Zobrazeno 1 - 10
of 28
pro vyhledávání: '"Tuğba Saraç-Sivrikoz"'
Autor:
Gürcan Türkyılmaz, Didar Kurt, Tuğba Saraç Sivrikoz, İbrahim Kalelioğlu, Recep Has, Atıl Yüksel
Publikováno v:
Journal of Clinical and Investigative Surgery, Vol 4, Iss 1, Pp 48-52 (2019)
Meconium peritonitis is a rare fetal disease due to the perforation of bowel in utero and sterile inflammatory reaction related to the extravasation of the meconium. Various classification systems have been published in the literature, and better out
Externí odkaz:
https://doaj.org/article/384261dbb5824336b4472b6e8eec5987
Autor:
Tuğba Saraç Sivrikoz, Selen Gürsoy Erzincan, Gürcan Türkyılmaz, Nihat Demirkol, Recep Has, İbrahim Kalelioğlu
Publikováno v:
Sağlık Bilimlerinde İleri Araştırmalar Dergisi / Journal of Advanced Research in Health Sciences. 6:10-16
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::766589139f80deb2c62ac3a663d42d3d
https://doi.org/10.26650/jarhs2023-1202942
https://doi.org/10.26650/jarhs2023-1202942
Publikováno v:
Experimed. 12:149-154
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4eadcf7cc6363cbf92597f76448fcaa4
https://doi.org/10.26650/experimed.1188882
https://doi.org/10.26650/experimed.1188882
Autor:
Tuğba Saraç Sivrikoz, Selen Gürsoy Erzincan, Lütfiye Selçuk Uygur, Çiğdem Kunt İşgüder, Savcı Telek, Recep Has, İbrahim Kalelioğlu
Publikováno v:
Journal of Istanbul Faculty of Medicine / İstanbul Tıp Fakültesi Dergisi.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b32d43836659011df05faeb49eddd2a9
https://doi.org/10.26650/iuitfd.1202881
https://doi.org/10.26650/iuitfd.1202881
Autor:
Hamdi Kale, Gozde Tutku Turgut, Çağrı Güleç, Gen Nishimura, Umut Altunoglu, Birsen Karaman, Tuğba Saraç Sivrikoz
Publikováno v:
American Journal of Medical Genetics Part A. 188:253-258
The lamin-B receptor (LBR) encodes a dual-functioning inner nuclear membrane protein essential for cholesterol biosynthesis and chromatin organization. LBR pathogenic variants cause distinct phenotypes due to the dual function of LBR, including Pelge
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::44787c5185a4418dac9b0f0360abf7ed
https://doi.org/10.1002/ajmg.a.62479
https://doi.org/10.1002/ajmg.a.62479
Autor:
Atıl Yüksel, Ibrahim Kalelioglu, Birsen Karaman, Tuğba Saraç Sivrikoz, Melike Kirgiz, Seher Başaran, Umut Altunoglu, Recep Has
Publikováno v:
Archives of Gynecology and Obstetrics. 305:323-342
We aimed to present the fetal ultrasound, cytogenetic/molecular testing and postmortem or postnatal clinical findings of cases with 22q11.2DS diagnosed prenatally. A retrospective medical record review of 48 prenatal cases diagnosed with 22q11.2DS we
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::665cccc8d3950acfab74a348cce6fa18
https://doi.org/10.1007/s00404-021-06125-4
https://doi.org/10.1007/s00404-021-06125-4
Autor:
Atıl Yüksel, Tayfun Oktar, Gürcan Türkyilmaz, Recep Has, Ibrahim Kalelioglu, Orhan Ziylan, Tuğba Saraç Sivrikoz, Emircan Erturk, Bilal Çetin
Publikováno v:
Journal of Obstetrics and Gynaecology. 41:1071-1075
We reviewed the records of 144 patients. The mean gestational age at first US diagnosis was 27.5 ± 4.3 weeks. An anomaly of the contralateral kidney was detected in 25% of cases. An extrarenal anomaly was detected in 13.8%. Karyotype analysis was pe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::550eb5fcdcb229e5a384d393f8f5d237
https://doi.org/10.1080/01443615.2020.1845631
https://doi.org/10.1080/01443615.2020.1845631
Autor:
Ibrahim Kalelioglu, Çiğdem Kunt İşgüder, Erhan Aygün, Tuğba Saraç Sivrikoz, Lutfiye Selcuk Uygu, Recep Has
Publikováno v:
Fetal and Pediatric Pathology. 41:451-456
Infantile fibrosarcoma (IFS) usually arises in the extremities during the first 12 months of life and responds well to surgery. It is unusual in the oropharynx or the prenatal period. Case report: ...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aa02bb264e568db055ba70b5f7fe1390
https://doi.org/10.1080/15513815.2020.1809038
https://doi.org/10.1080/15513815.2020.1809038
Autor:
Atıl Yüksel, Hasan Orhan Ziylan, Tuğba Saraç Sivrikoz, Recep Has, Didar Kurt, Halil İbrahim Kalelioğlu
Publikováno v:
Journal of Clinical Ultrasound. 48:350-356
Complete penoscrotal transposition is an extremely rare congenital anomaly and is usually associated with other urinary system abnormalities. Prenatal diagnosis is feasible by demonstrating perineal anatomy and its relation with scrotum and phallus.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3d55af0b831189e62296485e510e0393
https://doi.org/10.1002/jcu.22834
https://doi.org/10.1002/jcu.22834
Autor:
Ibrahim Kalelioglu, Tayfun Oktar, Recep Has, Emircan Erturk, Gürcan Türkyilmaz, Atıl Yüksel, Bilal Çetin, Tuğba Saraç Sivrikoz
Publikováno v:
Taiwanese Journal of Obstetrics & Gynecology, Vol 58, Iss 4, Pp 531-535 (2019)
Objective: We purposed to review prenatal diagnoses of ureterocele, to determine the sonographic findings and additional abnormalities, and to illustrate the pregnancy outcomes of these patients. Material and methods: We reviewed the records of 24 pa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::86ce0cab802c28d75be54bd9936f218d
http://www.sciencedirect.com/science/article/pii/S1028455919301226
http://www.sciencedirect.com/science/article/pii/S1028455919301226