Zobrazeno 1 - 5
of 5
pro vyhledávání: '"E. Berrin Yüksel-Konuk"'
Publikováno v:
Turkiye Klinikleri Journal of Medical Sciences. 31:115-121
Objective: To evaluate the expression of cyclooxygenase-2 (COX-2) and Ki-67 in primary and recurrent pterygia. Material and Methods: Pterygium excision together with limbal/conjunctival autografting was performed in primary and recurrent pterygium ca
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9f5902a5d2d8977d7354c4c03b6985bd
https://doi.org/10.5336/medsci.2009-12988
https://doi.org/10.5336/medsci.2009-12988
Autor:
Duygu Duman, Suna Tokgoz-Yilmaz, Hatice Ozturkmen-Akay, Seda Taşır-Yılmaz, Fazilet Altın, Asli Sirmaci, Hilal Özdağ, E. Berrin Yüksel-Konuk, Ismail Yilmaz, Müzeyyen Yıldırım, Suat Fitoz, Seyra Erbek, Burcu Öztürk-Hişmi, Mustafa Tekin, Abdullah Ayçiçek, Aylin Hasanefendioğlu-Bayrak, İdil Aslan, Filiz Basak Cengiz, Armagan Incesulu, Z. Serap Arıcı
Publikováno v:
International Journal of Pediatric Otorhinolaryngology. 73:699-705
Genome wide homozygosity mapping using Affymetrix 10K arrays revealed the DFNB7/11 locus including the TMC1 gene in 5 of 35 Turkish families with autosomal recessive nonsyndromic severe to profound congenital or prelingual-onset sensorineural hearing
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e2ee423f7bef9d0fea920aca5731be00
https://doi.org/10.1016/j.ijporl.2009.01.005
https://doi.org/10.1016/j.ijporl.2009.01.005
Publikováno v:
The Turkish journal of pediatrics. 50(3)
We report on a six-year-old boy with typical Rubinstein-Taybi syndrome (RSTS) phenotype. Clinical findings included mental and motor retardation, patent ductus arteriosus (PDA), undescended testes, hirsutism, broad thumbs with radial angulation and b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::8cd508c6a4900cae5c88f92ee25ed515
https://pubmed.ncbi.nlm.nih.gov/18773673
https://pubmed.ncbi.nlm.nih.gov/18773673
Autor:
Öztan Yasun, E. Berrin Yüksel-Konuk, Suat Fitoz, Hilal Özdağ, Asli Sirmaci, Nejat Akar, Seda Taşır Yılmaz, Bora İnceoğlu, İdil Aslan, Filiz Basak Cengiz, Mustafa Tekin, Burcu Ozturk Hismi
We identified nine individuals from three unrelated Turkish families with a unique autosomal recessive syndrome characterized by type I microtia, microdontia, and profound congenital deafness associated with a complete absence of inner ear structures
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::befa7e0aeb93575d25e75e787adeef44
https://avesis.gazi.edu.tr/publication/details/e893510d-d872-43ec-82e2-21b0db731bf8/oai
https://avesis.gazi.edu.tr/publication/details/e893510d-d872-43ec-82e2-21b0db731bf8/oai
Publikováno v:
European journal of endocrinology. 155(5)
Objective: The aim of this study is to evaluate the expression of cycloocygenase-2 (COX-2) in orbital fibroadipose connective tissue in Graves’ ophthalmopathy (GO) patients, and investigate the associations between COX-2 expression and GO character
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a2ef5033e62247c254891617706d9be1
https://pubmed.ncbi.nlm.nih.gov/17062883
https://pubmed.ncbi.nlm.nih.gov/17062883