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53. A child presenting with bullous emphysema

Author

Özsezen, Beste, primary, Tural, Dilber Ademhan, additional, Üner, Meral, additional, Özcan, H. Nursun, additional, Nurullayev, Elnur, additional, Emiralioğlu, Nagehan, additional, Soyer, Tutku, additional, Orhan, Diclehan, additional, Yalçın, Ebru, additional, Doğru, Deniz, additional, Özçelik, Uğur, additional, and Kiper, Nural, additional

Published
2022
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55. Evaluation of Clinical Findings in Children with Chylothorax: A Descriptive Study.

Author

Büyükşahin, Halime Nayir, Emiralioğlu, Nagehan, Özcan, H. Nursun, Sunman, Birce, Güzelkaş, İsmail, Alboğa, Didem, Erdal, Meltem Akgül, Kutluk, Tezer, Kurucu, Nilgün, Yalçın, Ebru, Doğru, Deniz, Özçelik, Ugur, and Kiper, Nural

Subjects
*CHYLOTHORAX, *BONE resorption, *RESEARCH methodology, *CHILDREN'S hospitals, *TERTIARY care, *RETROSPECTIVE studies, *SYMPTOMS, *DESCRIPTIVE statistics, *DATA analysis software, *DISEASE risk factors, *DISEASE complications, *CHILDREN
Abstract

Objective: Chylothorax refers to the presence of chyle in the pleural space. There are multiple etiologies of chylothorax. Our aim in this study was to evaluate the clinical manifestations, causes, and treatment of chylothorax in childhood and also to show the differences between the 2 age groups admitted to a tertiary care children’s hospital. The second aim was to evaluate the clinical and radiologic features of patients diagnosed as having Gorham-Stout disease via chylothorax. Materials and Methods: The archives were reviewed for chylothorax documented in the last 31 years. Twenty-two patients (11 girls and 11 boys) were included. Patients were divided into 2 groups: the younger group aged under 24 months and the older group aged over 24 months. Results: A total of 22 patients had chylothorax, and 10 were aged younger than 24 months. In the younger group, etiologies were in order congenital heart surgery, congenital chylothorax, and Gorham-Stout disease. In the older group, etiologies were Gorham-Stout disease, congenital heart surgery, heart failure, heart transplantation, thrombus, intestinal lymphangiectasia, and idiopathic. The most common treatment in the younger group was the medium-chain triglyceride diet (70%), and in the older group, it was sirolimus (50%). Conclusion: There is a wide variety of underlying etiologies in childhood, so a multidisciplinary approach is important to identify the underlying diagnosis. The common etiologies were postoperative and Gorham-Stout disease in our study. All patients with Gorham-Stout disease had a good prognosis. Gorham-Stout disease should be considered in patients of any age with a diagnosis of chylothorax who have bone lesions. [ABSTRACT FROM AUTHOR]

Published
2023
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56. The role of flexible bronchoscopy in the diagnostic pathway of children with unexplained peripheral eosinophilia.

Author

Hızal, Mina, Eryilmaz Polat, Sanem, Emiralioğlu, Nagehan, Cinel, Guzin, Yalcin, Ebru, Dogru, Deniz, Ozcelik, Ugur, and Kiper, Nural

Subjects
LUNG disease diagnosis, PNEUMONIA, PROTEINS, CLINICAL pathology, CYTOMEGALOVIRUSES, GENETIC mutation, BODY fluids, RETROSPECTIVE studies, PEDIATRICS, B cell lymphoma, SEVERE combined immunodeficiency, DESCRIPTIVE statistics, PULMONARY eosinophilia, BRONCHOSCOPY, EPIDEMIOLOGICAL research, CHILDREN
Abstract

Background: Many possible underlying causes can be seen in children with unexplained peripheral eosinophilia (UPE) with suspected pulmonary involvement. Here, we aimed to demonstrate the clinical characteristics and diagnoses of children evaluated for UPE who underwent diagnostic bronchoscopy. Methods: Thirty‐one children who underwent diagnostic bronchoscopy for UPE between 2006–2018 were included. Demographic characteristics, bronchoscopy findings and final diagnosis, and treatments were evaluated. Results: The median age at the time of diagnosis was 5 (0.25–17.5) years. The final diagnoses of 26 patients were as follows: immunodeficiency (n = 6); hyper‐IgE syndromes (n = 4), DOCK8 deficiency + HES (idiopathic hypereosinophilic syndrome; n = 1), and severe combined immunodeficiency (n = 1), HES (n = 3), idiopathic chronic eosinophilic pneumonia (ICEP; n = 3), idiopathic pulmonary hemosiderosis (n = 1), B cell lymphoma (n = 1). In one child, an integrin α3 mutation + cytomegalovirus (CMV) pneumonia was detected. Congenital pneumonia was found in one patient, and parasitic infection in another. In two, eosinophilia was attributed to underlying asthma and atopy. In four, the underlying reasons could not be elucidated. Two children with HES and one with ICEP were lost to follow‐up. There was no significant relationship between the peripheral eosinophil count at the time of diagnosis and the percentage of bronchoalveolar lavage eosinophils (BAL). Bronchoscopy contributed to the management of 14 (53.9%) patients. Conclusions: Bronchoscopy has potential diagnostic contribution in patients with UPE suspected of having pulmonary involvement. Numerous various underlying causes may be present in this patient group. There is no relation between peripheral eosinophil count and BAL eosinophil percentage. [ABSTRACT FROM AUTHOR]

Published
2023
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59. Specifying pediatric pulmonary hemorrhage: Suggestion of a diagnostic algorithm as guide to disease subcategories

Author

Knoflach, Katrin, primary, Rapp, Christina, additional, Seidl, Elias, additional, Schwerk, Nicolaus, additional, Wetzke, Martin, additional, Carlens, Julia, additional, Kiper, Nural, additional, Emiralioğlu, Nagehan, additional, Buchvald, Frederik, additional, Madsen Ring, Astrid, additional, Robinson, Peter N, additional, and Griese, Matthias, additional

Published
2021
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60. The effect of lung diseases on pulmonary hypertension and the effect of pulmonary hypertension on the lung

Author

Güzelkaş, Ismail, primary, Özsezen, Beste, additional, Ademhan Tural, Dilber, additional, Sunman, Birce, additional, Nayır Büyükşahin, Halime, additional, Aypar, Ebru, additional, Karagöz, Tevfik, additional, Emiralioğlu, Nagehan, additional, Yalçın, Ebru, additional, Doğru, Deniz, additional, Özçelik, Uğur, additional, and Kiper, Nural, additional

