21 results on '"Çelmeli, Fatih"'
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2. Therapeutic modalities and clinical outcomes in a large cohort with LRBA deficiency and CTLA4 insufficiency
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Taghizade, Nigar, Babayeva, Royala, Kara, Altan, Karakus, Ibrahim Serhat, Catak, Mehmet Cihangir, Bulutoglu, Alper, Haskologlu, Zehra Sule, Akay Haci, Idil, Tunakan Dalgic, Ceyda, Karabiber, Esra, Bilgic Eltan, Sevgi, Yorgun Altunbas, Melek, Sefer, Asena Pinar, Sezer, Ahmet, Kokcu Karadag, Sefika Ilknur, Arik, Elif, Karali, Zuhal, Ozhan Kont, Aylin, Tuzer, Can, Karaman, Sait, Mersin, Selver Seda, Kasap, Nurhan, Celik, Enes, Kocacik Uygun, Dilara Fatma, Aydemir, Sezin, Kiykim, Ayca, Aydogmus, Cigdem, Ozek Yucel, Esra, Celmeli, Fatih, Karatay, Emrah, Bozkurtlar, Emine, Demir, Semra, Metin, Ayse, Karaca, Neslihan Edeer, Kutukculer, Necil, Aksu, Guzide, Guner, Sukru Nail, Keles, Sevgi, Reisli, Ismail, Kendir Demirkol, Yasemin, Arikoglu, Tugba, Gulez, Nesrin, Genel, Ferah, Kilic, Sara Sebnem, Aytekin, Caner, Keskin, Ozlem, Yildiran, Alisan, Ozcan, Dilek, Altintas, Derya Ufuk, Ardeniz, Fatma Omur, Dogu, Esin Figen, Ikinciogullari, Kamile Aydan, Karakoc-Aydiner, Elif, Ozen, Ahmet, and Baris, Safa
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- 2023
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3. Monogenic early-onset lymphoproliferation and autoimmunity: Natural history of STAT3 gain-of-function syndrome
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Aleshkevich, Svetlana, Allende, Luis M., Atkinson, T. Prescott, Atschekzei, Faranaz, Aydemir, Sezin, Aygunes, Utku, Barlogis, Vincent, Baumann, Ulrich, Belko, John, Bezrodnik, Liliana, Biebl, Ariane, Broderick, Lori, Bunin, Nancy J., Caldirola, Maria Soledad, Castelle, Martin, Celmeli, Fatih, Charbonnier, Louis-Marie, Chatila, Talal A., Chellapandian, Deepak, Cokugras, Haluk, Conlon, Niall, Cox, Fionnuala, Crickx, Etienne, Dalgic, Buket, ASH Dalm, Virgil, Danielian, Silvia, Dominguez-Pinilla, Nerea, Dujovny, Tal, Ebbo, Mikael, Eken, Ahmet, Esty, Brittany, Fabre, Alexandre, Fischer, Alain, Hannibal, Mark, Huppert, Laura, Ikeda, Marc D., Jolles, Stephen, Jolly, Kent W., Jones, Neil, Kanariou, Maria, Karakoc-Aydiner, Elif, Karamantziani, Theoni, Kelaidi, Charikleia, Keogan, Mary, Pac Kisaarslan, Ayşenur, Kiykim, Ayca, Klocperk, Adam, Kotsonis, Kosmas, Kuzmenko, Natalia, Leroy, Sylvie, Lianou, Dimitra, Longhurst, Hilary, Lorenz, Myriam Ricarda, Maffucci, Patrick, Manson, Ania, Marchal, Sarah, Malphettes, Marion, Marega, Lia Furlaneto, Mauracher, Andrea A., Meesilpavikai, Kornvalee, Miller, Holly, Mombourquette, Joy, Morgan, Noel G., Mukhina, Anna, Nathalie, Aladjidi, Nelken, Brigitte, Nolan, David, Norlin, Anna-Carin, Oleastro, Matias, Ozcan, Alper, Pasquet, Marlene, Pegler, José