• Nail Changes In Patients With Inflammatory Bowel Diseases 

      Ekiz, Ozlem; Celik, Ebru; Balta, Ilknur; Sen, Bilge Bulbul; Rifaioglu, Emine Nur; Demir, Mehmet; Ekiz, Fuat; Basar, Omer; Yuksel, Osman (Tubitak Scientific & Technical Research Council Turkey, 2016)
      Background/aim: Inflammatory bowel disease (IBD) is a group of inflammatory conditions of the colon and small intestine. To our knowledge, no studies to date pertain to the profile of nail changes in IBD, except for ...
    • Nasal Natural Killer/T-Cell Lymphoma With Skin, Eye, And Peroneal Nerve Involvement 

      Türker, Burcu; Uz, Burak; Işık, Metin; Bektaş, Özlen; Demiroğlu, Haluk; Sayınalp, Nilgün; Üner, Aysegül; Özcebe, Osman İlhami (2012)
      Nasal-type natural killer (NK)/T-cell lymphoma (NKTL) is a rare disease strongly associated with Epstein-Barr virus and is often localized to the upper aerodigestive tract at presentation. Extranodal NKTL may involve any ...
    • Nasal Nitric Oxide Levels In Primary Ciliary Dyskinesia, Cystic Fibrosis And Healthy Children 

      Guney, Elif; Emiralioglu, Nagehan; Cinel, Guzin; Yalcin, Ebru; Dogru, Deniz; Kiper, Nural; Ozcelik, Hayriye Ugur (2019)
      Primary ciliary dyskinesia (PCD) is a rare, inherited disorder characterized by recurrent respiratory tract infections. The measurement of nasal nitric oxide (nNO) is an important test for the diagnosis of PCD. In this ...
    • Natural History And Early Diagnosis Of Lad-1/Variant Syndrome 

      Kuijpers, Taco W.; van Bruggen, Robin; Kamerbeek, Nanne; Tool, Anton T. J.; Hicsonmez, Gonul; Gurgey, Aytemiz; Karow, Axel; Verhoeven, Arthur J.; Seeger, Karl; Sanal, Ozden; Niemeyer, Charlotte; Roos, Dirk (Amer Soc Hematology, 2007)
      The syndrome of leukocyte adhesion deficiency (LAD) combined with a severe Glanzmann-type bleeding disorder has been recognized as a separate disease entity. The variability in clinical and cell biological terms has remained ...
    • Natural History Of Congenital Generalized Lipodystrophy: A Nationwide Study From Turkey 

      Akinci, Bans; Onay, Huseyin; Demir, Tevfik; Ozen, Samim; Kayserili, Hulya; Akinci, Gulcin; Nur, Banu; Tuysuz, Beyhan; Ozbek, Mehmet Nun; Gungor, Adem; Simsir, Ilgin Yildirim; Altay, Canan; Demir, Leyla; Simsek, Enver; Atmaca, Murat; Topaloglu, Haluk; Bilen, Habib; Atmaca, Hulusi; Atik, Tahir; Cavdar, Umit; Altunoglu, Umut; Aslanger, Ayca; Mihci, Ercan; Secil, Mustafa; Saygili, Fusun; Comlekci, Abdurrahman; Garg, Abhimanyu (Oxford Univ Press, 2016)
      Context: Congenital generalized lipodystrophy (CGL) is a rare autosomal recessive disorder characterized by near-total lack of body fat. Objective: We aimed to study natural history and disease burden of various subtypes ...
    • Natural History Of T1N0M0 Hepatocellular Carcinoma: Large-Scale Study In The United States 

      Al-Shamsi, Humaid O.; Abdel-Wahab, Reham; Hassan, Manal M.; Shalaby, Ahmed S.; Dahbour, Ibrahim; Lacin, Sahin; Mahvash, Armeen; Odisio, Bruno C.; Murthy, Ravi; Avritscher, Rony; Abdelsalam, Mohamed E.; Rashid, Asif; Vauthey, Jean-Nicolas; Aloia, Thomas A.; Conrad, Claudius; Chun, Yun Shin; Krishnan, Sunil; Das, Prajnan; Koay, Eugene J.; Amin, Hesham M.; Yao, James C.; Kaseb, Ahmed O. (Karger, 2017)
      Background: Hepatocellular carcinoma (HCC) prognosis depends on clinicopathological features in addition to the treatment provided. We aimed to assess the natural history of TNM stage I HCC tumors which received different ...
    • Naturally Acquired Hepatitis a Antibodies After Haematopoetic Stem Cell Transplantation 

