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Browsing Dahili Tıp Bilimleri Bölümü Makale Koleksiyonu by Title 
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Browsing Dahili Tıp Bilimleri Bölümü Makale Koleksiyonu by Title

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Now showing items 2176-2195 of 2905

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    • R141C Mutation Of Notch3 Gene In Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts And Leukoencephalopathy 

      Onder, Halil; Kurtcu, Kemal; Arsava, Ethem Murat; Topcuoglu, Mehmet Akif (2017)
    • Radiation For Etmr: Literature Review And Case Series Of Patients Treated With Proton Therapy 

      Jaramillo, Sergio; Grosshans, David R.; Philip, Nancy; Varan, Ali; Akyüz, Canan; McAleer, Mary Frances; Mahajan, Anita; McGovern, Susan L. (2018)
      • ETMRs are rare but highly aggressive tumors occurring in young children. • The role of radiation in the treatment of ETMRs is poorly defined. ...
    • Radioembolization for the Treatment of Unresectable Liver Cancer: Initial Experience at A Single Center 

      Peynircioglu, Bora; Cil, Barbaros; Bozkurt, Fani; Aydemir, Ece; Ugur, Oemer; Balkanci, Ferhun (Turkish Soc Radiology, 2010)
      PURPOSE Radioembolization with yttrium-90 microsphere (Y-90) therapy with SIR-Spheres (R) (Sirtex Medical, Lane Cove, Australia) was approved by the Turkish Ministry of Health in April 2008. In this study, we present the ...
    • Radiofrequency Ablation for Lung Tumors: Outcomes, Effects on Survival, and Prognostic Factors 

      Akhan, Okan; Guler, Ezgi; Akinci, Devrim; Ciftci, Turkmen; Kose, Ilgaz Cagatay (Turkish Soc Radiology, 2016)
      PURPOSE We aimed to evaluate the survival benefit achieved with radiofrequency (RF) ablation of primary and metastatic lung tumors and determine significant prognostic factors for recurrence-free survival. METHODS Forty-nine ...
    • Radiographic Manifestations of the Temporomandibular Joint in A Case of Proteus Syndrome 

      Yilmaz, E.; Kansu, O.; Ozgen, B.; Akcicek, G.; Kansu, H. (British Inst Radiology, 2013)
      Proteus syndrome is a rare disorder with progressive asymmetrical and disproportionate overgrowth of various tissues of the body. The syndrome is characterized by a wide range of malformations, including craniofacial ...
    • Radiological Study of Pleural Changes in Relation to Mesothelioma in Turkey 

      Hillerdal, G; Barış, YI (British Med Journal Publ Group, 1983)
    • Randomized Multicenter Comparison of Conventional Anticoagulation Versus Antiplatelet Therapy in Unplanned and Elective Coronary Stenting - The Full Anticoagulation Versus Aspirin and Ticlopidine (Fantastic) Study 

      Bertrand, ME; Legrand, V; Boland, J; Fleck, E; Bonnier, J; Emmanuelson, H; Vrolix, M; Missault, L; Chierchia, S; Casaccia, M; Niccoli, L; Oto, A; White, C; Webb-Peploe, M; Van Belle, E; McFadden, EP (Lippincott Williams & Wilkins, 1998)
      Background-Dual therapy with ticlopidine and aspirin has been shown to be as effective as or more effective than conventional anticoagulation in patients with an optimal result after implantation of intracoronary metallic ...
    • Randomized Phase Iii Study Comparing Irinotecan Combined with 5-Fluorouracil and Folinic Acid to Cisplatin Combined with 5-Fluorouracil in Chemotherapy Naive Patients with Advanced Adenocarcinoma of the Stomach or Esophagogastric Junction 

      Dank, M; Zaluski, J; Barone, C; Valvere, V; Yalcin, S; Peschel, C; Wenczl, M; Goker, E; Cisar, L; Wang, K; Bugat, R. (2008)
    • Rap1-Mediated Mek/Erk Pathway Defects in Kabuki Syndrome 

