Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Ozlem Boybeyi-Turer"'
Autor:
Gül Durmuş, Ozlem Boybeyi-Turer, Hatice Nursun Özcan, Onur Gözmen, Hüseyin Demirbilek, Tutku Soyer
Publikováno v:
European Journal of Pediatric Surgery Reports, Vol 10, Iss 01, Pp e80-e83 (2022)
The fusion of gonadal structures with internal organs is very rare. The close proximity between the left gonad and spleen during embryogenesis may result in splenogonadal fusion (SGF). Moreover, the trapping of hepatocyte-destined mesenchyme cells in
Externí odkaz:
https://doaj.org/article/53cb8031ac3b4422b01122ad7f38247d
Autor:
Ozlem Boybeyi-Turer, Hasan Tolga Çelik, Umut Ece Arslan, Tutku Soyer, Feridun Cahit Tanyel, Sibel Kiran
Publikováno v:
PLoS ONE, Vol 16, Iss 2, p e0247003 (2021)
Infantile hypertrophic pyloric stenosis (IHPS) is one of the hallmark pediatric surgical diseases. However, its etiology remains incompletely understood. By systematically reviewing the literature, we aim to clarify the effect of the effect of occupa
Externí odkaz:
https://doaj.org/article/16aa3aaeea6a4a4d9fcc421faff69c88
Publikováno v:
European Journal of Pediatric Surgery Reports, Vol 08, Iss 01, Pp e35-e38 (2020)
Prostatic utricle (PU) is incomplete regression of Müllerian duct and may cause recurrent urinary tract infections (UTIs), stone formation, postvoid dribbling, and recurrent epididymitis. Although surgical excision is recommended to avoid complicati
Externí odkaz:
https://doaj.org/article/e4a3033b9afe4e6a952c74781aaa8844
Publikováno v:
Journal of Clinical Ultrasound. 51:447-451
Foreign body aspiration (FBA) has a wide clinical spectrum, patients may be asymptomatic or present with cardiopulmonary arrest. Radiological imaging methods are used in addition to history and physical examination findings for certain diagnosis. Lun
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8d169d97f1756add703d6d30a2ee778f
https://doi.org/10.1002/jcu.23306
https://doi.org/10.1002/jcu.23306
Autor:
Ozlem, Boybeyi-Turer, Yasemin, Ozsurekci, Sibel Lacinel, Gurlevik, Pembe Derin, Oygar, Tutku, Soyer, Feridun Cahit, Tanyel
Publikováno v:
Surgery Today. 52:1313-1319
To evaluate the management of children with severe gastrointestinal symptoms during the disease course of COVID-19 and multisystem inflammatory syndrome (MIS-C).After ethical approval, we reviewed the medical records, retrospectively, of children wit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::05ae0920cc1345b96e05bd183f666874
https://doi.org/10.1007/s00595-022-02512-9
https://doi.org/10.1007/s00595-022-02512-9
Autor:
Jens Dingemann, Julia Quitmann, Umut Arslan, Michaela Dellenmark-Blom, Sinem Aydoner, Cigdem Ulukaya Durakbasa, Ozlem Boybeyi Turer, Tutku Soyer
Publikováno v:
Turk J Gastroenterol
BACKGROUND: This study reports the feasibility, validity, and reliability of the Turkish versions of the Esophageal-Atresia-Quality-of-Life (EA-QOL) questionnaires, which were originally developed in Sweden and Germany. METHODS: After translation fro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fababb8489234d9072120b933189916a
https://doi.org/10.5152/tjg.2021.201005
https://doi.org/10.5152/tjg.2021.201005
Publikováno v:
Congenital Anomalies. 61:208-211
Congenital esophageal web is a very rare type of esophageal atresia (EA) and is considered as Type IV atresia in Kluth's classification. Type IV EA is further classified into subgroups according to the location of web and the presence of tracheoesoph
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::48dea4d80b0d6dfc024a5b0be01e4d79
https://doi.org/10.1111/cga.12441
https://doi.org/10.1111/cga.12441
Autor:
Tutku Soyer, Ozlem Boybeyi-Turer, Mert Calis, Alev Ozon, Gülen Eda Utine, Gül Özyüksel, Ozlem Pelin Simsek Kiper, Gonul Buyukyilmaz
Publikováno v:
European Journal of Plastic Surgery. 44:709-712
Urorectal septum malformation sequence (URSM) is a rare congenital anomaly of caudal end of mesoderm. There is usually a single or no opening in the perineum. An infant with dysmorphic facial features, ambiguous genitalia, meningomyelocele, pes equin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8e955714d02a96d537be6680776a3652
https://doi.org/10.1007/s00238-020-01769-y
https://doi.org/10.1007/s00238-020-01769-y
Autor:
Ozlem Boybeyi-Turer, Tutku Soyer
Publikováno v:
Indian Journal of Surgery.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::250df607e45ba84138a13e49e483431d
https://doi.org/10.1007/s12262-022-03393-5
https://doi.org/10.1007/s12262-022-03393-5
Autor:
Ozlem, Boybeyi-Turer, Irem, Iyigun, Murat, Cagan, Hasan Tolga, Celik, Ozgur, Ozyuncu, Tutku, Soyer
Publikováno v:
Congenital anomaliesREFERENCES. 61(6)
Congenital esophageal web is a very rare type of esophageal atresia (EA) and is considered as Type IV atresia in Kluth's classification. Type IV EA is further classified into subgroups according to the location of web and the presence of tracheoesoph
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ef4f5f35c788699ce4f304c2701d545d
https://pubmed.ncbi.nlm.nih.gov/34273127
https://pubmed.ncbi.nlm.nih.gov/34273127