Zobrazeno 1 - 10
of 40
pro vyhledávání: '"Burhan Balta"'
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
Autor:
Gozde Ozcan, Burhan Balta, Ahmet Ercan Sekerci, Osman A Etoz, Claudia Martinuzzi, Ozlem Kara, Lorenza Pastorino, Fatma Kocoglu, Omer Ulker, Murat Erdogan
Publikováno v:
Indian Journal of Pathology and Microbiology, Vol 59, Iss 3, Pp 335-338 (2016)
Gorlin–Goltz syndrome (GGS) is an uncommon autosomal dominant inherited disorder which comprises the triad of basal cell carcinomas (BCCs), odontogenic keratocysts, and musculoskeletal malformations. Besides this triad, neurological, ophthalmic, en
Externí odkaz:
https://doaj.org/article/ee2704a075ff4f6fa53566c1b8046d27
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
Autor:
Memoona Ramzan, Duygu Duman, LeShon Chere Peart Hendricks, Shengru Guo, Ahmet Mutlu, Mahmut Tayyar Kalcioglu, Serhat Seyhan, Claudia Carranza, Murtaza Bonyadi, Nejat Mahdieh, Muzeyyen Yildirim-Baylan, Erick Figueroa-Ildefonso, Ozgul Alper, Tahir Atik, Abdurrahman Ayral, Nazim Bozan, Burhan Balta, Christian Rivas, Gabrielle N. Manzoli, Fabiola Huesca-Hernandez, Raja A. H. Kuchay, Merve Durgut, Guney Bademci, Mustafa Tekin
Hearing loss (HL) is a common heterogeneous trait that involves variants in more than 200 genes. In this study, we utilized exome (ES) and genome sequencing (GS) to effectively identify the genetic cause of presumably non-syndromic HL in 322 families
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7b34b9d561748a50db02b17e2cdc5635
https://hdl.handle.net/20.500.12866/13603
https://hdl.handle.net/20.500.12866/13603
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
Autor:
Murat ERDOĞAN, Hakan GÜMÜŞ, Didem Behice ÖZTOP, Burhan BALTA, Keziban KORKMAZ BAYRAM, Munis DÜNDAR
Publikováno v:
Volume: 44, Issue: 2 165-171
Cumhuriyet Medical Journal
Cumhuriyet Medical Journal
Cyclin-dependent kinase-like 5 (CDKL5, OMIM 300203), also known as STK9 (serine/threonine kinase 9), is a gene that is thought to play a role in the production of proteins involved in the normal development of the brain, although its function is not
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8c38be2946ba162dcb0ec5c82726e667
https://dergipark.org.tr/tr/pub/cmj/issue/70991/1121531
https://dergipark.org.tr/tr/pub/cmj/issue/70991/1121531
Publikováno v:
Molecular Biology Reports. 47:1835-1843
Familial Mediterranean fever is an auto inflammatory genetic disease involving especially Turks, Armenians, Arabs and non-Ashkenazi Jews and caused by variants in the MEFV gene. In this study, we aimed to evaluate the distribution and frequency of cl
Autor:
Sevgi Pekcan, Murat Faik Erdogan, Gizem Akıncı Gönen, Fatih Süheyl Ezgü, Burhan Balta, Ayse Gul Zamani, Mehmet Köse, Mahmut Selman Zamani, Ayse Tana Aslan, Melih Hangül, Tuğba Şişmanlar Eyüpoğlu, Tugba Ramasli Gursoy, Aslihan Kiraz
Publikováno v:
Balkan Medical Journal, Vol 38, Iss 6, Pp 357-364 (2021)
BACKGROUND Cystic fibrosis, a pulmonary disease which is an autosomal recessive, inherited, multisystemic genetic disease commonly seen in the Caucasian race, is the most frequent cause of mortality and morbidity. So far, more than 2000 disease-causi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aed3e641d6e39dfdf6ab29c3ca21ba08
https://avesis.gazi.edu.tr/publication/details/0af87497-6585-42da-9f1c-4a903abd918b/oai
https://avesis.gazi.edu.tr/publication/details/0af87497-6585-42da-9f1c-4a903abd918b/oai