An Alternative Perspective to the FMF Clinic: MCP-1 (A-2518G) and CCR2 (G190A) Polymorphisms and MCP1 Expression von ÇİTLİ, Şenol, KOÇAK, Nadir

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Investigation of sub‐chromosomal changes in males with idiopathic azoospermia by chromosomal microarray analysis von Çitli, Şenol, Ceylan, Ahmet Cevdet, Erdemir, Fikret

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IL-1β, IL-18 and Caspase-1 Levels in Serum as an Early Marker in Familial Mediterranean Fever Patients with Attack and Attack-free Period von Köksal Deveci, Feyzanur Yıldırımtepe Çaldıran, Şenol Çitli, Ercan Çaçan

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IL-1β, IL-18 and Caspase-1 Levels in Serum as an Early Marker in Familial Mediterranean Fever Patients with Attack and Attack-free Period von Ercan Çaçan, Şenol Çitli, Feyzanur Yıldırımtepe Çaldıran, Köksal Deveci

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A novel INPP4A mutation with pontocerebellar hypoplasia, myoclonic epilepsy, microcephaly, and severe developmental delay von Özkan Kart, Pınar, Citli, Senol, Yildiz, Nihal, Cansu, Ali

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Faktör V Leiden ve Mthfr İkili Mutasyonu Bulunan Renal Ven Trombozlu Yenidoğan Olgusu von Altın, Hakan, Çitli, Şenol, Akçay, Ahmet

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A Rare Duplication in the PLAG1 Gene: A Case of Neonatal Diabetes von Hekimoğlu, Berna, Çitli, Şenol

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IL-17A, MCP-1, CCR-2, and ABCA1 polymorphisms in children with non-alcoholic fatty liver disease von Akbulut, Ulas Emre, Emeksiz, Hamdi Cihan, Citli, Senol, Cebi, Alper Han, Korkmaz, Hatice Ayca Ata, Baki, Gaye

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Importance and usage of chromosomal microarray analysis in diagnosing intellectual disability, global developmental delay, and autism; and discovering new loci for these disorders von Ceylan, Ahmet Cevdet, Citli, Senol, Erdem, Haktan Bagis, Sahin, Ibrahim, Acar Arslan, Elif, Erdogan, Murat

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Akut Koroner Sendromlu Genç Hastalarda Monosit Kemoatraktan Protein-1 ve CC Kemokin Reseptörü Tip 2 Gen Polimorfizmlerinin Klinik Önemi von TAŞCANOV, Mustafa Beğenç, ÇİTLİ, Şenol

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IL‐17A, MCP‐1, CCR‐2, and ABCA1 polymorphisms in children with non‐alcoholic fatty liver disease von Akbulut, Ulas Emre, Emeksiz, Hamdi Cihan, Citli, Senol, Cebi, Alper Han, Korkmaz, Hatice Ayca Ata, Baki, Gaye

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Geç Tanı Almış Komplet Virilize Bir 46,XX 11-Beta Hidroksilaz Eksikliği Olgusu von Emeksiz,Hamdi Cihan, Altın,Hakan, Çitli,Şenol

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Combination treatment of bortezomib and epirubicin increases the expression of TNFRSF10 A/B, and induces TRAIL-mediated cell death in colorectal cancer cells von Caldiran, Feyzanur, Berkel, Caglar, Yilmaz, Esra, Kucuk, Burak, Cacan, Aslihan Hatun, Citli, Senol, Canpolat, Emel, Cacan, Ercan

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Expanding the clinical and immunological phenotypes of PAX1-deficient SCID and CID patients von Yakici, Nalan, Kreins, Alexandra Y., Catak, Mehmet Cihangir, Babayeva, Royala, Erman, Baran, Kenney, Heather, Gungor, Hatice Eke, Cea, Pablo A., Kawai, Tomoki, Bosticardo, Marita, Delmonte, Ottavia Maria, Adams, Stuart, Fan, Yu-Tong, Pala, Francesca, Turkyilmaz, Ayberk, Howley, Evey, Worth, Austen, Kot, Hakan, Sefer, Asena Pinar, Kara, Altan, Bulutoglu, Alper, Bilgic-Eltan, Sevgi, Altunbas, Melek Yorgun, Bayram Catak, Feyza, Karakus, Ibrahim Serhat, Karatay, Emrah, Tekeoglu, Sidem Didar, Eser, Metin, Albayrak, Davut, Citli, Senol, Kiykim, Ayca, Karakoc-Aydiner, Elif, Ozen, Ahmet, Ghosh, Sujal, Gohlke, Holger, Orhan, Fazil, Notarangelo, Luigi D., Davies, E. Graham, Baris, Safa