Published
2021
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61. Diffuse alveolar haemorrhage in children: an international multicentre study

Author

Ring, Astrid, primary, Schwerk, Nicolaus, additional, Kiper, Nural, additional, Aslan, Ayse Tana, additional, Aurora, Paul, additional, Ayats, Roser, additional, Azevedo, Inês, additional, Bandeira, Teresa, additional, Carlens, Julia, additional, Castillo-Corullon, Silvia, additional, Cobanoglu, Nazan, additional, Elnazir, Basil, additional, Emiralioğlu, Nagehan, additional, Eyuboglu, Tugba Sismanlar, additional, Gursoy, Tugba Ramasli, additional, Hogg, Claire, additional, Karadag, Bülent, additional, Látalová, Vendula, additional, Krenke, Katarzyna, additional, Lange, Joanna, additional, Osona, Borja, additional, Proesmann, Marijke, additional, Reix, Philippe, additional, Renoux, Marie-Catherine, additional, Roditis, Léa, additional, Rubak, Sune, additional, Rumman, Nisreen, additional, Thumerelle, Caroline, additional, Weiss, Laurence, additional, Yalcın, Ebru, additional, Zirek, Fazilcan, additional, Bush, Andy, additional, Clement, Annick, additional, Buchvald, Frederik Fouirnaies, additional, Griese, Matthias, additional, Nathan, Nadia, additional, and Nielsen, Kim Gjerum, additional

Published
2021
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62. Case Series of COVID-19 Disease in Pediatric Chronic Lung Diseases

Author

Güzelkaş, Ismail, primary, Emiralioğlu, Nagehan, additional, Ademhan Tural, Dilber, additional, Özsezen, Beste, additional, Sunman, Birce, additional, Nayır Büyükşahin, Halime, additional, Yalçın, Ebru, additional, Doğru, Deniz, additional, Özçelik, Uğur, additional, and Kiper, Nural, additional

Published
2021
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64. Çocukluk Çağı Akciğer Hastalıklarında Sağlıklı Beslenmenin Önemi.

Author

EMİRALİOĞLU, Nagehan and ASLAN, Dilek

Abstract

Nutrition has an important role in the development of the lungs. Malnutrition, which causes adverse effects on many systems, especially its effects on respiratory system development and lung diseases can lead to permanent impairment in respiratory functions in older ages. Prevention of malnutrition in childhood, early recognition and necessary interventions will contribute to reducing morbidity and mortality. In this review article, it is aimed to discuss the effects of nutrition on lung development, the effects of malnutrition on the frequency of lung diseases in children and the clinical course of these diseases, to evaluate nutritional suggestions and solutions to prevent malnutrition in childhood lung diseases, and to review the measures taken in this regard in the world. Although the effects of malnutrition in infancy and childhood on lung health and pulmonary functions are not known clearly, recent reports have shown that malnutrition in early childhood adversely affects the pulmonary functions. Besides, malnutrition has effects on both cellular and acquired immunity and on the frequency and risk of respiratory tract infections. Furthermore, all these influences increase the risk of developing chronic lung diseases. Majority of deaths due to respiratory diseases in childhood are preventable, however, it is important to take precautions and appropriate attitude in this regard. Supporting breastfeeding, adequate nutrition of the mother during pregnancy, supporting the intake of micronutrients, controlling the nutritional status in the early period in chronic respiratory diseases and taking precautions will positively affect the prognosis of patients in older ages. In conclusion, evaluation of the growth, adequate weight gain and height in the routine follow-up of children have an important role in terms of early interventions in preventable conditions. [ABSTRACT FROM AUTHOR]

Published
2022
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66. Uyku apnesi saptanan Down sendrom’lu hastalarda solunum Destek cihazı uyumunun değerlendirilmesi

Author

GARİBZADEH HIZAL, Mina, ERYILMAZ POLAT, Sanem, EMİRALİOĞLU, Nagehan, ADEMHAN TURAL, Dilber, ÖZSEZEN, Beste, SUNMAN, Birce, GÖZMEN, Onur, YALÇIN, Ebru, DOĞRU, Deniz, KİPER, Nural, and ÖZÇELİK, Uğur

Subjects
Medicine, Down Sendromu,Obstruktif uyku apne sendromu,Polisomnografi,Non-invaziv ventilasyon, Tıp
Abstract

AMAÇ: Obstruktif uyku apne sendromu Down Sendromlu çocuklarda sıklıkla izlenmektedir ve önemli bir morbidite nedenidir. Bu çalışmada Down Sendromu tanısı ile izlenen ve uyku apnesi nedeni ile solunum destek cihazı kullanan hastaların demografik özellikleri, polisomnografik karakteristikleri ve non-invaziv solunum destek tedaviye olan uyum düzeylerinin değerlendirilmesi amaçlandı.GEREÇ VE YÖNTEMLER: 2016-2019 yılları arasında Down Sendromu tanısı ile izlenmekte olan ve Hacettepe Üniversitesinde yapılan polisomnografi sonrasında solunum destek cihazı önerilen ve en az bir yıldır cihaza sahip hastalar çalışmaya dahil edildi. Kayıtları retrospektif olarak incelendi ve demografik özellikleri, polisomongrafik karakteristikleri ve solunum destek cihazı uyumları araştırıldı.BULGULAR: En az bir yıldır solunum destek cihazına sahip olan 20 Down Sendromlu hasta çalşmaya dahil edildi. Hastaların yaş ortalaması 4.45±4.09 idi. Hastaların 14’ünde (%60,9) horlama, 11’inde apne (%47.8) ve 11’inde ( 47.8) gece sık uyanma şikayeti vardı. Hastaların 5’inde (%25) PSG öncesi adenotonsillektomi öyküsü mevcut idi. Polisomnografi sonucunda hastaların 3’ünde orta ve 17’sinde ağır obstruktif uyku apne sendromu saptandı. Ortalama apne-hipopne indeksi değeri 33.26±46.87 olarak tespit edildi. Bir yıllık dönemde hastaların %30’un non-invazif uyumunun iyi (>4 saat/gece) olduğu saptandı. TARTIŞMA: Çalışmamız down sendromlu çocuklarda her yaşta solunum desteği gerektirecek uyku apnesinin görüldüğünü ve bu durumun bazı hastalarda asemptomatik olabileceğini göstermektedir. Çalışmamızda hastaların sadece %30’unda uzun dönemde non-invazif alet uyumunun yeterli olduğunu görmelmektedir.