Roberto, Picard, Capucine, Polychronopoulou, Sophia, Quartier, Pierre, Quesada, Juan Francisco, Ramakers, Jan, Randall, Katrina L., Rao, V. Koneti, Remiker, Allison, Resin, Geraldine, Richmond, Peter, Rieux-Laucat, Frederic, Rodina, Yulia, Rohrlich, Pierre, Sachs, Johnathan, Sakovich, Inga, Santarlas, Christopher, Sari, Sinan, Sawicki, Gregory, Schauer, Uwe, Scheffler Mendoza, Selma C., Schvetz, Oksana, Schmidt, Reinhold Ernst, Schwarz, Klaus, Sediva, Anna, Sinclair, Kyle, Slatter, Mary, Sleasman, John, Stergiou, Katerina, Suratannon, Narissara, Tanita, Kay, Thompson, Grace, Travis, Stephen, Trojan, Timothy, Tsinti, Maria, Unal, Ekrem, Urdinez, Luciano, Vazquez-Gomez, Felisa, Villa, Mariana, Weinrich, Michael, Weiss, Mitchell J., Wright, Benjamin, Yilmaz, Ebru, Zachova, Radana, Zhang, Yu, Leiding, Jennifer W., Vogel, Tiphanie P., Santarlas, Valentine G.J., Mhaskar, Rahul, Smith, Madison R., Carisey, Alexandre, Vargas-Hernández, Alexander, Silva-Carmona, Manuel, Heeg, Maximilian, Rensing-Ehl, Anne, Neven, Bénédicte, Hadjadj, Jérôme, Hambleton, Sophie, Ronan Leahy, Timothy, Cunningham-Rundles, Charlotte, Dutmer, Cullen M., Sharapova, Svetlana O., Taskinen, Mervi, Chua, Ignatius, Hague, Rosie, Klemann, Christian, Kostyuchenko, Larysa, Morio, Tomohiro, Thatayatikom, Akaluck, Ozen, Ahmet, Scherbina, Anna, Bauer, Cindy S., Flanagan, Sarah E., Gambineri, Eleonora, Giovannini-Chami, Lisa, Heimall, Jennifer, Sullivan, Kathleen E., Allenspach, Eric, Romberg, Neil, Deane, Sean G., Prince, Benjamin T., Rose, Melissa J., Bohnsack, John, Mousallem, Talal, Jesudas, Rohith, Santos Vilela, Maria Marluce Dos, O’Sullivan, Michael, Pachlopnik Schmid, Jana, Průhová, Štěpánka, Rees, Matthew, Su, Helen, Bahna, Sami, Baris, Safa, Bartnikas, Lisa M., Chang Berger, Amy, Briggs, Tracy A., Brothers, Shannon, Bundy, Vanessa, Chan, Alice Y., Chandrakasan, Shanmuganathan, Christiansen, Mette, Cole, Theresa, Cook, Matthew C., Desai, Mukesh M., Fischer, Ute, Fulcher, David A., Gallo, Silvanna, Gauthier, Amelie, Gennery, Andrew R., Gonçalo Marques, José, Gottrand, Frédéric, Grimbacher, Bodo, Grunebaum, Eyal, Haapaniemi, Emma, Hämäläinen, Sari, Heiskanen, Kaarina, Heiskanen-Kosma, Tarja, Hoffman, Hal M., Gonzalez-Granado, Luis Ignacio, Guerrerio, Anthony L., Kainulainen, Leena, Kumar, Ashish, Lawrence, Monica G., Levin, Carina, Martelius, Timi, Neth, Olaf, Olbrich, Peter, Palma, Alejandro, Patel, Niraj C., Pozos, Tamara, Preece, Kahn, Lugo Reyes, Saúl Oswaldo, Russell, Mark A., Schejter, Yael, Seroogy, Christine, Sinclair, Jan, Skevofilax, Effie, Suan, Daniel, Suez, Daniel, Szabolcs, Paul, Velasco, Helena, Warnatz, Klaus, Walkovich, Kelly, Worth, Austen, Seppänen, Mikko R.J., Torgerson, Troy R., Sogkas, Georgios, Ehl, Stephan, Tangye, Stuart G., Cooper, Megan A., Milner, Joshua D., and Forbes Satter, Lisa R.
