Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Bülent Zülfikar"'
Autor:
Bülent Zülfikar, Johnny Mahlangu, Salim Mohamed Nekkal, Cecil Ross, Noppacharn Uaprasert, Jerzy Windyga, Carmen Escuriola Ettingshausen, Bettina Ploder, Aurelia Lelli, Hanna T. Gazda
Publikováno v:
TH Open, Vol 08, Iss 03, Pp e273-e282 (2024)
Background Activated prothrombin complex concentrate (aPCC) is indicated for bleed treatment and prevention in patients with hemophilia with inhibitors. The safety and tolerability of intravenous aPCC at a reduced volume and faster infusion rates wer
Externí odkaz:
https://doaj.org/article/d6aef7dc90ac43e488c3d85c23242dd4
Autor:
Kaan Kavaklı, Süha Süreyya Özbek, Ali Bülent Antmen, Fahri Şahin, Şevkiye Selin Aytaç, Alphan Küpesiz, Bülent Zülfikar, Mehmet Sönmez, Ümran Çalışkan, Can Balkan, Tuğana Akbaş, Taner Arpacı, İpek Tamsel, Turgut Seber, Berna Oğuz, Can Çevikol, Mesut Bulakçı, Polat Koşucu, Demet Aydoğdu, İlgen Şaşmaz, Gülen Tüysüz, Başak Koç, Hüseyin Tokgöz, Zuhal Demirci, Burcu Özkan
Publikováno v:
Turkish Journal of Hematology, Vol 38, Iss 2, Pp 101-110 (2021)
Objective: This study aimed to observe the preventive effect of prophylactic treatment on joint health in people with hemophilia (PwH) and to investigate the importance of integration of ultrasonographic examination into clinical and radiological eva
Externí odkaz:
https://doaj.org/article/ca5ed396cb0a42fea2f11a3b6008d5e6
Autor:
Kaan Kavaklı, Bülent Antmen, Vahap Okan, Fahri Şahin, Selin Aytaç, Can Balkan, Ergül Berber, Zühre Kaya, Alphan Küpesiz, Bülent Zülfikar
Publikováno v:
Therapeutic Advances in Hematology, Vol 13 (2022)
Haemophilia is an X-linked lifelong congenital bleeding disorder that is caused by insufficient levels of factor VIII (FVIII; haemophilia A) or factor IX (FIX; haemophilia B) and characterized by spontaneous and trauma-related bleeding episodes. The
Externí odkaz:
https://doaj.org/article/64567dd6d59d469caa672f083dcdb98a
Autor:
Ayşegül Ünüvar, Serap Karaman, Deniz Tuğcu, Melike Sezgin Evim, Arzu Akçay, İbrahim Eker, Funda Tayfun Küpesiz, Namık Özbek, Mehmet Ertem, Sultan Aydın, Zuhal Keskin, Yusuf Ziya Aral, Zülfükar Gördü, Murat Elli, Ayşe Özkan Karagenç, Burcu Belen Apak, Hülya Uzel, Murat Söker, Tuba Karapınar, Yeşim Oymak, Nihal Karadaş, Alper Özcan, Ersin Töret, Ülker Koçak, Sinan Akbayram, Şule Ünal Cangül, Aylin Canbolat Ayhan, Tiraje Celkan, Bülent Zülfikar, Rejin Kebudi, Şadan Hacısalihoğlu, Erol Erduran, Sema Aylan Gelen, Nazan Sarper, Fatih Erbey, Emin Kürekçi, Hüseyin Gülen, Barış Yılmaz, Ömer Doğru, Ahmet Koç, Selma Ünal, Hüseyin Tokgöz, Canan Albayrak, Yılmaz Ay, Fatih Orhan, Davut Albayrak, Neslihan Karakurt, Betül Orhaner, Emine Türkkan, Yıldız Yıldırmak, Hadi Geylani, Begüm Koç, Ahmet Fayik Öner, Çetin Timur, Hale Ören
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 43, Iss , Pp S55-S56 (2021)
Objective: A questionnaire form was prepared by the Turkish Pediatric Hematology Society- Subcommittee of Hemostasis, Thrombosis and Hemophilia to determine the current approaches in the diagnosis and treatment of childhood ITP in our country. Our ai
Externí odkaz:
https://doaj.org/article/0eb80f230816404ab892c71ef0fed017
Publikováno v:
JCRPE, Vol 11, Iss 2, Pp 173-180 (2019)
Objective:Increased risk of unfavorable cardiovascular risk factors has been recognised in ageing patients with haemophilia (PwH), but needs further studies in younger patients. The purpose of this study was to assess obesity, hypertension (HT), meta
Externí odkaz:
https://doaj.org/article/2a271b2b4f554d5b938ac09ac870cfa5
Publikováno v:
Turkish Journal of Hematology, Vol 37, Iss 1, Pp 62-63 (2020)
Externí odkaz:
https://doaj.org/article/e6602903aea04ff28d7388c4ab6ea006
Autor:
İnanç Değer Fidancı, Bülent Zülfikar, Kaan Kavaklı, M. Cem Ar, Yurdanur Kılınç, Zafer Başlar, Server Hande Çağlayan
Publikováno v:
Turkish Journal of Hematology, Vol 31, Iss 1, Pp 17-24 (2014)
OBJECTIVE: A severe complication in the replacement therapy of hemophilia A (HA) patients is the development of alloantibodies (inhibitors) against factor VIII, which neutralizes the substituted factor. The primary genetic risk factors influencing th
Externí odkaz:
https://doaj.org/article/6b0ddb0d7b264ab9807c7d3153020d58
Publikováno v:
Turkish Journal of Hematology, Vol 30, Iss 1, Pp 19-24 (2013)
Objective: To assess the hemostatic efficacy of a new local hemostatic agent, Ankaferd Blood Stopper (ABS), for the control of bleeding following tooth extraction in hemophiliacs. Materials and Methods: Simple tooth extractions were performed in 27 h
Externí odkaz:
https://doaj.org/article/45d717f3f8d34c0c9429f090eeb0bc9b
Autor:
Ahmet Salduz, Özcan Kaya, Halil İbrahim Balci, Turgut Akgul, Fatih Dikici, Bülent Zülfikar, Mehmet Kocaoğlu
Publikováno v:
Case Reports in Orthopedics, Vol 2016 (2016)
The management of nonunion and limb length discrepancy has remained a constant challenge in hemophilic patients. In this study, we aimed to present the treatment of femur infected nonunion and limb length discrepancy in a twenty-seven-year-old patien
Externí odkaz:
https://doaj.org/article/66a2a5bc520942a6ac255d7ea1d2dc5c
Publikováno v:
Turkish Journal of Hematology, Vol 29, Iss 1, Pp 40-47 (2012)
OBJECTIVE: The aim of this study was to evaluate the efficiency of two local haemostatic agents administered together with preoperative dose of replacement therapy for oral surgical procedures in patients with bleeding disorders METHODS: Twenty-one p
Externí odkaz:
https://doaj.org/article/7506ed163c594e36a40e7698a5f727cc