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Başlık için Araştırma Çıktıları | Pubmed İndeksli Yayınlar Koleksiyonu listeleme

Başlık için Araştırma Çıktıları | Pubmed İndeksli Yayınlar Koleksiyonu listeleme

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  • 2018 Annual Report of the European Liver Transplant Registry 
    Adam, R; Karam, V; Cailliez, V; Grady, JGO; Mirza, D; Cherqui, D; Klempnauer, J; Salizzoni, M; Pratschke, J; Jamieson, N; Hidalgo, E; Paul, A; Andujar, RL; Lerut, J; Fisher, L; Boudjema, K; Fondevila, C; Soubrane, O; Bachellier, P; Pinna, AD; Berlakovich, G; Bennet, W; Pinzani, M; Schemmer, P; Zieniewicz, K; Romero, CJ; De Simone, P; Ericzon, BG; Schneeberger, S; Wigmore, SJ; Prous, JF; Colledan, M; Porte, RJ; Yilmaz, S; Azoulay, D; Pirenne, J; Line, PD; Trunecka, P; Navarro, F; Lopez, AV; De Carlis, L; Pena, SR; Kochs, E; Duvoux, C (2018)
    The purpose of this registry study was to provide an overview of trends and results of liver transplantation (LT) in Europe from 1968 to 2016. These data on LT were collected prospectively from 169 centers from 32 countries, ...
  • 2018 Annual Report of the European Liver Transplant Registry 
    Adam, R; Karam, V; Cailliez, V; Grady, JGO; Mirza, D; Cherqui, D; Klempnauer, J; Salizzoni, M; Pratschke, J; Jamieson, N; Hidalgo, E; Paul, A; Andujar, RL; Lerut, J; Fisher, L; Boudjema, K; Fondevila, C; Soubrane, O; Bachellier, P; Pinna, AD; Berlakovich, G; Bennet, W; Pinzani, M; Schemmer, P; Zieniewicz, K; Romero, CJ; De Simone, P; Ericzon, BG; Schneeberger, S; Wigmore, SJ; Prous, JF; Colledan, M; Porte, RJ; Yilmaz, S; Azoulay, D; Pirenne, J; Line, PD; Trunecka, P; Navarro, F; Lopez, AV; De Carlis, L; Pena, SR; Kochs, E; Duvoux, C (2018)
    The purpose of this registry study was to provide an overview of trends and results of liver transplantation (LT) in Europe from 1968 to 2016. These data on LT were collected prospectively from 169 centers from 32 countries, ...
  • 2019 Turkish Hypertension Consensus Report 
    Aydogdu, S; Guler, K; Bayram, F; Altun, B; Derici, U; Abaci, A; Tukek, T; Sabuncu, T; Arici, M; Erdem, Y; Ozin, B; Sahin, I; Erturk, S; Bitigen, A; Tokgozoglu, L (2019)
    The Turkish Hypertension Consensus Report was prepared for the first time in 2015 to adapt the European and American international guidelines to our clinical practice and to create a practical report that could be a basic ...
  • 2DOF multi-objective optimal tuning of disturbance reject fractional 
    Ozbey, N; Yeroglu, C; Alagoz, BB; Herencsar, N; Kartci, A; Sotner, R (2020)
    This study presents a Fractional Order Proportional Integral Derivative Acceleration (FOPIDA) controller design methodology to improve set point and disturbance reject control performance. The proposed controller tuning ...
  • 3D Analysis of D-RaCe and Self-Adjusting File in Removing Filling 
    Simsek, N; Ahmetoglu, F; Keles, A; Bulut, ET; Er, K (2014)
    The aim of this study was to compare the efficacy of D-RaCe files and a self-adjusting file (SAF) system in removing filling material from curved root canals instrumented and filled with different techniques by using ...
  • 3D Micro-CT Analysis of Void and Gap Formation in Curved Root Canals 
    Simsek, N; Keles, A; Ahmetoglu, F; Akinci, L; Er, K (2017)
    Objective: This study used microcomputed tomography (micro-CT) to compare the volumes of voids and gaps in curved root canals instrumented and filled using various techniques.
  • 3D micro-CT analysis of void formations and push-out bonding strength of 
    Uzun, IH; Malkoc, MA; Keles, A; Ogreten, AT (2016)
    PURPOSE. To investigate the void parameters within the resin cements used for fiber post cementation by micro-CT (mu CT) and regional push-out bonding strength. MATERIALS AND METHODS. Twenty-one, single and round shaped ...
  • (3R, 3'R)-zeaxanthin protects the retina from photo-oxidative damage via 
    Sahin, K; Akdemir, F; Orhan, C; Tuzcu, M; Gencoglu, H; Sahin, N; Ozercan, IH; Ali, S; Yilmaz, I; Juturu, V (2019)
    Purpose: Zeaxanthin protects the macula from ocular damage due to light or radiation by scavenging harmful reactive oxygen species. In the present study, zeaxanthin product (OmniXan (R); OMX), derived from paprika pods ...
