Zobrazeno 1 - 10
of 66
pro vyhledávání: '"Göksel Leblebisatan"'
Autor:
Ahmet Yöntem, Göksel Leblebisatan, Dinçer Yıldızdaş, Hatice İlgen Şaşmaz, Sevcan Erdem, Fadli Demir, Engin Melek, Aysun Karabay Bayazıt
Publikováno v:
Journal of Pediatric Research, Vol 8, Iss 3, Pp 251-256 (2021)
Aim:In this retrospective study, our objective was to evaluate children with arterial or venous thromboembolism, who were treated with tissue plasminogen activator (tPA) in our hospital.Materials and Methods:The medical records of 56 tPA treatments a
Externí odkaz:
https://doaj.org/article/a87f1772bebe4bb6858527f789b61896
Autor:
Ayça Koca Yozgat, Göksel Leblebisatan, Sinan Akbayram, Simge Çınar Özel, Zeynep Karakaş, Erol Erduran, Şebnem Yılmaz, Ülker Koçak, Şule Ünal, Gül Nihal Özdemir, Meryem Albayrak, Emine Zengin, Yeşim Oymak, Özcan Bör, Hasan Fatih Çakmaklı, Murat Söker, Dilek Gürlek Gökçebay, Hüseyin Tokgöz, Barış Malbora, Serap Karaman, Tiraje Celkan, İlgen Şaşmaz, Neşe Yaralı, Hale Ören, Ayşegül Ünüvar
Publikováno v:
Turkish Journal of Hematology, Vol 37, Iss 3, Pp 139-144 (2020)
Objective: Immune thrombocytopenia (ITP) is a rare autoimmune disease and hematologic disorder characterized by reduced platelet counts that can result in significant symptoms, such as bleeding, bruising, epistaxis, or petechiae. The thrombopoietin r
Externí odkaz:
https://doaj.org/article/0659ce0b12024b1d800b0a65ac28cbd5
Publikováno v:
Journal of Contemporary Medicine, Vol 9, Iss 3, Pp 197-202 (2019)
Introduction: Our aim was to compare NT-proBNP levels and cardiac functions after iron therapy in children with congenital cyanotic heart disease who had iron deficiency anemia.Materials and Methods: We included 40 children with pre-established cyano
Externí odkaz:
https://doaj.org/article/114c97c6ffcd42d9b128578702895513
Publikováno v:
Journal of Pediatric Emergency and Intensive Care Medicine, Vol 4, Iss 1, Pp 38-41 (2017)
A 10-year-old male patient with a fall-related soft tissue injury of the lateral lower left extremity was admitted to the emergency room with the complaints of flank pain, chest pain, respiratory distress and fever developing two days later. The pati
Externí odkaz:
https://doaj.org/article/bd3f2b093f234fb79e847c54e54f926c
Publikováno v:
Turkish Journal of Hematology, Vol 30, Iss 3, Pp 283-289 (2013)
Objective: Cardiac failure due to iron overload remains the most common cause of death in patients with beta-thalassemia major. This study aimed to evaluate myocardial function in children with beta-thalassemia major using standard echocardiography t
Externí odkaz:
https://doaj.org/article/d2dcb947d4fd4e9cb0f786d7794a018f
Autor:
Göksel Leblebisatan, Ali Bay, Noriko Mitsuiki, Osamu Ohara, Kenichi Honma, Kohsuke İmai, Shigeaki Nonoyama
Publikováno v:
Turkish Journal of Hematology, Vol 28, Iss 02, Pp 139-141 (2011)
Wiskott-Aldrich syndrome (WAS) is a clinical condition characterized by thrombocytopenia, eczema, and life-threatening infections. In some cases autoimmunity-related problems and even malignancy might be seen; however, some patients have milder clini
Externí odkaz:
https://doaj.org/article/0f6c25e4579c4c339b32bb7020b9fac5
Autor:
Banu İnce, Göksel Leblebisatan, Hatice İlgen Şaşmaz, Adnan Barutçu, Aysun Uğuz, İsa Burak Güney
Publikováno v:
Journal of Surgery and Medicine. 6:640-642
Hemophilia A is a hereditary hemorrhagic disorder associated with bleeding episodes and characterized by deficiency or dysfunction of coagulation protein factor VIII. Cancer incidence was found to increase in hemophilic patients. A case of a 6-year o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cfb21c186e0edb8aaf322c8431d8c1ee
https://doi.org/10.28982/josam.999565
https://doi.org/10.28982/josam.999565
Autor:
Fadli Demir, Aysun Karabay Bayazit, Dincer Yildizdas, Ahmet Yontem, Göksel Leblebisatan, Engin Melek, Sevcan Erdem, Hatice Şaşmaz
Publikováno v:
Journal of Pediatric Research, Vol 8, Iss 3, Pp 251-256 (2021)
Aim:In this retrospective study, our objective was to evaluate children with arterial or venous thromboembolism, who were treated with tissue plasminogen activator (tPA) in our hospital.Materials and Methods:The medical records of 56 tPA treatments a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ec37cf829f4294428e86c1d8c8515d91
https://doaj.org/article/a87f1772bebe4bb6858527f789b61896
https://doaj.org/article/a87f1772bebe4bb6858527f789b61896
Autor:
Adnan Barutçu, Fadli Demir, Serife Leblebisatan, Metin Cil, Göksel Leblebisatan, Hatice Şaşmaz
Publikováno v:
Journal of Pediatric Hematology/Oncology. 43:e774-e776
Wiskott-Aldrich syndrome (WAS) is a rare X-linked primary immunodeficiency disorder that is characterized by a triad of microthrombocytopenia, severe immunodeficiency, and eczema. We report the case of a 7-year-old male patient with chronic thrombocy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::644fd8ffee3f37a400fccf225ad3f0e5
https://doi.org/10.1097/mph.0000000000001932
https://doi.org/10.1097/mph.0000000000001932
Publikováno v:
Journal of Contemporary Medicine. 9:197-202
Introduction: Our aim was to compare NT-proBNP levels and cardiac functions after iron therapy in children with congenital cyanotic heart disease who had iron deficiency anemia.Materials and Methods: We included 40 children with pre-established cyano
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::511446d53ac4807b8ab96c7c470b4ccc
https://doi.org/10.16899/jcm.598034
https://doi.org/10.16899/jcm.598034