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Publikováno v:
Medical Journal of Suleyman Demirel University. 2018, Vol. 25 Issue 4, p400-406. 7p.
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
Autor:
Yasemin Ardicoglu Akisin, Nejat Akar
We read with great interest the paper on ‘A report of Hb Fontainebleau [α21 (B2) Ala > Pro] as a result of founder effect Phenomenon’ that appeared in a recent issue of the journal with great interest by Jalalia et al. However, although they dis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a1e0f614e3eda8af384151b77026a0fd
http://hdl.handle.net/20.500.11851/3712
http://hdl.handle.net/20.500.11851/3712
Publikováno v:
Volume: 49, Issue: 2 180-183
Zeynep Kamil Tıp Bülteni
Zeynep Kamil Tıp Bülteni
Amaç: Folat metabolik yolağı nükleotid sentezi ve DNA metilasyonu için gerekli olduğundan lösemi gelişimde önemli rol oynamaktadır. Folat eksikliği, DNA kırıklarına sebep olmaktadır. Bu yüzden folatla ilişkili polimorfizmler, çocukl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f31fabff069eb0f30b8cde0d8f872cc3
https://doi.org/10.16948/zktipb.379688
https://doi.org/10.16948/zktipb.379688
Publikováno v:
Turkish Journal of Hematology
Turkish Journal of Hematology, Vol 34, Iss 1, Pp 93-98 (2017)
Turkish Journal of Hematology, Vol 34, Iss 1, Pp 93-98 (2017)
Objective: Ankaferd hemostat (Ankaferd Blood Stopper®, ABS)- induced pharmacological modulation of essential erythroid proteins can cause vital erythroid aggregation via acting on fibrinogen gamma. Topical endoscopic ABS application is effective in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fc271a5583cb9a53b63723d04f9e58e6
http://europepmc.org/articles/PMC5451695
http://europepmc.org/articles/PMC5451695
Autor:
Baysun, Şahika, Akar, M Nejat
Publikováno v:
Journal of Paediatrics and Child Health
[No abstract available]
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e69887131656b7de47dc7f70e4d0d145
https://doi.org/10.1111/jpc.15105
https://doi.org/10.1111/jpc.15105
Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 21, Iss 1, Pp 1-2 (2020)
[No abstract available]
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::475fc2e98e56c7919a6a9312a175aa6c
http://hdl.handle.net/20.500.11851/3711
http://hdl.handle.net/20.500.11851/3711
Publikováno v:
Journal of Pediatric Research, Vol 6, Iss 1, Pp 86-87 (2019)
[No abstract available]
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2b0c3668c5cd018880bb99cb16794461
http://hdl.handle.net/20.500.11851/3779
http://hdl.handle.net/20.500.11851/3779