Published
2020

69. Acute exacerbations in children's interstitial lung disease.

Author

Seidl, Elias, Schwerk, Nicolaus, Carlens, Julia, Wetzke, Martin, Emiralioğlu, Nagehan, Kiper, Nural, Lange, Joanna, Krenke, Katarzyna, Szepfalusi, Zsolt, Stehling, Florian, Baden, Winfried, Hämmerling, Susanne, Jerkic, Silvija-Pera, Proesmans, Marijke, Ullmann, Nicola, Buchvald, Frederik, Knoflach, Katrin, Kappler, Matthias, chILD EU collaborators, and Griese, Matthias

Abstract

Introduction: Acute exacerbations (AEs) increase morbidity and mortality of patients with chronic pulmonary diseases. Little is known about the characteristics and impact of AEs on children's interstitial lung disease (chILD).Methods: The Kids Lung Register collected data on AEs, the clinical course and quality of life (patient-reported outcomes - PRO) of rare paediatric lung diseases. Characteristics of AEs were obtained.Results: Data of 2822 AEs and 2887 register visits of 719 patients with chILD were recorded. AEs were characterised by increased levels of dyspnoea (74.1%), increased respiratory rate (58.6%) and increased oxygen demand (57.4%). Mostly, infections (94.4%) were suspected causing an AE. AEs between two register visits revealed a decline in predicted FEV1 (median -1.6%, IQR -8.0 to 3.9; p=0.001), predicted FVC (median -1.8%, IQR -7.5 to 3.9; p=0.004), chILD-specific questionnaire (median -1.3%, IQR -3.6 to 4.5; p=0.034) and the physical health summary score (median -3.1%, IQR -15.6 to 4.3; p=0.005) compared with no AEs in between visits. During the median observational period of 2.5 years (IQR 1.2-4.6), 81 patients died. For 49 of these patients (60.5%), mortality was associated with an AE.Conclusion: This is the first comprehensive study analysing the characteristics and impact on the clinical course of AEs in chILD. AEs have a significant and deleterious effect on the clinical course and health-related quality of life in chILD. [ABSTRACT FROM AUTHOR]

Published
2022
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70. Healthcare resource utilisation and medical costs for children with interstitial lung diseases (chILD) in Europe.

Author

Seidl, Elias, Schwerk, Nicolaus, Carlens, Julia, Wetzke, Martin, Cunningham, Steve, Emiralioğlu, Nagehan, Kiper, Nural, Lange, Joanna, Krenke, Katarzyna, Ullmann, Nicola, Krikovszky, Dora, Maqhuzu, Phillen, Griese, Charlotte A., Schwarzkopf, Larissa, Griese, Matthias, and chILD-EU collaborators

Subjects
RESEARCH, RESEARCH methodology, MEDICAL care costs, INTERSTITIAL lung diseases, EVALUATION research, PATIENTS' attitudes, COMPARATIVE studies, LONGITUDINAL method
Abstract

Background: No data on healthcare utilisation and associated costs for the many rare entities of children's interstitial lung diseases (chILD) exist. This paper portrays healthcare utilisation structures among individuals with chILD, provides a pan-European estimate of a 3-month interval per-capita costs and delineates crucial cost drivers.Methods: Based on longitudinal healthcare resource utilisation pattern of 445 children included in the Kids Lung Register diagnosed with chILD across 10 European countries, we delineated direct medical and non-medical costs of care per 3-month interval. Country-specific utilisation patterns were assessed with a children-tailored modification of the validated FIMA questionnaire and valued by German unit costs. Costs of care and their drivers were subsequently identified via gamma-distributed generalised linear regression models.Results: During the 3 months prior to inclusion into the registry (baseline), the rate of hospital admissions and inpatient days was high. Unadjusted direct medical per capita costs (€19 818) exceeded indirect (€1 907) and direct non-medical costs (€1 125) by far. Country-specific total costs ranged from €8 713 in Italy to €28 788 in Poland. Highest expenses were caused by the disease categories 'diffuse parenchymal lung disease (DPLD)-diffuse developmental disorders' (€45 536) and 'DPLD-unclear in the non-neonate' (€47 011). During a follow-up time of up to 5 years, direct medical costs dropped, whereas indirect costs and non-medical costs remained stable.Conclusions: This is the first prospective, longitudinal study analysing healthcare resource utilisation and costs for chILD across different European countries. Our results indicate that chILD is associated with high utilisation of healthcare services, placing a substantial economic burden on health systems. [ABSTRACT FROM AUTHOR]

Published
2022
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72. KISTIK FIBROZISTE AKCIĞER NAKLI: ÜLKEMIZDEKI IHTIYAÇ,ENDIKASYON VE KONTRENDIKASYON DURUMLARI

Author

HARMANCI, KORAY, ÇAKIR, ERKAN, KÖSE, MEHMET, KILINÇ, AYŞE AYZIT, EMİRALİOĞLU, NAGEHAN, TAMAY, ZEYNEP ÜLKER, YÜKSEL, HASAN, ÖZCAN, GİZEM, TOPAL, ERDEM, ÖZDOĞAN, ŞEBNEM, ŞİŞMANLAR EYÜBOĞLU, TUĞBA, PEKCAN, SEVGİ, DEMİR, ESEN, YAZAN, HAKAN, CİNEL, GÜZİN, CAN, DEMET, ASLAN, AYŞE TANA, ALTINTAŞ, DERYA UFUK, KORKMAZ EKREN, PERVİN, RAMASLI GÜRSOY, TUĞBA, ONAY, ZEYNEP REYHAN, BİNGÖL, AYŞEN, DOĞRU ERSÖZ, DENİZ, SAPAN, NİHAT, ÇELEBİOĞLU, EBRU, TUĞCU, GÖKÇEN DİLŞA, ÖZDEMİR, ALİ, ÖZÇELİK, HAYRİYE UĞUR, YALÇIN, ELMAS EBRÜ, ŞEN, VELAT, ÇALTEPE, GÖNÜL, ÇOBANOĞLU, FATMA NAZAN, KILIÇ, MEHMET, and ERCAN, ÖMÜR