      Boegershausen, Nina; Tsai, I-Chun; Pohl, Esther; Kiper, Pelin Ozlem Simsek; Beleggia, Filippo; Percin, E. Ferda; Keupp, Katharina; Matchan, Angela; Milz, Esther; Alanay, Yasemin; Kayserili, Hulya; Liu, Yicheng; Banka, Siddharth; Kranz, Andrea; Zenker, Martin; Wieczorek, Dagmar; Elcioglu, Nursel; Prontera, Paolo; Lyonnet, Stanislas; Meitinger, Thomas; Stewart, A. Francis; Donnai, Dian; Strom, Tim M.; Boduroglu, Koray; Yigit, Goekhan; Li, Yun; Katsanis, Nicholas; Wollnik, Bernd (Amer Soc Clinical Investigation Inc, 2015)
      The genetic disorder Kabuki syndrome (KS) is characterized by developmental delay and congenital anomalies. Dominant mutations in the chromatin regulators lysine (K)-specific methyltransferase 2D (KMT2D) (also known as ...
    • Rapid Evolution and Spread of Carbapenemases Among Enterobacteriaceae in Europe 

      Canton, R.; Akova, M.; Carmeli, Y.; Giske, C. G.; Glupczynski, Y.; Gniadkowski, M.; Livermore, D. M.; Miriagou, V.; Naas, T.; Rossolini, G. M.; Samuelsen, O.; Seifert, H.; Woodford, N.; Nordmann, P. (Elsevier Sci Ltd, 2012)
      Plasmid-acquired carbapenemases in Enterobacteriaceae, which were first discovered in Europe in the 1990s, are now increasingly being identified at an alarming rate. Although their hydrolysis spectrum may vary, they hydrolyse ...
    • Rare Occupational Cause of Nasal Septum Perforation: Nickel Exposure 

      Bolek, Ertugrul Cagri; Erden, Abdulsamet; Kulekci, Cagri; Kalyoncu, Umut; Karadag, Omer (Nofer Inst Occupational Medicine, Sw, 2017)
      Many etiologies are held accountable for nasal septum perforations. Topical nasal drug usage, previous surgeries, trauma, nose picking, squamous cell carcinoma, some rheumatological disorders such as granulomatosis with ...
    • Ras Oncoprotein Expression in Erionite- and Asbestos-Induced Turkish Malignant Pleural Mesothelioma Patients - A Pilot Study 

      Olut, A; Firat, P; Ertugrul, D; Gungen, Y; Emri, S (W B Saunders Co Ltd, 2001)
    • Rasgrp1 Deficiency Causes Immunodeficiency With Impaired Cytoskeletal Dynamics 

      Salzer, Elisabeth; Cagdas, Deniz; Hons, Miroslav; Mace, Emily M.; Garncarz, Wojciech; Petronczki, Ozlem Yuce; Platzer, Rene; Pfajfer, Laurene; Bilic, Ivan; Ban, Sol A.; Willmann, Katharina L.; Mukherjee, Malini; Supper, Verena; Hsu, Hsiang Ting; Banerjee, Pinaki P.; Sinha, Papiya; McClanahan, Fabienne; Zlabinger, Gerhard J.; Pick, Winfried F.; Gribben, John G.; Stockinger, Hannes; Bennett, Keiryn L.; Huppa, Johannes B.; Dupre, Loic; Sanal, Ozden; Jager, Ulrich; Sixt, Michael; Tezcan, Ilhan; Orange, Jordan S.; Boztug, Kaan (Nature Publishing Group, 2016)
      RASGRP1 is an important guanine nucleotide exchange factor and activator of the RAS-MAPK pathway following T cell antigen receptor (TCR) signaling. The consequences of RASGRP1 mutations in humans are unknown. In a patient ...
    • Reactivation of Camp Pathway by Pde4D Inhibition Represents A Novel Druggable Axis for Overcoming Tamoxifen Resistance in Er-Positive Breast Cancer 

      Mishra, Rasmi R.; Belder, Nevin; Ansari, Suhail A.; Kayhan, Merve; Bal, Hilal; Raza, Umar; Ersan, Pelin G.; Tokat, Unal M.; Eyupoglu, Erol; Saatci, Ozge; Jandaghi, Pouria; Wiemann, Stefan; Uner, Aysegul; Cekic, Caglar; Riazalhosseini, Yasser; Sahin, Ozgur (Amer Assoc Cancer Research, 2018)
      Purpose: Tamoxifen remains an important hormonal therapy for ER-positive breast cancer; however, development of resistance is a major obstacle in clinics. Here, we aimed to identify novel mechanisms of tamoxifen resistance ...
    • Real World Survival Data of A Rare Malignancy: Anal Cancer Results in Hiv Negative Patients From Turkey 

      Esin, Ece; Yildiz, Ferah; Lacin, Sahin; Karakas, Yusuf; Gültekin, Melis; Dizdar, Ömer; Yalçin, Şuayib (Aves, 2018)
      Background/Aims: An organ preservation approach using chemoradiotherapy has been established for anal cancer. This retrospective cohort study aimed to define the clinico-demographic characteristics and outcomes of cases ...
    • Real-Time In Vivo Control Of Neural Membrane Potential By Electro-Ionic Modulation 