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- 2023
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4. Genetic Analysis of a Cohort of 275 Patients with Hyper-IgE Syndromes and/or Chronic Mucocutaneous Candidiasis
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Frede, Natalie, Rojas-Restrepo, Jessica, Caballero Garcia de Oteyza, Andrés, Buchta, Mary, Hübscher, Katrin, Gámez-Díaz, Laura, Proietti, Michele, Saghafi, Shiva, Chavoshzadeh, Zahra, Soler-Palacin, Pere, Galal, Nermeen, Adeli, Mehdi, Aldave-Becerra, Juan Carlos, Al-Ddafari, Moudjahed Saleh, Ardenyz, Ömür, Atkinson, T. Prescott, Kut, Fulya Bektas, Çelmeli, Fatih, Rees, Helen, Kilic, Sara S., Kirovski, Ilija, Klein, Christoph, Kobbe, Robin, Korganow, Anne-Sophie, Lilic, Desa, Lunt, Peter, Makwana, Niten, Metin, Ayse, Özgür, Tuba Turul, Karakas, Ayse Akman, Seneviratne, Suranjith, Sherkat, Roya, Sousa, Ana Berta, Unal, Ekrem, Patiroglu, Turkan, Wahn, Volker, von Bernuth, Horst, Whiteford, Margo, Doffinger, Rainer, Jouhadi, Zineb, and Grimbacher, Bodo
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- 2021
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5. Genetic, immunological, and clinical features of patients with bacterial and fungal infections due to inherited IL-17RA deficiency
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Lévy, Romain, Okada, Satoshi, Béziat, Vivien, Moriya, Kunihiko, Liu, Caini, Chai, Louis Yi Ann, Migaud, Mélanie, Hauck, Fabian, Ali, Amein Al, Cyrus, Cyril, Vatte, Chittibabu, Patiroglu, Turkan, Unal, Ekrem, Ferneiny, Marie, Hyakuna, Nobuyuki, Nepesov, Serdar, Oleastro, Matias, Ikinciogullari, Aydan, Dogu, Figen, Asano, Takaki, Ohara, Osamu, Yun, Ling, Mina, Erika Della, Bronnimann, Didier, Itan, Yuval, Gothe, Florian, Bustamante, Jacinta, Boisson-Dupuis, Stéphanie, Tahuil, Natalia, Aytekin, Caner, Salhi, Aicha, Muhsen, Saleh Al, Kobayashi, Masao, Toubiana, Julie, Abel, Laurent, Li, Xiaoxia, Camcioglu, Yildiz, Celmeli, Fatih, Klein, Christoph, AlKhater, Suzan A., Casanova, Jean-Laurent, and Puel, Anne
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- 2016
6. Diagnosis of immunodeficiency caused by a purine nucleoside phosphorylase defect by using tandem mass spectrometry on dried blood spots
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la Marca, Giancarlo, Canessa, Clementina, Giocaliere, Elisa, Romano, Francesca, Malvagia, Sabrina, Funghini, Silvia, Moriondo, Maria, Valleriani, Claudia, Lippi, Francesca, Ombrone, Daniela, Della Bona, Maria Luisa, Speckmann, Carsten, Borte, Stephan, Brodszki, Nicholas, Gennery, Andrew R., Weinacht, Katja, Celmeli, Fatih, Pagel, Julia, de Martino, Maurizio, Guerrini, Renzo, Wittkowski, Helmut, Santisteban, Ines, Bali, Pawan, Ikinciogullari, Aydan, Hershfield, Michael, Notarangelo, Luigi D., Resti, Massimo, and Azzari, Chiara
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- 2014
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7. CARD9 Mutation in a Patient with Candida albicans Meningoencephalitis; A Case Report
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Kuruoğlu, Tuba, primary, Çelik, Merve, additional, Çelmeli, Fatih, additional, and Tanyel, Esra, additional
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- 2021
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8. Candida albicans meningoensefaliti olan bir hastada card9 mutasyonu; bir olgu raporu
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Kuruoğlu, Tuba, Çelik, Merve, Tanyel, Esra, Çelmeli, Fatih, OMÜ, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümü, Kuruoğlu, Tuba, Çelik, Merve, and Tanyel, Esra
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Candida albicans meningoensefaliti ,primer immün yetmezlik ,CARD9 eksikliği ,CARD9 deficiency ,Candida albicans meningoencephalitis ,primary immunodeficiency ,Microbiology - Abstract