Published
2020

73. Indications and contraindications for lung transplantation of cystic fibrosis patients in Turkey

Author

YALÇIN, ELMAS EBRÜ, YÜKSEL, HASAN, TAMAY, ZEYNEP ÜLKER, EMİRALİOĞLU, NAGEHAN, KÖSE, MEHMET, HARMANCI, KORAY, DOĞRU ERSÖZ, DENİZ, ÖZDEMİR, ALİ, RAMASLI GÜRSOY, TUĞBA, TUĞCU, GÖKÇEN DİLŞA, ÇELEBİOĞLU, EBRU, SAPAN, NİHAT, BİNGÖL, AYŞEN, DEMİR, ESEN, ALTINTAŞ, DERYA UFUK, YAZAN, HAKAN, KILINÇ, AYŞE AYZIT, ERCAN, ÖMÜR, ŞEN, VELAT, ÖZÇELİK, HAYRİYE UĞUR, ONAY, ZEYNEP REYHAN, ASLAN, AYŞE TANA, ŞİŞMANLAR EYÜBOĞLU, TUĞBA, ÇAKIR, ERKAN, ÇOBANOĞLU, FATMA NAZAN, ÖZDOĞAN, ŞEBNEM, PEKCAN, SEVGİ, KILIÇ, MEHMET, ÇALTEPE, GÖNÜL, KORKMAZ EKREN, PERVİN, CAN, DEMET, CİNEL, GÜZİN, TOPAL, ERDEM, and ÖZCAN, GİZEM

Abstract

Proof systems for the Relativized Propositional Calculus are defined andcompared.

Published
2020

74. Comparison of clinical findings of the patients with cystic fibrosis in terms of diagnosed with and without neonatal screening

Author

TOPAL, ERDEM, ŞEBNEM, ÖZDOĞAN, KILIÇ, MEHMET, RAMASLI GÜRSOY, TUĞBA, ONAY, ZEYNEP REYHAN, ASLAN, AYŞE TANA, ŞİŞMANLAR EYÜBOĞLU, TUĞBA, ÇAKIR, ERKAN, ÇOBANOĞLU, FATMA NAZAN, PEKCAN, SEVGİ, CİNEL, GÜZİN, DOĞRU ERSÖZ, DENİZ, ÖZÇELİK, HAYRİYE UĞUR, YALÇIN, ELMAS EBRÜ, ŞEN, VELAT, ERCAN, ÖMÜR, KILINÇ, AYŞE AYZIT, YAZAN, HAKAN, ALTINTAŞ, DERYA UFUK, DEMİR, ESEN, BİNGÖL, AYŞEN, SAPAN, NİHAT, ÇELEBİOĞLU, EBRU, TUĞCU, GÖKÇEN DİLŞA, ÖZDEMİR, ALİ, HARMANCI, KORAY, KÖSE, MEHMET, EMİRALİOĞLU, NAGEHAN, TAMAY, ZEYNEP ÜLKER, YÜKSEL, HASAN, ÖZCAN, GİZEM, CAN, DEMET, KORKMAZ EKREN, PERVİN, and ÇALTEPE, GÖNÜL

Abstract

Proof systems for the Relativized Propositional Calculus are defined andcompared.

Published
2020

75. YENİDOĞAN TARAMASI İLE TANI ALAN VE ALMAYAN KİSTİKFİBROZİSLİ HASTALARIN KLİNİK ÖZELLİKLERİNİN KARŞILAŞTIRILMASI

Author

CAN, DEMET, ÖZÇELİK, HAYRİYE UĞUR, DOĞRU ERSÖZ, DENİZ, ÖZDEMİR, ALİ, HARMANCI, KORAY, KÖSE, MEHMET, EMİRALİOĞLU, NAGEHAN, TAMAY, ZEYNEP ÜLKER, YÜKSEL, HASAN, ÖZCAN, GİZEM, TOPAL, ERDEM, KORKMAZ EKREN, PERVİN, ÇALTEPE, GÖNÜL, KILIÇ, MEHMET, ÖZDOĞAN, ŞEBNEM, ONAY, ZEYNEP REYHAN, ASLAN, AYŞE TANA, ŞİŞMANLAR EYÜBOĞLU, TUĞBA, RAMASLI GÜRSOY, TUĞBA, ÇAKIR, ERKAN, ÇOBANOĞLU, FATMA NAZAN, PEKCAN, SEVGİ, CİNEL, GÜZİN, YALÇIN, ELMAS EBRÜ, ŞEN, VELAT, ERCAN, ÖMÜR, KILINÇ, AYŞE AYZIT, YAZAN, HAKAN, ALTINTAŞ, DERYA UFUK, DEMİR, ESEN, BİNGÖL, AYŞEN, SAPAN, NİHAT, ÇELEBİOĞLU, EBRU, and TUĞCU, GÖKÇEN DİLŞA

Published
2020

76. What we learned about COVID-19 so far? notes from underground

Author

Arikan, Huseyin, Karaoglanoglu, Selen, Yuksel, Aycan, KARADOĞAN, DİLEK, Celik, Selma, Esendagli, Dorina, ÖZDEN SERTÇELİK, ÜMRAN, AKGÜN, Metin, Aydin, Asena, Gurkan, Canan Gunduz, Toptay, Huseyin, Akyil, Fatma Tokgoz, Onyilmaz, Tugba Asli, Kaya, Ilknur, Polat, Demet, Ataoglu, Ozlem, Er, Berrin, Ercelik, Merve, Gulhan, Pinar Yildiz, Karcioglu, Oguz, Kusbeci, Tuba Ciftci, Kizilirmak, Deniz, Er, Aslihan Banu, Kilinc, Mukaddes, Gunaydin, Fatma Esra, Gurz, Selcuk, Cakmakci, Selin, Develi, Elif, Ozakinci, Hilal, YILMAZ KARA, BİLGE, Marim, Feride, Toreyin, Zehra Nur, Serifoglu, Irem, Gursoy, Tugba Ramasli, EMİRALİOĞLU, NAGEHAN, Eyuboglu, Tugba Sismanlar, RTEÜ, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümü, Karadoğan, Dilek, and Kara, Bilge Yılmaz

