagnosis and Management Guidelines for Inborn Errors of Immunity
Baris, Safa, Abolhassani, Hassan, Massaad, Michel J, Al-Nesf, Maryam, Chavoshzadeh, Zahra, Keles, Sevgi, Reisli, Ismail, Tahiat, Azzeddine, Shendi, Hiba Mohammad, Elaziz, Dalia Abd, Belaid, Brahim, Al Dhaheri, Fatima, Haskologlu, Sule, Dogu, Figen, Ben-Mustapha, Imen, Sobh, Ali, Galal, Nermeen, Meshaal, Safa, Elhawary, Rabab, El-Marsafy, Aisha, Alroqi, Fayhan J, Al-Saud, Bandar, Al-Ahmad, Mona, Al Farsi, Tariq, Al Sukaiti, Nashat, Al-Tamemi, Salem, Mehawej, Cybel, Dbaibo, Ghassan, ElGhazali, Gehad, Kilic, Sara Sebnem, Genel, Ferah, Kiykim, Ayca, Musabak, Ugur, Artac, Hasibe, Guner, Sukru Nail, Boukari, Rachida, Djidjik, Reda, Kechout, Nadia, Cagdas, Deniz, El-Sayed, Zeinab Awad, Karakoc-Aydiner, Elif, Alzyoud, Raed, Barbouche, Mohamed Ridha, Adeli, Mehdi, Wakim, Rima Hanna, Reda, Shereen M, Ikinciogullari, Aydan, Ozen, Ahmet, Bousfiha, Aziz, Al-Mousa, Hamoud, Rezaei, Nima, Al-Herz, Waleed, Geha, Raif S
Published in The journal of allergy and clinical immunology in practice (Cambridge, MA) (01.01.2023)
Published in The journal of allergy and clinical immunology in practice (Cambridge, MA) (01.01.2023)
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European internet-based patient and research database for primary immunodeficiencies: results 2006-2008
Gathmann, B, Grimbacher, B, Beauté, J, Dudoit, Y, Mahlaoui, N, Fischer, A, Knerr, V, Kindle, G
Published in Clinical and experimental immunology (01.09.2009)
Published in Clinical and experimental immunology (01.09.2009)
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Journal Article
Conference Proceeding
Type III bare lymphocyte syndrome associated with a novel RFXAP mutation: a case report
Gokturk, B., Artac, H., van Eggermond, M. J., van den Elsen, P., Reisli, İ.
Published in International journal of immunogenetics (01.08.2012)
Published in International journal of immunogenetics (01.08.2012)
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Journal Article
A Novel Homozygous Mutation With Different Clinical Presentations in 2 IRAK-4–Deficient Siblings: First Case With Recurrent Salmonellosis and Non-Hodgkin Lymphoma
Gokturk, B, Casanova, JL, Picard, C, Ayvaz, D Cagdas, Erman, B, Tezcan, I, Ozdemir, H, Ozel, A, Reisli, I
Published in Journal of investigational allergology & clinical immunology (01.01.2018)
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Published in Journal of investigational allergology & clinical immunology (01.01.2018)
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