• Tetralogy Of Fallot - Born To Be Bad? 

      Alpat, Safak; Önder, Sevgen Ç; Sargon, Mustafa F; Güvener, Murat; Yılmaz, Mustafa; Doğan, Rıza; Demircin, Metin; Paşaoğlu, İlhan (2015)
    • Thalassemia-free and graft-versus-host-free survival: outcomes of hematopoietic stem cell transplantation for thalassemia major, Turkish experience 

      Yesilipek, MA; Uygun, V; Kupesiz, A; Karasu, G; Ozturk, G; Ertem, M; Şaşmaz, İ; Daloğlu, H; Güler, E; Hazar, v; Fisgin, T; Sezgin, G; Kansoy, S; Kuskonmaz, Baris; Akıncı, B; Özbek, N; İnce, EÜ; Öztürkmen, S,; Yalçın, K; Anak, S; Bozkurt, C; Karakükçü, M; Küpeli, S; Albayrak, D; Öniz, H; Aksoylar, S; Okur, FV; Albayrak, C; Yenigürbüz, FD; Bozkaya, İO; İleri, T; Gürsel, O; Karagün, BŞ; Kintrup, GT; Çelen, S; Elli, M; Aksoy, BA; Yılmaz, E; Tanyeli, A; Akyol, ŞT; Siviş, ZÖ; Özek, G; Uçkan, D; Kartal, İ; Atay, D; Bilir, ÖA; Çakmaklı, HF; Kürekçi, E; Malbora, B; Akbayram, S; Demir, HA; Kılıç, SÇ; Güneş, AM; Zengin, E; Özmen, S; Antmen, AB (2022-05)
      We report the national data on the outcomes of hematopoietic stem cell transplantation (HSCT) for thalassemia major (TM) patients in Turkey on behalf of the Turkish Pediatric Stem Cell Transplantation Group. We retrospectively ...
    • The 8p11 Myeloproliferative Syndrome in A 3-year-Old Child 

      Kuskonmaz, Baris; Kafalı, Candaş; Akcoren, Zuhal; Karabulut, Halil G; Akalın, İbrahim; Tuncer, A Murat (Elsevier, 2007)
      We read the interesting report by Wong et al. describing 8p11 stem cell syndrome in a 14-year-old Chinese boy [1]. We wish to report our recent observations on a 3-year-old boy with T-cell lymphoma who was referred to the ...
    • The Activation of Rage and Nf-Kb in Nerve Biopsies of Patients with Axonal and Vasculitic Neuropathy 

      Bekircan-Kurt, Can Ebru; Tan, Ersin; Ozdamar, Sevim Erdem (Aves, 2015)
      Introduction: The receptor for advanced glycation end products (RAGE) is a pattern recognition receptor expressed in tissues and cells, which plays a role in immunity. The activation of RAGE results in the translocation ...
    • The Activities Of Turkish Civil Defence Search And Rescue Units From 1986 To 2007 

      Aydogdu, Serkan; Altintas, Kerim Hakan (Professional Medical Publications, 2011)
      Objective: The objective was to determine the activities of Civil Defence Search and Rescue (SAR) Units. Methodology: This descriptive study was conducted at the General Directorate of Civil Defence in Ankara, Turkey, from ...
    • The Added Value of Diffusion Magnetic Resonance Imaging in the Diagnosis and Posttreatment Evaluation of Skull Base Chordomas 

      Guler, Ezgi; Ozgen, Burce; Mut, Melike; Soylemezoglu, Figen; Oguz, Kader Karli (Thieme Medical Publ Inc, 2017)
      Objectives To determine the use of diffusion-weighted imaging (DWI) in the pre- and posttreatment evaluation of skull base chordomas. Design Retrospective study. Setting Tertiary care university hospital. Participants In ...
    • The Age-Mortality Curve of Endemic Pleural Mesothelioma in Karain, Central Turkey 

