Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Mahmut Çerkez Ergoren"'
Publikováno v:
Biomedicines, Vol 12, Iss 3, p 695 (2024)
Chronic venous insufficiency (CVI) is a common medical condition characterized by impaired functioning of the venous system in the lower extremities. It leads to various symptoms, including varicose veins, leg edema, and skin pigmentation. It is beli
Externí odkaz:
https://doaj.org/article/8480e2a1a4964efa9c637b3a98f4dfab
Publikováno v:
Genetic Syndromes ISBN: 9783319668161
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8cda70a4d57d97a1e5c3ac4af1cab309
https://doi.org/10.1007/978-3-319-66816-1_1781-1
https://doi.org/10.1007/978-3-319-66816-1_1781-1
Autor:
Gulten Tuncel, Burcin Sanlıdag, Eray Dirik, Tugba Baris, Mahmut Cerkez Ergoren, Sehime Gulsun Temel
Publikováno v:
Global Medical Genetics, Vol 10, Iss 03, Pp 240-246 (2023)
Spinal muscular atrophy (SMA) is a rare, recessively inherited neurodegenerative disorder caused by the presence of pathogenic variants in the SMN gene. As it is the leading inherited cause of infant mortality, identification of SMN gene pathogenic v
Externí odkaz:
https://doaj.org/article/d393add898a843b9b163c7108e2bbea4
Autor:
Ibrahim Boga, Sebnem Ozemri Sag, Nilgun Duman, Sevda Yesim Ozdemir, Mahmut Cerkez Ergoren, Kubilay Dalci, Cem Mujde, Cem Kaan Parsak, Cagla Rencuzogullari, Ozge Sonmezler, Orcun Yalav, Adem Alemdar, Lamiya Aliyeva, Ozlem Bozkurt, Sibel Cetintas, Erdem Cubukcu, Adem Deligonul, Berkcan Dogan, Cemre Ornek Erguzeloglu, Turkkan Evrensel, Sehsuvar Gokgoz, Kazim Senol, Sahsine Tolunay, Esra Akyurek, Neslihan Basgoz, Nuriye Gökçe, Bilge Dundar, Figen Ozturk, Duygu Taskin, Mercan Demirtas, Murat Cag, Omer Diker, Polat Olgun, Sevcan Tug Bozdogan, Munis Dundar, Atil Bisgin, Sehime Gulsun Temel
Publikováno v:
European Journal of Breast Health, Vol 19, Iss 3, Pp 235-252 (2023)
Objective:Breast cancer (BC) is the most common cancer type in women and may be inherited, mostly in an autosomal dominant pattern. The clinical diagnosis of BC relies on the published diagnostic criteria, and analysis of two genes, BRCA1 and BRCA2,
Externí odkaz:
https://doaj.org/article/a71c390801df4f9498bd73b6b92a7cb8
Autor:
Aya Badeea Ismail, Mehmet Sait Dundar, Cemre Ornek Erguzeloglu, Mahmut Cerkez Ergoren, Adem Alemdar, Sebnem Ozemri Sag, Sehime Gulsun Temel
Publikováno v:
Biomedicines, Vol 12, Iss 5, p 968 (2024)
Alzheimer’s disease (AD) is a major global health challenge, especially among individuals aged 65 or older. According to population health studies, Turkey has the highest AD prevalence in the Middle East and Europe. To accurately determine the freq
Externí odkaz:
https://doaj.org/article/911415175df84fada0540492352d7bd9
Autor:
Ayhan Kubar, Sehime Gülsüm Temel, Serdar Beken, Gizem Onder, Ozden Hatirnaz, Ayse Korkmaz, Yasemin Alanay, Ugur Ozbek, Sebnem Ozemri Sag, Mahmut Cerkez Ergoren, Elif Kubar, Candan Zeynep Sonmezalp, Ozlem Doğan
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 11, Iss 12, Pp n/a-n/a (2023)
Abstract Background Nucleic acid‐based assays provide an opportunity to screen for genetically encoded diseases like spinal muscular atrophy (SMA), before the onset of symptoms. Nowadays, such assays could be easily utilized as high‐throughputs i
Externí odkaz:
https://doaj.org/article/8e9b296ac0c9461bbb8e809e7092feb7
Autor:
Begimai Mamurova, Gokce Akan, Evren Mogol, Ayla Turgay, Gulten Tuncel, Emine Unal Evren, Hakan Evren, Kaya Suer, Tamer Sanlidag, Mahmut Cerkez Ergoren
Publikováno v:
Global Medical Genetics, Vol 10, Iss 01, Pp 027-033 (2023)
A coronavirus disease 2019 (COVID-19) disease, caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), has created significant concern since December 2019 worldwide. The virus is known to be highly transmissible. Heterogenic clini
Externí odkaz:
https://doaj.org/article/914516cd73564b00b707c8f3f3c277ac
Autor:
Mahmut Cerkez Ergoren, Gokce Akan, Emrah Guler, Gulten Tuncel, Damla Akovalı, Emine Unal Evren, Hakan Evren, Huseyin Kaya Suer, Tamer Sanlidag
Publikováno v:
Global Medical Genetics, Vol 10, Iss 01, Pp 22-26 (2023)
Data consisting of millions of cases cannot still explain the immunopathogenesis mechanism between severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection and host cell for ongoing coronavirus disease 2019 (COVID-19) pandemics. Epidemi
Externí odkaz:
https://doaj.org/article/b5242bce0c5b437f95923d0cba57a0ed
Publikováno v:
Global Medical Genetics, Vol 09, Iss 03, Pp 252-257 (2022)
Variants (Alfa, Gamma, Beta, and Delta) of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) are circulating worldwide. These variants of concerns share some common mutations but they also have distinguishing mutations. These mutations aff
Externí odkaz:
https://doaj.org/article/50436c61413e40b5aebc492cfea1673c
Publikováno v:
Global Medical Genetics, Vol 09, Iss 02, Pp 072-075 (2022)
Prenatal testing provides crucial information about the health status of fetuses as well as recommending better treatment. For the past decades, prenatal testing using chorionic villus sampling and amniocentesis were the two majorly used forms of inv
Externí odkaz:
https://doaj.org/article/4ca87a45db914346a27a210939680d10