Tam Metin / Full Text Q4 SCI-Expanded WOS:000708921000017 PMID: 34666665 Primer immün yetmezlikler; geniş bir yaş aralığında, hafif klinik tablolardan yaşamı tehdit eden ağır klinik durumlara kadar değişen bir yelpazede kendini gösteren bozukluklardır. Primer immün yetmezliklerin en yaygın komplikasyonlarından biri enfeksiyonlardır. “Caspase associated recruitment domain-9 (CARD9)” fungal immün yanıtta rol oynayan bir proteindir. CARD9 eksikliği, otozomal resesif kalıtım gösteren ve farklı klinik tablolara neden olabilen primer immün yetmezlik bozukluklarından biridir. Yüzeyel veya derin dermatofitoz, invaziv feohifomikoz, kutanöz mukormikoz, ekstrapulmoner aspergilloz, mukokutanöz veya invaziv kandidiyaz gibi çeşitli fungal enfeksiyonlar ile ilişkilendirilmiştir. CARD9 eksikliğinde en sık görülen enfeksiyonlar Candida spp. kaynaklıdır. Bu raporda CARD9 eksikliğine bağlı gelişen Candida albicans meningoensefaliti olgusu sunulmuştur. Otuz yedi yaşında erkek hastanın öyküsünde bilinen hastalığı ve ilaç kullanımı olmamakla birlikte çocukluğundan beri tekrarlayan oral kandidiyaz ve kutanöz fungal enfeksiyon geçirdiği, iki ay önce de C.albicans meningoensefaliti tanısıyla lipozomal amfoterisin B tedavisi aldığı öğrenilmiştir. Klinik iyileşme sonrasında vorikonazol tedavisiyle taburcu edildiği ancak taburcu olduktan sonra vorikanazol tedavisini kestiği ve kontrole gitmediği öğrenilmiştir. Taburcu edildikten 1.5 ay sonra baş ağrısı, kusma ve bilinç değişikliği şikayetleriyle tekrar başvuran hastanın ateşi ve ense sertliği olmayıp Kerning ve Bruzinski belirtisi negatif saptanmıştır. Beyin bilgisayarlı tomografisinde (BT) hidrosefali tespit edilmesi üzerine eksternal ventriküler drenaj (EVD) kateteri takılmıştır. Beyin omurilik sıvısı (BOS) incelemesinde eritrosit sayısı 340/mm3 olarak saptanmış, lökosit görülmemiştir. BOS protein düzeyi 28 mg/dl, BOS glukoz düzeyi 59 mg/dl (eş zamanlı kan glukoz düzeyi 104 mg/dl) idi. BOS’un Gram boyamasında maya ya da bakteri, Ziehl-Neelsen boyamada ise asite dirençli bakteri görülmemiştir. Hastanın önceki yatışında çalışılan BOS örneğinden yapılan Mycobacterium tuberculosis kültüründe üreme olmadığı öğrenilmiştir. Serumda insan bağışıklık yetmezlik virüs antikoru negatif bulunmuştur. Hastanın kontrol BOS kültüründe flukonazole duyarlı C.albicans üremesinin öğrenilmesi üzerine EVD kateteri değiştirilerek lipozomal amfoterisin B tedavisi başlanmıştır. BOS kültürü tekrarlanmış, takiplerinde tekrar edilen BOS kültürlerinde flukonazole duyarlı C.albicans üremesi devam etmiştir. Yapılan beyin manyetik rezonans (MR) görüntülemede apse lehine patoloji saptanmamıştr. Mevcut lipozomal amfoterisin B tedavisine flukonazol eklenmiştir. Anne ve babası üçüncü dereceden akraba olan hastada ve kardeşlerinde tekrarlayan mukokutanöz fungal enfeksiyon öyküsü olması CARD9 eksikliğini düşündürmüştür. Kan örneklerinden çalışılan moleküler testte hastada ve kız kardeşinde CARD9 eksikliğine bağlı homozigot p.Q295X mutasyonu saptanmıştır. Ancak hasta, hastaneye yatışının 62. gününde gecikmiş tanı, tekrarlayan C.albicans meningoensefaliti nedeniyle gelişen serebral komplikasyonlar ve granülosit koloni uyarıcı faktör (G-CSF) tedavisini alamaması sonucu, yetersiz tedavi gibi nedenlerle yaşamını yitirmiştir. CARD9 eksikliğinde gelişen inatçı fungal enfeksiyonlar ciddi komplikasyonlara ve mortaliteye sebep olmaktadır. CARD9 eksikliğinin Türk popülasyonundaki sıklığı ve ülkemizde tanı testinin yapılmaması göz önünde bulundurulduğunda tanı konulamayan, mortalite ya da morbiditeyle seyreden birçok hasta olabileceğini düşündürmektedir. Sonuç olarak bu olgu invaziv fungal enfeksiyonlar için bilinen risk faktörü taşımayan çocuk ve yetişkinlerde, etkili antifungal tedaviye rağmen tekrarlayan ya da devam eden inatçı invaziv fungal enfeksiyon durumunda CARD9 eksikliğinin göz önünde bulundurulmasını vurgulamak amacıyla sunulmuştur. Primary immunodeficiencies are disorders that cause clinical findings ranging from mild diseases to life-threatening diseases in a wide age range. Infections are the most common complications of primary immunodeficiencies. Caspase associated recruitment domain-9 (CARD9) is a protein that plays a role in fungal immune response. CARD9 deficiency is one of the primary immunodeficiency disorders that show autosomal recessive inheritance and can cause different clinical pictures. It has been associated with various fungal infections such as superficial or deep dermatophytosis, invasive pheohifomycosis, cutaneous mucormycosis, extrapulmonary aspergillosis, mucocutaneous or invasive candidiasis. The most common infections in CARD9 deficiency are caused by Candida spp. In this report, a case of Candida albicans meningoencephalitis due to CARD9 deficiency was presented. It was learned from the medical story that a 37 years old male patient had no known disease or drug use, but had recurrent oral candidiasis and cutaneous fungal infections since childhood, and received