      Saracci, R; Simonato, L; Baris, Y; Artvinli, M; Skidmore, J. (1982)
    • The Arid1B Spectrum In 143 Patients: From Nonsyndromic Intellectual Disability To Coffin-Siris Syndrome 

      van der Sluijs, Pleuntje J.; Jansen, Sandra; Vergano, Samantha A.; Adachi-Fukuda, Miho; Alanay, Yasemin; AlKindy, Adila; Baban, Anwar; Bayat, Allan; Beck-Woedl, Stefanie; Berry, Katherine; Bijlsma, Emilia K.; Bok, Levinus A.; Brouwer, Alwin F. J.; van der Burgt, Ineke; Campeau, Philippe M.; Canham, Natalie; Chrzanowska, Krystyna; Chu, Yoyo W. Y.; Chung, Brain H. Y.; Dahan, Karin; De Rademaeker, Marjan; Destree, Anne; Dudding-Byth, Tracy; Earl, Rachel; Elcioglu, Nursel; Elias, Ellen R.; Fagerberg, Christina; Gardham, Alice; Gener, Blanca; Gerkes, Erica H.; Grasshoff, Ute; van Haeringen, Arie; Heitink, Karin R.; Herkert, Johanna C.; den Hollander, Nicolette S.; Horn, Denise; Hunt, David; Kant, Sarina G.; Kato, Mitsuhiro; Kayserili, Hulya; Kersseboom, Rogier; Kilic, Esra; Krajewska-Walasek, Malgorzata; Lammers, Kylin; Laulund, Lone W.; Lederer, Damien; Lees, Melissa; Lopez-Gonzalez, Vanesa; Maas, Saskia; Mancini, Grazia M. S.; Marcelis, Carlo; Martinez, Francisco; Maystadt, Isabelle; McGuire, Marianne; McKee, Shane; Mehta, Sarju; Metcalfe, Kay; Milunsky, Jeff; Mizuno, Seiji; Moeschler, John B.; Netzer, Christian; Ockeloen, Charlotte W.; Oehl-Jaschkowitz, Barbara; Okamoto, Nobuhiko; Olminkhof, Sharon N. M.; Orellana, Carmen; Pasquier, Laurent; Pottinger, Caroline; Riehmer, Vera; Robertson, Stephen P.; Roifman, Maian; Rooryck, Caroline; Ropers, Fabienne G.; Rosello, Monica; Ruivenkamp, Claudia A. L.; Sagiroglu, Mahmut S.; Sallevelt, Suzanne C. E. H.; Sanchis Calvo, Amparo; Simsek-Kiper, Pelin O.; Soares, Gabriela; Solaeche, Lucia; Sonmez, Fatma Mujgan; Splitt, Miranda; Steenbeek, Duco; Stegmann, Alexander P. A.; Stumpel, Constance T. R. M.; Tanabe, Saori; Uctepe, Eyyup; Utine, G. Eda; Veenstra-Knol, Hermine E.; Venkateswaran, Sunita; Vilain, Catheline; Vincent-Delorme, Catherine; Vulto-van Silfhout, Anneke T.; Wheeler, Patricia; Wilson, Golder N.; Wilson, Louise C.; Wollnik, Bernd; Kosho, Tomoki; Wieczorek, Dagmar; Eichler, Evan; Pfundt, Rolph; de Vries, Bert B. A.; Clayton-Smith, Jill; Santen, Gijs W. E. (2019)
      Purpose: Pathogenic variants in ARID1B are one of the most frequent causes of intellectual disability (ID) as determined by large-scale exome sequencing studies. Most studies published thus far describe clinically diagnosed ...
    • The Arid1B Spectrum In 143 Patients: From Nonsyndromic Intellectual Disability To Coffin-Siris Syndrome (Vol 21, Pg 1295, 2019) 

