Zobrazeno 1 - 10
of 112
pro vyhledávání: '"Zuhal AKÇÖREN"'
Autor:
Ozge Surmeli-Onay, Selin Yakarisik, Ayse Korkmaz, Zuhal Akcoren, Aysel Yuce, Heiko Runz, Miriam Stampfer, Murat Yurdakok
Publikováno v:
Pediatrics and Neonatology, Vol 54, Iss 5, Pp 344-347 (2013)
Niemann–Pick type C (NPC; OMIM 257219) disease is a neurodegenerative lysosomal storage disorder characterized by accumulation of unesterified cholesterol in the lysosomal/late endosomal system. This autosomal recessive disorder occurs in approxima
Externí odkaz:
https://doaj.org/article/7964b9ba3495446fba2d1e449fb644e2
Autor:
Baran Erman, Ivan Bilic, Tatjana Hirschmugl, Elisabeth Salzer, Deniz Çagdas, Saliha Esenboga, Zuhal Akcoren, Ozden Sanal, Ilhan Tezcan, Kaan Boztug
Publikováno v:
Haematologica, Vol 100, Iss 6 (2015)
Externí odkaz:
https://doaj.org/article/790d18b9d1904a4ebd13a7fc4ee2912f
Autor:
Duygu Demirtaş, Emre Ünal, İlkay S. İdilman, Zuhal Akçören, Mehmet Akif Göktaş, Meryem Seda Boyraz, Sevilay Karahan, Diclehan Orhan, Mithat Haliloğlu, Muşturay Karçaaltıncaba, Hasan Özen
Publikováno v:
Insights into Imaging, Vol 14, Iss 1, Pp 1-8 (2023)
Key points 1. MRE has high sensitivity and specificity in evaluating liver fibrosis in children. 2. MRE-LS is significantly correlated with histological Ishak fibrosis stage. 3. Comparing to other parameters, only MRE-LS is a predictor of fibrosis st
Externí odkaz:
https://doaj.org/article/684fe933677a4795ad62d8ec72006516
Autor:
Begül YAĞCI-KÜPELİ, Arbay Ozden CİFTCİ, Bilgehan YALÇIN, Mithat HALİLOGLU, Zuhal AKÇÖREN, Münevver BÜYÜKPAMUKÇU
Publikováno v:
Cukurova Medical Journal, Vol 38, Iss 2, Pp 333-337 (2013)
İnfantil fibröz hamartom sıklıkla hayatın ilk yılında görülen, nadir ve benign bir subkutan tümördür. Hastalar genellikle üst ekstremite yerleşimli ağrısız ve hızlı büyüyen bir kitle nedeniyle başvurmaktadır. Kitlenin radyoloji
Externí odkaz:
https://doaj.org/article/41a9a6da7b8742a6841577e4468dd686
Autor:
Gözdem Kaykı, Diclehan Orhan, Bora Gülhan, Rezan Topaloğlu, Zuhal Akçören, Ali Düzova, Fatih Özaltın, Seza Özen, Yelda Bilginer, Şafak Güçer
Publikováno v:
The Turkish journal of pediatrics. 64(1)
Crescentic glomerulonephritis (CGN) is a rapidly progressive and rare cause of glomerulonephritis in childhood. The aim of this study is to evaluate demographic data of children with crescentic glomerulonephritis, to classify the etiologies and to in
Autor:
Haluk Topaloglu, Erdal Sag, Safak Gucer, Beril Talim, Diclehan Orhan, Seza Ozen, Gülsev Kale, Zuhal Akçören, Yelda Bilginer, Goknur Haliloglu
Publikováno v:
Rheumatology International. 41:77-85
Juvenile dermatomyositis (JDM) is an inflammatory myopathy which causes severe morbidity and high mortality if untreated. In this study, we aimed to define the T-helper cell profile in the muscle biopsies of JDM patients. Muscle biopsies of twenty-si
Autor:
Ömer Ertekin, Zuhal Akçören
Publikováno v:
Kafkas Journal of Medical Sciences. 10:32-38
Autor:
Ozgur Deren, Safak Gucer, Zuhal Akçören, Selma Yildirim, Murat Cagan, Özgür Özyüncü, Gulenay Gencosmanoglu Turkmen
Publikováno v:
Fetal and pediatric pathology. 41(5)
One-third of fetal soft tissue tumors are malignant and include congenital fibrosarcoma (CF). We report two fetal CFs arising in the posterior mediastinum. Case Presentation: In case 1, the CF resulted in a mediastinal shift, extensive infiltration o
Autor:
Evrim Yilmaz, Hülya Demir, Diclehan Orhan, Hayriye Hizarcioglu, Zeren Baris, Yusuf Aydemir, Zuhal Akçören
Publikováno v:
OSMANGAZİ JOURNAL OF MEDICINE.
Inlet patch (IP) is an area of heterotopic gastric mucosa located in proximal esophagus. Although the majority of IP are asymptomatic, they may be associated with digestive and respiratory symptoms. We aimed to assess prevalence, endoscopic and histo
Autor:
Yilmaz Yildiz, Hatice Serap Sivri, Helle Highland Nygaard, Ayşegül Tokatlı, Zuhal Akçören, Rikke Katrine Jentoft Olsen
Publikováno v:
Yıldız, Y, Olsen, R K J, Sivri, H S, Akçören, Z, Nygaard, H H & Tokatlı, A 2018, ' Post-mortem detection of FLAD1 mutations in 2 Turkish siblings with hypotonia in early infancy ', Neuromuscular Disorders, vol. 28, no. 9, pp. 787-790 . https://doi.org/10.1016/j.nmd.2018.05.009
Inherited defects of vitamin B2 (riboflavin) metabolism may cause different phenotypes with common biochemical markers of multiple acyl-CoA dehydrogenase deficiency (MADD). Most recently, mutations in FLAD1, which encodes flavin adenine dinucleotide