liposomal amphotericin B treatment with the diagnosis of C.albicans meningoencephalitis two months ago. It was learned that he was discharged with voriconazole treatment after clinical improvement, and he stopped the voriconazole treatment after discharge and did not go for follow-up. The patient, who reapplied 1.5 months after discharge with complaints of headache, vomiting and altered consciousness, did not have fever and neck stiffness, and Kerning and Bruzinski sign was negative. An external ventricular drainage (EVD) catheter was inserted after hydrocephalus was detected in the brain computerized tomography (CT). In the cerebrospinal fluid (CSF) examination, erythrocyte count was detected as 340/mm3, and no leukocytes were seen. CSF protein level was 28 mg/dl, CSF glucose level was 59 mg/dl (simultaneous blood glucose level was 104 mg/dl). There was no yeast or bacteria in CSF Gram staining and no acidfast bacteria in Ziehl-Neelsen staining. It was learned that there was no growth in the Mycobacterium tuberculosis culture made from CSF sample taken at the first admission of the patient. Serum human immunodeficiency virus antibody was negative. Upon learning of fluconazole-susceptible C.albicans growth in the control CSF culture of the patient, the EVD catheter was changed, and liposomal amphotericin B treatment was started. CSF culture was repeated. Fluconazole-susceptible C.albicans continued to grow in CSF cultures repeated in the follow-ups. No pathology in favor of abscess was detected in the brain magnetic resonance imaging. Fluconazole was added to the current liposomal amphotericin B treatment. Having a history of recurrent mucocutaneous fungal infection in the patient and his siblings, whose parents were third-degree relatives, suggested CARD9 deficiency. In the molecular test studied from blood samples, homozygous p.Q295X mutation due to CARD9 deficiency was detected in the patient and his sister. However, the patient died on the 62nd day of hospitalization due to delayed diagnosis, cerebral complications due to recurrent C.albicans meningoencephalitis, and insufficient treatment as a result of failure to receive the granulocyte colony stimulating factor (G-CSF) treatment. Persistent fungal infections that develop in CARD9 deficiency cause serious complications and mortality. Considering the frequency of CARD9 deficiency in the Turkish population and the lack of diagnostic testing in our country, it is thought that there may be many patients who cannot be diagnosed and who progress with mortality or morbidity. In conclusion, this case was presented to emphasize the consideration of CARD9 deficiency in case of persistent invasive fungal infection or recurrent invasive fungal infection after treatment despite effective antifungal treatment in children and adults who do not have known risk factors for invasive fungal infections. https://pubmed.ncbi.nlm.nih.gov/34666665/
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- 2021
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9. Hematopoietic stem cell transplantation in CD40 ligand deficiency: A single‐center experience
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Uygun, Dilara Fatma Kocacık, primary, Uygun, Vedat, additional, Karasu, Gülsün Tezcan, additional, Daloğlu, Hayriye, additional, Öztürkmen, Seda Irmak, additional, Çelmeli, Fatih, additional, Törün, Selda Hançerli, additional, Özen, Ahmet, additional, Barış, Safa, additional, Aydıner, Elif Karakoç, additional, Yalçın, Koray, additional, Kılıç, Suar Çakı, additional, Hazar, Volkan, additional, Bingöl, Ayşen, additional, and Yeşilipek, Akif, additional
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- 2020
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10. The demographic datas of chronic granulomatous disease patients and the comparation of the clinical datas before and after interferon-gamma treatment in our country