      van der Sluijs, Pleuntje J.; Jansen, Sandra; Vergano, Samantha A.; Adachi-Fukuda, Miho; Alanay, Yasemin; AlKindy, Adila; Baban, Anwar; Bayat, Allan; Beck-Woedl, Stefanie; Berry, Katherine; Bijlsma, Emilia K.; Bok, Levinus A.; Brouwer, Alwin F. J.; van der Burgt, Ineke; Campeau, Philippe M.; Canham, Natalie; Chrzanowska, Krystyna; Chu, Yoyo W. Y.; Chung, Brain H. Y.; Dahan, Karin; De Rademaeker, Marjan; Destree, Anne; Dudding-Byth, Tracy; Earl, Rachel; Elcioglu, Nursel; Elias, Ellen R.; Fagerberg, Christina; Gardham, Alice; Gener, Blanca; Gerkes, Erica H.; Grasshoff, Ute; van Haeringen, Arie; Heitink, Karin R.; Herkert, Johanna C.; den Hollander, Nicolette S.; Horn, Denise; Hunt, David; Kant, Sarina G.; Kato, Mitsuhiro; Kayserili, Hulya; Kersseboom, Rogier; Kilic, Esra; Krajewska-Walasek, Malgorzata; Lammers, Kylin; Laulund, Lone W.; Lederer, Damien; Lees, Melissa; Lopez-Gonzalez, Vanesa; Maas, Saskia; Mancini, Grazia M. S.; Marcelis, Carlo; Martinez, Francisco; Maystadt, Isabelle; McGuire, Marianne; Mckee, Shane; Mehta, Sarju; Metcalfe, Kay; Milunsky, Jeff; Mizuno, Seiji; Moeschler, John B.; Netzer, Christian; Ockeloen, Charlotte W.; Oehl-Jaschkowitz, Barbara; Okamoto, Nobuhiko; Olminkhof, Sharon N. M.; Orellana, Carmen; Pasquier, Laurent; Pottinger, Caroline; Riehmer, Vera; Robertson, Stephen P.; Roifman, Maian; Rooryck, Caroline; Ropers, Fabienne G.; Rosello, Monica; Ruivenkamp, Claudia A. L.; Sagiroglu, Mahmut S.; Sallevelt, Suzanne C. E. H.; Calvo, Amparo Sanchis; Simsek-Kiper, Pelin O.; Soares, Gabriela; Solaeche, Lucia; Sonmez, Fatma Mujgan; Splitt, Miranda; Steenbeek, Duco; Stegmann, Alexander P. A.; Stumpel, Constance T. R. M.; Tanabe, Saori; Uctepe, Eyyup; Utine, G. Eda; Veenstra-Knol, Hermine E.; Venkateswaran, Sunita; Vilain, Catheline; Vincent-Delorme, Catherine; Vulto-van Silfhout, Anneke T.; Wheeler, Patricia; Wilson, Golder N.; Wilson, Louise C.; Wollnik, Bernd; Kosho, Tomoki; Wieczorek, Dagmar; Eichler, Evan; Pfundt, Rolph; de Vries, Bert B. A.; Clayton-Smith, Jill; Santen, Gijs W. E. (2019)
    • The Association Between Vitamin D Levels And Infections In Patients With Primary Immunodeficiency 

      Gur Cetinkaya, Pinar; Ayvaz, Deniz Cagdas; Cuzdanci, Hacer; Tezcan, Ilhan (2019)
      Introduction: Vitamin D is a hormone responsible in the regulation of immune response. This study was designed to assess the relationship of vitamin D deficiency on the development of infections in patients with primary ...
    • The Association of Cognitive Impairment with Gray Matter Atrophy and Cortical Lesion Load in Clinically Isolated Syndrome 

      Diker, Sevda; Has, Arzu Ceylan; Kurne, Asli; Gocmen, Rahsan; Oguz, Kader Karli; Karabudak, Rana (Elsevier Sci Ltd, 2016)
      Background: Multiple sclerosis can impair cognition from the early stages and has been shown to be associated with gray matter damage in addition to white matter pathology. Objectives: To investigate the profile of cognitive ...
    • The Behavior Rating Inventory of Executive Function and Continuous Performance Test in Preschoolers with Attention Deficit Hyperactivity Disorder 