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Corrigendum to "Expanding the clinical and immunological phenotypes of PAX1-deficient SCID and CID patients" [Clinical Immunology 255 (2023) 109757] von Yakici, Nalan, Kreins, Alexandra Y, Catak, Mehmet Cihangir, Babayeva, Royala, Erman, Baran, Kenney, Heather, Eke-Gungor, Hatice, Cea, Pablo A, Kawai, Tomoki, Bosticardo, Marita, Delmonte, Ottavia Maria, Adams, Stuart, Fan, Yu-Tong, Pala, Francesca, Turkyilmaz, Ayberk, Howley, Evey, Worth, Austen, Kot, Hakan, Sefer, Asena Pinar, Kara, Altan, Bulutoglu, Alper, Bilgic-Eltan, Sevgi, Yorgun Altunbas, Melek, Bayram Catak, Feyza, Karakus, Ibrahim Serhat, Karatay, Emrah, Tekeoglu, Sidem Didar, Eser, Metin, Albayrak, Davut, Citli, Senol, Kiykim, Ayca, Karakoc-Aydiner, Elif, Ozen, Ahmet, Ghosh, Sujal, Gohlke, Holger, Orhan, Fazil, Notarangelo, Luigi D, Davies, E Graham, Baris, Safa

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Prevalence of known mutations in the MEFV gene in a population screening with high rate of carriers von Ozdemir, Oztürk, Sezgin, Ilhan, Kurtulgan, Hande Kucuk, Candan, Ferhan, Koksal, Binnur, Sumer, Haldun, Icagasioglu, Dilara, Uslu, Atilla, Yildiz, Fazilet, Arslan, Sulhattin, Cetinkaya, Selma, Citli, Senol, Oztemur, Zekeriya, Kayatas, Mansur

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ASD with the Bor Syndrome: A Case Report von Yaylaci, Ferhat, Sahbudak, Begum, Citli, Senol, Kilit, Neriman

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A novel INPP4A mutation with pontocerebellar hypoplasia, myoclonic epilepsy, microcephaly, and severe developmental delay von Özkan Kart, Pınar, Citli, Senol, Yildiz, Nihal, Cansu, Ali

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Corrigendum to “Expanding the clinical and immunological phenotypes of PAX1-deficient SCID and CID patients” [Clinical Immunology 255 (2023) 109757] von Yakici, Nalan, Kreins, Alexandra Y, Catak, Mehmet Cihangir, Babayeva, Royala, Erman, Baran, Kenney, Heather, Eke-Gungor, Hatice, Cea, Pablo A, Kawai, Tomoki, Bosticardo, Marita, Delmonte, Ottavia Maria, Adams, Stuart, Fan, Yu-Tong, Pala, Francesca, Turkyilmaz, Ayberk, Howley, Evey, Worth, Austen, Kot, Hakan, Sefer, Asena Pinar, Kara, Altan, Bulutoglu, Alper, Bilgic-Eltan, Sevgi, Yorgun Altunbas, Melek, Bayram Catak, Feyza, Karakus, Ibrahim Serhat, Karatay, Emrah, Tekeoglu, Sidem Didar, Eser, Metin, Albayrak, Davut, Citli, Senol, Kiykim, Ayca, Karakoc-Aydiner, Elif, Ozen, Ahmet, Ghosh, Sujal, Gohlke, Holger, Orhan, Fazil, Notarangelo, Luigi D, Davies, E Graham, Baris, Safa

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Expanding the clinical and immunological phenotypes of PAX1-deficient SCID and CID patients von Yakici, Nalan, Kreins, Alexandra Y, Catak, Mehmet Cihangir, Babayeva, Royala, Erman, Baran, Kenney, Heather, Gungor, Hatice Eke, Cea, Pablo A, Kawai, Tomoki, Bosticardo, Marita, Delmonte, Ottavia Maria, Adams, Stuart, Fan, Yu-Tong, Pala, Francesca, Turkyilmaz, Ayberk, Howley, Evey, Worth, Austen, Kot, Hakan, Sefer, Asena Pinar, Kara, Altan, Bulutoglu, Alper, Eltan, Sevgi Bilgic, Altunbas, Melek Yorgun, Bayram, Feyza, Karakus, Ibrahim Serhat, Karatay, Emrah, Tekeoglu, Sidem Didar, Eser, Metin, Albayrak, Davut, Citli, Senol, Kiykim, Ayca, Karakoc-Aydiner, Elif, Ozen, Ahmet, Ghosh, Sujal, Gohlke, Holger, Orhan, Fazil, Notarangelo, Luigi D, Davies, E Graham, Baris, Safa

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