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Filiz, Serkan, Kocacık Uygun, Dilara Fatma, Sanal, Özden, Camcıoğlu, Yıldız, Somer, Ayper, Barlan, Işıl, Kılıç, Şebnem, Reisli, İsmail, Patıroğlu, Türkan, Yıldıran, Alişan, Artaç, Hasibe, Metin, Ayşe, Aksu, Güzide, Genel, Ferah, Öztürk, Can, Çelmeli, Fatih, Bingöl, Ayşen, Yeğin, Olcay, Dilara Fatma Kocacık Uygun: 0000-0002-7669-434X, Özden Sanal: 0000-0003-3463-7555, Yıldız Camcıoğlu: 0000-0002-4796-6828, Ayper Somer: 0000-0002-7827-1113, Şebnem Kılıç: 0000-0001-8571-2581, İsmail Reisli: 0000-0001-8247-6405, Alişan Yıldıran: 0000-0002-2918-6238, Hasibe Artaç: 0000-0002-9807-2605, Ayşe Metin: 0000-0002-0731-5799, Güzide Aksu: 0000-0003-2714-0903, Ferah Genel: 0000-0002-9976-067X, Fatih Çelmeli: 0000-0002-2983-5058, Ayşen Bingöl: 0000-0002-0886-3332, Reisli, İ., Filiz, S., Kocacık Uygun, D. F., Sanal, Ö., Camcıoğlu, Y., Somer, A., Barlan, I., Kılıç, Ş., Patıroğlu, T., Yıldıran, A., Artaç, H., Metin, A., Aksu, G., Genel, F., Öztürk, C., Çelmeli, F., Bingöl, A., Yeğin, O. (2013). Ülkemizde kronik granülomatöz hastalık tanılı olguların demografik verileri ve interferon-gama tedavisi öncesi ve sonrası klinik verilerinin karşılaştırılması. Astım Allerji İmmünoloji, 11, 3, 153-161., and Necmettin Erbakan Üniversitesi Meram Tıp Fakültesi, Dahili Tıp Bilimleri Bölümü Çocuk Sağlığı ve Hastalıkları Anabilim Dalı
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İnterferon-gama ,Immunologic diseases ,İmmünolojik bozukluk - Abstract
Giriş: Kronik granülomatöz hastalık (KGH): Fagositik hücrelerin, bazı bakteri ve mantarları fagosite ettikten sonra öldürememesiyle karakterize heterojen, kalıtsal primer bir immünyetmezlik hastalığıdır. Doğal ve kazanılmış bağışıklık yanıtta rol oynayan interferon-gama (INF-), KGH tedavisinde uzun yıllardır kullanılmasına rağmen etkinliği hala tartışılmaktadır. Gereç ve Yöntem: Çalışmamızda, 14 immünoloji merkezinde KGH tanısıyla takip edilen toplam 57 hastanın demografik verileri, infeksiyöz ve granülomatöz komplikasyonlar gibi klinik bulgularına ait verileri, INF- tedavisi öncesi ve sonrası anket formları üzerinden değerlendirildi. Bulgular: Çalışmaya alınan 57 hastanın 14’ü kadın ve 43’ü erkekti. Yaş ortalaması 10.9 7.4 yıl iken tanı yaşı ortalaması ise 4.9 4.8 yıl olarak saptandı. Hastaların 56’sında akrabalık öyküsü ve 60’ında ise ailede primer immünyetmezlik (PİY) öyküsü vardı. Olguların %95’i trimetoprim-sülfametoksazol (TMP-SMX) ve %89.5’i itrakonazol tedavisi alırken %60’ı INF-? kullanıyordu. INF-? alanlarda, almayanlara göre ciddi infeksiyon, pnömoni, yumuşak doku infeksiyonu ve lenfadenit gibi infeksiyöz komplikasyonların sıklığının daha az olduğu görüldü. Ayrıca, INF-? alanlarda, aspergillozis infeksiyonu, organ apsesi, granülomatöz reaksiyon sıklığının daha az olduğu saptandı. Hastaların KGH alt tiplerine göre yıllık infeksiyöz komplikasyonları karşılaştırıldığında; gp91phox alt tipinde INF-? alan grupta infeksiyon sıklığının daha az olduğu görüldü. Sonuç: KGH’li olguların demografik ve klinik özelliklerini yansıtan çalışmamız göstermiştir ki, KGH’de INF profilaksisi tedavisi, infeksiyöz ve granülomatöz komplikasyon sıklığını azaltmakta ve bu tedavi özellikle gp91phox alt tipinde etkili olmaktadır., Objective: Chronic granulomatous disease (CGD) is a genetically heterogeneous primary immunodeficiency that is characterised by bacteria and fungal infections with defective phagocytosis. Interferongamma (INF-γ) has diverse roles in the innate and adaptive responses. Despite several decades of work on INF treatment in CGD, contraversy remains about its use. Materials and Methods: Fifty seven patients with CGD from 14 immunology centers were enrolled to our multi-center study. A questionnaire including patients demographic datas and clinical manifestations such as infectious and granulomatous complications up to enrolment was obtained before and after INF therapy. Results: Fifty seven patients 14 girls and 34 boys aged from 2-35 years were enrolled. The mean age of diagnosis were of the patient’s family had consanguineous marriage and 60 had a primary immunodeficiency history. Ninety five of the patients were treated with trimethoprim-sulfamethoxazole and 89.5 of them with itraconazol while 60 of them were received INF treatment. The patients receiving INF therapy tend to have lower infectious complications like severe infections, pneumonia, soft tissue infections and lymphadenitis. Aspergillus infection, tissue abcesses and granulomatous complications were also lower in this group. The annual infectious complications according to CGD subtypes, were also lower in gp91phox with receiving INF therapy. Conclusion: The demographic and clinical data of CGD patients in our study indicate that INF prophylaxis treatment decreases the infectious and granulomatous complications in some majority of CGD patients especially in gp91phox.