      Çak, H. Tuna; Çengel Kültür, S. Ebru; Gökler, Bahar; Öktem, Ferhunde; Taşkıran, Candan (2017)
      Objective The aim of this study is to examine performance-based measures and behavioral ratings of executive functions (EF) as a component of preschool attention deficit hyperactivity disorder (ADHD). Methods Twenty-one ...
    • The Bone and Mineral Disorder of Children Undergoing Chronic Peritoneal Dialysis 

      Borzych, Dagmara; Rees, Lesley; Ha, Il Soo; Chua, Annabelle; Valles, Patricia G.; Lipka, Maria; Zambrano, Pedro; Ahlenstiel, Thurid; Bakkaloglu, Sevcan A.; Spizzirri, Ana P.; Lopez, Laura; Ozaltin, Fatih; Printza, Nikoleta; Hari, Pankaj; Klaus, Guenter; Bak, Mustafa; Vogel, Andrea; Ariceta, Gema; Yap, Hui Kim; Warady, Bradley A.; Schaefer, Franz (Elsevier Science Inc, 2010)
      The mineral and bone disorder of chronic kidney disease remains a challenging complication in pediatric end-stage renal disease. Here, we assessed symptoms, risk factors and management of this disorder in 890 children and ...
    • The Cardiovascular Comorbidity in Children with Chronic Kidney Disease (4C) Study: Objectives, Design, and Methodology 

      Querfeld, Uwe; Anarat, All; Bayazit, Aysun K.; Bakkaloglu, Aysin S.; Bilginer, Yelda; Caliskan, Salim; Civilibal, Mahrnut; Doyon, Anke; Duzova, Ali; Kracht, Daniela; Litwin, Mieczyslaw; Melk, Anette; Mir, Sevgi; Sozeri, Betul; Shroff, Rukshana; Zeller, Rene; Wuehl, Elke; Schaefer, Franz (Amer Soc Nephrology, 2010)
      Background and objectives: Children and adolescents with chronic kidney disease (CKD) are at high risk for cardiovascular morbidity and mortality. A systemic arteriopathy and cardiomyopathy has been characterized in pediatric ...
    • The Challenge Of Treating Pulmonary Vasculitis In Behcet Disease: Two Pediatric Cases 

      Demir, Selcan; Sag, Erdal; Akca, Ummusen Kaya; Hazirolan, Tuncay; Bilginer, Yelda; Ozen, Seza (2019)
      Behcet disease (BD) is a multisystemic autoinflammatory disorder characterized by recurrent mucocutaneous, ocular, musculoskeletal, gastrointestinal, central nervous system, and vascular manifestations. Pulmonary arterial ...
    • The Challenge Of Treating Pulmonary Vasculitis In Behcet'S Disease: Two Pediatric Cases 

      Demir, Selcan; Sag, Erdal; Akca, Ummusen Kaya; Hazirolan, Tuncay; Bilginer, Yelda; Ozen, Seza (2019)
    • The Challenges Of The Health Care Providers In Refugee Settings: A Systematic Review 

      Kavukcu, Nurtac; Altintas, Kerim Hakan (2019)
      Background: All over the world, migration is affecting millions of people who either choose or are forced to leave their countries of origin. Health is considered to be one of the important aspects of migration that is ...
    • The Characteristics Of Pediatric Behcet'S Disease In Turkey Versus Israel 

      Butbul, Yonatan; Batu, Ezgi Deniz; Sonmez, Hafize Emine; Sozeri, Betul; Ayaz, Nuray Aktay; Baba, Limor; Amarilyo, Gil; Simsek, Seval; Harel, Liora; Karadag, Serife Gul; Bilginer, Yelda; Ozen, Seza (2019)
    • The Clinical and Laboratory Evaluation of Familial Hemophagocytic Lymphohistiocytosis and the Importance of Hepatic and Spinal Cord Involvement: A Single Center Experience 

      Beken, Burcin; Aytac, Selin; Balta, Gunay; Kuskonmaz, Baris; Uckan, Duygu; Unal, Sule; Cetin, Mualla; Gumruk, Fatma (2018)
      Familial hemophagocytic lymphohistiocytosis is an autosomal recessive, life-threatening condition characterized by defective immune response. A retrospective analysis was performed on 57 patients diagnosed with familial ...