      Yalcin, Sıdıka Songul; Kondolot, Meda; Goker, Hakan; Kuskonmaz, Baris; Karacan, Y; Cetin, Mualla; Aksu, Salih; Tezcan, Ilhan; Uckan, Duygu (Cambridge University Press, 2011)
      Haematopoietic stem cell transplant (HSCT) recipients lose immune memory of exposure to infectious agents and vaccines accumulated throughout their lifetime and therefore need to be revaccinated. We aimed to evaluate the ...
    • Nbeal2 Is Mutated In Gray Platelet Syndrome And Is Required For Biogenesis Of Platelet Alpha-Granules 

      Gunay-Aygun, Meral; Falik-Zaccai, Tzipora C; Vilboux, Thierry; Zivony-Elboum, Yifat; Gumruk, Fatma; Cetin, Mualla; Khayat, Morad; Boerkoel, Cornelius F; Kfir, Nehama; Huang, Yan; Maynard, Dawn; Dorward, Heidi; Berger, Katherine; Kleta, Robert; Anikster, Yair; Arat, Mutlu; Freiberg, Andrew S; Kehrel, Beate E; Jurk, Kerstin; Cruz, Pedro; Mullikin, Jim C; White, James G; Huizing, Marjan; Gahl, William A (2011)
      Gray Platelet Syndrome (GPS) is an autosomal recessive bleeding disorder with large platelets that lack α-granules. We found that mutations of NBEAL2 (neurobeachin-like 2), encoding a BEACH/ARM/WD40 domain protein, cause ...
    • Necrotizing Fasciitis Secondary To Bevacizumab Treatment For Metastatic Rectal Adenocarcinoma 

      Şendur, Mehmet A. N.; Aksoy, Sercan; Özdemir, Nuriye Yıldırım; Zengin, Nurullah (2014)
      Bevacizumab is a recombinant humanized monoclonal antibody that selectively blocks the activity of vascular endothelial growth factor (VEGF) receptor and it is used in metastatic colorectal patients. We present here a case ...
    • Necrotizing Pneumonia Caused By Streptococcus Pneumoniae Serotype 3 Despite Pcv13 

      Alkan, Gulsum; Emiroglu, Melike; Dagi, Hatice T.; Gurbuz, Venhar; Ceyhan, Mehmet (2019)
      Streptococcus pneumoniae is the most common cause of complicated pneumonia. Pneumococcal necrotizing pneumonia (PNP) is a rare and serotype related complication. Serotypes 1, 3, 14, 15, 19A and 33 were the most reported ...
    • Need For Comprehensive Hormonal Workup In The Management Of Adrenocortical Tumors In Children 

      Gönç, E. Nazlı; Özön, Zeynep Alev; Çakır, Meltem Didem; Alikaşifoğlu, Ayfer; Kandemir, Nurgün (2014)
      Ob­jec­ti­ve: Clinical findings do not reflect the excess hormonal status in adrenocortical tumors (ACTs) in children. Identification of abnormal hormone secretion may help provide the tumor marker and delineate those ...
    • Needlestick Injury To A Patient 

      Onal, E; Tanriover, M; Guven, G. (2008)
    • Neisseria Meningitidis Serogroup X St-5799 (St-22 Complex) In Turkey: A Unique Pediatric Case 

      Tanir, Gonul; Ozsurekci, Yasemin; Lucidarme, Jay; Durmus, Sevgi Yasar; Lekshmi, Aiswarya; Akisoglu, Ozlem; Aycan, Ahmet Emre; Borrow, Ray; Ceyhan, Mehmet (Taylor & Francis Inc, 2018)
      Although outbreaks of Neisseria meningitidis serogroup X occured in a couple of African countries, a limited number of serogroup X meningococcal cases were reported in America and Europe as well as Turkey. Additionally, ...
    • Neoadjuvant Chemotherapy Improves Survival In Patients With Locally Advanced Nasopharyngeal Carcinoma 

      Basaran, Hamit; Cengiz, Mustafa; Yazici, Gozde; Susulu, Nilda; Aksoy, Sercan; Hosal, Ali Sefik; Gullu, Ibrahim H.; Ozyigit, Gokhan (2019)
      This study aimed to evaluate survival in patients with locally advanced nasopharyngeal carcinoma. The records of 407 patients with locally advanced nasopharyngeal carcinoma treated retrospectively reviewed. Patients were ...
    • Neocentric Small Supernumerary Marker Chromosomes (Ssmc) - Three More Cases And Review Of The Literature 