  • 46,XY Sex Development Defect due to a Novel Homozygous (Splice Site) 
    Ciftci, N; Kayas, L; Camtosun, E; Akinci, A (2022)
    The enzyme 17-beta-hydroxysteroid dehydrogenase type 3 (17 beta-HSD3) catalyzes the biosynthesis of testosterone (T) from Delta 4-androstenedione, and plays an important role in the final steps of androgen synthesis. 17 ...
  • 8 Melatonin, quercetin and resveratrol attenuates oxidative 
    Elbe, H; Esrefoglu, M; Vardi, N; Taslidere, E; Ozerol, E; Tanbek, K (2015)
    In this study, effects of melatonin, quercetin and resveratrol on hepatocellular injury in streptozotocin (STZ)-induced experimental diabetes were aimed to be investigated by histological and biochemical methods. Thirty-five ...
  • 8 Melatonin, quercetin and resveratrol attenuates oxidative 
    Elbe, H; Esrefoglu, M; Vardi, N; Taslidere, E; Ozerol, E; Tanbek, K (2015)
    In this study, effects of melatonin, quercetin and resveratrol on hepatocellular injury in streptozotocin (STZ)-induced experimental diabetes were aimed to be investigated by histological and biochemical methods. Thirty-five ...
  • A 9-year follow-up of a girl with pyridoxine (vitamin B6)-dependent 
    Dogan, M; Dogan, DG; Kahraman, AS; Ozcan, O; Yakinci, C; Alkan, A (2012)
    Being an extremely rare condition makes the diagnosis of pyridoxine-dependent seizures (PDS) difficult. Early diagnosis of PDS is very important to prevent unwanted clinical outcomes. Elevated levels of glutamate and ...
  • A 9-year follow-up of a girl with pyridoxine (vitamin B6)-dependent 
    Dogan, M; Dogan, DG; Kahraman, AS; Ozcan, O; Yakinci, C; Alkan, A (2012)
    Being an extremely rare condition makes the diagnosis of pyridoxine-dependent seizures (PDS) difficult. Early diagnosis of PDS is very important to prevent unwanted clinical outcomes. Elevated levels of glutamate and ...
  • A bioactive product lipoxin A4 attenuates liver fibrosis in an 
    Kurtoglu, EL; Kayhan, B; Gul, M; Kayhan, MA; Karaca, ZM; Yesilada, E; Yilmaz, S (2019)
    Background/Aims: Lipoxin A4 (LXA4), an anti-inflammatory lipid mediator, regulates leukocyte cellular activity and activates gene transcription. The therapeutic effect of LXA4 on liver fibrosis and its mechanism on the ...
  • A bioactive product lipoxin A4 attenuates liver fibrosis in an 
    Kurtoglu, EL; Kayhan, B; Gul, M; Kayhan, MA; Karaca, ZM; Yesilada, E; Yilmaz, S (2019)
    Background/Aims: Lipoxin A4 (LXA4), an anti-inflammatory lipid mediator, regulates leukocyte cellular activity and activates gene transcription. The therapeutic effect of LXA4 on liver fibrosis and its mechanism on the ...
  • A Case of Cleidocranial Dysplasia with a Novel Mutation and Growth 
    Camtosun, E; Akinci, A; Demiral, E; Tekedereli, I; Sigirci, A (2019)
    Cleidocranial dysplasia (CCD) is a rare congenital autosomal dominant skeletal disorder that is characterized by hypoplasia or aplasia of clavicles, failure of cranial suture closure, dental anomalies, short stature and ...
  • A Case of Cleidocranial Dysplasia with a Novel Mutation and Growth 
    Camtosun, E; Akinci, A; Demiral, E; Tekedereli, I; Sigirci, A (2019)
    Cleidocranial dysplasia (CCD) is a rare congenital autosomal dominant skeletal disorder that is characterized by hypoplasia or aplasia of clavicles, failure of cranial suture closure, dental anomalies, short stature and ...
  • A Case of Cleidocranial Dysplasia with a Novel Mutation and Growth 
    Camtosun, E; Akinci, A; Demiral, E; Tekedereli, I; Sigirci, A (2019)
    Cleidocranial dysplasia (CCD) is a rare congenital autosomal dominant skeletal disorder that is characterized by hypoplasia or aplasia of clavicles, failure of cranial suture closure, dental anomalies, short stature and ...
  • A Case of Cleidocranial Dysplasia with a Novel Mutation and Growth 
    Camtosun, E; Akinci, A; Demiral, E; Tekedereli, I; Sigirci, A (2019)
    Cleidocranial dysplasia (CCD) is a rare congenital autosomal dominant skeletal disorder that is characterized by hypoplasia or aplasia of clavicles, failure of cranial suture closure, dental anomalies, short stature and ...
  • A Case of Cleidocranial Dysplasia with a Novel Mutation and Growth 
    Camtosun, E; Akinci, A; Demiral, E; Tekedereli, I; Sigirci, A (2019)
    Cleidocranial dysplasia (CCD) is a rare congenital autosomal dominant skeletal disorder that is characterized by hypoplasia or aplasia of clavicles, failure of cranial suture closure, dental anomalies, short stature and ...