Zobrazeno 1 - 10
of 60
pro vyhledávání: '"Hüseyin GÜLEN"'
Publikováno v:
Journal of Pediatric Research, Vol 11, Iss 3, Pp 185-188 (2024)
All-trans retinoic acid (ATRA), a derivative of vitamin A, has dramatically altered the treatment landscape for acute promyelocytic leukemia (APL). APL is characterized by the abnormal maturation of myeloid cells, which become arrested at the promyel
Externí odkaz:
https://doaj.org/article/906355b70e864180a4ea52df31bfa528
Autor:
Sedef Alpdoğan, Hüseyin Gülen
Publikováno v:
Journal of Pediatric Research, Vol 10, Iss 4, Pp 278-284 (2023)
Aim: To determine the risk factors associated with chronic childhood immune thrombocytopenia (ITP). Materials and Methods: We retrospectively analyzed the medical records of 123 children with ITP who were admitted to our Department of Pediatric Hemat
Externí odkaz:
https://doaj.org/article/dbbfbe6462e5407a8a7df5b388b2f02f
Autor:
Emine Zengin, Nazan Sarper, Arzu Yazal Erdem, Işık Odaman Al, Melike Sezgin Evim, Neşe Yaralı, Burcu Belen, Arzu Akçay, Ayşen Yıldırım, Tuba Hilkay Karapınar, Adalet Meral Güneş, Sema Aylan Gelen, Hale Ören, Lale Olcay, Birol Baytan, Hüseyin Gülen, Gülyüz Öztürk, Mehmet Fatih Orhan, Yeşim Oymak, Sibel Akpınar, Özlem Tüfekçi, Meryem Albayrak, Burçak Tatlı Güneş, Aylin Canpolat, Namık Özbek
Publikováno v:
Turkish Journal of Hematology, Vol 38, Iss 4, Pp 294-305 (2021)
Objective: This study aimed to evaluate systemic thrombolysis experiences with recombinant tissue plasminogen activator (rtPA). Materials and Methods: Retrospective data were collected from 13 Turkish pediatric hematology centers. The dose and durati
Externí odkaz:
https://doaj.org/article/e6651da5e2b34eb7b892f7bbb80c64ac
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
Autor:
Arzu Çalışkan Polat, Yeşim Yiğit, Esra Nagehan Akyol Önder, Ayşen Türedi Yıldırım, Pelin Ertan, Hüseyin Gülen
Publikováno v:
Journal of Pediatric Research, Vol 7, Iss 4, Pp 365-367 (2020)
Transfusion-related acute lung injury (TRALI) is a non-cardiac pulmonary edema presenting with severe dyspnea, hypoxia and bilateral diffuse infiltrates on chest X-ray. It usually occurs within the first 6 hours following the administration of plasma
Externí odkaz:
https://doaj.org/article/51c0862fd4a340d0948aedf8bbdfc542
Publikováno v:
Journal of Pediatric Research, Vol 7, Iss 3, Pp 264-266 (2020)
Eosinophilic gastroenteropathies are rare disorders. An 18-year-old girl presented to the hospital with abdominal pain and distension. Abdominal tenderness and grade 2 ascites, serious peripheral eosinophilia and high immunoglobulin E level were foun
Externí odkaz:
https://doaj.org/article/59319bbd3c1647bab7fc7276ffea3611
Publikováno v:
Journal of Behçet Uz Children's Hospital, Vol 9, Iss 3, Pp 263-267 (2019)
Introduction: Sweet syndrome is characterized by fever, arthralgia, neutrophilic leukocytosis and painful erythematous plaques, which occur mostly on the face and upper extremities. It is a rare skin disease characterized by dense neutrophilic infilt
Externí odkaz:
https://doaj.org/article/2affba8919304c3a8915fd4708f8d124
Publikováno v:
Journal of Pediatric Research, Vol 5, Iss 4, Pp 225-227 (2018)
Severe congenital neutropenia is a hereditary disease characterized by a low number of neutrophils occurring from the first months of life leading to severe infections. It is rare but threatens life because of severe infections. For this reason, earl
Externí odkaz:
https://doaj.org/article/86f6afcde95a4bb9bbe2c2ee2924706a
Publikováno v:
Turkish Journal of Hematology, Vol 28, Iss 01, Pp 63-67 (2011)
We report two male cases (4- and 5-years-old) of intrathecal methotrexate overdose. The two boys with acute lymphoblastic leukemia were to receive intrathecal injection of methotrexate. Instead of the prescribed 12 mg, they both received a dose of 12
Externí odkaz:
https://doaj.org/article/f2c122812da74c4b9a5dd91d7cd71fd5
Autor:
Burçak Tatlı Güneş, Arzu Yazal Erdem, Arzu Akcay, Hüseyin Gülen, Hale Ören, Birol Baytan, Işık Odaman Al, Mehmet Fatih Orhan, Sema Aylan Gelen, Burcu Belen, Namik Ozbek, T. Karapınar, Aylin Canpolat, Özlem Tüfekçi, Melike Sezgin Evim, Yeşim Oymak, Gülyüz Öztürk, Lale Olcay, Ayşen Türedi Yıldırım, Nazan Sarper, Adalet Meral Güneş, Meryem Albayrak, Emine Zengin, Sibel Akpınar, Neşe Yaralı
Publikováno v:
Turkish Journal of Hematology
This study aimed to evaluate systemic thrombolysis experiences with recombinant tissue plasminogen activator (rtPA).Retrospective data were collected from 13 Turkish pediatric hematology centers. The dose and duration of rtPA treatment, concomitant a