Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Hilmi Isi"'
Publikováno v:
Dicle Medical Journal, Vol 45, Iss 2, Pp 219-222 (2018)
Volume: 45, Issue: 2 219-222
Dicle Tıp Dergisi
Volume: 45, Issue: 2 219-222
Dicle Tıp Dergisi
Klinefeltersendromu ilk tanımlanan kromozom bozukluğu olup temel olarak hipergonadotropikhipogonadizm ve önükoid vücut yapısı ile karakterizedir. Sıklığı 500-1000 canlı doğumda birdir. Klinefelter sendromunun genel özelliklerini uzun bo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4803b114fdb44590ccbee9c2dc80007a
https://hdl.handle.net/20.500.12809/8247
https://hdl.handle.net/20.500.12809/8247
Autor:
Turgay Budak, Mahmut Balkan, Hilmi Isi, M. Nail Alp, Mehmet Fidanboy, Sevgi Kalkanli, Halit Akbas
Publikováno v:
Journal of Pediatric Genetics. :243-246
We report a case of complete tetraploidy in amniotic fluid culture obtained at 17 wk of pregnancy. Amniocentesis was performed in this pregnancy because of a high-risk maternal serum screening result and abnormal ultrasound findings. Amniotic fluid w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::52a8f8e20f0403934d8f21c565912876
https://doi.org/10.3233/pge-12039
https://doi.org/10.3233/pge-12039
Publikováno v:
Turkiye Klinikleri Journal of Medical Sciences. 32:1554-1559
Objective: We aimed to prospectively evaluate the effects of pegylated interferon alpha2a and alpha-2b therapy on chromosomal aberrations and mitotic index in patients with chronic hepatitis B. Material and Methods: Fifty patients with chronic hepati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8e6390556bd9d8680e1b9bf7ba66b250
https://doi.org/10.5336/medsci.2011-26395
https://doi.org/10.5336/medsci.2011-26395
Autor:
Mehmet Fidanboy, Turgay Budak, Abdullah Gedik, Ayşegül Türkyılmaz, Halit Akbas, Sevgi Kalkanli, Hilmi Isi, M N Alp, Selda Şimşek, Mahmut Balkan, Diclehan Oral
Publikováno v:
Genetics and Molecular Research. 9:1094-1103
We reviewed cytogenetic studies performed on 4216 patients who were referred to the Cytogenetics Unit at Dicle University Hospital, Diyarbair, Southeast Turkey, between 2000 and 2009. The cases were grouped according to the reason of referral for cyt
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f9717d1c1ad46e337b56e47304efd6b0
https://doi.org/10.4238/vol9-2gmr827
https://doi.org/10.4238/vol9-2gmr827
Autor:
Hilmi Isi, S. Akdeniz, Selahattin Tekes, Mahmut Balkan, Tuba Gökdoğan Edgünlü, Mehmet Emin Erdal, Turgay Budak, Özlem İzci Ay, B. Sula, Diclehan Oral
Publikováno v:
Biotechnology & Biotechnological Equipment. 24:2014-2019
Behcet's disease (BD) is a chronic, multisystemic inflammatory disease. The specific etiology of BD remains elusive, but the interaction between infectious-agent exposure and genetic factors may have a role. In this report, we aim to investigate the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d6ff47209250b90775bdbf6705b89f4b
https://doi.org/10.2478/v10133-010-0055-x
https://doi.org/10.2478/v10133-010-0055-x
Autor:
Hilmi Isi, G. Ates, C. Sinir, Mehmet Emin Erdal, Özlem İzci Ay, Gözde Türköz, T. Yildiz, Diclehan Oral
Publikováno v:
Biotechnology & Biotechnological Equipment. 24:1638-1643
Asthma is a chronic inflammatory disorder of the airways in which many cells and cellular elements play a role. Like other atopic diseases, asthma is a complex disorder caused by interactions between multiple genes of small to modest effect and equal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e6d5cc4098dfa09f59a4024caa241444
https://doi.org/10.2478/v10133-010-0018-2
https://doi.org/10.2478/v10133-010-0018-2
Autor:
Hilmi Isi, Timucin Cil, Abdullah Altintas, Orhan Ayyildiz, Sabri Batun, Semir Pasa, Nurten Akdeniz, Murat Yurt
Publikováno v:
Annals of Hematology. 86:727-731
Factor V Leiden (FV-Leiden) and prothrombin gene mutations (FII G20210A) are well-established independent risk factors for thrombosis. In the recent years, many studies have suggested that these mutations are associated with an increased risk of recu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::14ccbbe20a6b2bc490065e1e84f81abd
https://doi.org/10.1007/s00277-007-0327-1
https://doi.org/10.1007/s00277-007-0327-1
Publikováno v:
Dicle Medical Journal, Vol 32, Iss 3, Pp 149-152 (2005)
Case was 14 years-old girl having complaints of growth retardations and primary amenorrhea. In the physical and gynecological examinations; her height and weight were 130 cm and 45 kg, respectively and secondary sex characteristics were infantile and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doajarticles::bcad721c27af4f087a260e0fd63f7e41
http://4181.indexcopernicus.com/fulltxt.php?ICID=888055
http://4181.indexcopernicus.com/fulltxt.php?ICID=888055
Publikováno v:
Dicle Medical Journal, Vol 31, Iss 3, Pp 1-6 (2004)
Beginning with the therapeutic dose and increasing three differentdoses and three different periods of time Bleomycin (Bleomycin 0.3 μg/ml, 3μg/ml and 30 μg/ml, 6,24, 48 hours) were added to blood which was beingcultured on 5 samples who were expo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doajarticles::8a1168af40a930599bb2d68d291e4bd0
http://4181.indexcopernicus.com/fulltxt.php?ICID=887940
http://4181.indexcopernicus.com/fulltxt.php?ICID=887940
Publikováno v:
Dicle Medical Journal, Vol 31, Iss 2, Pp 4-8 (2004)
Beginning with the therapeutic dose and increasing three differentdoses and three different periods of time Bleomycin (Bleomycin 0.3 μg/ml, 3μg/ml and 30 μg/ml, 6, 24, 48 hours) were added to blood which was beingcultured on 5 samples who were exp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doajarticles::378a011ebc9901837393d4859ff8ad56
http://4181.indexcopernicus.com/fulltxt.php?ICID=887895
http://4181.indexcopernicus.com/fulltxt.php?ICID=887895