• A Rare Cause of Elevated Chitotriosidase Activity: Glycogen Storage Disease Type IV 

      Hizarcioglu-Gulsen, Hayriye; Yüce, Aysel; Akcoren, Zuhal; Berberoglu-Ates, Burcu; Aydemir, Yusuf; Sag, Erdal; Ceylaner, Serdar (Springer-Verlag Berlin, 2014)
      Human chitinolytic enzyme named "chitotriosidase" takes part in the defense mechanism against pathogens and the homeostasis of innate immunity. Chitotriosidase was firstly reported to be markedly high in plasma of patients ...
    • Cobalamin C Disease Missed By Newborn Screening In A Patient With Low Carnitine Level 

      Ahrens-Nicklas, Rebecca C.; Serdaroglu, Esra; Muraresku, Colleen; Ficicioglu, Can (Springer-Verlag Berlin, 2015)
      Cobalamin C (CblC) disease is the most common inherited disorder of intracellular cobalamin metabolism. It is a multisystemic disorder mainly affecting the eye and brain and characterized biochemically by methylmalonic ...
    • Covid-19 Pandemi Raporu (20 Mart-20 Kasım 2020) 

      İnkaya, Ahmet Çağkan; Er, Ahmet Görkem; Demir, Ahmet Uğur; Ertenli, Ali İhsan; Alp, Alpaslan; Topeli İskit, Arzu; Erdoğdu, Batuhan; Farisoğulları, Bayram; Halaçlı, Burçin; Balam Doğu, Burcu; Şahan, Ceyda; Can Güven, Deniz; Er, Ahmet Görkem; Demir, Ahmet Uğur; Ortaç Ersoy, Ebru; Aladağ Karakulak, Elifcan; Bilgin, Emre; Kara, Emre; Parlak, Erkan; Özkara, Feride; Metan, Gökhan; Telli Dizman, Gülçin; Haberal, Güldehan; Göker, Hakan; Oral, Hakan; Pat Altıok, Hilal; Ozarlı, İrem; Sönmezer, Meliha Çağla; Gülhan Halil, Meltem; Hafızoğlu, Merve; Durusu Tanrıöver, Mine; Akova, Murat; Özdede, Murat; Cankurtaran, Mustafa; Velet, Mustafa; Özer, Necla; Koç, Neriman Sıla; Sayınalp, Nilgün; Çalık Başaran, Nursel; Uyaroğlu, Oğuz Abdullah; Erkin Çınar, Olgu; Keskin, Onur; Özcebe, Osman İlhami; Dizdar, Ömer; Karadağ, Ömer; Uzun, Ömrüm; Dikçınar Yücesoy, Seda Nihal; Dağdelen, Selçuk; Ünal, Serhat; Özusta, Şeyda; Şendur, Süleyman Nahit; Kav, Taylan; Yıldırım, Tolga; Kalyoncu, Umut; Büyükaşık, Yahya; Şener, Yusuf Ziya; Arık, Zafer; Taş, Zahit (Hacettepe İç Hastalıkları Derneği, 2021)
      31 Aralık 2019 tarihinde Çin’de ortaya çıkan ve kısa sürede tüm dünyayı etkileyen SARS-Coronavirus-2 etkenine bağlı COVID-19’un Dünya Sağlık Örgütü tarafından pandemi ilan edildiği dönem ile eş zamanlı olarak, ülkemizde ...
    • Mutation Spectrum Of Fumarylacetoacetase Gene And Clinical Aspects Of Tyrosinemia Type I Disease 

      Dursun, A.; Ozgul, R. K.; Sivri, S.; Tokatli, A.; Guzel, A.; Mesci, L.; Kilic, M.; Aliefendioglu, D.; Ozcay, F.; Gunduz, M.; Coskun, T. (Springer-Verlag Berlin, 2011)
      Tyrosinemia type I (OMIM 276700) is a rare, autosomal recessive disorder caused by a deficiency in the fumarylacetoacetate hydrolase (FAH) enzyme. This study examined the spectrum of FAH gene mutation in 32 patients with ...
    • Novel Mutations In The Pc Gene In Patients With Type B Pyruvate Carboxylase Deficiency 

      Ostergaard, Elsebet; Duno, Morten; Moller, Lisbeth Birk; Kalkanoglu-Sivri, H. Serap; Dursun, Ali; Aliefendioglu, Didem; Leth, Helle; Dahl, Marianne; Christensen, Ernst; Wibrand, Flemming (Springer-Verlag Berlin, 2013)
      We have investigated seven patients with the type B form of pyruvate carboxylase (PC) deficiency. Mutation analysis revealed eight mutations, all novel. In a patient with exon skipping on cDNA analysis, we identified a ...
    • Pregnancy and Lactation Outcomes in a Turkish Patient With Lysinuric Protein Intolerance 

      Ünal, Özlem; Coşkun, Turgay; Orhan, Diclehan; Tokatl, Ayşegül; Dursun, Ali; Hismi, Burcu; Özyüncü, Özgür; Sivri, Serap Hatice Kalkanoglu (Springer-Verlag Berlin, 2014)
      Maternal lysinuric protein intolerance (LPI) is associated with increased risk of anemia, toxemia, and retarded growth in fetus during pregnancy, and bleeding complications during delivery. There has been limited number ...