Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Tekin Güney"'
Autor:
Erol Sener, Zeki Çatav, Mehmet Özatik, Seref Alp Kucuker, Sinan Sabit Kocabeyoğlu, Simten Dagdas, Tekin Güney, Burcu Demırkan, Servet Turgut, Fatih Yamac, Abdulkadir Yılmaz, Doğan Emre Sert, Mehmet Karahan
Publikováno v:
Genel Tıp Dergisi, Vol 32, Iss 6, Pp 719-723 (2022)
Abstract Background/Aims: In this study, the results of patients who had orthotopic heart transplantation (OHT) in acute rejection who admitted to our clinic with decompensated heart failure and who could not undergo endomyocardial biopsy (EMB) were
Externí odkaz:
https://doaj.org/article/d94d41614b184c15af92de1aa4999c57
Publikováno v:
Balkan Medical Journal, Vol 38, Iss 3, Pp 194-194 (2021)
Externí odkaz:
https://doaj.org/article/ef47a96f3d814070b660e6a9970f4176
Publikováno v:
Journal of Ankara University Faculty of Medicine. 75:204-210
Autor:
Aydan Akdeniz, Ayşegül Ünüvar, Muhlis Cem Ar, Esra Pekpak, Arzu Akyay, Özgür Mehtap, Fatma Keklik Karadağ, Can Acıpayam, Ali Doğan, Ömer Ekinci, Sultan Aydın Köker, Canan Albayrak, Ufuk Demirci, Tekin Güney, Meltem Kurt, Serap Karaman, Özge Şahin Kimyon, Sinan Albayrak, Yurday Öncül, Serkan Ünal, Fahri Şahin, Rumeysa Tuna, Bulent Zulfikar, Burcu Belen Apak, Elif Gülsüm Ümit, Ahmet Muzaffer Demir
Publikováno v:
Scandinavian Journal of Clinical and Laboratory Investigation. 82:28-36
Introduction: Inherited factor VII (FVII) deficiency (FVIID) is the most common of inherited rare bleeding disorders. Other determinants of clinical severity apart from FVII level (FVIIL) include genetic and environmental factors. We aimed to identif
Autor:
Eren Arslan Davulcu, Zühal Demirci, Umut Yılmaz, Muhlis Cem Ar, Hava Üsküdar Teke, Volkan Karakuş, Rafiye Çiftçiler, Cem Selim, İrfan Yavaşoğlu, Salih Sertaç Durusoy, Vahap Okan, Aydan Akdeniz, Alkım Yolcu, İsmet Aydoğdu, Tekin Güney, Asu Fergün Yılmaz, Fahri Şahin
Acquired hemophilia A (AHA) is a rare disease caused by autoantibodies inhibiting factor VIII (FVIII) activity. Although the conditionis usually idiopathic, there may be other underlying diseases. Treatment consists of two steps: treatment of acute b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::744f6e5495a4b4fba10e552e50e10563
https://hdl.handle.net/11454/76288
https://hdl.handle.net/11454/76288
Publikováno v:
Turkish journal of haematology : official journal of Turkish Society of Haematology. 39(1)
Autor:
Çağrı Yayla, Ozcan Ozeke, Mehmet Timur Selçuk, Sefa Ünal, Koray Demirtaş, Ahmet Akdi, Mustafa Karanfil, Tekin Güney, Ahmet Göktuğ Ertem
Publikováno v:
Blood pressure monitoring. 25(2)
AIMS Polycythemia vera increases the risk of hypertension, but there is limited information about the effect on daily blood pressure fluctuations. This study aimed to demonstrate how diurnal blood pressure rhythm is affected in polycythemia vera pati
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 44, Iss , Pp S18- (2022)
Objective: There is limited data in the literature on the mental health of newly diagnosed hematological cancer (HC) patients in COVID-19 pandemic. This study evaluates the mental health statuses of HC inpatients diagnosed during the COVID-19 pandemi
Externí odkaz:
https://doaj.org/article/b5ef741a9257443782612627746b018c
Publikováno v:
Turkish Journal of Hematology, Vol 39, Iss 1, Pp 74-75 (2022)
Externí odkaz:
https://doaj.org/article/428b587e7c144bc5bfc7d343697ba70a
Publikováno v:
Nasza Dermatologia Online, Vol 8, Iss 4, Pp 453-456 (2017)
Blastic plasmacytoid dendritic cell neoplasm (BPDCN) is a rare and aggressive hematological malignancy characterized by proliferation of plasmacytoid dendritic cell precursors. Herein, we describe a 65-year-old male presented with a 6 month history o
Externí odkaz:
https://doaj.org/article/fb256c1bb7e44c12adb1f257aeb32108