Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Ayşen Türedi YILDIRIM"'
Autor:
Ayşen Türedi YILDIRIM, Yeşim OYMAK, Yöntem YAMAN, Osman SAATÇİ, Rana MALATYALI, Serra KAMER, Hüdaver ALPER
Publikováno v:
Cukurova Medical Journal, Vol 39, Iss 4, p 0 (2014)
Lösemili hastalarda yoğun kemoterapi, intratekal metotrexate tedavileri ve proflaktik santral sinir sistemi radyoterapisine rağmen ekstramedüller relapslar görülebilmektedir. Akut lenfoblastik lösemili hastalarda izole optik sinir relapsı nad
Externí odkaz:
https://doaj.org/article/0734c5f2488045dea7e69f8aea686a8d
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:
Ayşen TÜREDİ YILDIRIM, Hüseyin GÜLEN, Yeşim YİĞİT, Ahmet ÖZBİLGİN, Serkan BAŞTEMİR, Fatih DÜZGÜN
Publikováno v:
Turkish Journal of Pediatric Disease.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::93afc73b2d2de92046f672c591c9e027
https://doi.org/10.12956/tjpd.2015.149
https://doi.org/10.12956/tjpd.2015.149
Publikováno v:
Hitit Medical Journal, Vol 4, Iss 3, Pp 132-134 (2022)
Porfiriler hem biyosentezinde görevli enzimlerin doğuştan yada kazanılmış bozukluğu, yada eksikliği sonucu oluşan, periferik ve santral sinir sistemini etkileyebilen, farklı alt tipleri olan, nadir görülen metabolik hastalıklardır. Akut
Externí odkaz:
https://doaj.org/article/327486d0322c41f8a8c594671f98ef42
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 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
Autor:
Aysen Turedi Yildirim, Yesim Oymak, Yontem Yaman, Osman Saatci, Rana Malatyali, Serra Kamer, Hudaver Alper
Publikováno v:
Çukurova Üniversitesi Tıp Fakültesi Dergisi, Vol 39, Iss 4, Pp 894-899 (2014)
Notwithstanding extensive chemotherapy, intrathecal methotrexate treatments and prophylactic central nervous system radiotherapy, extramedullary relapses can still be seen in leukemia patients. Isolated optic nerve relapses, one of its symptoms being
Externí odkaz:
https://doaj.org/article/fae109a90719437294b27b26d318e335
Publikováno v:
Cukurova Medical Journal, Vol 38, Iss 4, Pp 805-808 (2013)
Nörofibromatoziz tip 1 (NF1) endokrin bozuklukların eşlik ettiği otozomal dominant geçişli multisistem bir hastalıktır. Nörofibromatoziz tip 1 ve hipertiroidizm birlikteliği nadir görülen bir durumdur. Bugüne kadar yayınlanmış olgular
Externí odkaz:
https://doaj.org/article/807e379c154247359a1a28e226eefdc5
Publikováno v:
Çukurova Üniversitesi Tıp Fakültesi Dergisi, Vol 38, Iss 4, Pp 805-808 (2013)
Neurofibromatosis type 1 (NF1) is an autosomal dominant inherited multisystem disease associated with several endocrine disorders. Association of NF1 and hyperthyroidism is extremely rare. All previously reported cases were in adult age group. Herein
Externí odkaz:
https://doaj.org/article/4b8ebf6df3824bc888e6b8bc303ba7c3