PUBLICATIONS 1.S.S. Yalçın, D. Çağdaş, K Yurdakök, CŞ Şener, "Right-Sided Duane Retraction Syndrome Associated With Multiple Malformations", Pediatrics International (ISI) , Cilt 45, 577-579 pp., 2003. D.N. Cagdas, S Gucer, G Kale, A Duzova, S Ozen, "Familial Mediterranean fever and mesangial proliferative glomerulonephritis: report of a case and review of the literature", Pediatric Nephrology (ISI) , Cilt 20, 1352-1354 pp., 2005. F.A. Pac, D.N. Cagdas, "Treatment of Massive Cardiac Thrombi in a Patient with Protein C and S Defficiency", Blood Coagulation and Fibrinolysis (ISI) , Cilt 18, 699-702 pp., 2007. G. Seçmeer, A.O. Ciftçi, G. Kanra, M. Ceyhan, A. Kara, A.B. Cengiz, N Kiper, M Haliloğlu, U Ozçelik, DN Cağdaş, "Community-acquired pneumonia and parapneumonic effusions in developing countries.", Turkish Journal of Pediatrics (ISI) , Cilt 50(1), 51-7 pp., 2008. D Cağdaş, A Celiker, S Ozer, "Premature ventricular contractions in normal children", Turkish Journal of Pediatrics (ISI) , Cilt 50(3), 260-264 pp., 2008. DN Çağdaş, Aİ. Parlar, F.A. Pac, U. Tutun, M. Pac, S. Balcı, "A Turkish Family With Ellis-Van Creveld Syndrome in Six Siblings; Linkage Analysis On 4p16 Region (D4S3360-D4S2366).", Genetic Counseling (ISI) , Cilt 19(4), 387-95 pp., 2008. DN Cağdaş, FA Paç, "Cardiac Chest Pain in Children", Anadolu Kardiyoloji Dergisi (ISI) , Cilt 9(5), 401-406 pp., 2009 . FA Paç, DN Cagdas, "Congenital Left ventricular apical diverticulum.", Anadolu Kardiyoloji Dergisi (ISI) , Cilt 8(1), 91 pp., 2008. DN Cağdaş, FA Paç, E Cakal, "Glucocorticoid-induced diabetic ketoacidosis in acute rheumatic fever.", Journal of Cardiovascular Pharmacology and Therapeutics (ISI) , Cilt 13(4), 298-300 pp., 2008. FA Paç, DN Cağdaş, "Ventricular septal diverticule and ventricular septal defect after penetrating cardiac trauma", Anadolu Kardiyoloji Dergisi (ISI) , Cilt 9(1), 62-3 pp., 2009. DN Cağdaş, FA Paç, "A case of cardiac valvular dysplasia", Anadolu Kardiyoloji Dergisi (ISI) , Cilt 9(6), E22-3 pp., 2009. F.A. Paç, D. Çağdaş, M. Akdoğan, N.İ. Zengin, N. Şaşmaz, "Hepatopulmonary Syndrome associated with Budd-Chiari Syndrome: Report of a case and review of the literature.", Anadolu Kardiyoloji Dergisi (ISI), Cilt 10(3), 286-288 pp., 2010. Damla Hanoglu D, Tuba Turul Ozgür, Deniz Ayvaz, Yavuz Köker, Ozden Sanal. Chronic granulomatous disease presenting with hypogammaglobulinemia. J Investig Allergol Clin Immunol. 