Subjects
SARS-CoV-2, Review, Real-Time PCR, Hydroxychloroquine
Abstract

The novel coronavirus pandemic poses a major global threat to public health. Our knowledge concerning every aspect of COVID-19 is evolving rapidly, given the increasing data from all over the world. In this narrative review, the Turkish Thoracic Society Early Career Taskforce members aimed to provide a summary on recent literature regarding epidemiology, clinical findings, diagnosis, treatment, prevention, and control of COVID-19. Studies revealed that the genetic sequence of the novel coronavirus showed significant identity to SARS-CoV and MERS-CoV. Angiotensin-converting enzyme 2 receptor is an important target of the SARS-CoV-2 while entering an organism. Smokers were more likely to develop the disease and have a higher risk for ICU admission. The mean incubation period was 6.4 days, whereas asymptomatic transmission was reported up to 25 days after infection. Fever and cough were the most common symptoms, and cardiovascular diseases and hypertension were reported to be the most common comorbidities among patients. Clinical manifestations range from asymptomatic and mild disease to severe acute respiratory distress syndrome. Several patients showed typical symptoms and radiological changes with negative RT-PCR but positive IgG and IgM antibodies. Although radiological findings may vary, bilateral, peripherally distributed, ground-glass opacities were typical of COVID-19. Poor prognosis was associated with older age, higher Sequential Organ Failure Assessment score, and high D-dimer level. Chloroquine was found to be effective in reducing viral replication in vitro. Likewise, protease inhibitors, including lopinavir/ritonavir, favipiravir, and nucleoside analogue remdesivir were proposed to be the potential drug candidates in COVID-19 management. Despite these efforts, we still have much to learn regarding the transmission, treatment, and prevention of COVID-19.

Published
2020

77. FARS1‐related disorders caused by bi‐allelic mutations in cytosolic phenylalanyl‐tRNA synthetase genes: Look beyond the lungs!

Author

Schuch, Luise A., primary, Forstner, Maria, additional, Rapp, Christina K., additional, Li, Yang, additional, Smith, Desiree E. C., additional, Mendes, Marisa I., additional, Delhommel, Florent, additional, Sattler, Michael, additional, Emiralioğlu, Nagehan, additional, Taskiran, Ekim Z., additional, Orhan, Diclehan, additional, Kiper, Nural, additional, Rohlfs, Meino, additional, Jeske, Tim, additional, Hastreiter, Maximilian, additional, Gerstlauer, Michael, additional, Torrent‐Vernetta, Alba, additional, Moreno‐Galdó, Antonio, additional, Kammer, Birgit, additional, Brasch, Frank, additional, Reu‐Hofer, Simone, additional, and Griese, Matthias, additional

Published
2021
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78. Üçüncü Basamak Bir Merkezin Pediatrik Tüberküloz Verilerinin Ulusal Tüberküloz Bildirim Sistemi Verileri İle Karşılaştırılması

Author

METE YEŞİL, Ayşe, primary, YALÇIN, Ebru, additional, ADEMHAN TURAL, Dilber, additional, EMİRALİOĞLU, Nagehan, additional, ÖZSEZEN, Beste, additional, KABASAKAL, Erhan, additional, YILDIRIM, Ayşegül, additional, DOĞRU, Deniz, additional, ÖZÇELİK, Uğur, additional, and KİPER, Nural, additional

Published
2021
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81. The Importance of Flexible Bronchoscopy in Difficult-to-treat Asthma from a Pediatric Pulmonology Perspective.

Author

Büyükşahin, Halime Nayir, Emiralioğlu, Nagehan, Tural, Dilber Ademhan, Özsezen, Beste, Sunman, Birce, Güzelkaş, İsmail, Yalçın, Ebru, Doğru, Deniz, Özçelik, Uğur, and Kiper, Nural

Subjects
*ASTHMA diagnosis, *ASTHMA treatment, *DRUG therapy for tuberculosis, *LUNG abnormalities, *MYCOBACTERIUM, *CHEST X rays, *BRONCHOALVEOLAR lavage, *CROSS-sectional method, *TRACHEOMALACIA, *PHYSICAL therapy, *DIFFERENTIAL diagnosis, *RETROSPECTIVE studies, *RESPIRATORY organ sounds, *BRONCHITIS, *PROTON pump inhibitors, *PULMONOLOGY, *DESCRIPTIVE statistics, *COUGH, *ANTITUBERCULAR agents, *IPRATROPIUM (Drug), *COMPUTED tomography, *BACTERIAL diseases, *BRONCHOMALACIA, *BRONCHOSCOPY, *MICROBIAL sensitivity tests, *CHILDREN
Abstract

Objective: Asthma is the most common chronic lung disease in childhood. Difficult-to-treat asthma is defined as the continuation of symptoms or attacks of patients despite step 4 or 5 of Global Initiative for Asthma therapy. In the differential diagnosis of these patients, flexible fiberoptic bronchoscopy is recommended to exclude other lung diseases. In this study, we aimed to examine the clinical and radiologic features and flexible fiberoptic bronchoscopy findings of patients referred to our pediatric pulmonology department due to difficult-to-treat asthma and determine the effects of flexible fiberoptic bronchoscopy on the differential diagnosis and treatment. Materials and Methods: The demographic characteristics and flexible fiberoptic bronchoscopy results of 62 patients who were diagnosed as having difficult-to-treat asthma in our pediatric pulmonology department between January 2015 and June 2020 were evaluated retrospectively. The symptoms, history, medications, physical examination findings, pulmonary function tests, and radiologic findings of patients who underwent flexible fiberoptic bronchoscopy were evaluated. [ABSTRACT FROM AUTHOR]

Published
2022
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82. ERS International Virtual Congress 2021: Highlights from the Turkish Thoracic Society Early Career Members.

Author

Şenel, Merve Yumrukuz, Karadoğan, Dilek, Vardaloğlu, Ilgım, Develi, Elif, Çelik, Selma, Hızal, Mina, Özsezen, Beste, Öncel, Aslı, Can, İlknur, Hürsoy, Nur, Uyar, Kübra, Karakaş, Fatma Gülsüm, Er, Berrin, Asfuroğlu, Pelin, Gürsoy, Tuğba Ramaslı, Eyüboğlu, Tuğba Şişmanlar, Çakır, Eylül Pınar, Ademhan, Dilber, Karaoğlanoğlu, Selen, and Emiralioğlu, Nagehan

Subjects
TREATMENT of respiratory diseases, PULMONOLOGISTS, CONFERENCES & conventions, MEMBERSHIP, INFORMATION resources
Abstract

This review aimed to highlight some important points derived from the presentations of the European Respiratory Society 2021 Virtual International Congress by a committee formed by the Early Career Task Group of the Turkish Thoracic Society. We summarized a wide range of topics including current developments of respiratory diseases and provided an overview of important and striking topics of the congress. Our primary motivation was to give some up-to-date information and new developments discussed during congress especially for the pulmonologists who did not have a chance to follow the congress. This review also committed an opportunity to get an overview of the newest data in the diverse fields of respiratory medicine such as post-coronavirus disease 2019, some new interventional and technologic developments related to respiratory health, and new treatment strategies. [ABSTRACT FROM AUTHOR]

