Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Aslıhan Kiraz"'
Autor:
Murat Erdoğan, Mehmet Köse, Sevgi Pekcan, Melih Hangül, Burhan Balta, Aslıhan Kiraz, Gizem Akıncı Gönen, Ayşe Gül Zamani, Mahmut Selam Yıldırım, Tuğba Ramaslı Gürsoy, Fatih Ezgu, Tuğba Şişmanlar Eyüpoğlu, Ayse Tana Aslan
Publikováno v:
Balkan Medical Journal, Vol 38, Iss 6, Pp 357-364 (2021)
Externí odkaz:
https://doaj.org/article/ec5ce3ddafe34a4b840ad5e9b836d007
Publikováno v:
Ahi Evran Medical Journal, Vol 5, Iss 1, Pp 8-12 (2021)
Purpose: Recurrent pregnancy loss (RPL) is called as loss of two or more clinically defined pregnancies. The causes of RPL include chromosomal abnormalities, endocrinological disorders, autoimmune problems, uterine anomalies, and thrombophilic factor
Externí odkaz:
https://doaj.org/article/4c2b3ca85a64415ca629329ea1e1fe25
Publikováno v:
Turkish Journal of Hematology, Vol 36, Iss 1, Pp 25-28 (2019)
Objective: Hyperferritinemia cataract syndrome (HFCS) is an autosomal dominantly inherited disease characterized by increased serum ferritin levels and bilateral cataract formation in the early period of life. Heterozygote mutations in the 5' untrans
Externí odkaz:
https://doaj.org/article/56cfe4d84c77467a92931b89717214c1
Publikováno v:
Anatolian Journal of Cardiology, Vol 25, Iss 10, Pp 745-746 (2021)
Externí odkaz:
https://doaj.org/article/fecaa5e83a10456ea100ddc454a4075d
Publikováno v:
Tuberk Toraks. 71:34-40
Autor:
Aslıhan Kiraz, Ozlem Sezer, Adem Alemdar, Sezin Canbek, Nilgun Duman, Atıl Bisgin, Tulin Cora, Hatice Ilgın Ruhi, Mahmut Cerkez Ergoren, Bilgen Bilge Geçkinli, Sebnem Ozemri Sag, Hilmi Erdem Gözden, Ozlem Oz, Zuhal Mert Altıntaş, Sinem Yalcıntepe, Adem Keskin, Ayşegül Yabacı Tak, Şeyma Aktaş Paskal, Uğur Fahri Yürekli, Mercan Demirtas, Emine Unal Evren, Abdullah Hanta, Müşerref Başdemirci, Kaya Suer, Burhan Balta, Nadir Kocak, Halil Gürhan Karabulut, Havva Cobanogulları, Esra Arslan Ateş, Sevcan Tuğ Bozdoğan, Damla Eker, Sadiye Ekinci, Süleyman Nergiz, Timur Tuncalı, Serap Yagbasan, Ceren Alavanda, Nuket Yurur Kutlay, Hakan Evren, Murat Erdoğan, Sule Altıner, Tamer Sanlidag, Gizem Akıncı Gonen, Arzu Vicdan, Nazan Eras, Hatice Koçak Eker, Ozgür Balasar, Gulten Tuncel, Munis Dundar, Hakan Gurkan, Sehime Gulsun Temel
Thrombotic and microangiopathic effects have been reported in COVID-19 patients. This study examined the contribution of the hereditary thrombophilia factors Prothrombin (FII) and Factor V Leiden (FVL) genotypes to the severity of COVID-19 disease an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::012a2db7faa6ca88f32d5fd353b005ee
https://hdl.handle.net/11424/287280
https://hdl.handle.net/11424/287280
Publikováno v:
Volume: 23, Issue: 3 468-475
Kırıkkale Üniversitesi Tıp Fakültesi Dergisi
Kırıkkale Üniversitesi Tıp Fakültesi Dergisi
Objective: Infertility is defined as absence of a healthy baby or pregnancy despite a one-year regular unprotected sexual intercourse. While primary infertility is called the absence of pregnancy at all, secondary infertility is called inability of c
© 2022 Wiley Periodicals LLC.Beaulieu-Boycott-Innes syndrome (BBIS; MIM#613680) is a rare, autosomal recessive neurodevelopmental genetic disorder associated with pathogenic variants in the THOC6 gene (*615403). Intellectual disability, dysmorphic f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b2c9f14cd373ba4df1ab93b46600375e
https://avesis.kayseri.edu.tr/publication/details/5ca4f0c7-810d-479a-b9a0-d40c7139dd68/oai
https://avesis.kayseri.edu.tr/publication/details/5ca4f0c7-810d-479a-b9a0-d40c7139dd68/oai
Publikováno v:
Anatolian Journal of Cardiology, Vol 25, Iss 10, Pp 745-746 (2021)
Anatol J Cardiol
Anatol J Cardiol
Restrictive cardiomyopathy (RCM) is a rare disease characterized by restrictive filling and decreased diastolic volume of the heart. It is the rarest cardiomyopathy among all cardiomyopathies with approximately 2.5%–5% ratio (1). The prognosis is p
Autor:
Aslıhan Kiraz
Publikováno v:
The journal of Tepecik Education and Research Hospital.
Objective: This study aims to compare the diagnostic effectiveness of fragment analysis and next-generation sequencing methods in Familial Mediterranean Fever (FMF) disease. Data from the study will guide clinicians in the diagnosis of FMF patients M