Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Haydar Bağiş"'
Publikováno v:
Clinical Case Reports, Vol 9, Iss 4, Pp 1973-1976 (2021)
Abstract Ellis‐van Creveld syndrome 10‐year‐old Turkish girl and her parents were first degree cousins. A novel pathogenic variant (p.Glu1178Glyfs*82) was detected in the EVC2 gene in patient. She had no peg‐shaped teeth, multiple frenula, an
Externí odkaz:
https://doaj.org/article/6afd816257614977ad2fcb66ab344d28
Publikováno v:
Sakarya Tıp Dergisi, Vol 10, Iss 1, Pp 128-132 (2020)
Rett Sendromu (RS), normal gelişim basamaklarını takiben erken nörolojik regresyon ile tanınan ve kızlarda görülen nörogelişimsel bir hastalıktır. Klasik RS tanısı için; doğum öncesi, doğum sırası, doğum sonrası dönemleri ile i
Externí odkaz:
https://doaj.org/article/1a1785b0e54f45c0b9be887b8d243e2d
Autor:
Celal Güven, Eylem Taşkın, Önder Yumrutaş, Leyla Türker Şener, Fulya Dal, Mufide Ahbab, İbrahim Bozgeyik, Işıl Albeniz, Haydar Bağış, Mustafa Pehlivan, Fatih Üçkardeşler, Handan Akçakaya
Publikováno v:
Turkish Journal of Agriculture: Food Science and Technology, Vol 6, Iss 6, Pp 792-798 (2018)
One of the alternative therapeutic methods is herbal medicine. Leontice leontopetalum belongs to Berberidaceae family. The aim of study was investigated the extract of LL on human pancreatic beta cell-treated with STZ. Materials and methods: The huma
Externí odkaz:
https://doaj.org/article/276cc064c19545bca9f82c2d50188b65
Publikováno v:
Adıyaman Üniversitesi Sağlık Bilimleri Dergisi. 6:128-131
1p 36 delesyon sendromu en sık rastlanılan submikroskopik delesyon sendromlarından bir tanesidir. 1p 36 delesyon sendromlu hastalar; gelişimsel gecikme/zihinsel yetersizlik ve mikrobrakisefali, hipo/hipertelorizm, düz kaşlar, derin gözler, dü
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::000c5785461eaddff7d8c836fbd1a3d6
https://doi.org/10.30569/adiyamansaglik.641603
https://doi.org/10.30569/adiyamansaglik.641603
Publikováno v:
Turkish Journal of Pediatric Disease. :1-5
Aydın, Hilal (Balikesir Author)
Amaç: Fragile-X sendromunda değişen derecelerde zihinsel gerilik, uzun ve dar yüz, öne çıkan alın ve çene yapısı, büyük kulaklar temel bulgulardır. Bu çalışmada Fragile X sendromu tanısı konula
Amaç: Fragile-X sendromunda değişen derecelerde zihinsel gerilik, uzun ve dar yüz, öne çıkan alın ve çene yapısı, büyük kulaklar temel bulgulardır. Bu çalışmada Fragile X sendromu tanısı konula
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::72aea5555e8613ca834bccf118dbc89e
https://doi.org/10.12956/tchd.613271
https://doi.org/10.12956/tchd.613271
Here we report a Turkish child with Ellis-van Creveld syndrome whose presentation was short strature, hypodontia, narrow thorax, dysplastic nails, cardiac abnormality and polydactyly. Genetic analysis revealed novel homozygous mutation in the EVC2 ge
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::97d3e73f1a3f6c4b479b6e591bad01ae
https://doi.org/10.22541/au.160839989.99464782/v1
https://doi.org/10.22541/au.160839989.99464782/v1
Autor:
Ibrahim Bozgeyik, Celal Güven, Atilla Yildiz, Müfide Aydoğan Ahbab, Onder Yumrutas, Işıl Albeniz, Yusuf Özay, Haydar Bağiş, Leyla Türker Şener
Publikováno v:
Volume: 38, Issue: 3 516-524
Cumhuriyet Science Journal
Cumhuriyet Science Journal, Vol 38, Iss 3, Pp 516-524 (2017)
Cumhuriyet Science Journal
Cumhuriyet Science Journal, Vol 38, Iss 3, Pp 516-524 (2017)
Evernia prunastri (L.) Ach, belonging to Parmeliaceae, is animportant lichen species in Turkey. Previous studies was reported that E. prunastri have significantantioxidant, antimicrobial and anticancer compounds in its structure. Althoughantiprolifer
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::884c40de8ab9b2697a624c589853ff6b
https://dergipark.org.tr/tr/pub/csj/issue/31252/340502
https://dergipark.org.tr/tr/pub/csj/issue/31252/340502
Publikováno v:
Volume: 40, Issue: 2 157-162
Turkish Journal of Veterinary and Animal Sciences
Turkish Journal of Veterinary and Animal Sciences
Preimplantation genetic diagnosis is the detection of inherited diseases and the sex of embryos before implantation in the practice of human medicine as well as in veterinary medicine. The introduction of experimental animal embryo biopsy techniques
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2c2ddf28d2f670940cf1710ac037896a
https://app.trdizin.gov.tr/makale/TWpFek16UXlNZz09
https://app.trdizin.gov.tr/makale/TWpFek16UXlNZz09
Publikováno v:
Turkish Journal of Biology. 20:303-311
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f3b87d429f09e7ac41ee197884002676
https://doi.org/10.55730/1300-0152.2535
https://doi.org/10.55730/1300-0152.2535
Publikováno v:
Volume: 33, Issue: 5 393-399
Turkish Journal of Veterinary and Animal Sciences
Turkish Journal of Veterinary and Animal Sciences
BAGIS/0000-0002-1140-8058; WOS: 000271745600005 The objective of this study was to determine the effects of 3 chemical agents used sequentially and electrical stimuli on parthenogenetic activation of in vitro matured bovine oocytes and comparison wit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6f6d6cf097fa86c329e72e843405d1fc
https://hdl.handle.net/20.500.12712/19039
https://hdl.handle.net/20.500.12712/19039