Zobrazeno 1 - 10
of 49
pro vyhledávání: '"Ebru Yılmaz KESKİN"'
Autor:
İbrahim Cemal Maslak, Muhammed Burak Selver, Ömer Kaşkaya, Merve Bayrak Yıldırım, Ayşe Çiğdem Sivrice, Mahmut Keskin, Ebru Sagay, Ebru Yılmaz Keskin
Publikováno v:
Turkish Archives of Pediatrics, Vol 59, Iss 4, Pp 419-421 (2024)
Externí odkaz:
https://doaj.org/article/41c7e85d8ba848719ea714acf6eaa9b0
Autor:
Emel Uzunoğlu, Ebru Yılmaz Keskin
Publikováno v:
The Journal of Pediatric Academy, Vol 5, Iss 1, Pp 7-13 (2024)
Iron deficiency anemia (IDA) and β-thalassemia trait (BTT) are the most common causes of hypochromic microcytic anemia (HMA). Various erythrocyte indices that may help in the initial discrimination between IDA and BTT have been reported, but data ev
Externí odkaz:
https://doaj.org/article/a62df9063d8a4b4f8df121227e2b7fce
Autor:
Yılmaz Keskin, Ebru
Tez (doktora) -- Ondokuz Mayıs Üniversitesi, 2005 Libra Kayıt No: 17042 Denemede, 17 -metiltestosteron hormonu kullanımının lepistes balıklarında (Poecilia reticulata Peters, 1860) renk oluşumu ve üreme üzerine etkileri incelenmiştir.Üç
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______9773::d79f8fa628e4232661e721b2af4e4d45
http://libra.omu.edu.tr/tezler/17042.pdf
http://libra.omu.edu.tr/tezler/17042.pdf
Autor:
Tahir Atik, Esra Işık, Hüseyin Onay, Bilçağ Akgün, Moharram Shamsali, Kaan Kavaklo, Melike Evim, Gülen Tüysüz, Namık Yaşar Özbek, Fahri Şahin, Zafer Salcıoğlu, Canan Albayrak, Yeşim Oymak, Ekrem Ünal, Fatma Burcu Belen, Ebru Yılmaz Keskin, Can Balkan, Birol Baytan, Alphan Küpesiz, Vildan Culha, Tuba Nur Tahtakesen, Adalet Meral Güneş, Ferda Özkınay
Publikováno v:
Turkish Journal of Hematology, Vol 37, Iss 3, Pp 145-153 (2020)
Objective: Hemophilia A (HA) is the most severe X-linked inherited bleeding disorder caused by hemizygous mutations in the factor 8 (F8) gene. The aim of this study is to determine the mutation spectrum of the F8 gene in a large HA cohort from Turkey
Externí odkaz:
https://doaj.org/article/739b1796010f4465a28442c9b6243a1b
Publikováno v:
Journal of Contemporary Medicine, Vol 9, Iss 4, Pp 359-364 (2019)
AbstractAim: Analysis of the data of children following stem cell transplantation.Materials and Methods: A total of 44 children who received stem cell transplant between February 2009 and May 2011 were evaluated retrospectively. Results: Among the pa
Externí odkaz:
https://doaj.org/article/6d7c342c8c8a42c98744e9be5977b6e9
Publikováno v:
Turkish Journal of Hematology, Vol 36, Iss 4, Pp 299-301 (2019)
Externí odkaz:
https://doaj.org/article/c24600b57f364930bb050540bd028310
Autor:
Selman Kesici, Ebru Yılmaz Keskin, Samuel C.c. Chiang, Çiğdem Seher Kasapkara, Takuya Sekine, Meltem Akçaboy, Ali Fettah, Yenan T. Bryceson
Publikováno v:
Turkish Journal of Hematology, Vol 35, Iss 3, Pp 200-202 (2018)
Externí odkaz:
https://doaj.org/article/26bea762471348f4b78fe3fa296fc7b1
Autor:
Ebru Yılmaz Keskin, İdil Yenicesu
Publikováno v:
Turkish Journal of Hematology, Vol 32, Iss 1, Pp 1-14 (2015)
Demir, oksijenin taşınması, DNA sentezi ve hücre çoğalması gibi çeşitli biyolojik reaksiyonlar için vazgeçilmez olduğundan, yaşam için zorunludur. Demir metabolizması ve bu elementin düzenlenmesiyle ilgili bilgilerimiz, son yıllarda
Externí odkaz:
https://doaj.org/article/0adfb0c8f76941dabeb87d6f9296b4a0
Autor:
Mustafa Kılıç, David Stephen Cram, Ebru Yılmaz Keskin, Gonca Sandal, Deniz Torun, Asburce Olgac, Çiğdem Seher Kasapkara, Johannes Häberle
Publikováno v:
Journal of Pediatric Endocrinology and Metabolism. 33:1349-1352
Objectives Carbonic anhydrase VA (CAVA) deficiency is a rare autosomal recessive inborn error of metabolism that leads to acute metabolic crises, especially in the neonatal or infantile period. It is caused by a deficiency of the enzyme CAVA, which i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::32ff34aead313f97c0e72d59c5d7da4d
https://doi.org/10.1515/jpem-2020-0117
https://doi.org/10.1515/jpem-2020-0117
Autor:
Fahri Şahin, Ekrem Unal, Birol Baytan, Fatma Burcu Belen, Ferda Ozkinay, Yeşim Oymak, Vildan Çulha, Gülen Tüysüz, Adalet Meral Güneş, Kaan Kavakli, Bilçağ Akgün, Melike Sezgin Evim, Namik Ozbek, Alphan Kupesiz, Tahir Atik, Esra Isik, Hüseyin Onay, Moharram Shamsali, Can Balkan, Ebru Yılmaz Keskin, Zafer Salcioglu, Canan Albayrak, Tuba Nur Tahtakesen Güçer
Publikováno v:
Turkish Journal of Hematology
Turkish Journal of Hematology, Vol 37, Iss 3, Pp 145-153 (2020)
Turkish Journal of Hematology, Vol 37, Iss 3, Pp 145-153 (2020)
Objective Hemophilia A (HA) is the most severe X-linked inherited bleeding disorder caused by hemizygous mutations in the factor 8 (F8) gene. The aim of this study is to determine the mutation spectrum of the F8 gene in a large HA cohort from Turkey,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d0df3de9d9ceb05d09504bab5835f685
http://europepmc.org/articles/PMC7463214
http://europepmc.org/articles/PMC7463214