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- 2013
11. Late-Onset Congenital Diaphragmatic Hernia; Report of Three Cases
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Çelmeli, Fatih, primary, Palancı, Atiye Nil, additional, Şahin, Murat, additional, Saz, Eylem Ulaş, additional, and Türkkahraman, Doğa, additional
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- 2015
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12. Evaluation of ifn- γ response to cfp-10 and esat-6 antigens by elispot test in tuberculosis
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Çelmeli, Fatih, Yeğin, Olcay, and Çocuk Sağlığı ve Hastalıkları Anabilim Dalı
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bacterial infections and mycoses ,complex mixtures ,Çocuk Sağlığı ve Hastalıkları ,Child Health and Diseases - Abstract
Sadece Mycobacterium tuberculosis'e özgül CFP-10, ESAT-6 proteinlerini kullanarak bellek T hücrelerinin INF-γ sentezlemesini ELISPOT yöntemi ile test etmek, TBH'ndan LTBE ve BCG etkisinin atrılması merak uyandırmaktadır.Amacımız CFP-10 ve ESAT-6 proteinlerine INF- γ yanıtının aktif TBH, LTBE ve BCG etkisinden ayrımınında kullanılabilirliğini ELISPOT yöntemi ile test etmek. Ve aktif TBH'nda tedavi süresince test değişimlerini gözlemlemekti.Yöntem 84 aktif TB hastası, 104 LTBE olabilecek, TBH ile ev içi yakın temaslı, 71 şüpheli kontrol ve 68 sağlıklı kontrol grubuna INF-γ ELISPOT test uygulandı.Periferal kan mononükleer hücreleri PPD ve Mycobacterium tuberculosis'e özgül ESAT-6 ve CFP-10 antijenleri ile uyarıldı. IFN-γ ELISPOT sonuçları daha önceden Lalvani ve arkadaşlarının kriterlerine göre ölcüldü ve değerlendirildi. Tüm gruplar klinik ve radyolojik bulgular, AARB ve Mycobacterium tuberculosis kültür sonuçları takip edildi. IFN-γ ELISPOT sonuçlarında aktif TB hastalarında sağlıklı kontrol ve şüpheli kontrollere göre istatistiksel olarak anlamlı yüksek değerlere sahipti.(p
- Published
- 2009
13. Tip 1 diyabetli Türk çocuklarında CTLA-4 gen polimorfizmi
- Author
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Çelmeli, Fatih, Akçurin, Sema, and Çocuk Sağlığı ve Hastalıkları Anabilim Dalı
- Subjects
Çocuk Sağlığı ve Hastalıkları ,Child Health and Diseases - Abstract
44
- Published
- 2005
14. Suicide Behaviour After Montelukast Usage: A Case Report
- Author
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ÇELMELİ, Fatih, primary, ÇELMELİ, Gamze, additional, SÜRER ADANIR, Aslınur, additional, and TÜRKKAHRAMAN, Doğa, additional
- Published
- 2014
- Full Text
- View/download PDF
15. Transient Anisocoria During Wheezy Infant Treatment due to Ipratropium-Bromide
- Author
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Çelmeli, Fatih, primary, Çelik, Tamer, additional, Özkiraz, Servet, additional, and Çelik, Ümit, additional
- Published
- 2012
- Full Text
- View/download PDF
16. Geç Başlangıçlı Konjenital Diyafragma Hernisi; Üç Olgunun Sunumu.
- Author
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Çelmeli, Fatih, Palancı, Atiye Nil, Şahin, Murat, Saz, Eylem Ulaş, and Türkkahraman, Doğa
- Abstract
Congenital diaphragmatic hernia (CDH) is a congenital anomaly characterized by developmental defect of the diaphragm in the intrauterine period. Late onset CDH is defined as the CDH that presents after the first month of age. Here, we report three cases with late-onset CDH presenting with a variety of clinical manifestations, and who were treated successfully by surgery. [ABSTRACT FROM AUTHOR]
- Published
- 2015
- Full Text
- View/download PDF
17. Defining Severe Asthma In Childhood: A Descriptive Multicenter Study In Turkey
- Author
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Sekerel, Bulent Enis, Soyer, Ozge, Celmeli, Fatih, Canitez, Yakup, Keskin, Ozlem, Can, Demet, Catal, Ferhat, Kilic, Mehtap, Nalbantoglu, Burcin, Yologlu, Nail, Yavuz, Suleyman T., Guc, Belgin, Ozturk, Fadil, Karakoc, Gulbin, Asilsoy, Suna, Kilic, Mehmet, Razi, Cem, Zeyrek, Dost, Kuyucu, Semanur, Yuksel, Hasan, Cevit, Omer, Bingol, Aysen, Yazicioglu, Mehtap G., and Yenigun, Ayse
- Published
- 2014
- Full Text
- View/download PDF
18. Ãlkemizde kronik granülomatöz hastalık tanılı olguların demografik verileri ve interferon-gama tedavisi öncesi ve sonrası klinik verilerinin karşılaştırılması.
