Zobrazeno 1 - 10
of 51
pro vyhledávání: '"Ozturk, Ozdemir"'
Publikováno v:
In AEUE - International Journal of Electronics and Communications March 2023 161
Autor:
Malik Ejder Yildirim, Hande Kucuk Kurtulgan, Ozturk Ozdemir, Hasan Kilicgun, Didem S. Aydemir, Burak Baser, Ilhan Sezgin
Publikováno v:
Annals of Saudi Medicine, Vol 39, Iss 6, Pp 382-387 (2019)
BACKGROUND: Familial Mediterranean fever (FMF), an autosomal recessive, autoinflammatory disease that is common in Arabs, Jews, Armenians and Turks, is caused by mutations in the MEFV gene, which encodes a protein called pyrin. The disease is charact
Externí odkaz:
https://doaj.org/article/007e1e1917cc4faca68662cd59df76a7
Autor:
Jelena Velickovic, Fatma Silan, Firdevs Dincsoy Bir, Coskun Silan, Burcu Albuz, Ozturk Ozdemir
Publikováno v:
Autoimmunity, Vol 52, Iss 7-8, Pp 256-263 (2019)
Blau syndrome is an autosomal dominant rare disease caused by mutations in NOD2 gene. Less than 200 patients published with Blau Syndrome Worldwide. We reported a 41-year old female Turkish patient diagnosed as Blau syndrome. Granulomatous dermatitis
Externí odkaz:
https://doaj.org/article/e44b04f0c0f0414aa381821e38b14122
Publikováno v:
Family Practice and Palliative Care, Vol 4, Iss 1, Pp 1-6 (2019)
Introduction: The non-invasive prenataldiagnosis of the fetus RhD genotype in RhD incompatibility has a crucial rolein the prevention of increased anti-D immunoglobulin therapy for haemolyticdiseases in pregnant women carrying RhD negative fetus. It
Externí odkaz:
https://doaj.org/article/cf83de03c4424f21ae5fd893ccedbfb0
Publikováno v:
Twin Research and Human Genetics. :1-7
Parkinson’s disease (PD) is a complex disorder with a significant genetic component. Genetic variations associated with PD play a crucial role in the disease’s inheritance and prognosis. Currently, 31 genes have been linked to PD in the OMIM data
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::eb972b69600eaad2a2f155cd8891dda0
https://doi.org/10.1017/thg.2023.14
https://doi.org/10.1017/thg.2023.14
Publikováno v:
Aircraft Engineering and Aerospace Technology, 2018, Vol. 90, Issue 9, pp. 1438-1444.
Externí odkaz:
http://www.emeraldinsight.com/doi/10.1108/AEAT-07-2017-0175
Autor:
Fatma Silan, Romyla Bourouba, Taner Karakaya, Onur Yildiz, Baris Paksoy, Mine Urfali, Ozturk Ozdemir
Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 19, Iss 4, Pp 437-441 (2018)
Background: Rearrangements that occur mainly through the non-allelic homologous recombination (NAHR) during maternal meiosis in short arms of chromosome 8 is relatively associated with various clinical spectrum. Aim: The objective of this study was t
Externí odkaz:
https://doaj.org/article/73bc1d25823b4e519bd702dc73791dfd
Publikováno v:
Family Practice and Palliative Care, Vol 3, Iss 1, Pp 23-27 (2018)
Introduction: Thepresent study aimed to evaluate macular and choroidal thicknesses in childrenwith MEFV gene mutations.Methods: Thirty-five childrenwith MEFV gene mutations and 40 healthy controls were included in the study.MEFV gene profiles for the
Externí odkaz:
https://doaj.org/article/06f5d21b6b2b47a686ac2521603dc4ed
Publikováno v:
Hemoglobin. 46:87-90
Hemoglobinopathies are the most common single-gene disorders, and β-thalassemia (β-thal) imposes a tremendous health burden on Turkey. Thus, premarital carrier screening is obligatory in Turkey, as it is in some other countries. As a result of this
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e033d594896e5b8b484fd0c50a51dace
https://doi.org/10.1080/03630269.2022.2083968
https://doi.org/10.1080/03630269.2022.2083968
Autor:
Ceyhun Karpuz, Gulfem Balasu Firat Unuk, Pinar Ozturk Ozdemir, Alperen Cengiz, Ali Kursad Gorur
Publikováno v:
2023 IEEE Radio and Wireless Symposium (RWS).
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f0593106a33a41fde3c80590f3946238
https://doi.org/10.1109/rws55624.2023.10046308
https://doi.org/10.1109/rws55624.2023.10046308