      Soybaş, Zafer; Şimşek, Sefa; Erol, F.M. Betül; Erdoğan, U. Çiya; Şimşek, Esra N.; Şahin, Büşra; Marçalı, Merve; Aydoğdu, Bahattin; Elbüken, Çağlar; Melik, Rohat (2019)
      Theoretically, by controlling neural membrane potential (Vm) in vivo, motion, sensation, and behavior can be controlled. Until now, there was no available technique that can increase or decrease ion concentration in vivo ...
    • Rebound Thrombocytosis Following Induction Chemotherapy Is An Independent Predictor of A Good Prognosis in Acute Myeloid Leukemia Patients Attaining First Complete Remission 

      Malkan, Umit Yavuz; Gunes, Gursel; Isik, Ayse; Eliacik, Eylem; Etgul, Sezgin; Aslan, Tuncay; Balaban, Muruvvet Seda; Haznedaroglu, Ibrahim Celalettin; Demiroglu, Haluk; Goker, Hakan; Ozcebe, Osman Ilhami; Sayinalp, Nilgun; Aksu, Salih; Buyukasik, Yahya; Mahallesi, Mutlukent (Karger, 2015)
      There are very few data about the relationship between acute myeloid leukemia (AML) prognosis and bone marrow recovery kinetics following chemotherapy. In this study, we aimed to assess the prognostic importance and clinical ...
    • Recessive Lamc3 Mutations Cause Malformations of Occipital Cortical Development 

      Barak, Tanyeri; Kwan, Kenneth Y.; Louvi, Angeliki; Demirbilek, Veysi; Saygi, Serap; Tuysuz, Beyhan; Choi, Murim; Boyaci, Huseyin; Doerschner, Katja; Zhu, Ying; Kaymakcalan, Hande; Yilmaz, Saliha; Bakircioglu, Mehmet; Caglayan, Ahmet Okay; Oeztuerk, Ali Kemal; Yasuno, Katsuhito; Brunken, William J.; Atalar, Ergin; Yalcinkaya, Cengiz; Dincer, Alp; Bronen, Richard A.; Mane, Shrikant; Ozcelik, Tayfun; Lifton, Richard P.; Sestan, Nenad; Bilguevar, Kaya; Guenel, Murat (Nature Publishing Group, 2011)
      The biological basis for regional and inter-species differences in cerebral cortical morphology is poorly understood. We focused on consanguineous Turkish families with a single affected member with complex bilateral ...
    • Recessive Missense Mutations in Lamb2 Expand the Clinical Spectrum of Lamb2-Associated Disorders 

      Hasselbacher, K.; Wiggins, R. C.; Matejas, V.; Hinkes, B. G.; Mucha, B.; Hoskins, B. E.; Ozaltin, F.; Nuernberg, G.; Becker, C.; Hangan, D.; Pohl, M.; Kuwertz-Broeking, E.; Griebel, M.; Schumacher, V.; Royer-Pokora, B.; Bakkaloglu, A.; Nuernberg, P.; Zenker, M.; Hildebrandt, F. (Elsevier Science Inc, 2006)
      Congenital nephrotic syndrome is clinically and genetically heterogeneous. The majority of cases can be attributed to mutations in the genes NPHS1, NPHS2, and WT1. By homozygosity mapping in a consanguineous family with ...
    • Recessive Ttn Truncating Mutations Define Novel Forms of Core Myopathy with Heart Disease 

      Chauveau, Claire; Bonnemann, Carsten G.; Julien, Cedric; Kho, Ay Lin; Marks, Harold; Talim, Beril; Maury, Philippe; Arne-Bes, Marie Christine; Uro-Coste, Emmanuelle; Alexandrovich, Alexander; Vihola, Anna; Schafer, Sebastian; Kaufmann, Beth; Medne, Livija; Huebner, Norbert; Foley, A. Reghan; Santi, Mariarita; Udd, Bjarne; Topaloglu, Haluk; Moore, Steven A.; Gotthardt, Michael; Samuels, Mark E.; Gautel, Mathias; Ferreiro, Ana (Oxford Univ Press, 2014)
      Core myopathies (CM), the main non-dystrophic myopathies in childhood, remain genetically unexplained in many cases. Heart disease is not considered part of the typical CM spectrum. No congenital heart defect has been ...
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