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pro vyhledávání: '"Koçkara, Ayşe"'
Autor:
Koçkara, Ayşe Şeker
Nehcü’l-Ferâdîs, kırk hadis türünde yazılmış mensur bir eserdir. Kerderli Mahmud bin Ali tarafından759’dan önce yazıldığı düşünülmektedir. Eser, her biri onar fasıldan oluşan dört baptan meydanagelir. Birinci bapta Hz. Muham
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3120::cffc439a49e36cc4bb9d1d39e07810c3
https://hdl.handle.net/20.500.11857/2252
https://hdl.handle.net/20.500.11857/2252
Autor:
Koçkara, Ayşe Şeker1 (AUTHOR) doctrayse@gmail.com, Candan, Ferhan1 (AUTHOR), Hüzmeli, Can1 (AUTHOR), Kayataş, Mansur1 (AUTHOR), Alaygut, Demet2 (AUTHOR)
Publikováno v:
Renal Failure. 2013, Vol. 35 Issue 9, p1285-1288. 4p. 1 Black and White Photograph, 1 Chart.
Autor:
Koçkara, Ayşe1 (AUTHOR), Kayataş, Mansur1 (AUTHOR) mansurkay@yahoo.com
Publikováno v:
Renal Failure. 2013, Vol. 35 Issue 2, p291-294. 4p.
Autor:
Koçkara, Ayşe Şeker1 doctrayse@gmail.com, Kayataş, Mansur1, Huzmeli, Can1, Candan, Ferhan1, Gümüş, Cesur2
Publikováno v:
Case Reports in Medicine. 2013, p1-4. 4p.
Autor:
Şeker Koçkara, Ayşe
Akut dekompanse kalp yetersizliği (ADKY), kalp yetersizliği hastalarında majör hastaneye başvuru sebebi olup, her ADKY atağı, hastaların mortalite ve morbiditesini artırmaktadır. Yıllardır loop diüretikleri ADKY atağında ilk basamak te
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_____10208::239e2ebe393d037cd42bbf7a2c71716f
https://acikbilim.yok.gov.tr/handle/20.500.12812/605542
https://acikbilim.yok.gov.tr/handle/20.500.12812/605542
Publikováno v:
Case Reports in Medicine.
Autosomal dominant polycystic kidney disease (ADPKD) is the most common hereditary kidney disease and is responsible for 8–10% of patients with end-stage renal failure. The major extrarenal complications of ADPKD are cardiovascular abnormalities. I
Publikováno v:
European Journal of Rheumatology; Jun2018, Vol. 5 Issue 2, p145-146, 2p
Publikováno v:
European Journal of Rheumatology; 2017, Vol. 4 Issue 3, p14-15, 2p
Publikováno v:
European Journal of Rheumatology; 2016, Vol. 3 Issue 4, p10-11, 2p
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