Published
2022
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84. An example of national scientific collaboration during the COVID-19 pandemic: Turkish Thoracic Society Early Career Members Taskforce Group’s contribution to accessing reliable scientific knowledge

Author

Karadoğan, Dilek, primary, Emiralioğlu, Nagehan, additional, Akyil, Fatma, additional, Gürkan, Canan, additional, Yüksel, Aycan, additional, Marim, Feride, additional, Töreyin, Zehra, additional, Arikan, Hüseyin, additional, Eyüboğlu, Tuğba, additional, Şerifoğlu, İrem, additional, Sandal, Abdulsamet, additional, Gürsoy, Tuğba, additional, and Akgün, Metin, additional

Published
2020
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85. Lymphoid interstitial pneumonia should be suspected in children with autoimmune disease and immune deficiency

Author

Köseoğlu, Busra, primary, Emiralioğlu, Nagehan, additional, Ademhan, Dilber, additional, Özsezen, Beste, additional, Sunman, Birce, additional, Cinel, Guzin, additional, Özcan, Nursun, additional, Oğuz, Berna, additional, Orhan, Diclehan, additional, Yalçın, Ebru, additional, Doğru, Deniz, additional, Özçelik, Uğur, additional, and Kiper, Nural, additional

Published
2020
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88. CFTR mutations unidentified in CFTR2 database and their phenotypic characteristics: Data from cystic fibrosis registry of Turkey

Author

Cinel, Güzin, primary, Doğru, Deniz, additional, Çakır, Erkan, additional, Şişmanlar Eyüboğlu, Tuğba, additional, Çobanoğlu, Nazan, additional, Pekcan, Sevgi, additional, Yalçın, Ebru, additional, Kiper, Nural, additional, Şen, Velat, additional, Selimoğlu Şen, Hadice, additional, Ercan, Ömür, additional, Keskin, Özlem, additional, Bilgiç Eltan, Sevgi, additional, Muhammed Al Shadfan, Lina, additional, Yazan, Hakan, additional, Altıntaş, Derya Ufuk, additional, Şaşihüseyinoğlu, Şenay, additional, Sapan, Nihat, additional, Çekiç, Şükrü, additional, Çokuğraş, Haluk, additional, Ayzıt Atabek, Ayşe, additional, Ramaslı Gürsoy, Tuğba, additional, Aslan, Ayşe Tana, additional, Bingöl, Ayşen, additional, Başaran, Abdurrahman Erdem, additional, Özdemir, Ali, additional, Köse, Mehmet, additional, Hangül, Melih, additional, Emiralioğlu, Nagehan, additional, Tuğcu, Gökçen, additional, Yüksel, Hasan, additional, Yılmaz, Özge, additional, Orhan, Fazıl, additional, Gayretli aydın, Zeynep Gökçe, additional, Topal, Erdem, additional, Tamay, Zeynep, additional, Süleyman, Ayşe, additional, Can, Demet, additional, Bal, Cem Murat, additional, Çaltepe, Gönül, additional, and Özçelik, Uğur, additional

Published
2020
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89. Diverse clinical characteristics of Aspergillus growth in patients with cystic fibrosis

Author

Emiralioğlu, Nagehan, primary, Şener, Burçin, additional, Özçelik, Uğur, additional, Yalçın, Ebru, additional, Hızal, Mina Gharibzadeh, additional, Tuğcu, Gökçen, additional, Polat, Sanem Eryılmaz, additional, Akdağlı, Sevtap Arıkan, additional, Gülmez, Dolunay, additional, Doğan, Özlem, additional, Doğru, Deniz, additional, and Kiper, Nural, additional

Published
2020
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91. Patients eligible for modulator drugs: Data from cystic fibrosis registry of Turkey

Author

Çobanoğlu, Nazan, primary, Özçelik, Uğur, additional, Çakır, Erkan, additional, Şişmanlar Eyüboğlu, Tuğba, additional, Pekcan, Sevgi, additional, Cinel, Güzin, additional, Yalçın, Ebru, additional, Kiper, Nural, additional, Emiralioğlu, Nagehan, additional, Şen, Velat, additional, Şen, Hadice Selimoğlu, additional, Ercan, Ömür, additional, Çokuğraş, Haluk, additional, Kılınç, Ayşe Ayzıt, additional, Al Shadfan, Lina Muhammed, additional, Yazan, Hakan, additional, Altıntaş, Derya Ufuk, additional, Karagöz, Dilek, additional, Demir, Esen, additional, Kartal Öztürk, Gökçen, additional, Bingöl, Ayşen, additional, Başaran, Abdurrahman Erdem, additional, Sapan, Nihat, additional, Çekiç, Şükrü, additional, Çelebioğlu, Ebru, additional, Aslan, Ayşe Tana, additional, Gürsoy, Tuğba Ramaslı, additional, Tuğcu, Gökçen, additional, Özdemir, Ali, additional, Harmancı, Koray, additional, Yıldırım, Gonca Kılıç, additional, Köse, Mehmet, additional, Hangül, Melih, additional, Tamay, Zeynep, additional, Süleyman, Ayşe, additional, Yüksel, Hasan, additional, Yılmaz, Özge, additional, Özcan, Gizem, additional, Topal, Erdem, additional, Can, Demet, additional, Korkmaz Ekren, Pervin, additional, Çaltepe, Gönül, additional, Kılıç, Mehmet, additional, Özdoğan, Şebnem, additional, and Doğru, Deniz, additional

Published
2020
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94. Uzamış bakteriyel bronşit tanısı alan hastalarda immunolojik değerlendirme yapılmalı mıdır?