      Liehr, T.; Utine, G. E.; Trautmann, U.; Rauch, A.; Kuechler, A.; Pietracz, J.; Bocian, E.; Kosyakova, N.; Mrasek, K.; Boduroglu, K.; Weise, A.; Aktas, D. (Karger, 2007)
      Here we report on three new patients with neocentric small supernumerary marker chromosomes (sSMC) derived from chromosome 2, 13 and 15, respectively. The sSMC( 13) and sSMC( 15) had inverted duplicated shapes and the sSMC( ...
    • Neonatal Adrenal Insufficiency: Turkish Neonatal And Pediatric Endocrinology And Diabetes Societies Consensus Report 

      Yiğit, Şule; Türkmen, Münevver; Tuncer, Oğuz; Taşkın, Erdal; Güran, Tülay; Abacı, Ayhan; Çatlı, Gönül; Tarım, Ömer (2018)
      It is difficult to make a diagnosis of adrenal insufficiency in the newborn, because the clinical findings are not specific and the normal serum cortisol level is far lower compared to children and adults. However, ...
    • Neonatal Assessment In The Delivery Room – Trial To Evaluate A Specified Type Of Apgar (Test-Apgar) 

      Rüdiger, Mario; Braun, Nicole; Aranda, Jacob; Aguar, Marta; Bergert, Renate; Bystricka, Alica; Dimitriou, Gabriel; El-Atawi, Khaled; Ifflaender, Sascha; Jung, Philipp; Matasova, Katarina; Ojinaga, Violeta; Petruskeviciene, Zita; Roll, Claudia; Schwindt, Jens; Simma, Burkhard; Staal, Nanette; Valencia, Gloria; Vasconcellos, Maria Gabriela; Veinla, Maie; Vento, Máximo; Weber, Benedikt; Wendt, Anke; Yigit, Sule; Zotter, Heinz; Küster, Helmut (2015)
      Background Since an objective description is essential to determine infant’s postnatal condition and efficacy of interventions, two scores were suggested in the past but weren’t tested yet: The Specified-Apgar uses the 5 ...
    • Neonatal Effects Of Thyroid Diseases In Pregnancy And Approach To The Infant With Increased Tsh: Turkish Neonatal And Pediatric Endocrinology And Diabetes Societies Consensus Report 

      Özon, Alev; Tekin, Neslihan; Şıklar, Zeynep; Gülcan, Hande; Kara, Cengiz; Taştekin, Ayhan; Demir, Korcan; Koç, Esin; Evliyaoğlu, Olcay; Kurtoğlu, Selim (2018)
      Thyroid functions in the fetus and newborn carry importance in terms of the baby’s health and development of the central nervous system. Maternaliodine deficiency, exposure to iodine, thyroid diseases (Hashimoto thyroiditis, ...
    • Neonatal Screening For Congenital Adrenal Hyperplasia In Turkey: A Pilot Study With 38,935 Infants 

      Güran, Tülay; Tezel, Başak; Gürbüz, Fatih; Selver Eklioğlu, Beray; Hatipoğlu, Nihal; Kara, Cengiz; Şimşek, Enver; Çizmecioğlu, Filiz Mine; Ozon, Alev; Baş, Firdevs; Aydın, Murat; Darendeliler, Feyza (2019)
      Objective: Congenital adrenal hyperplasia (CAH) is the most common form of primary adrenal insufficiency in children. Neonatal screening for CAH is effective in detecting the salt-wasting (SW) form and in reducing mortality. ...
    • Nephropathic Cystinosis: An International Consensus Document 

      Emma, Francesco; Nesterova, Galina; Langman, Craig; Labbe, Antoine; Cherqui, Stephanie; Goodyer, Paul; Janssen, Mirian C.; Greco, Marcella; Topaloglu, Rezan; Elenberg, Ewa; Dohil, Ranjan; Trauner, Doris; Antignac, Corinne; Cochat, Pierre; Kaskel, Frederick; Servais, Aude; Wuehl, Elke; Niaudet, Patrick; Van't Hoff, William; Gahl, William; Levtchenko, Elena (Oxford Univ Press, 2014)
      Cystinosis is caused by mutations in the CTNS gene (17p13.2), which encodes for a lysosomal cystine/proton symporter termed cystinosin. It is the most common cause of inherited renal Fanconi syndrome in young children. ...