Zobrazeno 1 - 10
of 35
pro vyhledávání: '"Didem Torun"'
Autor:
Didem Torun Özkan, Nejat Akar
Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 19, Iss 3, Pp 271-272 (2018)
Macrothrombocytopenia is a congenital autosomal dominant blood disorder characterized by increased platelet size and decreased number of circulating platelets (Althaus and Greinacher, 2009). Here, we report a 32 year old beta thalassemia major patien
Externí odkaz:
https://doaj.org/article/8515f7e044714838a16fc7f5f2f5b1f1
Publikováno v:
Turkish Journal of Hematology, Vol 28, Iss 04, Pp 276-285 (2011)
Objective: Ankaferd® Blood Stopper (ABS) is an herbal extract that has historically been used as a hemostatic agent in traditional Turkish medicine. ABS is comprised of a standardized herbal mixture of T. vulgaris, G. glabra, V. vinifera, A. officin
Externí odkaz:
https://doaj.org/article/ab7f2a5d987f41629d32f1073468b2b3
Publikováno v:
Turkish Journal of Hematology, Vol 28, Iss 04, Pp 354-356 (2011)
Externí odkaz:
https://doaj.org/article/adaca48b63e74190afd4a686f467352b
Publikováno v:
Turkish Journal of Hematology, Vol 31, Iss 3, Pp 317-318 (2014)
Externí odkaz:
https://doaj.org/article/98d398dc2e9f441a9dac03b2d4cbd370
Autor:
OZKAN, Didem TORUN, AKIN, Dilara Fatma
Publikováno v:
Journal of Health Sciences / Sağlık Bilimleri Dergisi; Aug2024, Vol. 33 Issue 2, p224-234, 11p
Autor:
Yeşim Oymak, Didem Torun Ozkan, Abdullah Abdul Waheed, Uygar H. Tazebay, Zihni Onur Çalişkaner, Ayten Kandilci, Nejat Akar, Merve Tuzlakoglu Ozturk
Publikováno v:
Turkish Journal of Medical Sciences
Background/aim Macrothrombocytopenia is an autosomal dominant disorder characterized by increased platelet size and decreased number of circulating platelets. Membrane skeleton and the link between actin filaments of the skeleton and microtubules, wh
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4359b90e8850a6433c59c63fc387d742
https://doi.org/10.3906/sag-2003-259
https://doi.org/10.3906/sag-2003-259
Publikováno v:
Lokman Hekim Health Sciences. 1:14-31
Introduction: It has been aimed to analyze the role of pathogenic effects of mutation and expression anomalies occurring on diaphanous-related formin 1 (DIAPH1), WASP actin nucleation-promoting factor (WASP), myosin heavy chain 9 (MYH9), actinin alph
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2dfbd8fc05b9b2612e404842fc1eed90
https://doi.org/10.14744/lhhs.2021.70004
https://doi.org/10.14744/lhhs.2021.70004
Autor:
Nejat Akar, Didem Torun Ozkan
Publikováno v:
Turkish Journal of Clinics and Laboratory. 11:75-79
Protein C inhibitor is a non-specific serine protease inhibitor with extensive protease reactivity. Protein C inhibitor (SERPINA5, plasminogen activator inhibitor-3/PAI-3) is a secreted, extracellular clade A serpin. SERPINA5/PCI has originally been
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d13de8ef5843a47e6268a8470c8cb585
https://doi.org/10.18663/tjcl.645392
https://doi.org/10.18663/tjcl.645392
Publikováno v:
Acta Haematologica. 143:529-532
Introduction: Congenital afibrinogenemia is a rare autosomal recessive disorder characterized by bleeding that varies from mild to severe and by complete absence or extremely low levels of plasma and platelet fibrinogen. Hypofibrinogenemia is charact
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b3819346b0ffb2e441adc6488ba585df
https://doi.org/10.1159/000505174
https://doi.org/10.1159/000505174
Introduction: Congenital afibrinogenemia is a rare autosomal recessive disorder characterized by bleeding that varies from mild to severe and by complete absence or extremely low levels of plasma and platelet fibrinogen. Hypofibrinogenemia is charact
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______4483::18b7fa0186aae0a4d8c27d41369206eb
http://hdl.handle.net/20.500.11851/4008
http://hdl.handle.net/20.500.11851/4008