Author

Güzelkaş, İsmail, Emiralioğlu, Nagehan, Yalçın, Ebru, Ersöz, Deniz Doğru, Çağdaş, Deniz, Tezcan, İlhan, Özçelik, Uğur, and Kiper, Nural

Abstract

Protracted bacterial bronchitis is one of the major causes of chronic cough in childhood. Although immunodeficiencies are rare, they are conditions that should be investigated in the etiology of protracted bacterial bronchitis. In our study, we aimed to examine the results of the immunological evaluation in patients diagnosed with protracted bacterial bronchitis based on history, clinical, radiological and bronchoscopy findings. Thirty one patients who underwent flexible bronchoscopy with the suspicion of protracted bacterial bronchitis followed in Hacettepe University İhsan Doğramacı Children's Hospital between January 2011 and December 2014 were included in the study. The median age was 7 years (2.5-14 years). The mean duration of cough was 11 months (6-48 months). In bronchoscopy, purulent secretion was found in 51.6% of patients, bronchomalacia in 3.2%, and tracheomalacia in 3.2% of patients. When the immunoglobulin (Ig) levels were checked, it was discovered that 9.6% of the patients had low Ig G and 3.2% of the patients had low Ig A and one patient was diagnosed with agammaglobulinemia. Due to the development of bronchiectasis in protracted bacterial bronchitis, diagnosis and appropriate treatment are important. It is thought that immunological examination for the etiology of these patients will contribute to the diagnosis of underlying immunodeficiencies. [ABSTRACT FROM AUTHOR]

Published
2022

95. ULUSAL KİSTİK FİBROZİS KAYIT SİSTEMİ VERİLERİNE GÖRE ÜLKEMİZDE KFTR MUTASYON ÇEŞİTLİLİĞİ VE FENOTİPİK ÖZELLİKLERİ

Author

ASLAN, AYŞE TANA, BİNGÖL, AYŞEN, RAMASLI GÜRSOY, TUĞBA, HANGÜL, MELİH, ÇEKİÇ, ŞÜKRÜ, YÜKSEL, HASAN, YAZAN, HAKAN, AL SHADFAN, LİNA M, ELTAN, SEVGİ, KESKİN, ÖZLEM, ERCAN, ÖMÜR, SELİMOĞLU ŞEN, HADİCE, ŞEN, VELAT, ÖZDEMİR, ALİ, KİPER, EMİNE NURAL, YALÇIN, EBRU, PEKCAN, SEVGİ, ÇOBANOĞLU, FATMA NAZAN, ŞİŞMANLAR EYÜBOĞLU, TUĞBA, ÇAKIR, ERKAN, KÖSE, MEHMET, DOĞRU ERSÖZ, DENİZ, CİNEL, GÜZİN, TOPAL, ERDEM, TAMAY, ZEYNEP ÜLKER, BAŞARAN, ABDURRAHMAN ERDEM, SÜLEYMAN, AYŞE, CAN, DEMET, BAL, CEM, ÇALTEPE, GÖNÜL, ÖZÇELİK, HAYRİYE UĞUR, SAPAN, NİHAT, ŞAŞIHÜSEYİNOĞLU, ŞENAY, EMİRALİOĞLU, NAGEHAN, TUĞCU, GÖKÇEN DİLŞA, ÇOKUĞRAŞ, HALUK CEZMİ, AYZIT ATABEK, AYŞE, ALTINTAŞ, DERYA UFUK, YILMAZ, ÖZGE, ORHAN, FAZIL, and GAYRETLİ AYDIN, ZEYNEP GÖKÇE

Published
2019

96. Pseudo Bartter: The Most Common Complication in the Turkish National Cystic Fibrosis Registry

Author

ASLAN, AYŞE TANA, SÜLEYMAN, AYŞE, YILMAZ, ÖZGE, YÜKSEL, HASAN, CAN, DEMET, TUĞCU, GÖKÇEN DİLŞA, EMİRALİOĞLU, NAGEHAN, DOĞRU ERSÖZ, DENİZ, HANGÜL, MELİH, BAL, CEM MURAT, KÖSE, MEHMET, TAMAY, ZEYNEP ÜLKER, TOPAL, ERDEM, ÇALTEPE, GÖNÜL, ÖZÇELİK, HAYRİYE UĞUR, GAYRETLİ AYDIN, ZEYNEP GÖKÇE, ORHAN, FAZIL, Muhammed Al Shadfan, Lina, BİLGİÇ ELTAN, SEVGİ, KESKİN, ÖZLEM, ERCAN, ÖMÜR, SELİMOĞLU ŞEN, HADİCE, PEKCAN, SEVGİ, YALÇIN, ELMAS EBRU, KİPER, EMİNE NURAL, ŞEN, VELAT, ŞİŞMANLAR EYÜBOĞLU, TUĞBA, ÖZDEMİR, ALİ, BAŞARAN, ABDURRAHMAN ERDEM, BİNGÖL, AYŞEN, ÇAKIR, ERKAN, ÇOBANOĞLU, FATMA NAZAN, RAMASLI GÜRSOY, TUĞBA, AYZIT ATABEK, AYŞE, ÇOKUĞRAŞ, HALUK CEZMİ, ÇEKİÇ, ŞÜKRÜ, SAPAN, NİHAT, Şaşihüseyinoğlu, Şenay, ALTINTAŞ, DERYA UFUK, YAZAN, HAKAN, and CİNEL, GÜZİN

Published
2019

97. First results of Turkish National Cystic Fibrosis Registry

Author

KESKİN, ÖZLEM, SELİMOĞLU ŞEN, HADİCE, ERCAN, ÖMÜR, KİPER, EMİNE NURAL, ŞEN, VELAT, ASLAN, AYŞE TANA, DOĞRU ERSÖZ, DENİZ, ÇAKIR, ERKAN, ŞİŞMANLAR EYÜBOĞLU, TUĞBA, ÇOBANOĞLU, FATMA NAZAN, PEKCAN, SEVGİ, CİNEL, GÜZİN, YALÇIN, ELMAS EBRU, ÖZÇELİK, HAYRİYE UĞUR, ÇALTEPE, GÖNÜL, BAL, CEM MURAT, CAN, DEMET, SÜLEYMAN, AYŞE, TAMAY, ZEYNEP ÜLKER, TOPAL, ERDEM, GAYRETLİ AYDIN, ZEYNEP GÖKÇE, ORHAN, FAZIL, YILMAZ, ÖZGE, YÜKSEL, HASAN, TUĞCU, GÖKÇEN DİLŞA, EMİRALİOĞLU, NAGEHAN, HANGÜL, MELİH, KÖSE, MEHMET, ÖZDEMİR, ALİ, BAŞARAN, ABDURRAHMAN ERDEM, BİNGÖL, AYŞEN, RAMASLI GÜRSOY, TUĞBA, AYZIT ATABEK, AYŞE, ÇOKUĞRAŞ, HALUK CEZMİ, ÇEKİÇ, ŞÜKRÜ, SAPAN, NİHAT, ALTINTAŞ, DERYA UFUK, YAZAN, HAKAN, MUHAMMED AL SHADFAN, LİNA, and BİLGİÇ ELTAN, SEVGİ

