Zobrazeno 1 - 10
of 27
pro vyhledávání: '"Esra Altan"'
Autor:
Emine Ikbal Atli, Engin Atli, Cihan Inan, Gülizar Fusun Varol, Cisem Mail, Esra Altan Erbilen, Sinem Yalcintepe, Selma Demir, Hakan Gurkan
Publikováno v:
Taiwanese Journal of Obstetrics & Gynecology, Vol 61, Iss 3, Pp 504-509 (2022)
Objective: The 18q terminal deletion with inverted duplication is an extremely rare abnormality, with only three confirmed cases in Europe to date. Here, we report, for the first time, a case of de novo 18q inv-dup-del in a Turkish pregnant woman. Ca
Externí odkaz:
https://doaj.org/article/b84f7b60f23a418c9825d3a874cd3ba2
Publikováno v:
Journal of Pediatric and Neonatal Individualized Medicine, Vol 11, Iss 2, Pp e110226-e110226 (2022)
Krukenberg tumors (KTs) are 1-2% of all ovarian tumors, they are rare in pregnancy, and they have a poor prognosis since they are detected in advanced stages. We report 2 cases of KT in pregnancy. Bilateral giant solid adnexal masses were detected at
Externí odkaz:
https://doaj.org/article/dff7c4b64eba418ea66ecca149ff180f
Autor:
Cem Yener, Cenk Sayın, Cihan İnan, Hakan Gürkan, Emine İkbal Atlı, Engin Atlı, Esra Altan, Sinan Ateş, Füsun Varol
Publikováno v:
Taiwanese Journal of Obstetrics & Gynecology, Vol 60, Iss 2, Pp 350-354 (2021)
Objective: The objective of this study was to report the first case of prenatal diagnosis of the fetal 20p13 microdeletion syndrome in the literature. Case report: The mother was 31 years old and had a first trimester serum screening that indicated t
Externí odkaz:
https://doaj.org/article/f2ccc0731e6a4deab5bf805ed4d8517c
Publikováno v:
Namık Kemal Tıp Dergisi, Vol 8, Iss 2, Pp 170-176 (2020)
Aim:The nasal bone can be imaged with ultrasonography from the 10th week of pregnancy. In situations where the nasal bone is aplastic or hypoplastic, the risk of chromosomal anomalies increases. Thickening of the prenasal soft tissue is also apparent
Externí odkaz:
https://doaj.org/article/99d1f333e71b4ea0a4a00b79a379b209
Autor:
Gülşah Ilhan, Fatma Ferda Verit Atmaca, Esra Altan, Ali Galip Zebitay, Hamdullah Sozen, Hurkan Akyol, Meryem Kurek Eken
Publikováno v:
Journal of Family and Reproductive Health, Vol 10, Iss 4 (2017)
Objective: To evaluate whether systemic inflammatory markers (neutrophil to lymphocyte ratio (NLR), platelet to lymphocyte ratio (PLR) and red blood cell distribution width (RDW) to platelet ratio (RPR)) can be used as reliable markers for the diagno
Externí odkaz:
https://doaj.org/article/250d97b71b364c1991b27e8f4535ab38
Publikováno v:
Journal of Fetal Medicine. :71-74
Conjoined twins are an uncommon type of monoamniotic twins with an incidence of about 1.5 per 100,000 births worldwide. Non-janiceps is the extremely rare sub-type of cephalopagus which is reported as 1 in 58 of all conjoined twins or 1 in 3 million
Publikováno v:
Hamidiye Medical Journal. 3:40-45
Publikováno v:
Fetal and Pediatric Pathology. 41:1035-1040
Background: The coexistence of a hydatidiform mole and a fetus can occur in a multiple pregnancy, being less frequent in triplets and quadruplets because of their infrequency. With assisted reproduction, multiple pregnancies are becoming more frequen
Autor:
Emine Ikbal Atli, Engin Atli, Cem Yener, Füsun Varol, Sinan Ateş, Cenk Sayin, Esra Altan, Hakan Gurkan, Cihan Inan
Publikováno v:
Taiwanese Journal of Obstetrics & Gynecology, Vol 60, Iss 2, Pp 350-354 (2021)
Objective The objective of this study was to report the first case of prenatal diagnosis of the fetal 20p13 microdeletion syndrome in the literature. Case report The mother was 31 years old and had a first trimester serum screening that indicated the
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