Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Asuman Gedıkbaşi"'
Autor:
Bagdagul Aksu, Alberto Caldas Afonso, Ipek Akil, Harika Alpay, Bahriye Atmis, Ozlem Aydog, Sevcan Bakkaloglu, Aysun Karabay Bayazıt, Meral Torun Bayram, Ilmay Bilge, Ipek Kaplan Bulut, Ayse Pinar Goksu Cetinkaya, Elif Comak, Belde Kasap Demir, Nida Dincel, Osman Donmez, Mehmet Akif Durmus, Hasan Dursun, Ruhan Dusunsel, Ali Duzova, Pelin Ertan, Asuman Gedikbasi, Nilufer Goknar, Sercin Guven, Duygu Hacihamdioglu, Augustina Jankauskiene, Mukaddes Kalyoncu, Salih Kavukcu, Bahriye Uzun Kenan, Nuran Kucuk, Bahar Kural, Mieczysław Litwin, Giovanni Montini, William Morello, Lukasz Obrycki, Beyhan Omer, Ebru Misirli Ozdemir, Nese Ozkayin, Dusan Paripovic, Cemile Pehlivanoglu, Seha Saygili, Franz Schaefer, Susanne Schaefer, Ferah Sonmez, Yilmaz Tabel, Nesrin Tas, Mehmet Tasdemir, Ana Teixeira, Demet Tekcan, Rezan Topaloglu, Sebahat Tulpar, Ozde Nisa Turkkan, Berfin Uysal, Metin Uysalol, Renata Vitkevic, Sevgi Yavuz, Sibel Yel, Tarik Yildirim, Zeynep Yuruk Yildirim, Nurdan Yildiz, Selcuk Yuksel, Eray Yurtseven, Alev Yilmaz
Publikováno v:
Frontiers in Urology, Vol 3 (2024)
BackgroundCongenital anomalies of the kidney and urinary tract (CAKUT) are defined as structural malformations of the kidney and/or urinary tract. Heat shock proteins (HSPs) are expressed in the kidney in response to cellular changes, such as thermal
Externí odkaz:
https://doaj.org/article/a80c88e2313546b599114335aabc3870
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 17, Iss 1, Pp 1-10 (2022)
Abstract Objective Alström syndrome (ALMS) is a rare autosomal recessive genetic disorder that is caused by homozygous or compound heterozygous mutation in the ALMS1 gene. Dilated cardiomyopathy (DCM) is one of the well-recognized features of the sy
Externí odkaz:
https://doaj.org/article/c5028f6768bb450da73bbe2f99f54eb2
Autor:
Asuman Gedikbasi, Guven Toksoy, Meryem Karaca, Cagri Gulec, Mehmet Cihan Balci, Dilek Gunes, Seda Gunes, Ayca Dilruba Aslanger, Gokcen Unverengil, Birsen Karaman, Seher Basaran, Mubeccel Demirkol, Gulden Fatma Gokcay, Zehra Oya Uyguner
Publikováno v:
Frontiers in Genetics, Vol 14 (2023)
Background: Mitochondrial diseases are the most common group of inherited metabolic disorders, causing difficulties in definite diagnosis due to clinical and genetic heterogeneity. Clinical components are predominantly associated with pathogenic vari
Externí odkaz:
https://doaj.org/article/795cb8b594b04d13b3f30e2a251abb26
Autor:
Gonul Aciksari, Bulent Demir, Turgut Uygun, Asuman Gedikbasi, Orkide Kutlu, Adem Atici, Omer Faruk Baycan, Mehmet Kocak, Şeref Kul
Publikováno v:
İstanbul Kuzey Klinikleri, Vol 7, Iss 5, Pp 471-477 (2020)
OBJECTIVE: Although the underlying mechanism is not yet fully understood, Cardiac Syndrome X (CSX) is defined as microvascular dysfunction. Prolidase plays a role in collagen synthesis. Increased serum prolidase activity (SPA) has been shown to corre
Externí odkaz:
https://doaj.org/article/5711c104367847dda19b24f7137eff03
Publikováno v:
International Journal of Ophthalmology, Vol 10, Iss 11, Pp 1662-1668 (2017)