2011;21(4):310-2. Deniz Çağdaş, Tuba Turul Özgür, Gülten Türkkanı Asal, Patrick Revy, Jean-Pierre De Villartay, Mirjam van der Burg, Özden Sanal, İlhan Tezcan. Two SCID cases with Cernunnos-XLF deficiency successfully treated by hematopoietic stem cell transplantation., Pediatric Transplantation , 2011 , DOI: doi: 10.1111/j.1399-3046.2011.01491.x DN Çağdaş Ayvaz, F Nişancı Kılınç, FA Paç, E Çakal, "Anthropometric measurements and body composition analysis of obese adolescents with and without metabolic syndrome", Turkish Journal of Medical Sciences (ISI) , 267-274 pp., 2011 , DOI: 10.3906/sag-0909-254. Ozden Sanal, Huie Jing, Tuba Ozgur, Deniz Ayvaz, Dara M. Strauss-Albee, Sibel Ersoy-Evans, Ilhan Tezcan, Gulten Turkkani, Helen F. Matthews, Goknur Haliloglu, Aysel Yuce, Bilgehan Yalcin, Ozay Gokoz, Kader K. Oguz, Helen C. Su. Additional Diverse Findings Expand the Clinical Presentation of DOCK8 Deficiency. Journal of Clinical Immunology, 2012 DOI: 10.1007/s10875-012-9664-5 Fatma Nişancı, Deniz Çağdaş Ayvaz. Sağlık Meslek Lisesi Öğrencilerinin beslenme alışkanlıklarının beslenme bilgi düzeylerinin ve vücut kompozisyonlarının değerlendirilmesi. Türk Pediatri Arşivi, 2012 DOI: 10.4274/tpa.842. Fatma Nişancı, Deniz Çağdaş Ayvaz. Diet and physical activity interventions do have effects on body composition and metabolic syndrome parameters in overweight and obese adolescents and their mothers. Turkish Journal of Pediatrics 2013 May-Jun;55(3):292-9. Esther van de Vosse, Margje H. Haverkamp, Noe Ramirez-Alejo, Mónica Martinez-Gallo, Lizbeth Blancas-Galicia, Ayşe Metin, Ben Zion Garty, Çağman Sun-Tan, Arnon Broides, Roelof A. de Paus, Özlem Keskin, Deniz Çağdaş, Ilhan Tezcan, Encarna Lopez-Ruzafa,Juan I. Aróstegui, Jacov Levy,Francisco J. Espinosa-Rosales, Özden Sanal, Leopoldo Santos-Argumedo, Jean-Laurent Casanova, Stephanie Boisson-Dupuis, Jaap T. van Dissel, Jacinta Bustamante. IL-12Rβ1 deficiency: mutation update and description of the IL12RB1 variation database. Human Mutation 2013 Oct;34(10):1329-39. 20. Cağdaş D, Ozgür TT, Asal GT, Tezcan I, Metin A, Lambert N, de Saint Basile G, Sanal O. Griscelli syndrome types 1 and 3: analysis of four new cases and long-term evaluation of previously diagnosed patients. Eur J Pediatr. 2012 Oct;171(10):1527-31. Cavkaytar O, Cagdas Ayvaz D, Keskin O, Yilmaz EA, Buyuktiryaki, B,Sahiner UM, Yavuz ST, Tuncer A, Sackesen C, Sanal O. A Case of DOCK8 Deficient Hyper-IgE Syndrome Presenting Primarily With Eczema, Food Allergy, and Asthma. Pediatric Allergy, Immunology, and Pulmonology 2013; 26(1): 48-51 Yaman Bajin I, Çağdaş Ayvaz D, Ünal S, Turul Özgür T, Çetin M, Gümrük F, Tezcan I, Villartay JP, Sanal O. Atypical combined immunodeficiency due to Artemis defect: A case presenting as hyperimmunoglobulin M Syndrome and with LGLL. Molecular Immunology 2013 Dec;56(4):354-7. 23. Unal S, Sag E, Kuskonmaz B, Kesici S, Bayrakci B, Ayvaz DC, Tezcan I, Yalnızoglu D, Uckan D. Successful treatment of severe myasthenia gravis developed after allogeneic hematopoietic stem cell transplantation with plasma exchange and rituximab. Pediatr Blood Cancer. 2013 Oct 18. doi: 10.1002/pbc.24799.

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: deniz.ayvaz@hacettepe.edu.tr