Published
2019

98. Pseudo Bartter Syndrome: The most common complication in theTurkish National Cystic Fibrosis Registry

Author

ÖZDEMİR, ALİ, BAŞARAN, ABDURRAHMAN ERDEM, HANGÜL, MELİH, KÖSE, MEHMET, YÜKSEL, HASAN, YILMAZ, ÖZGE, SÜLEYMAN, AYŞE, ÇALTEPE, GÖNÜL, ORHAN, FAZIL, KILINÇ, AYŞE AYZIT, BİNGÖL, AYŞEN, TAMAY, ZEYNEP ÜLKER, CAN, DEMET, ÖZÇELİK, HAYRİYE UĞUR, GAYRETLİ AYDIN, ZEYNEP GÖKÇE, TOPAL, ERDEM, EMİRALİOĞLU, NAGEHAN, ASLAN, AYŞE TANA, TUĞCU, GÖKÇEN DİLŞA, BAL, CEM, AL SHADFAN, LİNA M, RAMASLI GÜRSOY, TUĞBA, ŞİŞMANLAR EYÜBOĞLU, TUĞBA, DOĞRU ERSÖZ, DENİZ, ÇAKIR, ERKAN, ÇOBANOĞLU, FATMA NAZAN, PEKCAN, SEVGİ, CİNEL, GÜZİN, YALÇIN, EBRU, KİPER, EMİNE NURAL, ŞEN, VELAT, SELİMOĞLU ŞEN, HADİCE, ERCAN, FATİH, KESKİN, ÖZLEM, ELTAN, SEVGİ, YAZAN, HAKAN, ALTINTAŞ, DERYA UFUK, ŞAŞIHÜSEYİNOĞLU, ŞENAY, SAPAN, NİHAT, ÇEKİÇ, ŞÜKRÜ, and ÇOKUĞRAŞ, HALUK CEZMİ

Published
2019

99. FIRST RESULTS OF TURKISH NATIONAL CYSTIC FIBROSIS REGISTRY

Author

YÜKSEL, HASAN, YILMAZ, ÖZGE, ÇOKUĞRAŞ, HALUK CEZMİ, BİNGÖL, AYŞEN, ASLAN, AYŞE TANA, CAN, DEMET, SÜLEYMAN, AYŞE, RAMASLI GÜRSOY, TUĞBA, ATABEK, AYŞE AYZIT, ORHAN, FAZIL, ÇEKİÇ, ŞÜKRÜ, SAPAN, NİHAT, ŞAŞİHÜSEYİNOĞLU, AYŞE ŞENAY, ALTINTAŞ, DERYA UFUK, YAZAN, HAKAN, LİNA MUHAMMED, AL SHADFAN, ozdemir, ali, ÖZÇELİK, HAYRİYE UĞUR, SEVGİ, BİLGİÇ ELTAN, ÇALTEPE, GÖNÜL, BAL, CEM MURAT, KÖSE, MEHMET, HANGÜL, MELİH, EMİRALİOĞLU, NAGEHAN, TUĞCU, GÖKÇEN DİLŞA, KESKİN, ÖZLEM, ERCAN, ÖMÜR, SELİMOĞLU ŞEN, HADİCE, BAŞARAN, ABDURRAHMAN ERDEM, DOĞRU ERSÖZ, DENİZ, TAMAY, ZEYNEP ÜLKER, ÇAKIR, ERKAN, ŞİŞMANLAR EYÜBOĞLU, TUĞBA, ÇOBANOĞLU, FATMA NAZAN, PEKCAN, SEVGİ, CİNEL, GÜZİN, YALÇIN, ELMAS EBRÜ, KİPER, EMİNE NURAL, ŞEN, VELAT, TOPAL, ERDEM, GAYRETLİ AYDIN, ZEYNEP GÖKÇE, and ÇAKIR, Erkan

Subjects
DOĞRU ERSÖZ D., ÇAKIR E., ŞİŞMANLAR EYÜBOĞLU T., ÇOBANOĞLU F. N. , PEKCAN S., CİNEL G., YALÇIN E., KİPER E. N. , ŞEN V., SELİMOĞLU ŞEN H., et al., -FIRST RESULTS OF TURKISH NATIONAL CYSTIC FIBROSIS REGISTRY-, 42nd EUROPEAN CYSTIC FIBROSIS CONFERENCE, LIVERPOOL, UNITED KINGDOM, 5 - 08 Haziran 2019, cilt.18, ss.73
Published
2019

100. Clinical Features of Cystic Fibrosis Patients with Chronic Liver Disease in the Turkish National Cystic Fibrosis Registry

Author

ÇEKİÇ, ŞÜKRÜ, KİPER, EMİNE NURAL, YALÇIN, ELMAS EBRÜ, CİNEL, GÜZİN, ŞEN, VELAT, SELİMOĞLU ŞEN, HADİCE, ERCAN, ÖMÜR, KESKİN, ÖZLEM, ELTAN, SEVGİ BİLGİÇ, LİNA MUHAMMED, AL SHADFAN, YAZAN, HAKAN, ALTINTAŞ, DERYA UFUK, ŞAŞİHÜSEYİNOĞLU, AYŞE ŞENAY, SAPAN, NİHAT, ÇOKUĞRAŞ, HALUK CEZMİ, ATABEK, AYŞE AYZIT, RAMASLI GÜRSOY, TUĞBA, ASLAN, AYŞE TANA, BİNGÖL, AYŞEN, BAŞARAN, ABDURRAHMAN ERDEM, OZDEMİR, ALİ, KÖSE, MEHMET, HANGÜL, MELİH, EMİRALİOĞLU, NAGEHAN, TUĞCU, GÖKÇEN DİLŞA, YÜKSEL, HASAN, YILMAZ, ÖZGE, ORHAN, FAZIL, GAYRETLİ AYDIN, ZEYNEP GÖKÇE, TOPAL, ERDEM, TAMAY, ZEYNEP ÜLKER, SÜLEYMAN, AYŞE, CAN, DEMET, BAL, CEM MURAT, ÇALTEPE, GÖNÜL, ÖZÇELİK, HAYRİYE UĞUR, PEKCAN, SEVGİ, ÇOBANOĞLU, FATMA NAZAN, ÇAKIR, ERKAN, DOĞRU ERSÖZ, DENİZ, and ŞİŞMANLAR EYÜBOĞLU, TUĞBA

Published
2019

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