AIM: To investigate the effect of pomegranate juice (PJ) intake on overall oxidation status in retinas of diabetic rats. METHODS: Twenty-seven rats were divided into four groups as control (CO), diabetic (DM), control treated with PJ (CO-PJ), and di
Externí odkaz:
https://doaj.org/article/a7b5aae5ebc2403bb17371e17bd6dce1
Autor:
Ismail Biyik, Fatma Nihan Turhan Caglar, Nilgun Isiksacan, Nursel Kocamaz, Pınar Kasapoglu, Asuman Gedikbasi, Faruk Akturk
Publikováno v:
International Journal of Hypertension, Vol 2018 (2018)
Introduction. Hypertension (HT) is a common serious condition associated with cardiovascular morbidity and mortality. The pathogenesis of HT is multifactorial and has been widely investigated. Besides the vascular, hormonal, and neurological factors,
Externí odkaz:
https://doaj.org/article/703fd2c211c84d299924bdbeb9c60a5b
Autor:
Nilgül Akalin, Yıldız Okuturlar, Özlem Harmankaya, Asuman Gedıkbaşi, Selçuk Sezıklı, Sibel Koçak Yücel
Publikováno v:
International Journal of Nephrology, Vol 2014 (2014)
Introduction. In this study, we aimed to demonstrate the correlation of FGF-23 levels with bone-mineral metabolism, anemia, and the treatment in dialysis patients. Methods. Eighty-nine patients with similar age, gender, dialysis duration, and dialysi
Externí odkaz:
https://doaj.org/article/ed5283138edb4ed1a2ab5de25a453080
Autor:
Meral Küçük Yetgin, Ani Agopyan, Ferit Kerim Küçükler, Asuman Gedikbaşı, Soner Yetgin, Fatma Çelik Kayapınar, Nurper Özbar, Bilal Biçer, Hasan Birol Çotuk
Publikováno v:
İstanbul Medical Journal, Vol 21, Iss 3, Pp 182-189 (2020)
Introduction:This present study aimed to examine the effects of long-term resistance exercise (REG) and aerobic exercise (AEG) on the adiponectin, insulin resistance, lipid profile and body composition in adolescent boys with obesity.Methods:Sixteen
Externí odkaz:
https://doaj.org/article/1a12e90ca0f04c3cb3b1cd4a81bf41c3
Autor:
Zeynep Yürük Yıldırım, Alev Yılmaz, Cemile Pehlivanoğlu, Asuman Gedikbaşı, Mehmet Yıldız, Ahmet Dirican, Rüveyde Bundak, Feyza Darendeliler, Sevinç Emre, Ahmet Nayır
Publikováno v:
JCRPE, Vol 11, Iss 2, Pp 157-163 (2019)
Objective:Histopathological changes in the kidney in type 1 diabetes mellitus (T1DM) begin before detection of microalbuminuria. Therefore, there is interest in finding a better biomarker for the early detection of diabetic kidney injury. The aim of
Externí odkaz:
https://doaj.org/article/d7efcdb1d32045419da069c13d00c435
Autor:
Bulent Demir, Esra Demir, Gonul Acıksarı, Turgut Uygun, Irem Kırac Utku, Asuman Gedikbasi, Ilker Murat Caglar, Osman Pirhan, Hande Oktay Tureli, Ersan Oflar, İsmail Ungan, Serkan Ciftci, Osman Karakaya
Publikováno v:
International Journal of Endocrinology, Vol 2014 (2014)
The risk for cardiovascular diseases and type 2 diabetes mellitus significantly increases in the patient population with metabolic syndrome (MeS). The present study aimed to investigate the association between the epicardial adipose tissue thickness
Externí odkaz:
https://doaj.org/article/8c2037ccba6041acad2858dde73477cc