- Author
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FİLİZ, Serkan, Kocacik Uygun, Dilara Fatma, Sanal, Özden, CamcioĞLu, Yıldız, Somer, Ayper, Barlan, Işıl, KiliÇ, Şebnem, ReİSlİ, İsmail, PatiroĞLu, Türkan, Yildiran, Alişan, ArtaÇ, Hasibe, MetİN, Ayşe, Aksu, Güzide, Genel, Ferah, ÖZtÜRk, Can, ÇElmelİ, Fatih, BİNgÖL, Ayşen, and YeĞİN, Olcay
- Abstract
Copyright of Asthma Allergy Immunology / Astim Allerji Immunoloji is the property of Turkish National Society of Allergy & Clinical Immunology and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)
- Published
- 2013
19. lkemizde kronik granlomatz hastalık tanılı olguların demografik verileri ve interferon-gama tedavisi ncesi ve sonrası klinik verilerinin karşılaştırılması.
- Author
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FİLİZ, Serkan, KOCACIK UYGUN, Dilara Fatma, SANAL, Özden, CAMCIOĞLU, Yıldız, SOMER, Ayper, BARLAN, Işıl, KILIÇ, Şebnem, REİSLİ, İsmail, PATIROĞLU, Türkan, YILDIRAN, Alişan, ARTAÇ, Hasibe, METİN, Ayşe, AKSU, Güzide, GENEL, Ferah, ÖZTÜRK, Can, ÇELMELİ, Fatih, BİNGÖL, Ayşen, and YEĞİN, Olcay
- Subjects
IMMUNOLOGIC diseases ,INTERFERONS ,RESEARCH methodology ,QUESTIONNAIRES - Abstract
Copyright of Asthma Allergy Immunology / Astim Allerji Immunoloji is the property of Turkish National Society of Allergy & Clinical Immunology and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)
- Published
- 2013
20. CTLA-4 (+49A/G) Polymorphism and Type-1 Diabetes in Turkish Children.
- Author
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Çelmeli, Fatih, Türkkahraman, Doğa, Özel, Deniz, Akçurin, Sema, and Yeğin, Olcay
- Subjects
- *
TYPE 1 diabetes , *DIABETES in children , *GENETIC polymorphisms , *CHILDREN , *ANTIGENS - Abstract
Objective: To evaluate the contribution of cytotoxic T-Iymphocyte antigen-4 (CTLA-4)+49A/G polymorphism to the susceptibility to type-1 diabetes (T1D) in Turkish children. Methods: A case-control study was designed to include 91 Turkish children with T1D and 99 healthy controls. CTLA-4 (+99A/G) gene polymorphism typing was done by PCR amplification followed by restriction fragment length polymorphism method. Results: The genotype and allele frequencies of the CTLA-4 (+99A/G) polymorphism in patients with T1D were not different from those in the controls (p>0.05). The allele frequency of G was 36.2% in patients with T1D, and 31.8% in controls (p>0.05). Additionally, this polymorphism was not associated with the clinical and laboratory characteristics of the patients with T1D (p>0.05). Conclusions: Our case-control study suggests that the CTLA-4 (+99A/G) gene polymorphism is not associated with T1D in the Turkish population. [ABSTRACT FROM AUTHOR]
- Published
- 2013
- Full Text
- View/download PDF
21. Montelukast Kullanımı Sonrası İntihar Düşüncesi ve Davranışı Gösteren Olgu.
- Author
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ÇELMELİ, Fatih, ÇELMELİ, Gamze, ADANIR, Aslı SÜRER, and TÜRKKAHRAMAN, Doğa
- Abstract
Montelukast, a leukotriene receptor antagonistis a commonly prescribed medication in management of asthma in children. It has been associated with increased risk of various neuropsychiatric events. Here, we report a young boy who presents a number of unusual neuropsychiatric events (suicide behavior) after montelukast usage. The complete resolution of the symptoms was seen upon the withdrawal of the medication. [ABSTRACT FROM AUTHOR]
- Published
- 2014
- Full Text
- View/download PDF
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